Journal of medicinal chemistry

Potential inhibitors of L-asparagine biosynthesis. 4. Substituted sulfonamide and sulfonylhydrazide analogs of L-asparagine

S Brynes, GJ Burckart, M Mokotoff

Index: Brynes,S. et al. Journal of Medicinal Chemistry, 1978 , vol. 21, p. 45 - 49

Full Text: HTML

Citation Number: 16

Abstract

Several N-substituted sulfonamides and"-substituted sulfonylhydrazides have been prepared as sulfur analogues of L-asparagine with the potential of acting as inhibitors of L- asparagine synthetase (ASase, from Novikoff hepatoma). L-Cystine was converted in known steps to N-carboxy-3-(sulfonylchloro)-~-alanine dibenzyl ester (1). Condensation of 1 with 0- benzylhydroxylamine, p-(fluorosulfonyl) benzylamine, or monoethyl fumarylhydrazide (S), ...

Related Articles:

A new procedure for preparation of carboxylic acid hydrazides

[Zhang, Xini; Breslav, Michael; Grimm, Jeffrey; Guan, Kailin; Huang, Aihua; Liu, Fuqiang; Maryanoff, Cynthia A.; Palmer, David; Patel, Mitul; Qian, Yun; Shaw, Charles; Sorgi, Kirk; Stefanick, Stephen; Xu, Dawei Journal of Organic Chemistry, 2002 , vol. 67, # 26 p. 9471 - 9474]

More Articles...