2,5-bis(3′-Indolyl)pyrroles, analogues of the marine alkaloid nortopsentin, were conveniently prepared through a three step procedure in good overall yields. Derivatives 1a and 1b exhibited concentration-dependent antitumor activity towards a panel of 42 human tumor cell lines with mean IC50 values of 1.54 μM and 0.67 μM, respectively. Investigating human tumor xenografts in an ex-vivo clonogenic assay revealed selective antitumor activity, whereas sensitive tumor models were scattered among various tumor histotypes.

Carbone, A., Parrino, B., Barraja, P., Spanò, V., Cirrincione, G., Diana, P., et al. (2013). Synthesis and Antiproliferative Activity of 2,5-bis(3′-Indolyl)pyrroles, Analogues of the Marine Alkaloid Nortopsentin. MARINE DRUGS, 11, 643-654 [10.3390/md11030643].

Synthesis and Antiproliferative Activity of 2,5-bis(3′-Indolyl)pyrroles, Analogues of the Marine Alkaloid Nortopsentin

CARBONE, Anna;PARRINO, Barbara;BARRAJA, Paola;SPANO', Virginia;CIRRINCIONE, Girolamo;DIANA, Patrizia;
2013-01-01

Abstract

2,5-bis(3′-Indolyl)pyrroles, analogues of the marine alkaloid nortopsentin, were conveniently prepared through a three step procedure in good overall yields. Derivatives 1a and 1b exhibited concentration-dependent antitumor activity towards a panel of 42 human tumor cell lines with mean IC50 values of 1.54 μM and 0.67 μM, respectively. Investigating human tumor xenografts in an ex-vivo clonogenic assay revealed selective antitumor activity, whereas sensitive tumor models were scattered among various tumor histotypes.
2013
Settore CHIM/08 - Chimica Farmaceutica
Carbone, A., Parrino, B., Barraja, P., Spanò, V., Cirrincione, G., Diana, P., et al. (2013). Synthesis and Antiproliferative Activity of 2,5-bis(3′-Indolyl)pyrroles, Analogues of the Marine Alkaloid Nortopsentin. MARINE DRUGS, 11, 643-654 [10.3390/md11030643].
File in questo prodotto:
File Dimensione Formato  
marinedrugs2013.pdf

Solo gestori archvio

Dimensione 543.72 kB
Formato Adobe PDF
543.72 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10447/72063
Citazioni
  • ???jsp.display-item.citation.pmc??? 20
  • Scopus 72
  • ???jsp.display-item.citation.isi??? 70
social impact