Enhanced cytotoxicity of indenyl molybdenum(II) compounds bearing a thiophene function

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F19%3A39914740" target="_blank" >RIV/00216275:25310/19:39914740 - isvavai.cz</a>

Nalezeny alternativní kódy

RIV/00216208:11150/19:10396155 RIV/00216208:11310/19:10396155 RIV/00179906:_____/19:10396155

Výsledek na webu

<a href="https://pubs.rsc.org/en/content/articlelanding/2019/dt/c9dt01698h#!divAbstract" target="_blank" >https://pubs.rsc.org/en/content/articlelanding/2019/dt/c9dt01698h#!divAbstract</a>

DOI - Digital Object Identifier

<a href="http://dx.doi.org/10.1039/c9dt01698h" target="_blank" >10.1039/c9dt01698h</a>

Jazyk výsledku

angličtina

Název v původním jazyce

Enhanced cytotoxicity of indenyl molybdenum(II) compounds bearing a thiophene function

Popis výsledku v původním jazyce

A series of six indenyl molybdenum compounds bearing a thiophenyl function in the side chain were prepared and characterized by analytical and spectroscopic methods. The structures of [(eta(5)-C9H6CH2C4H3S)(eta(3)-C3H5)Mo(CO)(2)] and [(eta(5)-C9H6CH2C4H3S)Mo(CO)(2)(bpy)][BF4] were determined by single-crystal X-ray diffraction. The compounds bearing N,N-chelating ligands exhibit increased cytotoxic activity against human leukemia cell lines MOLT-4; up to two orders of magnitude lower IC50 values were observed compared to analogues with unsubstituted indenyl, which clearly demonstrates the strong effect of the indenyl ligand modification on the biological activity of the molybdenum(ii) compounds. The highest cytostatic potential was observed for the complex bearing 4,7-diphenyl-1,10-phenanthtoline [(eta(5)-C9H6CH2C4H3S)Mo(CO)(2)(Ph(2)phen)][BF4] with IC50 (MOLT-4) = 0.19 +/- 0.02 mu M. Detailed regulation of the molecular and cellular mechanism by this derivative was investigated on the lung carcinoma cell line A549 and compared with the lung fibroblast cell line MRC-5. Rather unusual differences in the effects on tumor and non-tumor cell lines provide a unique insight into the cytostatic action of molybdenum(ii) complexes.

Název v anglickém jazyce

Enhanced cytotoxicity of indenyl molybdenum(II) compounds bearing a thiophene function

Popis výsledku anglicky

A series of six indenyl molybdenum compounds bearing a thiophenyl function in the side chain were prepared and characterized by analytical and spectroscopic methods. The structures of [(eta(5)-C9H6CH2C4H3S)(eta(3)-C3H5)Mo(CO)(2)] and [(eta(5)-C9H6CH2C4H3S)Mo(CO)(2)(bpy)][BF4] were determined by single-crystal X-ray diffraction. The compounds bearing N,N-chelating ligands exhibit increased cytotoxic activity against human leukemia cell lines MOLT-4; up to two orders of magnitude lower IC50 values were observed compared to analogues with unsubstituted indenyl, which clearly demonstrates the strong effect of the indenyl ligand modification on the biological activity of the molybdenum(ii) compounds. The highest cytostatic potential was observed for the complex bearing 4,7-diphenyl-1,10-phenanthtoline [(eta(5)-C9H6CH2C4H3S)Mo(CO)(2)(Ph(2)phen)][BF4] with IC50 (MOLT-4) = 0.19 +/- 0.02 mu M. Detailed regulation of the molecular and cellular mechanism by this derivative was investigated on the lung carcinoma cell line A549 and compared with the lung fibroblast cell line MRC-5. Rather unusual differences in the effects on tumor and non-tumor cell lines provide a unique insight into the cytostatic action of molybdenum(ii) complexes.

Druh

J_imp - Článek v periodiku v databázi Web of Science

CEP obor

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OECD FORD obor

10402 - Inorganic and nuclear chemistry

Projekt

—

Návaznosti

I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Rok uplatnění

2019

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Dalton Transactions

ISSN

1477-9226

e-ISSN

—

Svazek periodika

48

Číslo periodika v rámci svazku

30

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

13

Strana od-do

11361-11373

Kód UT WoS článku

000477957200019

EID výsledku v databázi Scopus

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