Quinoxaline chemistry. Part 13: 3-carboxy-2-benzylamino substituted quinoxalines and N-[4-[(3-carboxyquinoxalin-2-yl) aminomethyl]benzoyl]-L-glutamates: synthesis and evaluation of in vitro anticancer activity

Citation
P. Corona et al., Quinoxaline chemistry. Part 13: 3-carboxy-2-benzylamino substituted quinoxalines and N-[4-[(3-carboxyquinoxalin-2-yl) aminomethyl]benzoyl]-L-glutamates: synthesis and evaluation of in vitro anticancer activity, FARMACO, 55(2), 2000, pp. 77-86
Citations number
11
Categorie Soggetti
Pharmacology & Toxicology
Journal title
FARMACO
ISSN journal
0014827X → ACNP
Volume
55
Issue
2
Year of publication
2000
Pages
77 - 86
Database
ISI
SICI code
0014-827X(200002)55:2<77:QCP13S>2.0.ZU;2-U
Abstract
Among a new series of 28 3-carboxy or carbethoxy quinoxalines bearing a sub stituted benzylamino or N-[4-(aminomethyl)benzoyl]glutamate group on positi on 2 of the ring and various substituents at C-6, 7 positions, 21 were sele cted at the National Cancer Institute for evaluation of their in vitro anti cancer activity. The results obtained seem to confirm that the carboxy or c arbethoxy group on position 3 is not helpful, with a few exceptions, for th e anticancer activity. (C) 2000 Elsevier Science S.A. All rights reserved.