2014-07-18T11:58:36Z
2014-07-18T11:58:36Z
2008-09-03
2014-07-18T11:58:37Z
Several analogs of the cytotoxic thiopeptide IB-01211 or Mechercharmycin A (1) have been synthetized. The cytotoxicity of 1 and the synthetized analogs was evaluated against a panel of three human tumor cell lines. Thiopeptide 1 and the most active derivatives, 2 and 3c, were chosen for further studies like effects on cell cycle progression and induction of apoptosis. Interestingly, the inhibition of cell division and activation of a programmed cell death by apoptosis was detected.
Article
Accepted version
English
Compostos heterocíclics; Medicaments antineoplàstics; Síntesi de pèptids; Espectroscòpia de ressonància magnètica nuclear; Heterocyclic compounds; Antineoplastic agents; Peptide synthesis; Nuclear magnetic resonance spectroscopy
American Chemical Society
Versió postprint del document publicat a: http://dx.doi.org/10.1021/jm800513w
Journal of Medicinal Chemistry, 2008, vol. 51, num. 18, p. 5722-5730
http://dx.doi.org/10.1021/jm800513w
(c) American Chemical Society , 2008