Synthesis and antitumor activity of mechercharmycin A analogues


Autoria(s): Hernández, Delia; Altuna, Marta; Cuevas, Carmen; Aligué i Alemany, Rosa Maria; Albericio Palomera, Fernando; Álvarez Domingo, Mercedes
Contribuinte(s)

Universitat de Barcelona

Resumo

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.

Identificador

http://hdl.handle.net/2445/56045

Idioma(s)

eng

Publicador

American Chemical Society

Direitos

(c) American Chemical Society , 2008

info:eu-repo/semantics/openAccess

Palavras-Chave #Compostos heterocíclics #Medicaments antineoplàstics #Síntesi de pèptids #Espectroscòpia de ressonància magnètica nuclear #Heterocyclic compounds #Antineoplastic agents #Peptide synthesis #Nuclear magnetic resonance spectroscopy
Tipo

info:eu-repo/semantics/article

info:eu-repo/semantics/acceptedVersion