Evaluation of N-(phenylmethyl)-4-[5-(phenylmethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridin-4-yl]benzamide inhibitors of Mycobacterium tuberculosis growth

被引:22
|
作者
Wall, Michael D.
Oshin, Michael
Chung, Gavin A. C.
Parkhouse, Tony
Gore, Andrea
Herreros, Esperanza
Cox, Brian
Duncan, Ken
Evans, Brian
Everett, Martin
Mendoza, Alfonso
机构
[1] GlaxoSmithKline, Med Res Ctr, Stevenage SG1 2NY, Herts, England
[2] GlaxoSmithKline, Harlow CM19 5AW, Essex, England
[3] GlaxoSmithKline, E-28760 Madrid, Spain
关键词
Mycobacterium tuberculosis; imidazopiperidines; InhA;
D O I
10.1016/j.bmcl.2007.02.078
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The biological evaluation of imidazopiperidines as FAS II inhibitors of Mycobacterium tuberculosis growth has been carried out with a view to assessment of potential as lead compounds for the development of a new TB drug. A summary of the hit evaluation and current challenges is described herein. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2740 / 2744
页数:5
相关论文
共 50 条
  • [21] 4-(4-Fluorophenyl)-1-phenyl-3-(pyridin-4-yl)-1H-pyrazol-5-amine
    Abu Thaher, Bassam
    Koch, Pierre
    Schollmeyer, Dieter
    Laufer, Stefan
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O632 - U1589
  • [22] 1-{4-[(1-Isobutyl-1H-imidazo[4,5-c]quinolin-4yl)amino]phenyl}ethanone
    Dinesha
    Viveka, Shivapura
    Laxmeshwar, Sandeep S.
    Nagaraja, Gundibasappa Karikannar
    MOLBANK, 2012, (04)
  • [23] 3-Ethyl-5-(4-methoxyphenoxy)-2-(pyridin-4-yl)-3H-imidazo[4,5-b]pyridine
    Ranjith, S.
    SubbiahPandi, A.
    Suresh, A. D.
    Pitchumani, K.
    ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE, 2011, 67 : O1764 - U1337
  • [25] 4-(4-Fluorophenyl)-1-(4-nitrophenyl)3-(pyridin-4-yl)-1H-pyrazol-5-amine
    Abu Thaher, Bassam
    Koch, Pierre
    Schollmeyer, Dieter
    Laufer, Stefan
    ACTA CRYSTALLOGRAPHICA SECTION E-CRYSTALLOGRAPHIC COMMUNICATIONS, 2012, 68 : O633 - U1597
  • [26] Design, Synthesis and Antifungal Evaluation of N-Substituted-1-(3-chloropyridin-2-yl)-N-(pyridin-4-yl)-5-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives
    Wu, Zhibing
    Yang, Guangqian
    Zhao, Xin
    Wu, Jiangchun
    Wu, Shixi
    JOURNAL OF HETEROCYCLIC CHEMISTRY, 2019, 56 (01) : 234 - 238
  • [27] Enantioselective synthesis of 4,5,6,7-tetrahydro-4-oxo-benzofuran-5-yl acetate and 1-benzyl-4,5,6,7-tetrahydro-4-oxo-1(H)-indol-5-yl acetate using chemoenzymatic methods
    Demir, Ayhan S.
    Caliskan, Zerrin
    Sahin, Ertan
    JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC, 2007, 44 (3-4) : 87 - 92
  • [28] Anti-oxidant activity of 1-(1H-imidazo[4,5-c]pyridin-4-yl)ethenone, a Maillard reaction product derived from fructose and histidine
    Zhao, Kangyu
    Long, Xin
    Li, Junle
    Wang, Ying
    Lan, Ping
    Wang, Yong
    JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, 2024,
  • [29] Crystal structure of 1-(thiazolo[4,5-c]pyridin-2-yl)hydrazine, C6H6N4S
    Zhang, Yu
    ZEITSCHRIFT FUR KRISTALLOGRAPHIE-NEW CRYSTAL STRUCTURES, 2014, 229 (03): : 231 - 232
  • [30] 6-Phenyl-1H-imidazo[4,5-c]pyridine-4-carbonitrile as cathepsin S inhibitors
    Cai, Jiaqiang
    Baugh, Mark
    Black, Darcey
    Long, Clive
    Bennett, D. Jonathan
    Dempster, Maureen
    Fradera, Xavier
    Gillespie, Jonathan
    Andrews, Fiona
    Boucharens, Sylviane
    Bruin, John
    Cameron, Kenneth S.
    Cumming, Iain
    Hamilton, William
    Jones, Philip S.
    Kaptein, Allard
    Kinghorn, Emma
    Maidment, Maurice
    Martin, Iain
    Mitchell, Ann
    Rankovic, Zoran
    Robinson, John
    Scullion, Paul
    Uitdehaag, Joost C. M.
    Vink, Paul
    Westwood, Paul
    van Zeeland, Mario
    van Berkom, Leon
    Bastiani, Martijn
    Meulemans, Tommi
    BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2010, 20 (15) : 4350 - 4354