Efforts towards the development of new antitubercular agents: Potential for thiolactomycin based compounds

被引:26
作者
Kamal, Ahmed [1 ]
Azeeza, Shaik [1 ]
Malik, M. Shaheer [1 ]
Shaik, Ahmad Ali [1 ]
Rao, Maddamsetty V. [1 ]
机构
[1] Indian Inst Chem Technol, Div Organ Chem, Biol Chem Lab, Hyderabad 500007, Andhra Pradesh, India
关键词
D O I
10.18433/J36K5K
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Development of new chemotherapeutic drugs is the need of the hour to improve tuberculosis control, particularly in the developing world. In the last fourty years no new compound has been brought to the market for the treatment of tuberculosis. However, in recent years there is an enhanced activity in the research and development of new drugs for TB. Some compounds are presently in clinical development, while others are being investigated pre-clinically in an attempt to explore new molecules for the target based treatment of TB. Simultaneously some new targets are being identified and validated for their practical usefulness. Structures based on thiolactomycin could have considerable potential in the development of target based anti-TB agents. The present review provides an overview of the drugs that are being clinically used and the compounds that are in advanced stages of clinical as well as preclinical studies. We have also attempted to highlight the efforts that are being made in the development of new molecules based on thiolactomycin as lead compound, including studies from this laboratory.
引用
收藏
页码:56 / 80
页数:25
相关论文
共 156 条
[1]  
AMALIO T, 2000, DRUGS, V59, P171
[2]  
Amaral Leonard, 2004, In Vivo (Attiki), V18, P725
[3]   A diarylquinoline drug active on the ATP synthase of Mycobacterium tuberculosis [J].
Andries, K ;
Verhasselt, P ;
Guillemont, J ;
Göhlmann, HWH ;
Neefs, JM ;
Winkler, H ;
Van Gestel, J ;
Timmerman, P ;
Zhu, M ;
Lee, E ;
Williams, P ;
de Chaffoy, D ;
Huitric, E ;
Hoffner, S ;
Cambau, E ;
Truffot-Pernot, C ;
Lounis, N ;
Jarlier, V .
SCIENCE, 2005, 307 (5707) :223-227
[4]  
[Anonymous], 2008, GLOBAL TUBERCULOSIS, P51
[5]   INVITRO AND INVIVO ACTIVITIES OF THE NITROIMIDAZOLE CGI-17341 AGAINST MYCOBACTERIUM-TUBERCULOSIS [J].
ASHTEKAR, DR ;
COSTAPERIRA, R ;
NAGRAJAN, K ;
VISHVANATHAN, N ;
BHATT, AD ;
RITTEL, W .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1993, 37 (02) :183-186
[6]   The eukaryotic-like Ser/Thr protein kinases of Mycobacterium tuberculosis [J].
Av-Gay, Y ;
Everett, M .
TRENDS IN MICROBIOLOGY, 2000, 8 (05) :238-244
[7]   9-benzylpurines with inhibitory activity against Mycobacterium tuberculosis [J].
Bakkestuen, AK ;
Gundersen, LL ;
Langli, G ;
Liu, FS ;
Nolsoe, JMJ .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2000, 10 (11) :1207-1210
[8]   INHA, A GENE ENCODING A TARGET FOR ISONIAZID AND ETHIONAMIDE IN MYCOBACTERIUM-TUBERCULOSIS [J].
BANERJEE, A ;
DUBNAU, E ;
QUEMARD, A ;
BALASUBRAMANIAN, V ;
UM, KS ;
WILSON, T ;
COLLINS, D ;
DELISLE, G ;
JACOBS, WR .
SCIENCE, 1994, 263 (5144) :227-230
[9]   New horizons in the treatment of tuberculosis [J].
Barry, CE .
BIOCHEMICAL PHARMACOLOGY, 1997, 54 (11) :1165-1172
[10]   Use of genomics and combinatorial chemistry in the development of new antimycobacterial drugs [J].
Barry, CE ;
Slayden, RA ;
Sampson, AE ;
Lee, RE .
BIOCHEMICAL PHARMACOLOGY, 2000, 59 (03) :221-231