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Antitumor pentamethylcyclopentadienyl rhodium complexes of maltol and allomaltol: synthesis, solution speciation and bioactivity.
Volume 134, May 2014
Contents lists available at ScienceDirect
Journal of Inorganic Biochemistry
j o u r n a l h o m e p a g e : w w w. e l s ev i e r. c o m / l o c a t e / j i n o r g b i o
Contents
Jingnan Zhang, Qianqian Yu, Qian Li,
Licong Yang, Lanmei Chen,
Yanhui Zhou, Jie Liu
Journal of Inorganic Biochemistry 134 (2014)
1–11
[Ru(ip)3](ClO4)2·2H2O (complex 1) stabilizes the combination of bcl-2 G-quadruplex to form the antiparallel conformation
and causes cell apoptosis mediated by
caspase activation.
A ruthenium(II) complex capable of inducing
and stabilizing bcl-2 G-quadruplex formation
as a potential cancer inhibitor
Konstantis F. Konidaris, Georgios A. Dalkas,
Eugenia Katsoulakou, George Pairas,
Catherine P. Raptopoulou, Fotini N. Lamari,
Georgios A. Spyroulias, Evy Manessi-Zoupa
Journal of Inorganic Biochemistry 134 (2014)
12–19
ZnII/pyridyloxime complexes as potential
reactivators of OP-inhibited
acetylcholinesterase: In vitro and docking
simulation studies
Ricardo Cerón-Camacho,
Ronan Le Lagadec, Igor V. Kurnikov,
Alexander D. Ryabov
Journal of Inorganic Biochemistry 134 (2014)
20–24
A glance at the reactivity of osma(II)cycles
[Os(C–N)x(bpy)3 − x]m + (x = 0–3)
Covering a 1.8 V Potential Range toward
Peroxidase through Monte Carlo
Simulations (−C–N = o-2phenylpyridinato, bpy = 2,2′-bipyridine)
Elsevier Inc.
doi:10.1016/S0162-0134(14)00078-6
Novel ZnII/pyridyloxime complexes have
been synthesized, crystallographically
characterized and tested in vitro as potential reactivators of paraoxon-inhibited
acetylcholinesterase. The results have
been evaluated in the light of predicted
complex-enzyme interactions based on
docking simulation studies.
Mono, bis and tris-cyclometalated osmium complexes react fast with peroxidase;
theoretical analysis by Monte Carlo simulations suggests a plausible reaction
pathway.
Contents
Gabriella Tamasi, Caterina Bernini,
Gianfranco Corbini, Natalie F. Owens,
Luigi Messori, Federica Scaletti,
Lara Massai, Pietro Lo Giudice, Renzo Cini
Two original ruthenium(III)–oxicam
complexes showed in vivo higher antiedema and lower undesired effects when
compared to free ligands.
Journal of Inorganic Biochemistry 134 (2014)
25–35
Synthesis, spectroscopic and DFT structural
characterization of two novel
ruthenium(III) oxicam complexes. In vivo
evaluation of anti-inflammatory and gastric
damaging activities
Zumira A. Carneiro, Juliana C. Biazzotto,
Anamaria D.P. Alexiou, Sofia Nikolaou
Journal of Inorganic Biochemistry 134 (2014)
36–38
Nitric oxide photorelease from a trinuclear
ruthenium nitrosyl complex and its in vitro
cytotoxicity against melanoma cells
Jesús E. de A. Bojórquez-Quintal,
Lucila A. Sánchez-Cach, Ángela Ku-González,
Cesar de los Santos-Briones,
María de Fátima Medina-Lara,
Ileana Echevarría-Machado,
José A. Muñoz-Sánchez,
S.M. Teresa Hernández Sotomayor,
Manuel Martínez Estévez
The [Ru3O(CH3COO)6(4-pic)2(NO)]PF6
triruthenium nitrosyl cluster (1) reduces
B16F10 melanoma cell viability up to
90% when irradiated with visible light
(λ = 532 nm). The solvated species
does not reduce cell viability at all,
demonstrating that 1 acts as a pro-drug
by delivering NO, the actual active
species.
Aluminum has differential effects on in
vitro primary root growth, nutrient
content and phospholipase C activity in
Coffea arabica seedlings.
Journal of Inorganic Biochemistry 134 (2014)
39–48
Differential effects of aluminum on in vitro
primary root growth, nutrient content and
phospholipase C activity in coffee seedlings
(Coffea arabica)
Dileep A.K. Vezzu, Qun Lu, Yan-Hua Chen,
Shouquan Huo
Journal of Inorganic Biochemistry 134 (2014)
49–56
Cytotoxicity of cyclometalated platinum
complexes based on tridentate NCN and
CNN-coordinating ligands: Remarkable
coordination dependence
Drastic difference in cytotoxicity was found
between isomeric platinum complexes
(N^C^N)PtCl and (C^N^N)PtCl. The
N^C^N-coordinated Pt complex demonstrated remarkably higher t against a series
of human lung cancer cells and a prostate
cancer cell, which was attributed to the
trans effect of the carbon donor in
N^C^N-coordinated complex.
v
vi
Orsolya Dömötör, Sabine Aicher,
Melanie Schmidlehner, Maria S. Novak,
Alexander Roller, Michael A. Jakupec,
Wolfgang Kandioller,
Christian G. Hartinger,
Bernhard K. Keppler, Éva A. Enyedy
Journal of Inorganic Biochemistry 134 (2014)
57–65
Antitumor pentamethylcyclopentadienyl
rhodium c om plexes of ma ltol and
allomaltol: Synthesis, solution speciation
and bioactivity
Emina Mrkalić, Ariadni Zianna,
George Psomas, Maria Gdaniec,
Agnieszka Czapik,
Evdoxia Coutouli-Argyropoulou,
Maria Lalia-Kantouri
Journal of Inorganic Biochemistry 134 (2014)
66–75
Synthesis, characterization, thermal and
DNA-binding properties of new zinc
complexes with 2-hydroxyphenones
Ana M. Plutín, Raúl Mocelo,
Anislay Alvarez, Raúl Ramos,
Eduardo E. Castellano, Marcia R. Cominetti,
Angelica E. Graminha, Antonio G. Ferreira,
Alzir A. Batista,
Journal of Inorganic Biochemistry 134 (2014)
76–82
Contents
RhIII(Cp*)(L)Cl complexes of hydroxypyrones were prepared under standard
and microwave conditions and their
antiproliferative activity was tested
against cancer cell lines. Stoichiometry
and stability of the complexes were
characterized by combination of different methods in aqueous solution and
formation of mono complexes with
moderate stability was found.
Zinc complexes of the formulae
[Zn(keto)2(H2O)2] and [Zn(keto)2(enR)]
with 2-hydroxyphenones (ketoH) and
N,N′-donor ligands (enR) have been
synthesized and characterized. The
complexes bind tightly to CT DNA probably by intercalation and compete with
ethidium bromide for the intercalation
site of DNA.
The synthesis, characterization and the
cytotoxicity of Pd(II) complexes of N,Ndisubstituted-N′-acyl thioureas against
DU-145 (human prostate cancer cells),
MDA-MB-231 (human breast cancer
cells) and the toxicity against the L929
cell line (health cell line from mouse) are
reported in this article.
On the cytotoxic activity of Pd(II) complexes
of N,N-disubstituted-N′-acyl thioureas
Olga Mazuryk, Monika Maciuszek,
Grażyna Stochel, Franck Suzenet,
Małgorzata Brindell
Journal of Inorganic Biochemistry 134 (2014)
83–91
2-Nitroimidazole-ruthenium polypyridyl
complex as a new conjugate for cancer
treatment and visualization
Ru(II) complex bearing two 4,7-diphenyl-1,10-phenanthroline ligands and
2,2′-bipyridine anchoring 2-nitroimidazole was designed towards its application
in treatment and visualization of cancer.
Contents
Radka Křikavová, Jan Hošek,
Pavel Suchý Jr., Ján Vančo,
Zdeněk Trávníček
Journal of Inorganic Biochemistry 134 (2014)
92–99
Diverse in vitro and in vivo anti-inflammatory
effects of trichlorido-gold(III) complexes with
N6-benzyladenine derivatives
Rabbab Oun, Jane A. Plumb, Nial J. Wheate
Journal of Inorganic Biochemistry 134 (2014)
100–105
Au(III) complexes of the type [Au(HL1–5)
Cl3]∙nH2O involving N6-benzyladenine
derivatives were prepared and fully characterized. They showed negligible in vitro
cytotoxicity, moderate in vitro anti-inflammatory activity on LPS-activated
THP-1 macrophages, and significant in
vivo anti-oedematous activity, even exceeding the activity of gold-containing
metallodrug Auranofin.
A hydrogel-based delivery system of
PVA and gelatin is more effective for
delivering cucurbit[7]uril encapsulated
cisplatin compared with the free drug in
human ovarian tumour xenografts.
A cisplatin slow-release hydrogel drug
delivery system based on a formulation of
the macrocycle cucurbit[7]uril, gelatin and
polyvinyl alcohol
I.E. León, N. Butenko, A.L. Di Virgilio,
C.I. Muglia, E.J. Baran, I.Cavaco,
S.B. Etcheverry
Journal of Inorganic Biochemistry 134 (2014)
106–117
Vanadium and cancer treatment: Antitumoral
mechanisms of three oxidovanadium(IV)
complexes on a human osteosarcoma cell line
Bioactivity of three oxovanadium(IV)
complexes with oxodiacetate (oda) (a
multiple oxygen donor) and intercalating
DNA related ligands: odabipy and odaphen, was evaluated in the human osteosarcoma cell line (MG-63). Cytotoxicity,
genotoxicity, and mechanisms of action
correlated with the chemical structures.
VO(oda)phen was the most potent antitumoral complex of this series.
Early Career Focused Review
Yao-Sheng Chen, Wen-I Luo,
Chung-Ling Yang, Yi-Jung Tu,
Chun-Wei Chang, Chih-Hsiang Chiang,
Chi-Yao Chang, Sunney I. Chan,
Steve S.-F. Yu
Journal of Inorganic Biochemistry 134 (2014)
118–133
Controlled oxidation of aliphatic C\H bonds
in metallo-monooxygenases: Mechanistic
insights derived from studies on deuterated
and fluorinated hydrocarbons
Deuterated and fluorinated hydrocarbon
substrates are deployed to probe the high
regio-specificity and unusual stereo-selectivity in the efficient substrate oxidization mediated by the high-valent metal
active sites in three metalloproteins:
particulate methane monooxygenase
(pMMO), alkane hydroxylase (AlkB) and
cytochrome P450 BM3.
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