Analysis of β-amino alcohols as inhibitors of the potential anti-tubercular target N-acetyltransferase
摘要:
The synthesis and inhibitory potencies of a novel series of beta-amino alcohols, based on the hit-compound 3-[3`-(4 ''-cyclopent-2```-en-1```-ylphenoxy)-2`-hydroxypropyl]-5,5 dimethylimidazolidine-2,4-dione as specific inhibitors of mycobacterial N-acetyltransferase (NAT) enzymes are reported. Effects of synthesised compounds on growth of Mycobacterium tuberculosis have been determined. (c) 2010 Elsevier Ltd. All rights reserved.
Analysis of β-amino alcohols as inhibitors of the potential anti-tubercular target N-acetyltransferase
摘要:
The synthesis and inhibitory potencies of a novel series of beta-amino alcohols, based on the hit-compound 3-[3`-(4 ''-cyclopent-2```-en-1```-ylphenoxy)-2`-hydroxypropyl]-5,5 dimethylimidazolidine-2,4-dione as specific inhibitors of mycobacterial N-acetyltransferase (NAT) enzymes are reported. Effects of synthesised compounds on growth of Mycobacterium tuberculosis have been determined. (c) 2010 Elsevier Ltd. All rights reserved.
Kumar, Surat; Rastogi, Shri Nivas, Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1983, vol. 22, # 7, p. 659 - 663
作者:Kumar, Surat、Rastogi, Shri Nivas
DOI:——
日期:——
KUMAR, SURAT;RASTOGI, SRI, NIVAS, INDIAN J. CHEM., 1983, 22, N 7, 59-663
作者:KUMAR, SURAT、RASTOGI, SRI, NIVAS
DOI:——
日期:——
Analysis of β-amino alcohols as inhibitors of the potential anti-tubercular target N-acetyltransferase
作者:Elizabeth Fullam、Areej Abuhammad、David L. Wilson、Matthew C. Anderton、Steve G. Davies、Angela J. Russell、Edith Sim
DOI:10.1016/j.bmcl.2010.12.099
日期:2011.2
The synthesis and inhibitory potencies of a novel series of beta-amino alcohols, based on the hit-compound 3-[3`-(4 ''-cyclopent-2```-en-1```-ylphenoxy)-2`-hydroxypropyl]-5,5 dimethylimidazolidine-2,4-dione as specific inhibitors of mycobacterial N-acetyltransferase (NAT) enzymes are reported. Effects of synthesised compounds on growth of Mycobacterium tuberculosis have been determined. (c) 2010 Elsevier Ltd. All rights reserved.