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Cyclopentadienyl‐Based Anticancer Drugs: Improvement of Cytotoxic Activity through Functionalisation of the π Ligand
Author(s) -
Absolonová Monika,
Melounková Lucie,
Vinklárek Jaromír,
Honzíček Jan,
Dostál Libor,
Mrózek Ondřej
Publication year - 2021
Publication title -
chemmedchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.817
H-Index - 100
eISSN - 1860-7187
pISSN - 1860-7179
DOI - 10.1002/cmdc.202100060
Subject(s) - cyclopentadienyl complex , cytotoxic t cell , ligand (biochemistry) , chemistry , combinatorial chemistry , pharmacology , stereochemistry , medicine , biochemistry , receptor , in vitro , catalysis
Abstract Cytotoxic complexes containing molybdenum are widely studied as a potential substitution for commercially used drugs that often suffer from pronounced side effects and cellular resistance. Compounds of the type [(η 5 ‐Cp′)Mo(CO) 2 ( N , N L)][BF 4 ], where Cp is cyclopentadienyl and N , N L is a bidentate ligand, are well known for their strong anticancer activity. It is a generally accepted paradigm that the nature of the coordinated N , N L ligand has a major impact on the cytotoxicity. In this study, a series of new functionalised Cp complexes of molybdenum was synthesised from derivatised fulvenes as π‐ligand precursors. Indeed, the coordination sphere‘s modulation by various N , N ‐chelating ligands afforded species active toward leukemic cell line MOLT‐4 with IC 50 values depending on the character of the N , N ‐chelator used. However, following study clearly showed that functionalisation of the Cp ring with an amine moiety considerably improved cytotoxicity. These results are of crucial importance for the future design of highly active cytotoxic drugs, as modification of cyclopentadienyl is believed to have a minor effect on biological activity.