Premium
Synthesis and Biological Evaluation of α‐Tubulin‐Binding Pironetin Analogues with Enhanced Lipophilicity
Author(s) -
Carda Miguel,
Murga Juan,
DíazOltra Santiago,
GarcíaPla Jorge,
Paños Julián,
Falomir Eva,
Trigili Chiara,
Díaz J. Fernando,
Barasoain Isabel,
Marco J. Alberto
Publication year - 2013
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201201283
Subject(s) - chemistry , lipophilicity , stereocenter , stereochemistry , tubulin , mechanism of action , cytotoxic t cell , oligopeptide , mechanism (biology) , side chain , biological activity , pyrone , combinatorial chemistry , in vitro , microtubule , biochemistry , enantioselective synthesis , peptide , organic chemistry , philosophy , polymer , epistemology , microbiology and biotechnology , biology , catalysis
Abstract Four new lipophilic analogues of the natural pyrone pironetin have been prepared. The C 9 side‐chain of the latter has been replaced in one analogue by a 4‐phenylbutyl chain and in the other three analogues by C 13 or C 16 aliphatic chains, all of them bearing two stereogenic centres. Their cytotoxic activities and interactions with tubulin have been investigated. It was found that all four are cytotoxic towards two either sensitive or resistant tumoral cell lines with similar IC 50 values in each case, which indicates that, like the parent natural compound, they also display a covalent mechanism of action. However, one of them operates in all likelihood through a mechanism very similar to pironetin, whereas the other three seem to operate through a different mechanism.