Synthesis and antitumor activity of mechercharmycin A analogues

Fecha de publicación

2014-07-18T11:58:36Z

2014-07-18T11:58:36Z

2008-09-03

2014-07-18T11:58:37Z

Resumen

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.

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Artículo


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Inglés

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American Chemical Society

Documentos relacionados

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

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(c) American Chemical Society , 2008

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