Structure-activity relationships of anticancer ruthenium(II) complexes with substituted hydroxyquinolines.

VU Research Portal Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic cancer cells Cascioferro, Stella; Petri, Giovanna Li; Parrino, Barbara; Carbone, Daniela; Funel, Niccola; Bergonzini, Cecilia; Mantini, Giulia; Dekker, Henk; Geerke, Daan; Peters, Godefridus J.; Cirrincione, Girolamo; Giovannetti, Elisa; Diana, Patrizia published in European Journal of Medicinal Chemistry 2020 DOI (link to publisher) 10.1016/j.ejmech.2020.112088 document version Publisher's PDF, also known as Version of record document license Article 25fa Dutch Copyright Act Link to publication in VU Research Portal citation for published version (APA) Cascioferro, S., Petri, G. L., Parrino, B., Carbone, D., Funel, N., Bergonzini, C., Mantini, G., Dekker, H., Geerke, D., Peters, G. J., Cirrincione, G., Giovannetti, E., & Diana, P. (2020). Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic cancer cells. European Journal of Medicinal Chemistry, 189, 1-18. 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May. 2026 European Journal of Medicinal Chemistry 189 (2020) 112088 Contents lists available at ScienceDirect European Journal of Medicinal Chemistry journal homepage: http://www.elsevier.com/locate/ejmech Research paper Imidazo[2,1-b] [1,3,4]thiadiazoles with antiproliferative activity against primary and gemcitabine-resistant pancreatic cancer cells Stella Cascioferro a, 1, Giovanna Li Petri a, b, 1, Barbara Parrino a, Daniela Carbone a, Niccola Funel c, Cecilia Bergonzini b, Giulia Mantini b, Henk Dekker b, Daan Geerke d, Godefridus J. Peters b, Girolamo Cirrincione a, Elisa Giovannetti b, e, **, Patrizia Diana a, * degli Studi di Palermo, Via Archiraﬁ 32, 90123, Palermo, Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Universita Italy Department of Medical Oncology, Amsterdam University Medical Center, VU University Cancer Center Amsterdam, De Boelelaan 1117, 1081HV, Amsterdam, the Netherlands c Unit of Anatomic Pathology II, Azienda Ospedaliero-Universitaria Pisana, Via Roma 67, 56126, Pisa, Italy d AIMMS Division of Molecular Toxicology, Department of Chemistry and Pharmaceutical Sciences, Faculty of Sciences, VU University Amsterdam, De Boelelaan 1108, 1081 HZ, Amsterdam, the Netherlands e Fondazione Pisana per la Scienza, Via Ferruccio Giovannini 13, 56017, San Giuliano Terme, Pisa, Italy a b a r t i c l e i n f o a b s t r a c t Article history: Received 1 October 2019 Received in revised form 16 January 2020 Accepted 20 January 2020 Available online 25 January 2020 A new series of eighteen imidazo [2,1-b] [1,3,4]thiadiazole derivatives was efﬁciently synthesized and screened for antiproliferative activity against the National Cancer Institute (NCI-60) cell lines panel. Two out of eighteen derivatives, compounds 12a and 12h, showed remarkably cytotoxic activity with the half maximal inhibitory concentration values (IC50) ranging from 0.23 to 11.4 mM, and 0.29e12.2 mM, respectively. However, two additional compounds, 12b and 13g, displayed remarkable in vitro antiproliferative activity against pancreatic ductal adenocarcinoma (PDAC) cell lines, including immortalized (SUIT-2, Capan-1, Panc-1), primary (PDAC-3) and gemcitabine-resistant (Panc-1R), eliciting IC50 values ranging from micromolar to sub-micromolar level, associated with signiﬁcant reduction of cell-migration and spheroid shrinkage. These remarkable results might be explained by modulation of key regulators of epithelial-to-mesenchymal transition (EMT), including E-cadherin and vimentin, and inhibition of metalloproteinase-2/-9. High-throughput arrays revealed a signiﬁcant inhibition of the phosphorylation of 45 tyrosine kinases substrates, whose visualization on Cytoscape highlighted PTK2/FAK as an important hub. Inhibition of phosphorylation of PTK2/FAK was validated as one of the possible mechanisms of action, using a speciﬁc ELISA. In conclusion, novel imidazothiadiazoles show potent antiproliferative activity, mediated by modulation of EMT and PTK2/FAK. © 2020 Elsevier Masson SAS. All rights reserved. Keywords: Imidazo[2,1-b][1,3,4]thiadiazole derivatives Pancreatic ductal adenocarcinoma Antiproliferative activity Inhibition of migration Spheroids shrinkage Modulation of EMT PTK2/FAK 1. Introduction The synthesis of hybrid molecules, bearing two or more different biologically active scaffolds in a single structure, is * Corresponding author. Dipartimento di Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche (STEBICEF), Universit a degli Studi di Palermo, Via Archiraﬁ 32, 90123, Palermo, Italy ** Corresponding author. Department of Medical Oncology, Amsterdam University Medical Center, VU University Cancer Center Amsterdam, De Boelelaan 1117, 1081HV, Amsterdam, the Netherlands. E-mail addresses: e.giovannetti@amsterdamumc.nl (E. Giovannetti), patrizia. diana@unipa.it (P. Diana). 1 Equally contributed. https://doi.org/10.1016/j.ejmech.2020.112088 0223-5234/© 2020 Elsevier Masson SAS. All rights reserved. regarded as one of the most valuable approaches in drug development in order to obtain new therapeutic strategies to treat oncological diseases [1e3]. The design of anticancer drugs characterized by two moieties with antitumor activity led to the development of a number of molecules with improved biological potential compared to the parent compounds. In particular, hybrid anticancer drugs showed improved speciﬁcity, a greater ability to overcome drug-resistance mechanisms, better patient compliance and lower side effects [4,5]. The simultaneous presence of two pharmacophores often led to a synergism of the biological activities and therefore to the capability to act towards more than one target. Many examples of hybrid compounds with promising cytotoxic properties have been 2 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 reported in the latest years. Singla and collaborators described remarkable antiproliferative activity against the NCI-60 cell lines panel of benzimidazole-triazine hybrids 1 (Fig. 1) which showed IC50 values from the low micromolar to the nanomolar range [6]. The pyrimidine-triazole hybrids 2 (Fig. 1) exhibited potent anticancer activity against the B16eF10 murine melanoma cancer cell line due to their ability in reducing the pro-caspase 3 level while increasing the p53 and active-caspase 3 levels [7]. Pyrazolebenzofuran hybrids 3 (Fig. 1) emerged as promising anticancer compounds against human pancreatic (Panc-1 and PaCa-2 cells), lung (A549 and H-460), breast (MCF-7), colon (HT-29) and prostate (PC-3) cancer, with IC50 values in the range of 0.9e2.2 mM (Fig. 1) [8]. The imidazo [2,1-b] [1,3,4]thiadiazole nucleus has been considered a privileged scaffold for the development of molecules with various pharmacological activities, such as anticancer [9], analgesic [10], anti-leishmanial [11], antioxidant [12], antitubercular [13], anticonvulsant [14], and antibacterial [15,16]. Concerning the antitumor activity, many imidazo [2,1-b] [1,3,4] thiadiazole derivatives have been described as potent anticancer molecules acting on several targets against different tumor models. Compound 4 (Fig. 2) showed potent inhibitory activity (IC50 ¼ 1.2 nM) against the activin receptor-like kinase 5 (ALK5) proving to be selective toward the P38a kinase [17]. The imidazo [2,1-b] [1,3,4]thiadiazole-5-carbaldehyde 5 (Fig. 2) was three fold more potent than melphalan, used as reference drug, against murine (L1210) and human (CEM) leukemia cells as well as against immortalized cervical cancer (HeLa) cells, eliciting IC50 values of 0.89 mM, 0.75 mM and 0.90 mM, respectively [18]. In the last decade the indole ring has emerged among the scaffolds recognized as privileged pharmacophores for the development of new antitumor compounds [19e26]. The indole derivative 6 was described for its potent antiproliferative activity against diffuse malignant peritoneal mesothelioma (DMPM) cell. Nortopsentin analogue 6 potently inhibited CDK1 activity eliciting an IC50 value of 0.86 mM and consequently induced a marked cell cycle arrest at the G2/M phase, which was paralleled by an increase in the apoptotic rate [27]. Therefore, on the basis of the interesting anticancer properties described for imidazo [2,1-b] [1,3,4]thiadiazole and indole scaffolds, we decided to evaluate the cytotoxic activity of a library of thirtysix 3-(6-phenylimidazo [2,1-b] [1,3,4]thiadiazol-2-yl)-1H-indole derivatives. In particular derivative 7 (Fig. 3) was effective against all the tested cancer cell lines showing GI50 values ranging from 1.02 to 9.21 mM [28]. These preliminary results prompted further studies on nitrogen heterocyclic systems endowed with antitumor activity [29e35] and we synthesized eighteen new 3-(imidazo [2,1-b] [1,3,4]thiadiazol2-yl)-1H indole analogues in order to evaluate how structural modiﬁcations on the indole nucleus, introduction of an aldehyde group at the position 5 of the imidazothiadiazole scaffold or the replacement of the phenyl ring at the position 6 with a thiophene ring could inﬂuence the anticancer activity of this class of compounds. We decided to test our new compounds on clinically-relevant models of pancreatic ductal adenocarcinoma (PDAC). This tumor is an extremely aggressive neoplasm, predicted to become the second leading cause of cancer-related deaths before 2030 [36]. Cytotoxic chemotherapy remains the mainstay of treatment for most PDAC patients. Treatment with 5-ﬂuorouracil, leucovorin, irinotecan and oxaliplatin (FOLFIRINOX) or with a combination of gemcitabine and nab-paclitaxel, represent the standard-of-care for unresectable patients, and recent data support the use of FOLFIRINOX as adjuvant therapy after surgical resection [37]. However, PDAC is broadly chemoresistant, with a 5-year survival rate below 9%, and novel, more effective therapeutics for PDAC remain an important unmet need [38e40]. 2. Chemistry The new imidazothiadiazole derivatives 12e14 were efﬁciently synthesized following the synthetic route described in Scheme 1. The commercially available indole-3-carbonitrile 9a and the derivatives 9b-e, prepared by reaction of the appropriate 1H-indole Fig. 1. Chemical structures of benzimidazole-triazine hybrids 1, pyrimidine-triazole hybrids 2, pyrazole-benzofuran hybrids 3. S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 3 Fig. 2. Chemical structures of the anticancer compounds 4e6. Fig. 3. Hybrid compound 7 obtained by combining the two bioactive scaffolds indole and imidazothiadiazole. with chlorosulfonyl isocyanate (CSI), were subjected to a methylation for obtaining the corresponding 1-methyl-1H-indole-3carbonitriles 10a-e [16]. The 5-(1H-indol-3-yl)-1,3,4-thiadiazol-2amines 11a-j were obtained in excellent yields (92e100%) by treating the proper derivatives 9a-e or 10a-e with thiosemicarbazide. The 1,3,4-thiadiazol-2-amines 11a-j underwent a reaction with the appropriate a-bromoacetyl compounds in reﬂuxing ethanol to give the hydrobromide derivatives 12a-r. Some of such hydrobromides, 12a,b,d,e,f,h, were isolated as pure compounds (yields 55e68%) and were characterized without further puriﬁcations. Instead, hydrobromides 12c,g,i,j were treated with saturated aqueous NaHCO3 solution producing the corresponding free bases 13 which were puriﬁed by column chromatography providing specimens with suitable analytical and spectral data (yields 58e80%). Finally, the free bases 13k-r, prepared through the treatment of the corresponding hydrobromides 12 with saturated aqueous NaHCO3 solution, were subjected to a reaction of formylation using standard Vilsmeier conditions to give the imidazo [2,1-b] [1,3,4] thiadiazole derivatives 14k-r (yields 70e90%) (Table 1). Data on physicochemical properties of the compounds are reported in the Supplementary results and Supplementary Tables 1e2. Reagents and conditions: i) CH3CN, CSI, 0 C, 2 h, then DMF, 0 C, 1.5 h (98e100%); ii) DMF, (CH3O)2CO, K2CO3, 130 C, 3.5 h (98e100%); iii) triﬂuoroacetic acid, thiosemicarbazide, 60 C, 3.5 h 4 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 Table 1 New 3-(imidazo [2,1-b] [1,3,4]thiadiazol-2-yl)-1H-indole derivatives 12e14. Comp R R1 R2 Yield 12a 12b 12d 12e 12f 12h 13c 13g 13i 13j 14k 14l 14m 14n 14o 14p 14q 14r H H Br Cl Cl F Br F OCH3 OCH3 H H H H H H H Br H CH3 CH3 H CH3 CH3 H H H CH3 H CH3 H H H CH3 H H tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl tiophen-3-yl C6H5 C6H5 4-F-C6H4 3OCH3eC6H4 2,5-OCH3-C6H3 2,5-OCH3-C6H3 4-NO2-C6H4 2,5-OCH3-C6H3 57% 55% 68% 63% 68% 58% 58% 80% 58% 70% 71% 91% 81% 60% 82% 70% 75% 90% (98e100%); iv) anhydrous ethanol, reﬂux, 24 h (42e80%); v) NaHCO3 saturated aqueous solution (58e80%); vi) POCl3, DMF, 0e5 C, then compound 13, DMF, 70 C, 5 h. 3. Results and discussion 3.1. Antiproliferative activity The newly synthesized imidazo [2,1-b] [1,3,4]thiadiazoles 12a,b,d,e,f,h, 13c,g,i,j and 14k,l,n,o,p were submitted to the National Cancer Institute (NCI; Bethesda, MD) for the pharmacological evaluation of their antitumor activity. They were initially prescreened according to the NCI protocol at one-dose of 10 mM on the full panel of 60 human cancer cell lines derived from 9 cancer cell types and grouped into disease subpanels including leukemia, non-small cell lung, colon, central nervous system, melanoma, ovarian, renal, prostate, and breast cancers. The 12a and 12h derivatives were selected for further screening at ﬁve concentrations at 10-fold dilution (104-108 M) on the full panel. As shown in Table 2, both derivatives have interesting in vitro anticancer activity with GI50 values ranging from micromolar to sub-micromolar level, i.e., 0.23e11.4 mM, and 0.29e12.2 mM, respectively (Table 2). In order to expand the NCI panel, we evaluated the in vitro antiproliferative activity of the compounds 12a,b,d,e,f,h, 13c,g,i,j and 14k-r on a panel of PDAC cells, including SUIT-2, Capan-1 and Panc-1, by Sulforhodamine-B (SRB) assay. PDAC is indeed broadly chemoresistant tumor, with a 5-year survival rate below 9%, and novel, more effective therapeutics for PDAC remain an important unmet need. A pre-screening assay was initially performed at concentrations of 0.1, 1 and 16 mM. We then expanded the cytotoxicity test, using at least 8 different concentrations (from 125 nM to 16 mM) on the most promising compounds, in order to deﬁne more accurate halfmaximal inhibitory concentration (IC50) values. The compounds 12a,b,h and 13g exhibited remarkable antiproliferative activity on all the preclinical models with IC50 values in the range from 0.85 to 4.86 mM (Table 3). PDAC is notoriously resistant to chemotherapy or radiotherapy. For several decades, gemcitabine monotherapy has been used as a ﬁrst-line treatment for metastatic PDAC and is still a cornerstone of PDAC treatment in all stages of this disease. However, this drug has limited clinical effects caused by primary PDAC resistance, as well as by the development of resistance within a few weeks from treatment initiation [41]. Therefore, new therapeutic agents should be tested for their ability to circumvent gemcitabine chemoresistance. For this reason, we assessed the cytotoxic activity of the compounds 12a,b,h and 13g in the Panc-1R cells, a gemcitabineresistant sub-clone obtained by continuous incubation of Panc-1 with 1 mM of the drug [41]. Notably, all these compounds showed antiproliferative activity against Panc-1R, with IC50 ranging from 2.2 ± 0.37 mM (compound 12b) to 3.9 ± 0.25 mM (compound 13g) as reported in Fig. 4. Scheme 1. Synthesis of 3-(imidazo [2,1-b] [1,3,4]thiadiazol-2-yl)-1H-indole derivatives 12e14. S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 Table 2 GI50 and TGI of the compounds 12a and 12h.a Panel/Cell line 12a GI50 (mM) Leukemia CCRF-CEM 2.19 HL-60 (TB) 0.76 K-562 0.38 RPMI-8226 1.47 Non-Small Cell Lung Cancer A549/ATCC 1.72 EKVX 1.99 HOP-62 1.58 HOP-92 5.46 NCIeH226 9.94 NCIeH23 4.47 NCIeH322 M 4.85 NCIeH460 0.57 NCIeH522 0.75 Colon Cancer HCC-2998 2.99 HCT-116 0.63 HCT-15 0.49 HT29 0.41 KM12 0.50 SW-620 0.43 CNS Cancer SF-268 3.84 SF-295 1.74 SF-539 1.49 SNB-19 2.56 SNB-75 0.45 U251 1.21 Melanoma MALME-3M 10.4 M14 0.75 MDA-MB-435 0.23 SK-MEL-2 1.08 SK-MEL-28 4.74 SK-MEL-5 0.71 UACC-257 11.4 UACC-62 0.74 Ovarian Cancer IGROV1 1.79 OVCAR-3 0.92 OVCAR-4 4.42 OVCAR-5 4.27 OVCAR-8 2.72 NCI/ADR-RES 0.56 SK-OV-3 2.80 Renal Cancer 786e0 3.06 A498 5.97 ACHN 3.23 CAKI-1 1.00 RXF 393 2.05 SN12C 1.15 TK-10 5.21 UO-31 1.71 Prostate Cancer PC-3 2.07 DU-145 2.86 Breast Cancer MCF7 1.17 MDA-MB-231/ATCC 1.08 HS 578T 2.65 BT-549 2.87 MDA-MB-468 2.92 12h TGI (mM) GI50 (mM) TGI (mM) 27.2 20.9 39.9 15.4 2.54 1.34 0.45 3.01 >100 15.5 >100 27 >100 >100 39.9 >100 >100 >100 52.7 >100 >100 2.85 2.51 1.92 12.2 4.56 3.82 4.71 1.73 1.62 99.5 >100 23.1 76.9 35.8 >100 >100 17.1 24.5 26.7 70.6 15.6 10.2 10.5 >100 5.64 2.04 0.61 0.48 1.04 0.48 33.9 26.4 >100 14.8 >100 >100 >100 6.44 4.60 >100 8.09 17 6.58 2.24 2.18 3.44 1.29 2.76 >100 9.39 7.54 >100 6.45 17.9 36.9 15.8 0.68 23.8 44.0 15.1 98.3 18.7 1.81 1.05 0.29 1.59 7.23 1.80 7.90 1.93 31.6 >100 1.13 7.29 >100 12.9 >100 >100 >100 9.02 >100 76.4 >100 >100 82.7 1.93 2.06 5.77 8.24 4.53 0.99 3.47 >100 9.67 >100 84.4 >100 19.1 70.9 >100 23.6 52.5 >100 50.0 >100 33.5 >100 7.62 4.09 3.39 2.42 1.59 4.71 4.92 1.72 52.3 50.0 86.8 57.4 5.73 >100 19.4 >100 >100 >100 3.19 3.67 >100 31.6 20.2 7.88 >100 31.7 27.8 0.83 3.23 2.34 5.54 1.44 30.0 30.6 13.4 77.4 5.47 a Data obtained from the NCI in vitro disease-oriented human tumor cell line screen. [b] GI50: concentration that inhibit 50% net cell growth. [c] TGI total growth inhibition. 5 Our previous studies showed different genetic and epigenetic modiﬁcations, including splicing and phosphoproteomics aberrations [42,43], underlying the molecular mechanisms of gemcitabine-resistance, and further studies will be carried out to identify how our new compounds counteract these mechanisms. Moreover, the compounds 12a,b,h and 13g were tested on a primary patient-derived PDAC cell culture, PDAC-3 (Fig. 4B and C). This cellular model was chosen since our previous studies showed that its genetic and histological features were similar to the original tumor [44]. In order to maintain the original characteristics of the primary tumor, particularly from the genetic point of view, these cells have been kept in culture only for a few passages. As shown in Fig. 4B the new imidazothiadiazoles maintained their antiproliferative activity on PDAC-3 cells, with IC50 values slightly higher in comparison to the values reported on the previously mentioned cancer cell lines. The phase contrast microscopy images in Fig. 4C highlighted the antiproliferative activity of compounds 12a and 12b (central and right panel, respectively) compared to untreated cells (left picture) after 72 h of the treatment. Because of their remarkable antiproliferative activity the compounds 12a,b,h and 13g were selected for following mechanistic studies, in order to unravel the mechanisms underlying their anticancer activity. Despite compound 7 has shown interesting GI50 values against all the tested cancer cell lines in the NCI screening, preliminary biological evaluations of analogues 13k,l,n,p,r showed limited antiproliferative activity [28]. We evaluated the citotoxicity of the compounds 13m, 13o and 13q on SUIT-2, Capan-1 and Panc-1 but the IC50 values were above 16 mM. Finally, we performed additional experiments to evaluate the in vitro cytotoxicity of the new compounds 12a and 12b against the normal ﬁbroblasts Hs27. The results of these experiments allowed us to calculate the selectivity index (SI, IC50 non-tumor cell line/IC50 tumor cell line), which was 4.5 and 7.2 for compounds 12a and 12b, respectively, and therefore our compounds have SI similar to Gemcitabine and 5-ﬂuorouracil and were regarded as highly cancer selective compared to the primary pancreatic cells PDAC3 (Supplementary Table 3). 3.2. Volume reduction of PDAC-3-derived tumor spheres Two-dimensional cytotoxicity assay obviously provide a useful method to screen libraries of compounds with high-throughput efﬁciency, but they are not capable of resembling the complex architecture and biology of solid tumors, which grow in threedimensions (3D) [45]. For this reason we evaluated two of our most promising compounds (emerging from monolayer assay) on 3D spheroids of PDAC-3 cells. These primary cultures are indeed able to form spheroids that are more representative of the aggregation of tumor cells in vivo, as also reported in our previous studies [46]. We treated spheroids with compounds 12a and 12b after 3 days of growth, at 5-times the IC50, and we took a picture which represent the Day 1. Then the treatment was repeated every four days (Day 5 and Day 8) and pictures were taken immediately before that (Fig. 5A). Reduction of the size of spheroids was calculated by measuring their area with ImageJ. As shown in Fig. 5B, after ﬁve, but considerably more after eight days, both compounds clearly showed their ability to hinder the spheroids formation. This reduction is shown as the fold-change between treated spheroids compared to the controls and was statistically signiﬁcant (p-value < 0.0001). Therefore, these two compounds retained their activity in a 3D model. 6 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 Table 3 Antiproliferative activity of compounds 12a,b,d,e,f,h, 13c,g,i,j and 14k-r on SUIT-2, Capan-1 and Panc-1 cell lines. IC50a (mM) ± SEMb Cell lines Comp SUIT-2 Capan-1 Panc-1 12a 12b 12d 12e 12f 12h 13c 13g 13i 13j 14k 14l 14m 14n 14o 14p 14q 14r gemcitabine 5-ﬂuorouracil 0.85 ± 0.018 0.99 ± 0.078 >16 >16 >16 1.78 ± 0.017 >16 2.16 ± 0.039 >16 >16 9.56 ± 0.34 >16 7.93 ± 0.23 11.49 ± 0.36 13 ± 1.13 12.49 ± 0.18 5.32 ± 0.29 8.7 ± 0.20 0.01 ± 0.001 0.91 ± 0.15 1.19 ± 0.06 1.35 ± 0.04 >16 >16 >16 1.93 ± 0.25 >16 4.52 ± 0.48 >16 >16 10.5 ± 0.21 >16 8.83 ± 0.17 >16 >16 5.73 ± 0.086 6.1 ± 0.019 8.24 ± 0.08 0.02 ± 0.001 0.47 ± 0.13 1.70 ± 0.20 1.69 ± 0.10 >16 >16 >16 2.37 ± 0.028 >16 4.86 ± 0.5 >16 >16 12.41 ± 0.16 >16 10.53 ± 037 >16 >16 >16 3.61 ± 0.4 10.56 ± 0.11 0.15 ± 0.01 4.3 ± 0.42 a b The values are means ± SEM of three separate experiments. SEM: Standard Error of the Mean. Fig. 4. Representative growth curves of Panc-1R (A) and PDAC-3 (B) cells treated with the compounds 12a,b,h and 13g (from 0.125 to 16 mM). Points, mean values obtained from three independent experiments; bars, SEM. (C) Representative pictures of PDAC-3 cells after 72 h from the treatment at concentration of IC50 value. Left panel: untreated cells; central panel: cells treated with compound 12a; right panel: cells treated with compound 12b. Original magniﬁcation 20X. (D) IC50 values of compounds 12a,b,h and 13g on gemcitabine-resistant and primary PDAC-3 cells (aThe values are means of three separated experiments. bSEM: Standard Error Mean). 3.3. Reduction of cell migration Next to the lack of clinically relevant improvement in effective treatments, the high metastatic potential of PDAC is one of the main causes for the poor outcome of this disease [36]. The ability of the compounds 12a and 12b to inhibit the migratory behaviour of PDAC cells was investigated by scratch wound-healing assays on SUIT-2, Capan-1, Panc-1, Panc-1R and PDAC-3 cell lines. Brieﬂy, 5 104 cells/well were seeded into 96-well ﬂat-bottom plates in a volume of 100 mL and incubated for 24 h to create a monolayer. The scratches in the middle of the wells were created by scraping with a speciﬁc tool with needles. The cells were then treated with the compounds using 4x IC50 concentrations. These concentrations were chosen after preliminary experiments demonstrating that the exposure for 24 h did not result in proapoptotic or necrotic effects. The wound closure was monitored by phase-contrast microscopy and the pictures were captured immediately after scratch (T ¼ 0), and at 4, 8, 20 and 24 h from the S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 7 Fig. 5. Size reduction of PDAC-3 spheroids treated with compounds 12a and 12 b at 5-times the IC50 (i.e. 8.5 mM). (A) Representative pictures of PDAC-3 spheroids exposed to 12a and 12b, taken at day 1 of treatment, and after 5 and 8 days with an automated phase-contrast microscope. (B) Fold-change, corrected for control, of the spheroids size, at Day 1, Day 5 and Day 8. p-values were determined by Two-way ANOVA followed by Tukey’s multiple comparisons test, **** ¼ p < 0.0001. The values were obtained taking into account the mean values of the areas of at least ten different spheroids. treatment. As shown in Fig. 6AeD, the compounds 12a and 12b induced a remarkable reduction of cell migration rate in Panc-1R and SUIT-2 cell lines. The scratch area (mm2) was already wider in the treated cells compared to the untreated Panc-1R cells after 8 h of treatment. After 24 h from the beginning of the treatment we observed a reduction of the cell migration with a fold-change value of approximately 4 in both cell lines, SUIT-2 and Panc-1, treated with compounds 12a and 12b (Fig. 6A,B). Statistical analyses revealed that these differences were signiﬁcant, compared to the respective controls (i.e., untreated cells) in both cell lines. In particular, compared to untreated cells (set at 100%), the percentages of migration in cells treated with the compounds 12a and 12b were of 33.3% and 32%, respectively, in Panc-1R (Fig. 6C), and 34.9% and 41%, respectively, in SUIT-2 (Fig. 6D) after 24 h from the start of the treatment. The anti-migratory activity was also evident in Capan-1 and Panc-1 cells for which we observed similar statistically signiﬁcant results, with migration rates between 50% and 60% (Fig. 7AeC and Fig. 7AeD). Finally, as shown in the Supplementary data Fig. 1A, we detected lower migration rates (64% and 71%, respectively) compared to the control (set at 100%) also in the primary PDAC-3 cells treated with the compounds 12a and 12b. Overall, these data highlighted the ability of our compounds to signiﬁcantly reduce the rate of cell migration on all the PDAC preclinical models. Fig. 6. Modulation of the migration rate in Panc-1R and SUIT-2 cells treated with the compounds 12a and 12 b at concentration of 4x IC50. (A-B) Fold-changes in Panc-1R (A) and SUIT-2 (B) cells were determined by taking into consideration at least four scratch areas. All the P values were calculated with Student’s t-test. ****p < 0.0001, ***p < 0.001, **p < 0.01, *p < 0.05. (C-D) Percentages of migration monitored over time (0, 4, 8, 20 and 24 h) of Panc-1R (C) and SUIT-2 (D) cells treated with compound 12a and 12 b at concentration 4x IC50. Points, mean values obtained from the means of at least three different scratch areas. (E) Representative images of the wounds closure captured with the microscope at 0, 8 and 20 h on Panc-1R cells. Original magniﬁcation 5X. 8 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 Fig. 7. (A-D) Percentage of migration monitored over time (0, 4, 8, 20 and 24 h) of Capan-1 (A-B) and Panc-1 (C) cells treated with the compounds 12a and 12 b at concentrations of 4x IC50. Points, mean values obtained from the means of at least three different scratch areas. (D) (Table) List of P values that were calculated with Student’s t-test. ****p < 0.0001, ***p < 0.001, **p < 0.01, *p < 0.05, ns ¼ not signiﬁcant. 3.4. Modulation of epithelial mesenchymal transition events as assessed by qRT-PCR, western blot and gelatine zymography It is well known that epithelial-to-mesenchymal transition (EMT) events are essential for embryonic development and other physiological events, such as the response to several injuries. During EMT, epithelial cells undergo changes in their phenotypic tracts through the loss of polarity, cell-cell adhesion and extracellular matrix, and they acquire mesenchymal features including motility and invasiveness [47]. Several transcription factors within the cellular microenvironment regulate the expression of epithelial and mesenchymal marker genes, among which the most important include the zinc ﬁnger transcription factors SNAIL1 and SNAIL2, potent epithelial repressors belonging to the SNAIL superfamily, Ecadherin (CDH1) and N-cadherin (CDH12), calcium-dependent cell adhesion molecules, vimentin (VIM), type III intermediate ﬁlament (IF) protein typically expressed in mesenchymal cells, and ﬁnally, the matrix metalloproteinases (MMPs), enzymes involved in the breakdown of extracellular matrix [48]. Remarkably, their dysregulation induces a transition from the physiological function to the pathological one, including mechanisms underlying the origin and progression of tumors and tissue ﬁbrosis [49]. The loss of CDH1 expression is considered the hallmark of EMTs in cancer and recently, SNAIL1 and SNAIL2 have been identiﬁed as the major determinants for the repression of its transcription through the direct binding to the E-cadherin E-box promoter [50e52]. Simultaneously, the gain of mesenchymal markers, such as VIM, CDH12, MMPs and others occur [53]. In PDAC, these genes contribute to a crucial network of signalling pathways that contribute to the irreversible change of cell phenotype, both in metastasis and resistance to the chemotherapy [54]. Because of their outstanding effects against PDAC cell migration, we assessed the inﬂuence of the imidazothiadiazole derivatives 12a and 12b on these EMTs key regulator expression, in SUIT-2, Capan-1 and Panc-1 cells, using RT- qPCR, Western blot and gelatine zymography analyses. Capan-1 and SUIT-2 cells were selected for these experiments because preliminary analyses of the housekeeping protein GAPDH showed that using lysates of these cells the Western blot images were not “saturated” and were kept in the linear range (as revealed by exposing blots to increasing times and drawing a plot of intensity and time exposure). RT-qPCR reactions were performed in order to evaluate the modulation of the mRNA expression of SNAIL1, SNAIL2, CDH1, CDH12. Brieﬂy, SUIT-2 and Capan-1 cells (2.5 105/well) were seeded into 6-well plates and incubated for 24 h to form a conﬂuent monolayer. Then they were treated with the compounds 12a and 12 b at concentrations of 5x IC50. After 24 h, the cells were harvested using TRIzol, and we extracted the total RNA, which was used to synthesize, by reverse transcription, the cDNA for the PCR reactions. The expression levels were normalized to those of the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) housekeeping gene, whose expression was constant in all cells, as described previously [55]. As shown in Fig. 8A and B, the compounds 12a and 12b affected the genes leading EMTs. In both cell lines the mRNA levels of SNAIL1 and SNAIL2 were increased from 1.5 to approximately 1.9 fold compared to the GAPDH in the control cells, suggesting a low amount of protein expression and consequently, due to a negative feedback mechanism, CDH1 protein expression was upregulated, as reported in the Western blot analysis (Fig. 8C and D, Fig. 8G and Supplementary data Fig. 2). Instead, the protein expression of VIM and MMP2 were signiﬁcantly reduced. Finally, CDH12 protein expression did not noticeably change compared to the control. Furthermore, considering the pivotal role of MMPs in tumor invasion, through degradation of extracellular matrix components, we evaluated the effect of the compounds 12a and 12b on the proteolytic activity of MMP2 and MMP9 by using speciﬁc gelatine zymography assays. These assays showed a signiﬁcant decrease of the activity of MMP2 and MMP9 isolated from SUIT-2 and Capan- S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 9 Fig. 8. SNAIL1, SNAIL2, CDH1 and CDH12 mRNA expressions in SUIT-2 (A) and Capan-1 (B) cells treated with the compounds 12a and 12 b at 5x IC50 for 24 h. The expression levels were determined by RT-qPCR and the results were obtained by the delta-delta Ct (cycle threshold) analysis. The experiments were conducted in duplicates and the values are shown as means ± SD. (C-D) SNAIL1, SNAIL2, CDH1, CDH12, VIM and MMP2 protein levels expression in SUIT-2 (C) and Capan-1 (D) cells treated with compounds 12a and 12b. The protein levels were determined after 24 h of treatment at concentration 5x IC50 value by densitometric analysis of the Western Blot performed using ImageJ. All the P values were determined by Tukey’s multiple comparisons test. ****p < 0.0001, ***p < 0.001, **p < 0.01, *p < 0.05. (E-F) Gelatine zymography analysis of media from SUIT-2 and Capan-1 cells incubated with serum-free medium for 24 h. The enzymatic activity of MMP2 and MMP9 was determined by densitometric analysis. The cells were treated with the compounds 12a and 12 b at concentration 5x IC50 value for 24 h ****p < 0.0001, ***p < 0.001. (G) Representative image of CDH1 expression determined by Western blot analysis in Capan-1 cells treated with the compounds 12a and 12 b at 5x IC50 concentrations after 24 h. 1 cells exposed to the compounds. In particular, the activities of the MMP2 and MMP9 enzymes were decreased by about 50% after 24 h of treatment compared to the control (Fig. 8E and F). However, as shown in the Supplementary data Fig. 3, the areas of lysis created by the proteolytic activities of both enzymes isolated from Panc1 cells treated with compounds 12a and 12b were not signiﬁcantly wider compared to the control. 3.5. Proﬁling of inhibition of kinase activity To investigate the potential mechanism of action of our compounds, we performed a high-throughput analysis with the Pamgene tyrosine kinase peptide substrate array (PamChip). The PamChip consists of 4 identical arrays, each of which contains 144 peptide sequences immobilized on a porous ceramic membrane (Fig. 9A). Each of these sequences harbours one or more phosphorylation sites, derived from literature or computational predictions. Finally, speciﬁc ﬂuorescently labelled anti-phospho antibodies are used to detect the amount of phosphorylated protein by tyrosine kinases from our samples. The compound 12b signiﬁcantly inhibited the phosphorylation of 45 peptide substrates in SUIT-2 cells, and we visualized on 10 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 Fig. 9. (A) Representative images of pictures taken at the end point of the control array (left) and the treated array (right). (B) Network visualization obtained with Cytoscape of the signiﬁcant proteins containing differentially phosphorylated peptides, color legend indicates the signiﬁcance level of each protein. (C) Barplot of PTK2 phosphorylation in the control vs treated with 5x IC50 of 12b. (For interpretation of the references to color in this ﬁgure legend, the reader is referred to the Web version of this article.) Cytoscape a network highlighting the interactions between proteins containing the phosphorylated peptides. Notably, PTK2/FAK emerged as an important hub between those proteins (Fig. 9B). In particular, the phosphorylation of PTK2/FAK showed a more than 2fold inhibition after treatment with compound 12b, with FDR <0.01 (Fig. 9C). This result prompted us to validate the inhibition of phosphorylation of PTK2/FAK as one of the possible mechanisms of action of our compound, using a speciﬁc ELISA assay, as detailed in the following paragraphs. 3.6. Inhibition of PTK2/FAK as assessed by ELISA The focal adhesion kinase (FAK), also known as protein tyrosine kinase 2 (PTK2), is a downstream non-receptor tyrosine kinase able to mediate information from extracellular matrix into the cytoplasmatic compartment, through a linker with intracellular tails of integrins [56]. FAK controls several cellular processes, including survival, proliferation and motility. However, its overexpression is correlated with many aspects of the tumorigenesis. For instance, FAK regulates the development of metastasis, driving adhesion, invasion and migration events. Furthermore, the translocation of FAK in the nucleus induces the arrest of p53 activity and its downstream gene transcription [57]. In PDAC, FAK coordinates several signalling pathways involved in growth and metastasis processes [58]. Notably, a recent study reported the ability of the indole-3-carbinol to affect EMTs genes and reduce FAK mRNA expression in MCF-7 cells [59]. Thereby, we conducted a quantitative analysis by the Enzyme-Linked Immunosorbent Assay (ELISA) to investigate whether our imidazothiadiazole compounds could reduce FAK phosphorylation at tyrosine residue 397 (FAK [pY397]), which is essential for the kinase activity of this protein. This assay was carried out on lysates of SUIT-2, Capan-1 and Panc-1 cells treated with compounds 12a and 12 b at concentrations of 5x IC50s for 24 h. As shown in Fig. 10, these ELISA experiments showed a reduction of p-FAK in all the PDAC cell lines, with fold-change values ranging from 0.4 to 0.5. Similar results were observed in the Western blot analyses of the same compounds (Supplementary Fig. 4). These results suggest that FAK is a target of our compounds and might explain how they can then suppress FAK-driven migration, and growth in PDAC cells. 4. Conclusions A new series of hybrid molecules, 12a,b,d,e,f,h, 13c,g,i,j and 14kr compounds bearing in the same structure the imidazo [2,1-b] [1,3,4]thiadiazole and indole scaffolds were efﬁciently synthesized and evaluated for their antiproliferative activity and mechanism of action on a panel of PDAC cells, namely SUIT-2, Capan-1 and Panc-1. Among the synthesized imidazothiadiazoles, compounds 12a,b,d,e,f,h, 13c,g,i,j and 14k,l,n,o,p were screened by the NCI on the full panel of sixty human cancer cells at concentration of 10 mM. Notably, compounds 12a and 12h displayed relevant antiproliferative activity eliciting GI50 values in the range from micro-to sub-micromolar levels. In addition, compounds 12b and 13g considerably reduced PDAC cell proliferation in SUIT-2, Capan-1, Panc-1, Panc-1R (gemcitabine-resistant) and in the primary cells PDAC-3, growing as monolayers or as spheroids. Noteworthy, compounds 12a,b,h and 13g are characterized by a thiophene ring at position 6 of the imidazothiadiazole scaffold, suggesting the importance of this ring for the pharmacological activity. However, in order to conﬁrm the role of aldehyde for the antiproliferative activity future studies in 14a-j compounds are warranted. Through wound-healing assays we found remarkably reduction of cell migration in all the PDAC preclinical models when treated with the most promising compounds 12a and 12b. These effects might be explained by modulation of key regulators of EMT, including E-cadherin and vimentin, as well as by the inhibition of MMP-2/-9 activities. Finally, high-throughput analysis with kinase arrays revealed a signiﬁcant inhibition of the phosphorylation of 45 tyrosine kinases substrates, whose visualization on Cytoscape S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 11 Fig. 10. Inhibition of FAK/PTK2 phosphorylation by compounds 12a and 12b. Modulation of phosphorylated-FAK (pFAK) at tyrosine residue 397 by compounds 12a and 12b on Panc-1 (A), Capan-1 (B) and SUIT-2 (C) cells. The amount of pFAK was measured in cell lysates after 24 h from the treatment with compounds 12a and 12 b at 5x IC50s. All the P values were calculated with Student’s t-test, *p < 0.05. highlighted PTK2/FAK as an important hub between those proteins. These results were validated using a speciﬁc ELISA assay, which demonstrated the inhibition of phosphorylation of PTK2/FAK. Altogether these results support the high potential of this type of compounds against EMT and PTK2/FAK, which play a key role in the aggressiveness of pancreatic cancer [55]. In order to support our experimental ﬁndings we also investigated the molecular structure of FAK. Unfortunately complete crystal structures of the molecule are not available; e.g. the Tyr397 part is lacking in the published structures, which may be due to the high ﬂexibility of this region of the molecule. This means that proper molecular docking is not yet feasible. 5. Experimental section 5.1. Chemistry All melting points were taken on a Büchi-Tottoly capillary apparatus and are uncorrected. IR spectra were determined in bromoform with a Shimadzu FT/IR 8400S spectrophotometer. 1H and 13C NMR spectra were measured at 200 and 50.0 MHz, respectively, in DMSO‑d6 solution, using a Bruker Avance II series 200 MHz spectrometer. Column chromatography was performed with Merck silica gel 230e400 mesh ASTM or with Büchi Sepacor chromatography module (prepacked cartridge system). Elemental analyses (C, H, N) were within ±0.4% of theoretical values and were performed with a VARIO EL III elemental analyzer. The LC/HRMS have been obtained on a Thermo Q-Exactive system equipped with a Dionex 3000 chromatographic system. 5.1.1. Synthesis of 1H-indole-3-carbonitriles (9b-e) A solution of the suitable indole 8 (5.10 mmol) in anhydrous acetonitrile (4.5 mL) was treated dropwise with chlorosulfonyl isocyanate (CSI) (0.44 mL, 5.10 mmol). The reaction mixture was maintained at 0 C under stirring for 2 h, then, anhydrous dimethylformamide (DMF) (2.8 mL, 36.39 mmol) was slowly added and the mixture was stirred at 0 C for 1.5 h. The resulting solution was poured into crushed ice. The solid obtained was ﬁltered and dried (yields 98e100%). Analytical and spectroscopic data for compounds 9b-e are in agreement with those previously reported [60]. 5.1.2. Synthesis of 1-methylindole-3-carbonitriles (10a-e) To a solution of the suitable 3-cyanoindole 9 (7.03 mmol) in anhydrous DMF (10 mL) 3.61 mmol of K2CO3 and dimethyl carbonate (1.8 mL, 21.4 mmol) were added and the mixture was heated at 130 C for 3.5 h. After cooling (0e5 C), water and ice (25 mL) was slowly added under stirring. The oily suspension obtained was extracted with diethyl ether (3 10 mL), the organic phase was washed with water and brine, dried over Na2SO4 and the solvent evaporated at reduced pressure to obtain the 3-cyano-1methylindoles 10 in excellent yields. Analytical and spectroscopic data are in accordance to those reported in literature [16]. 5.1.3. Synthesis of 5-(1H-indol-3-yl)-1,3,4-thiadiazol-2-amines (11a-j) A mixture of the suitable indole-3-carbonitrile 9a-e or 10a-e (5 mmol), thiosemicarbazide (5 mmol) and triﬂuoroacetic acid (5 mL) was heated under stirring at 60 C for 3.5 h. The reaction mixture was then poured into ice and neutralized with NaHCO3 saturated solution. The solid obtained was ﬁltered off, washed with water, cyclohexane and diethyl ether to give 5-(1H-indol-3-yl)1,3,4-thiadiazol-2-amines 11a-j in excellent yields. Analytical and spectroscopic data for the derivatives 11a-f are in accordance to those reported in literature [16]. 5.1.3.1. 5-(5-Methoxy-1H-indol-3-yl)-1,3,4-thiadiazol-2-amine (11g). Light yellow solid. Yield: 98%, m.p. 216e217 C IR: 3604 (NH), 3558 (NH2) cm 1; 1HNMR (200 MHz, DMSO‑d6) d: 3.79 (3H, s, CH3), 6.88 (1H, dd, J ¼ 2.4, 8.8 Hz, AreH), 7.39 (1H, d, J ¼ 8.8 Hz, AreH), 7.53 (1H, d, J ¼ 2.3 Hz, AreH), 8.02 (1H, s, AreH), 8.58 (2H, bs, NH2), 12.07 (1H, bs, NH). 13C NMR (50 MHz, DMSO‑d6) d: 55.2 (q), 101.9 (d), 105.7 (s), 112.9 (d), 113.0 (d), 124.4 (s), 128.7 (d), 131.5 (s), 152.2 (s), 154.7 (s), 166.5 (s). Anal. Calcd for C11H10N4OS (MW: 246.29): C, 53.64; H, 4.09; N, 22.75. Found: C, 53.72; H, 4.16; N, 22.98. 5.1.3.2. 5-(5-Methoxy-1-methyl-1H-indol-3-yl)-1,3,4-thiadiazol-2amine (11h). Light yellow solid. Yield: 99%, m.p. 205e206 C IR: 3381 (NH2) cm 1; 1HNMR (200 MHz, DMSO‑d6) d: 3.80 (6H, s, CH3, OCH3), 6.90 (1H, dd, J ¼ 2.5, 8.8 Hz, AreH), 7.13 (2H, s, NH2), 7.41 (1H, d, J ¼ 8.9 Hz, AreH), 7.61 (1H, d, J ¼ 2.4 Hz, AreH), 7.81 (1H, s, AreH). 13C NMR (50 MHz, DMSO‑d6) d: 32.8 (q), 55.3 (q), 102.3 (d), 106.0 (s), 111.2 (d), 112.5 (d), 124.9 (s), 130.7 (d), 132.0 (s), 152.2 (s), 154.6 (s), 165.4 (s). Anal. Calcd for C12H12N4OS (MW: 260.31): C, 55.37; H, 4.65; N, 21.52. Found: C, 55.42; H, 4.80; N, 21.78. 5.1.3.3. 5-(5-Fluoro-1H-indol-3-yl)-1,3,4-thiadiazol-2-amine (11i). Light yellow solid. Yield: 98%, m.p. 257 C IR: 3609 (NH), 3461 (NH2) cm 1; 1HNMR (200 MHz, DMSO‑d6) d: 7.03e7.12 (1H, m, AreH), 7.33e750 (3H, m, AreH, NH2), 7.80 (1H, dd, J ¼ 2.5, 10.0 Hz, AreH), 7.95 (1H, s, AreH), 11.79 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 105.4 (d, J ¼ 24 Hz), 107.4 (s, J ¼ 4.5 Hz), 110.7 (d, J ¼ 25.5 Hz), 113.1 (d, J ¼ 10 Hz), 124.4 (s, J ¼ 11 Hz), 128.6 (d), 130.1 (s), 152.0 (s), 159.9 12 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 (s), 165.9 (s). Anal. Calcd for C10H7FN4S (MW: 234.25): C, 51.27; H, 3.01; N, 23.92. Found: C, 51.38; H, 3.25; N, 24.12. 5.1.3.4. 5-(5-Fluoro-1-methyl-1H-indol-3-yl)-1,3,4-thiadiazol-2amine (11j). Light orange solid. Yield: 98%, m.p. 183 C. IR: 3471 (NH2) cm 1; 1HNMR (200 MHz, DMSO‑d6) d: 3.85 (3H, s, CH3), 7.12e7.21 (1H, m, AreH), 7.59 (1H, dd, J ¼ 4.4, 9.9 Hz, AreH), 7.76 (2H, dd, J ¼ 2.5, 9.8 Hz, AreH), 8.10 (2H, s, NH2). 13C NMR (50 MHz, DMSO‑d6) d: 33.14 (q), 105.4 (s), 105.5 (d, J ¼ 24 Hz), 110.9 (d, J ¼ 26 Hz), 112.0 (d, J ¼ 9.5 Hz), 124.3 (s), 124.5 (s), 133.1 (d), 151.4 (s), 155.7 (s). Anal. Calcd for C11H9FN4S (MW: 248.28): C, 53.21; H, 3.65; N, 22.57. Found: C, 53.38; H, 3.88; N, 22.72. 5.1.4. General procedure for the synthesis of 3-(6-phenylimidazo [2,1-b] [1,3,4]thiadiazol-2-yl)-1H-indole derivatives (12 and 13) A mixture of 5-(1H-indol-3-yl)-1,3,4-thiadiazol-2-amine 11a-j (0.92 mmol) and the suitable a-bromoacetyl derivative (0.92 mmol) in 40 mL of anhydrous ethanol was stirred at reﬂux for 24 h. After cooling at room temperature the desired product 12 was ﬁltered off and washed with cold ethanol. Derivatives 12a,b,d-f,h were isolated as pure compounds and were characterized without further puriﬁcations. Whereas, compounds 12c,g,i,j were treated with saturated aqueous NaHCO3 solution to give the corresponding free bases 13 which were puriﬁed by silica gel column chromatography eluting by petroleum ether:ethyl acetate, 1:1. Analytical and spectroscopic data for the derivatives 12k-r are in accordance to those reported in literature [16]. 5.1.4.1. 3-[6-(Thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]1H-indole hydrobromide (12a). White solid, yield: 57%, m.p. 288e289 C, IR cm1: 3630 (NH), 3458 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 7.27e7.34 (2H, m, 2xAr-H), 7.54e7.59 (2H, m, 2xAr-H), 7.68 (1H, dd, J ¼ 2.9, 5.0 Hz, AreH), 7.89 (1H, dd, J ¼ 1.1, 2.8 Hz, AreH), 8.16 (1H, dd, J ¼ 2.8, 6.2 Hz, AreH), 8.42 (1H, d, J ¼ 3.0 Hz, AreH), 8.71 (1H, s, AreH), 10.63 (1H, bs, NH), 12.24 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 106.06 (s), 110.68 (d), 112.62 (d), 120.30 (d), 120.52 (d), 121.65 (d), 123.31 (d), 123.71 (s), 125.47 (d), 127.24 (d), 130.00 (d), 133.78 (s), 136.70 (s), 139.17 (s), 142.45 (s), 158.13 (s). Anal. Calcd for C16H11BrN4S2 (MW: 403.32): C, 47.65; H, 2.75; N, 13.89. Found: C, 47.74; H, 2.83; N, 13.95. LC-HRMS: 323.04979 m/z. 5.1.4.4. 5-Chloro-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole hydrobromide (12e). Whitish solid, yield: 63%, m.p. 276e277 C, IR cm1: 3285 (NH), 3168 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 7.32 (1H, d, J ¼ 2.1 Hz, AreH), 7.52e7.68 (3H, m, AreH), 7.83 (1H, m, AreH), 8.15 (1H, d, J ¼ 1.9 Hz, AreH), 8.46 (1H, d, J ¼ 2.9 Hz, AreH), 8.71 (1H, s, AreH), 9.19 (1H, bs, NH), 12.37 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 92.15 (s), 99.49 (s), 106.10 (s), 110.43 (d), 114.24 (d), 119.58 (d), 120.27 (d), 121.37 (s), 123.35 (d), 124.74 (s), 125.80 (d), 126.17 (s), 126.67 (d), 131.35 (d), 134.16 (s), 135.22 (s). Anal. Calcd for C16H10BrClN4S2 (MW: 437.76): C, 43.90; H, 2.30; N, 12.80. Found: C, 43.99; H, 2.41; N, 12.91. LCHRMS: 357.00452 m/z. 5.1.4.5. 5-Chloro-1-methyl-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole hydrobromide (12f). Whitish solid, yield: 68%, m.p. 324e325 C, IR cm1: 2625e2496 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 3.87(3H, s, CH3), 7.36 (1H, d, J ¼ 2.0 Hz AreH), 7.51 (1H, m, J ¼ 4.5 Hz AreH), 7.60e7.68 (2H, m, AreH), 7.82 (1H, d, J ¼ 1.8 Hz, AreH), 8.07 (1H, d, J ¼ 1.9 Hz, AreH), 8.45 (1H, s, AreH), 8.64 (1H, bs, NH), 8.68 (1H, s, AreH). 13C NMR (50 MHz, DMSO‑d6) d: 33.41 (q), 104.61 (s), 110.72 (d), 112.84 (d), 119.60 (d), 120.50 (d), 123.24 (d), 124.87 (s), 125.38 (d), 126.61 (s), 127.23 (d), 133.73 (s), 134.73 (d), 135.75 (s), 139.26 (s), 142.19 (s), 157.10 (s). Anal. Calcd for C17H12BrClN4S2 (MW: 451.79): C, 45.19; H, 2.68; N, 12.40. Found: C, 45.25; H, 2.74; N, 12.45. LC-HRMS: 371.02017 m/z. 5.1.4.6. 5-Fluoro-1-methyl-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole hydro-bromide (12h). White solid, yield: 58%, m.p. 286e287 C, IR cm1: 2713e2485 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 3.88 (3H, s, CH3), 7.20 (1H, td, J ¼ 2.4, 9.2 Hz, AreH), 7.54 (1H, d, J ¼ 5.0 Hz, AreH), 7.59e7.69 (2H, m, AreH), 7.78 (1H, dd, J ¼ 2.3, 9.6 Hz, AreH), 7.86 (1H, d, J ¼ 2.3 Hz, AreH), 8.47 (1H, s, AreH), 8.67 (1H, s, AreH), 10.04 (H, bs, NH). 13C NMR (50 MHz, DMSO‑d6) d: 33.50 (q), 104.74 (d), 104.83 (s), 105.35 (d, J ¼ 6.2 Hz), 110.73 (d), 111.45 (d, J ¼ 26.1 Hz), 112.65 (d, J ¼ 26.1 Hz), 120.84 (d), 124.15 (s), 124.37 (s), 125.39 (d), 127.36 (s), 133.08 (s), 133.93 (s), 135.03 (d), 140.25 (s, J ¼ 180.3 Hz), 157.62 (s). Anal. Calcd for C17H12BrFN4S2 (MW: 435.33): C, 46.90; H, 2.78; N, 12.87. Found: C, 47.01; H, 2.87; N, 12.95. LC-HRMS: 355.04926 m/z. 5.1.4.2. 1-Methyl-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole hydrobromide (12b). Greenish yellow solid, yield: 55%, m.p. 317e318 C, IR cm1: 2650 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 3.91 (3H, s, CH3), 6.50 (1H, bs, NH), 7.32e7.41 (2H, m, 2xAr-H), 7.55 (1H, d, J ¼ 4.9 Hz, AreH),7.61e7.66 (2H, m, 3xAr-H), 7.81 (1H, d, J ¼ 2.4 Hz, AreH), 8.16 (1H, dd, J ¼ 2.4, 6.2 Hz, AreH), 8.38 (1H, s, AreH), 8.60 (1H, s, AreH). 13C NMR (50 MHz, DMSO‑d6) d: 33.14 (q), 99.50 (s), 105.39 (s), 110.30 (d), 111.01 (d), 119.59 (d), 120.44 (s), 121.77 (d), 123.23 (d), 124.06 (s), 125.53 (d), 126.74 (d), 132.95 (s), 133.28 (d), 135.53 (s), 137.25 (s), 141.09 (d). Anal. Calcd for C17H13BrN4S2 (MW: 417.35): C, 48.92; H, 3.14; N, 13.42. Found: C, 48.85; H, 3.22; N, 13.51. LC-HRMS: 337.05688 m/z. 5.1.4.7. 5-Bromo-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole (13c). Whitish solid, yield: 58%, m.p. 299e300 C, IR cm1: 3535e3633 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 7.39e7.44 (1H, m, AreH), 7.50e7.54 (2H, m, AreH), 7.59e7.63 (1H, m, AreH), 7.75 (1H, dd, J ¼ 1.1, 1.1 Hz, AreH), 8.32 (2H, d, J ¼ 1.7 Hz, AreH), 8.60 (1H, s, AreH), 12.29 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 99.49 (s), 106.21 (s), 110.38 (d), 114.03 (s), 114.59 (d), 119.34 (d), 122.61 (d), 125.46 (d), 125.77 (d), 126.72 (d), 130.65 (d), 135.45 (s), 135.98 (s), 141.65 (s), 142.62 (s), 156.42 (s). Anal. Calcd for C16H9BrN4S2 (MW: 401.30): C, 47.89; H, 2.26; N, 13.96. Found: C, 47.95; H, 2.31; N, 14.04. LC-HRMS: 402.95081 m/z. 5.1.4.3. 5-Bromo-1-methyl-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole hydrobromide (12d). Whitish solid, yield: 68%, m.p. 318e319 C, IR cm1: 2697e2500 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 3.87 (3H, s, CH3), 7.43e7.68 (4H, m, AreH), 7.81e7.83 (1H, m, AreH), 8.24 (1H, d, J ¼ 1.76 Hz, AreH), 8.38 (1H, bs, NH), 8.43 (1H, s, AreH), 8.69 (1H, s, AreH). 13C NMR (50 MHz, DMSO‑d6) d: 33.39 (q), 104.55 (s), 110.72 (d), 113.26 (d), 114.60 (s), 120.41 (d), 122.63 (d), 125.38 (d), 125.49 (s), 125.80 (d), 127.21 (d), 133.90 (s), 134.58 (d), 136.01 (s), 139.42 (s), 142.21 (s), 157.02 (s). Anal. Calcd for C17H12Br2N4S2 (MW: 496.24): C, 41.15H, 2.44; N, 11.29. Found: C, 41.22; H, 2.52; N, 11.41. LC-HRMS: 416.96634 m/z. 5.1.4.8. 5-Fluoro-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole (13g). Yellow solid, yield: 80%, m.p. 260e261 C, IR cm1: 3630 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 7.16 (1H, td, J ¼ 2.5, 9.2 Hz, AreH), 7.52e7.63 (3H, m, 3xAr-H), 7.75e7.77 (1H, m, AreH), 7.84 (1H, dd, J ¼ 2.4, 9.8 Hz, AreH), 8.38 (1H, d, J ¼ 2.9 Hz, AreH), 8.55 (1H, s, AreH), 12.24 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 99.40 (s), 104.61 (s), 105.78 (s), 111.36 (d), 113.77 (s), 120.20 (d), 123.70 (s), 123.96 (s), 126.46 (d), 128.11 (d), 131.63 (s), 133.24 (s), 135.45 (d), 138.25 (d), 140.74 (d), 145.68 (d). Anal. Calcd for C16H9FN4S2 (MW: 340.4): C, 56.45; H, 2.66; N, 16.46. Found: C, 56.51; H, 2.71; N, 16.56. LC-HRMS: 341.03256 m/z. S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 5.1.4.9. 5-Methoxy-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole (13i). Yellow solid, yield: 58%, m.p. 255e256 C, IR cm1: 3628 (NH). 1HNMR (200 MHz, DMSO‑d6) d: 3.85 (3H, s, CH3), 6.95 (1H, dd, J ¼ 2.4, 8.8 Hz, AreH), 7.44 (1H, d, J ¼ 8.8 Hz, AreH), 7.52e7.65 (3H, m, AreH), 7.75 (1H, dd, J ¼ 1.0, 2.8 Hz AreH), 8.24 (1H, d, J ¼ 3.0 Hz, AreH), 8.55 (1H, s, AreH), 12.00 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 55.32 (q), 102.18 (d), 106.35 (s), 110.30 (d), 113.09 (d), 113.30 (d), 119.24 (d), 124.34 (s), 125.52 (d), 126.66 (d), 129.59 (d), 131.61 (s), 136.07 (s), 141.49 (s), 142.55 (s), 155.09 (s), 157.08 (s). Anal. Calcd for C17H12N4OS2 (MW: 352.43): C, 57.93; H, 3.43; N, 15.90. Found: C, 57.88; H, 3.52; N, 15.99. LC-HRMS: 353.05377 m/z. 5.1.4.10. 5-Methoxy-1-methyl-3-[6-(thiophen-3-yl)imidazo[2,1-b] [1,3,4]thiadiazol-2-yl]-1H-indole (13j). Yellow solid, yield: 60%, m.p. 213e214 C, 1HNMR (200 MHz, DMSO‑d6) d: 3.86 (6H, s, OCH3, CH3), 6.99 (1H, dd, J ¼ 2.5, 7.7 Hz, AreH), 7.50e7.64 (4H, m, AreH), 7.75 (1H, d, J ¼ 3.2 Hz, AreH), 8.26 (1H, s, AreH), 8.55 (1H, s, AreH). 13C NMR (50 MHz, DMSO‑d6) d: 33.24 (q, CH3), 55.38 (q, CH3), 99.49 (s), 102.32 (d), 105.06 (s), 110.35 (d), 111.90 (d), 112.96 (d), 119.24 (d), 124.61 (s), 125.52 (d), 126.67 (d), 132.30 (s), 133.03 (d), 136.00 (s), 141.46 (s), 142.43 (s), 155.37 (s), 156.63 (s). Anal. Calcd for C18H14N4OS2 (MW: 366.46): C, 58.99; H, 3.85; N, 15.29. Found: C, 59.07; H, 3.91; N, 15.37. LC-HRMS: 367.06955 m/z. 5.1.5. General procedure for the synthesis 2-(1H-indol-3-yl)-6phenylimidazo[2,1-b] [1,3,4]thiadiazole-5-carbaldehydes 14k-r Vilsmeier reagent was prepared at 0 C by adding dropwise POCl3 (0.11 mL) into a stirred DMF anhydrous (0.08 mL). The appropriate derivative 13 (0.5 mmol) in 2 mL of DMF anhydrous was added and the solution was heated at 70 C under stirring for 5h. The reaction mixture was poured onto ice and the corresponding aldehyde 14 was ﬁltered off and puriﬁed by silica gel column chromatography eluting by petroleum ether:ethyl acetate, 3:7. Derivatives 14l, 14q were characterized only by 1HNMR spectra due to their poor solubility. 5.1.5.1. 2-(1H-indol-3-yl)-6-phenylimidazo[2,1-b] [1,3,4]thiadiazole5-carbaldehyde (14k). White solid, yield: 70%, m.p. 285e286 C, IR cm1: 2918 (NH), 1683 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 7.30 (1H, m, AreH), 7.52 (2H, d, J ¼ 6.8 Hz, AreH), 8.01 (2H, d, J ¼ 5.8 Hz, AreH), 8.27e8.30 (3H, m, AreH), 8.41 (2H, d, J ¼ 3.0 Hz, AreH), 10.08 (1H, s, CHO), 12.20 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 106.20 (s), 112.64 (d), 120.65 (d), 121.70 (d), 123.36 (d), 123.47 (s), 123.80 (s), 128.67 (4xd), 129.41 (d), 130.10 (d), 132.38 (s), 136.68 (s), 148.53 (s), 153.45 (s), 159.38 (s), 177.31 (d). Anal. Calcd for C19H12N4OS (MW: 344.39): C, 66.26; H, 3.51; N, 16.27. Found: C, 66.35; H, 3.59; N, 16.41. LC-HRMS: 345.08148 m/z. 5.1.5.2. 2-(1-Methyl-1H-indol-3-yl)-6-phenylimidazo[2,1-b] [1,3,4] thiadiazole-5-carbaldehyde (14l). White solid, yield: 91%, m.p. 233e234 C, IR cm1: 1560 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 3.90 (3H, s, CH3), 7.31e7.59 (6H, m, AreH), 7.87e8.41(4H, m, AreH), 10.07 (1H, s, CHO). Anal. Calcd for C20H14N4OS (MW: 358.4): Composition: C, 67.02; H, 3.94; N, 15.63. Found: C, 67.28; H, 4.11; N, 15.75. LC-HRMS: 214.09023 m/z. 5.1.5.3. 6-(4-Fluorophenyl)-2-(1H-indol-3-yl)imidazo[2,1-b] [1,3,4] thiadiazole-5-carbaldehyde (14m). White solid, yield: 81%, m.p. 255e256 C, IR cm1:3158 (NH), 1560 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 7.28e7.38 (4H, m, AreH), 7.52e7.55 (1H, m, AreH), 8.08e8.11 (2H, m, AreH), 8.26e8.29 (1H, m, AreH), 8.40 (1H, s, AreH), 10.09 (1H, s, CHO), 12.19 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 99.5 (s), 106.1 (s), 112.5 (d), 115.3 (d), 115.8 (d), 120.6 13 (d), 121.7 (d), 123.3 (d), 123.8 (2xs), 128.9 (s), 130.2 (d), 130.7 (d), 130.9 (d), 136.7 (s), 148.2 (s), 151.8 (s), 159.4 (s), 177.3 (d). Anal. Calcd for C19H11FN4OS (MW: 362.38): C, 62.97; H, 3.06; N, 15.46. Found: C, 63.05; H, 3.11; N, 15.53. LC-HRMS: 363.07043 m/z. 5.1.5.4. 2-(1H-indol-3-yl)-6-(3-methoxyphenyl)imidazo[2,1-b] [1,3,4] thiadiazole-5-carbaldehyde (14n). White solid, yield: 60%, m.p. 278e279 C, IR cm1: 3308 (NH), 1560 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 3.84 (3H, s, CH3), 7.06 (1H, d, J ¼ 6.7 Hz, AreH), 7.29e7.32 (2H, m, AreH), 7.41e7.46 (1H, m, AreH), 7.55 (1H, dd, J ¼ 3.1, 5.8 Hz, AreH), 7.61 (2H, m, AreH), 8.30 (1H, m, AreH), 8.42 (1H, d, AreH), 10.10 (1H, s, CHO), 12.20 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 55.2 (q), 99.49 (s), 106.2 (s), 113.5 (2xd), 120.7 (d), 121.0 (d), 121.7 (d), 123.3 (d), 123.6 (s), 123.8 (s), 129.7 (2xd), 130.1 (d), 133.7 (s), 136.7 (s), 153.0 (s), 159.3 (s), 159.4 (s), 177.3 (d). Anal. Calcd for C20H14N4O2S (MW: 374.42): C, 64.16; H, 3.77; N, 14.96. Found: C, 64.25; H, 3.51; N, 15.13. LC-HRMS: 375.09232 m/z. 5.1.5.5. 6-(2,5-Dimethoxyphenyl)-2-(1H-indol-3-yl)imidazo[2,1-b] [1,3,4]thiadiazole-5-carbaldehyde (14o). Yellow solid, yield: 82%, m.p. 268e269 C, IR cm1: 1561 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 3.75 (3H, s, CH3), 3.77 (3H, s, CH3), 7.02e7.18 (3H, m, AreH), 7.32 (2H, dd, J ¼ 2.9, 5.8 Hz, AreH), 7.55e7.58 (1H, m, AreH), 8.28 (2H, d, J ¼ 5.5 Hz, AreH), 8.42 (1H, s, AreH), 9.76 (1H, s, CHO), 12.21 (1H, s, NH). 13C NMR (50 MHz, DMSO‑d6) d: 55.5 (q), 55.9 (q), 99.5 (s), 106.2 (s), 112.5 (d), 113.1 (d), 116.1 (d), 116.3 (2xd), 120.62 (s), 121.7 (d), 122.1 (s), 123.3 (d), 123.8 (s), 130.0 (d), 136.7 (s), 148.7 (s), 150.4 (s), 153.1 (s), 159.2 (s), 177.6 (d). Anal. Calcd for C21H16N4O3S (MW: 404.44): C, 62.36; H, 3.99; N, 13.85. Found: C, 62.49; H, 4.05; N, 13.63. LC-HRMS: 405.10297 m/z. 5.1.5.6. 6-(2,5-Dimethoxyphenyl)-2-(1-methyl-1H-indol-3-yl)imidazo[2,1-b] [1,3,4]thiadiazole-5-carbaldehyde (14p). White solid, yield: 70%, m.p. 216e217 C, IR cm1: 1667 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 3.75 (3H, s, CH3), 3.77 (3H, s, CH3), 3.92 (3H, s, CH3), 7.06 (1H, dd, J ¼ 2.9, 5.8 Hz, AreH), 7.17 (2H, m, AreH), 7.36e7.39 (2H, t, J ¼ 4.0 Hz, AreH), 7.64 (1H, d, J ¼ 8.8 Hz, AreH), 8.27 (1H, d, J ¼ 10.4 Hz, AreH), 8.43 (1H, s, AreH), 9.76 (1H, s, CHO). 13C NMR (50 MHz, DMSO‑d6) d: 33.2 (q), 55.5 (q), 55.97 (q), 99.5 (s), 105.1 (s), 108.5 (d), 111.1 (d), 113.1 (d), 116.1 (s), 116.3 (d), 118.73 (d), 120.68 (d), 122.0 (d), 123.4 (d), 123.9 (s), 124.1 (s),136.2 (s),137.3 (s), 148.6 (s), 150.4 (s), 153.0 (s), 158.8 (s), 177.6 (d). Anal. Calcd for C22H18N4O3S (MW: 418.47): C, 63.14; H, 4.34; N, 13.39. Found: C, 63.21; H, 4.43; N, 13.48. LC-HRMS: 419.11682 m/z. 5.1.5.7. 2-(1H-indol-3-yl)-6-(4-nitrophenyl)imidazo[2,1-b] [1,3,4] thiadiazole-5-carbaldehyde (14q). Yellow solid, yield: 75%, m.p. 314e315 C, IR cm1: 3311 (NH), 1561 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 7.31 (2H, d, J ¼ 2.9 Hz, AreH), 7.52 (1H, s, AreH), 8.34e8.43 (5H, m, AreH), 10.21 (1H, s, CHO), 12.23 (1H, s, NH). Anal. Calcd for C19H11N5O3S (MW: 389.39): C, 58.61; H, 2.85; N, 17.99. Found: C, 58.82; H, 2.73; N, 18.09. LC-HRMS: 390.06683 m/z. 5.1.5.8. 2-(5-Bromo-1H-indol-3-yl)-6-(2,5-dimethoxyphenyl)imidazo[2,1-b] [1,3,4]thiadiazole-5-carbaldehyde (14r). White solid, yield: 90%, m.p. 250e251 C, IR cm1: 3268 (NH), 1654 (CO). 1HNMR (200 MHz, DMSO‑d6) d: 3.76 (6H, d, J ¼ 3.9 Hz, 2xCH3), 7.08e7.18 (3H, m, AreH), 7.42e7.56 (2H, m, AreH), 8.45 (2H, d, J ¼ 10.3 Hz, AreH), 9.76 (1H, s, CHO), 12.38 (1H, bs, NH). 13C NMR (50 MHz, DMSO‑d6) d: 55.3 (q), 55.9 (q), 99.5 (s), 105.9 (s), 108.2 (s), 114.3 (s), 116.1 (d), 116.3 (d), 122.0 (s), 122.9 (d), 123.9 (s), 125.5 (s), 126.0 (d), 131.2 (d), 135.5 (s), 141.6 (d), 150.3 (s), 150.7 (d), 153.3 (s), 158.7 (s), 178.6 (d). Anal. Calcd for C21H15BrN4O3S (MW: 483.33): C, 52.18; H, 3.13; N, 11.59. Found: C, 52.39; H, 3.21; N, 11.70. LC-HRMS: 485.01031 m/z. 14 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 5.2. Biology 5.2.1. Drugs and chemicals The synthesized imidazothiadiazole compounds 12e14 were dissolved in DMSO. The medium, foetal bovine serum (FBS), penicillin (50 IU mL1) and streptomycin (50 mg mL1) were from Gibco (Gaithersburg, MD, USA). All other chemicals were from Sigma (Zwijndrecht, the Netherlands). 5.2.2. Cell culture Capan-1 and Panc-1 cell lines, were purchased at the ATCC (Manassas, VA, USA), while SUIT-2 cells were a generous gift from Dr. Adam Frampton (Imperial College, London, UK). Panc-1R cells, a gemcitabine-resistant sub-clone obtained by continuous incubation of Panc-1 with 1 mM of this drug, were achieved as described previously [41]. The primary PDAC-3 culture was isolated from a patient at Pisa Hospital as described previously [61]. The cell lines were tested for their authentication by STRePCR, performed by BaseClear (Leiden, the Netherlands). The cells were cultured in RPMI-1640 (Roswell Park Memorial Institute 1640) supplemented with 10% heat-inactivated FBS, 1% penicillin/streptomycin, or in DMEM (Dulbecco’s Modiﬁed Eagle’s Medium), supplemented with 10% heat-inactivated FBS, 1% HEPES. The cells were kept in a humidiﬁed atmosphere of 5% CO2 and 95% air at 37 C and harvested with trypsin-EDTA. Not all these preclinical models allowed to perform the different experiments to check antitumor properties of new compounds. In particular, PDAC-3 cells were selected to form spheroids which are more representative of the aggregation of tumor cells in vivo, as also reported in our previous studies. All the PDAC cells, i.e., Panc-1R, SUIT-2 and PDAC-3, but also Panc-1 and Capan-1 cells were selected for the wound-healing assay because in all these cells the exposure for 24 h with our compounds did not result in pro-apoptotic or necrotic effects, allowing a reliable analysis of the results. Capan-1 and SUIT-2 cells were selected for Western blot, zymography and PCR assays because preliminary analyses of the housekeeping protein GAPDH at the Western blot showed that using lysates of these cells the Western blot images were not “saturated” and were kept in the linear range (as revealed by exposing blots to increasing times and drawing a plot of intensity and time exposure). SUIT-2 cells were selected for the PamChip array because of the lowest background noise observed in preliminary experiments. 5.2.3. Cell growth inhibition The in vitro antiproliferative activity of the new imidazothiadiazole compounds 12a,b,d,e,f,h, 13c,g,i,j and 14k-r was evaluated on a panel of pancreatic cancer cells by Sulforhodamine-B (SRB) assay, both for primary cell cultures (PDAC-3) and for the immortalized cell lines (SUIT-2, Capan-1, Panc-1 and Panc-1R), following a previously described protocol [42]. The cytotoxicity of the new compounds 12a and 12b was also evaluated in the normal ﬁbroblast cells Hs27. The results of these experiments allowed us to calculate the selectivity index (SI, IC50 non-tumor cell line/IC50 tumor cell line). Cells were seeded into a 96-well ﬂat-bottom plates in triplicate in a volume of 100 mL (3 103 cells/well for SUIT-2, Panc-1, Panc-1R and PDAC-3 cell lines, 5 103 cells/well for Capan-1 cells, and 8 103 cells/well for Hs27 cells) and incubated for 24 h at 37 C to create a conﬂuent monolayer. Then, the cells were treated with 100 mL of the compounds dissolved in DMSO at different concentration (125e16000 nM) for 72 h at 37 C, 5% CO2 and 100% humidity. At the end of incubation period, the cells were ﬁxed with 25 mL of 50% cold trichloroacetic acid (TCA) and kept for at least 60 min at 4 C. Then, the plates were emptied and washed gently with deionized water, dried at room temperature (RT) overnight and stained with 50 mL of 0.4% SRB solution in 1% acetic acid for 15 min at RT. The excess of SRB stain was removed and the plates were washed with a 1% acetic acid solution and let dry at RT overnight. The SRB staining was dissolved in 150 mL of tris(hydroxymethyl)aminomethane solution pH ¼ 8.8 (TRIS base), and the absorbance was measured at wavelengths of 490 nm and 540 nm. Cell growth inhibition was calculated as the percentage of drug treated cells versus vehicle-treated cells (“untreated cells or control”) OD (corrected for OD before drug addiction, “day-0”). The 50% inhibitory concentration of cell growth (IC50) was calculated by non-linear least squares curve ﬁtting (GraphPad PRISM, Intuitive Software for Science, San Diego, CA). In the NCI protocol IC50 is named GI50 (50% growth inhibitory concentration). 5.2.4. Wound-healing assay The in vitro scratch wound-healing assay was performed as previously described [62]. SUIT-2, Capan-1, Panc-1 and Panc-1R cells were seeded in 96-well ﬂat-bottom plates at the density of 5 104 cells/well in 100 mL. After 24 h of pre-incubation at 37 C, 5% CO2 and 100% humidity, the cell monolayers were scratched using a speciﬁc tool with multiple needles to create scratches of constant width. After removal of the detached cells by washing with phosphate buffered saline (PBS) solution, in the control wells the medium was replaced with only medium while the medium added with the compounds of interest in the experimental wells. The wound conﬂuence was monitored by phase-contrast microscopy (Universal Grab 6.3 software, Digital Cell Imaging Labs, Keerbergen, Belgium) integrated to the Leica DMI300B (Leica Microsystems, Eindhoven, Netherlands) migration station and the pictures were captured immediately after scratch (T ¼ 0), and 4, 8, 20 and 24 h from the treatment. The results were analyzed with the Scratch Assay 6.2 software (Digital Cell Imaging Labs). 5.2.5. Spheroid assay PDAC-3 spheroids were grown in CELLSTAR®96-well cell repellent U-bottom plates (Greiner Bio-One, Cat No. 650970, Kremsmünster, Austria). Cells were seeded at the density of 2 104 cells per well, and incubated at 37 C, 5% CO2 for 72 h in order to let the spheroids form. Before the treatment a picture of the plate was taken with an automated phase-contrast microscope DMI300B (Leica Microsystems, Eindhoven, Netherlands), and the subsequent pictures were taken every two days. After 72 h of incubation the culture medium was replaced with medium added with compounds of interest, which were diluted to the ﬁnal concentration of 8.5 mM (5x the IC50, obtained with previous growth-inhibition assay). Despite the careful pipetting, tilting the plate and placing the pipette tip on the side of the well, the structure of the spheroid was disturbed so we decided to centrifuge the plate at 200xRCF, for 3 min at RT (Rotixa 500RS, Hettich Zentrifugen Technology, Tuttlingen, Germany). The treatment was repeated after four days, to ensure the availability of nutrients, and so was the centrifuge. Pictures were analyzed with ImageJ Software (U.S. National Institute of Health, Bethesda, Maryland, USA) to determine the area of the spheroids treated and compare it to the area of the untreated spheroids, as described previously [63]. 5.2.6. RNA isolation RNA was extracted from SUIT-2, Capan-1 and Panc-1 cells according to TRIzol-chloroform protocol as described previously [64]. Cells were seeded in a 6-well plate in a density of 2.5 105 cells/ well and kept at 37 C, with a constant level of CO2 (5%) and 100% humidity for 24 h. Subsequently, the cells were treated for 24 h with the compounds of interest at concentration 5x IC50 and stored for an additional 24 h in the incubator. The cells were then S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 harvested by 250 mL of TRIzol reagent. After precipitation with isopropanol and washing with 70% ethanol, the total RNA appeared as a white gel-like pellet at the bottom of the tube. RNA yields and integrity were determined by measuring optical density at 260 nm with a Thermo Scientiﬁc NanoDrop 1000™ Spectrophotometer, controlled by ND1000 software. Instead, the test for detection of contaminations by protein or by organic compounds, thiocyanates and phenolate ions was performed by measuring absorbance at 280 and 230 nm, respectively. 5.2.7. Reverse transcription (RT) and quantitative real-time PCR (qRT-PCR) For qRT-PCR, complementary DNA (cDNA) synthesis was performed according to manufacturer’s protocol Thermo Scientiﬁc™ First Strand cDNA Synthesis Kit. For the reverse transcriptase reactions, 1.5 mg of mRNA was added to a 1 mL of random hexamer primer and, ﬁnally, water nuclease free up to a ﬁnal volume of 11 mL. Therefore, 5X Reaction Buffer (4 mL), RiboLock RNase Inhibitor (20 U/mL) (1 mL), 10 nM dNTP Mix (2 mL) and M-MuLV Reverse Transcriptase (20 U/mL) (2 mL) components were added (all provided by Kit). The mixture was incubated for 5 min at 25 C followed by 60 min at 37 C. Subsequently, the reaction was terminated by heating at 70 C for 5 min. The DNA samples obtained (20 mL) were diluted 1:10 and used immediately for the RT-PCR assay. RT-PCR reactions were performed using the commercial TaqMan® Universal PCR Master Mix kit. For the RT-PCR, 25 mL of total mix per well is needed. Therefore, 12.5 mL of Universal Master Mix 2X (AmpliTaq Gold DNA Polymerase, dNTPs with dUTP, passive reference, and optimized buffer components), 1 mL of Primers and TaqMan® probe, 6.5 mL of H2O and 5 mL of cDNA sample were loaded in duplicate on a 96-well PCR plate and the ampliﬁcation was carried out in a GeneAmp 5700 Sequence Detection System. Samples were ampliﬁed by following the thermal cycle conditions for 40 cycles: an initial incubation at 50 C for 2 min to prevent the reampliﬁcation of carry-over PCR products by AmpErase uracil-Nglycosylase, followed by incubation at 95 C for 10 min to suppress AmpErase UNG activity and denature the DNA, followed by annealing and extension at 60 C for 1 min. Primers and probes were obtained from Applied Biosystems Assay-on Demand Gene expression products to amplify the following genes: SNAIL1 (Hs00195591_m1), SNAIL2 (Hs00950344_m1), CDH1 (Hs010 23894_m1), CDH12 (Hs00362037_m1). GAPDH (Hs02758991_g1) has been used as housekeeping gene to normalize the ampliﬁcations. All reactions were performed in duplicate using the ABI PRISM7500 sequence detection system instrument (AppliedBiosystems). The cycle threshold (Ct) was determined and gene expression levels relative to that of GAPDH were calculated by the 2DDCT method, as described previously. 5.2.8. Western blot and gelatine zymography The protein expression of SNAIL1, SNAIL2, CDH1, CDH12, and VIM in SUIT-2, PANC-1 and Capan-1 cells treated with compounds 12a and 12b was evaluated by Western Blot analysis as described previously [65]. All the primary antibodies were from Cell Signalling Technology (Beverly, MA). Additional Western blot analyses were performed in order to evaluate the phosphorylation of FAK, using the Phospho-FAK (Tyr397) Antibody #3283 (Cell Signalling Technology). The activity of MMP2 and MMP9 was evaluated by gelatine zymography, as described previously [65]. PDAC cells (106) were seeded in Petri dishes and incubated with serum-free medium for 24 h, with or without the selected compounds at 5x IC50. Medium was harvested and centrifuged (1500 rpm for 5 min) in order to remove cellular debris. The collected media were then mixed with SDS-PAGE buffer 4X without reducing agent and underwent 15 electrophoresis in 10% polyacrylamide gel containing 1 mg/mL gelatine. After 1 h, the gel was exposed to renaturating buffer (50 mM Tris-HCl pH 7, 6.5 mM CaCl2, 1 mM ZnCl2, 2.5% Triton X-100) for 15 min, washed with washing buffer (50 mM Tris-HCl pH 7, 6.5 mM CaCl2, 1 mM ZnCl2) and ﬁnally incubated with developing buffer (50 mM Tris-HCl pH 7, 6.5 mM CaCl2, 1 mM ZnCl2, 1% Triton X100, 0.02% NaN3) for 16 h at 37 C. The staining was then performed using 0.25% Coomassie Brilliant Blue R-250 solution containing 45% methanol and 10% glacial acetic acid for 4 h, washed with a solution of 10% glacial acetic acid and 45% methanol for 2 h. The areas of protease activity were detected as clear bands and the activity of MMPs was assessed by densitometric scanning and quantitative analysis using ImageJ software (National Institutes of Health, Bethesda, MD, US). 5.2.9. PamChip® kinase activity proﬁling A PamChip array with 144 kinase peptides substrates (#86312 PamGene International B.V., ‘s-Hertogenbosch, The Netherlands) was used to test the change in tyrosine kinase activity when using the 12b compound. This experiment was performed with SUIT2 cells in biological duplicates (two untreated samples and two treated samples with 12b compound), as described previously [66,67]. 5.2.10. Preparation of cell lysates Cells were grown in 25 cm2 ﬂasks until they reached 80% of conﬂuence, at 37 C and 5% of CO2, then SUIT-2 cells were treated with 5 mM of 12b (5x IC50), and the medium of control cells was replaced with fresh medium. Treatment lasted 24 h, and then cells were lysed with 100 mL x 106 cells of M-PER lysis buffer containing: M-PER Mammalian Extraction Buffer (Thermo Scientiﬁc, Rockford, IL, USA), Halt protease Inhibitor cocktail, EDTA free (Complete Mini EDTA-free Protease Inhibitor Cocktail, Roche #11836170001), Halt Phosphatase Inhibitor Cocktail (Thermo Fisher #78420) both diluted 1:100, for at least 15 min at 4 C. The lysates were collected in 1.5 mL tubes, which were centrifuged (at 4 C, 16000g) for 15 min, and the supernatants were collected and stored at 80 C until use. Protein concentration of the samples was determined using Bio-Rad protein Assay, based on the method of Bradford (BioRad, Hercules, CA). 5.2.11. Tyrosine kinase activity proﬁling Lysates for the PamChips were prepared in order to reach a concentration of 10 mg protein/array, and they were added to the MasterMix (PamGene reagent kit 32116) containing: PK buffer 10x, BSA solution 100x, PTK additive 10x, 1 M DTT solution, Complete Mini EDTA-free Protease Inhibitor Cocktail, Halt Phosphatase Inhibitor Cocktail 400x (Thermo Fisher), PY-20-FITC (ﬂuorescent labelled antibody), 4 mM ATP solution. Samples were added to the MasterMix immediately prior to loading on the chip. Before loading the samples, the PamStation®12 instrument performed a blocking step with 25 mL of 2% BSA on each array followed by three wash steps with PK buffer, then 40 mL of each sample mix was loaded in duplicate onto the arrays. During incubation at 30 C, the sample mix was pumped up and down through the array once per minute for 60 cycles. Repeated ﬂuorescent imaging of each array was performed with a 12-bit CCD camera, monitoring ﬂuorescence intensities in real time. 5.2.12. PamGene data analysis The intensity of each spot at the end point was evaluated through an open source software (ScanAnalyze) and subsequently corrected for local background noise. Since the negative control was a negative value, all the intensities were subjected to a minimal shift to have the negative control equal to zero. 16 S. Cascioferro et al. / European Journal of Medicinal Chemistry 189 (2020) 112088 One duplicate of the treated samples was excluded from the analysis due to bad quality data ending with two controls and one treated samples. To maintain a balance and statistical power for the differential analysis, one extra sample for the control group was generated using the median of the two samples and adding a constant k while 2 extra samples for the treated group were generated adding a different constant k to the treated sample. The differential analysis was performed by a Student t-test in R (version 3.6.1) and the p.value was corrected by FDR. The signiﬁcant peptides were selected applying a cutoff on FDR <0.01. Visualization of differentially phosphorylated protein was performed in Cytoscape (version 3.5.0) and the barplot for PTK2 phosphorylation was generated in R (version 3.6.1). 5.2.13. Enzyme-Linked Immunosorbent Assay (ELISA) for phosphorylated FAK (pFAK) kinase The pFAK level at tyrosine residue 397 was detected and quantiﬁed using Enzyme-Linked Immunosorbent Assay (ELISA). The assay was conducted using Invitrogen™ FAK [pY397] ELISA Kit (Cat. # KHO0441) according to the manufacturer’s protocol. Supernatants from Panc-1, Capan-1 and SUIT-2 cells were collected after 24 h from the treatment with imidazothiadiazole compounds 12a and 12 b at concentration 5x IC50 value. The absorbance was read at 450 nm. We performed a parallel ELISA test using the wellknown FAK inhibitor defactinib (5 mM). This drug reduced the FAK/ PTK2 phosphorylation of 65%, supporting the use of this method in order to check the inhibition of pFAK. 5.2.14. Statistics All SRB, PCR, Western blot, and zymography assays were carried out in triplicate and repeated at least three times, whereas the percentages of cell migration were calculated taking into account at least six scratch areas. The data was evaluated using the GraphPad Prism version 7 software (GraphPad Software, San Diego, CA, USA). Data is expressed as mean values ± SEM and analyzed by the Student t-test. Declaration of competing interest The authors declare that they have no known competing ﬁnancial interests or personal relationships that could have appeared to inﬂuence the work reported in this paper. Acknowledgments This work was partially supported in the collections and analysis of data by the following grants: CCA Foundation 2015 and 2018 grants, KWF Dutch Cancer Society grants (KWF project#10401 and #11957) and AIRC/Start-Up grant (to E.G.). The Authors would like to thank Btissame El Hassouni, MSc (VUmc, Amsterdam, The Netherlands) for the support with the work on the cell culture experiments. We thank the members of the Drug Discovery Commitee of the EORTC-PAMM group for the useful discussion and support. Appendix A. Supplementary data Supplementary data to this article can be found online at https://doi.org/10.1016/j.ejmech.2020.112088. List of abbreviations CDH1 CDH12 CSI E-cadherin N-cadherin chlorosulfonyl isocyanate DMF Dimethylformamide DMPM diffuse malignant peritoneal mesothelioma DMSO Dimethyl sulfoxide ELISA enzyme-linked immunosorbent assay EMT epithelial mesenchymal transition FAK focal adhesion kinase FBS foetal bovine serum FDR false discovery rate GI50 growth inhibition of 50% of cells IC50 inhibitory concentration 50% MMP-2/9 matrix metalloproteinases-2/9 NCI National Cancer Institute PDAC pancreatic ductal adenocarcinoma PTK2 protein tyrosine kinase 2 RT room temperature SD standard deviation SEM standard error media SI selectivity index SNAIL-1/2 zinc ﬁnger protein-1/2 TGI total growth inhibition VIM vimentin References [1] K. Nepali, S. Sharma, M. Sharma, P.M.S. Bedi, K.L. Dhar, Rational approaches, design strategies, structure activity relationship and mechanistic insights for anticancer hybrids, Eur. J. Med. Chem. 77 (2014) 422e487, https://doi.org/ 10.1016/j.ejmech.2014.03.018. [2] C. 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