Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/74014
Type: Artigo de periódico
Title: Synthesis and antitumor activity of beta-carboline 3-(substituted-carbohydrazide) derivatives
Author: Barbosa, VA
Formagio, ASN
Savariz, FC
Foglio, MA
Spindola, HM
de Carvalho, JE
Meyer, E
Sarragiotto, MH
Abstract: A series of beta-carboline derivatives bearing a substituted-carbohydrazide moiety at C-3 were synthesized and evaluated for their antitumor activity against eight human cancer cell lines. The beta-carboline N-(substituted-benzylidene)carbohydrazides showed, in general, a greater antitumor activity than their N-(alkylidene)carbohydrazide analogues. The N-9-methylation of beta-carboline N-(substituted-benzylidene) carbohydrazides resulted in a decrease of antitumor activity. Among compounds tested, the benzylidene-carbohydrazides 3, 4, 11, 13, 16, 21 and 22 were the most active, possessing IC50 less than 10 mu M for six of the eight tumor cell lines assayed. The derivative 4 displayed the most significant activity toward all tested cell lines, with a remarkable cytotoxicity against renal (786-0) cell lines (IC50 = 0.04 mu M). Compound 4 was assayed for its in vivo antineoplastic activity in the Ehrlich solid carcinoma assay. (C) 2011 Elsevier Ltd. All rights reserved.
Subject: beta-Carboline derivatives
Carbohydrazides
Antitumor activity
Ehrlich tumor
Country: Inglaterra
Editor: Pergamon-elsevier Science Ltd
Rights: fechado
Identifier DOI: 10.1016/j.bmc.2011.08.059
Date Issue: 2011
Appears in Collections:Artigos e Materiais de Revistas Científicas - Unicamp

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