Literature DB >> 22297115

Inhibitors of acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). Part 1: Hit to lead evaluation of a novel arylsulfonamide series.

Oluyinka M Green1, Andrew R McKenzie, Adam B Shapiro, Ludovic Otterbein, Haihong Ni, Arthur Patten, Suzanne Stokes, Robert Albert, Sameer Kawatkar, Jason Breed.   

Abstract

A novel arylsulfonamide-containing series of compounds represented by 1, discovered by highthroughput screening, inhibit the acetyltransferase domain of N-acetylglucosamine-1-phosphate-uridyltransferase/glucosamine-1-phosphate-acetyltransferase (GlmU). X-ray structure determination confirmed that inhibitor binds at the site occupied by acetyl-CoA, indicating that series is competitive with this substrate. This letter documents our early hit-to-lead evaluation of the chemical series and some of the findings that led to improvement in in-vitro potency against Gram-negative and Gram-positive bacterial isozymes, exemplified by compound 40.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22297115     DOI: 10.1016/j.bmcl.2012.01.016

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  2 in total

1.  Structure of uridine diphosphate N-acetylglucosamine pyrophosphorylase from Entamoeba histolytica.

Authors:  Thomas E Edwards; Anna S Gardberg; Isabelle Q H Phan; Yang Zhang; Bart L Staker; Peter J Myler; Donald D Lorimer
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-04-21       Impact factor: 1.056

2.  Action of Dicumarol on Glucosamine-1-Phosphate Acetyltransferase of GlmU and Mycobacterium tuberculosis.

Authors:  Xiuyan Han; Changming Chen; Qiulong Yan; Liqiu Jia; Ayaz Taj; Yufang Ma
Journal:  Front Microbiol       Date:  2019-08-20       Impact factor: 5.640

  2 in total

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