» Articles » PMID: 22421275

Tuberculosis: the Drug Development Pipeline at a Glance

Overview
Journal Eur J Med Chem
Specialty Chemistry
Date 2012 Mar 17
PMID 22421275
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Tuberculosis is a major disease causing every year 1.8 million deaths worldwide and represents the leading cause of mortality resulting from a bacterial infection. Introduction in the 60's of first-line drug regimen resulted in the control of the disease and TB was perceived as defeating. However, since the progression of HIV leading to co-infection with AIDS and the emergence of drug resistant strains, the need of new anti-tuberculosis drugs was not overstated. However in the past 40 years any new molecule did succeed in reaching the market. Today, the pipeline of potential new treatments has been fulfilled with several compounds in clinical trials or preclinical development with promising activities against sensitive and resistant Mycobacterium tuberculosis strains. Compounds as gatifloxacin, moxifloxacin, metronidazole or linezolid already used against other bacterial infections are currently evaluated in clinical phases 2 or 3 for treating tuberculosis. In addition, analogues of known TB drugs (PA-824, OPC-67683, PNU-100480, AZD5847, SQ609, SQ109, DC-159a) and new chemical entities (TMC207, BTZ043, DNB1, BDM31343) are under development. In this review, we report the chemical synthesis, mode of action when known, in vitro and in vivo activities and clinical data of all current small molecules targeting tuberculosis.

Citing Articles

Pretomanid for tuberculosis treatment: an update for clinical purposes.

Occhineri S, Matucci T, Rindi L, Tiseo G, Falcone M, Riccardi N Curr Res Pharmacol Drug Discov. 2022; 3:100128.

PMID: 36105740 PMC: 9461242. DOI: 10.1016/j.crphar.2022.100128.


Exploration of 4-aminopyrrolo[2,3-d]pyrimidine as antitubercular agents.

Jesumoroti O, Beteck R, Jordaan A, Warner D, Legoabe L Mol Divers. 2022; 27(2):753-765.

PMID: 35598185 PMC: 9124159. DOI: 10.1007/s11030-022-10453-1.


Identification of a new series of benzothiazinone derivatives with excellent antitubercular activity and improved pharmacokinetic profiles.

Xiong L, Gao C, Shi Y, Tao X, Rong J, Liu K RSC Adv. 2022; 8(20):11163-11176.

PMID: 35541526 PMC: 9078972. DOI: 10.1039/c8ra00720a.


Chemical Classes Presenting Novel Antituberculosis Agents Currently in Different Phases of Drug Development: A 2010-2020 Review.

Angula K, Legoabe L, Beteck R Pharmaceuticals (Basel). 2021; 14(5).

PMID: 34068171 PMC: 8152995. DOI: 10.3390/ph14050461.


Structure-based drug design, synthesis and screening of MmaA1 inhibitors as novel anti-TB agents.

Veeravarapu H, Malkhed V, Mustyala K, Vadija R, Malikanti R, Vuruputuri U Mol Divers. 2020; 25(1):351-366.

PMID: 32533514 DOI: 10.1007/s11030-020-10107-0.