Mechanisms of action and therapeutic efficacies of the lipophilic antimycobacterial agents clofazimine and bedaquiline

MC Cholo, MT Mothiba, B Fourie… - Journal of Antimicrobial …, 2016 - academic.oup.com
Abstract Drug-resistant (DR)-TB is the major challenge confronting the global TB control
programme, necessitating treatment with second-line anti-TB drugs, often with limited …

The mur enzymes chink in the armour of Mycobacterium tuberculosis cell wall

Y Shinde, I Ahmad, S Surana, H Patel - European Journal of Medicinal …, 2021 - Elsevier
Tuberculosis (TB) transmitted by Mycobacterium tuberculosis (Mtb) is one of the top 10
causes of death globally. Currently, the widespread occurrence of resistance toward Mtb …

[HTML][HTML] Prevalence of Mycobacterium tuberculosis resistant to bedaquiline and delamanid in China

W He, C Liu, D Liu, A Ma, Y Song, P He, J Bao… - Journal of global …, 2021 - Elsevier
Objectives The new antituberculous drugs delamanid and bedaquiline form the last line of
defence against drug-resistant tuberculosis (TB). Understanding the background prevalence …

Structural Simplification of Bedaquiline: the Discovery of 3‐(4‐(N,N‐Dimethylaminomethyl)phenyl)quinoline‐Derived Antitubercular Lead Compounds

C He, L Preiss, B Wang, L Fu, H Wen, X Zhang… - …, 2017 - Wiley Online Library
Bedaquiline (BDQ) is a novel and highly potent last‐line antituberculosis drug that was
approved by the US FDA in 2013. Owing to its stereo‐structural complexity, chemical …

Routes of Synthesis of Carbapenems for Optimizing Both the Inactivation of l,d-Transpeptidase LdtMt1 of Mycobacterium tuberculosis and the Stability toward …

L Iannazzo, D Soroka, S Triboulet… - Journal of Medicinal …, 2016 - ACS Publications
Combinations of β-lactams of the carbapenem class, such as meropenem, with clavulanate,
a β-lactamase inhibitor, are being evaluated for the treatment of drug-resistant tuberculosis …

Bedaquiline, Delamanid, Linezolid, Clofazimine, and Capreomycin MIC Distributions for Drug Resistance Mycobacterium tuberculosis in Shanghai, China

Y Guo, J Yang, W Wang, X Wu, B Wan… - Infection and Drug …, 2023 - Taylor & Francis
Background New antituberculosis drugs have recently been approved for the treatment of
multidrug-resistant tuberculosis TB (MDR-TB). We aimed to describe the distributions of …

[HTML][HTML] Identification of novel benzoxa-[2, 1, 3]-diazole substituted amino acid hydrazides as potential anti-tubercular agents

AK Brown, AKB Aljohani, JH Gill, PG Steel, JD Sellars - Molecules, 2019 - mdpi.com
Discovery and development of new therapeutic options for the treatment of Mycobacterium
tuberculosis (Mtb) infection are desperately needed to tackle the continuing global burden of …

A highly efficient way to recycle inactive stereoisomers of Bedaquiline into two previous intermediates via base-catalyzed Csp3Csp3 bond cleavage

DL Kong, Y Huang, LY Ren, WH Feng - Chinese Chemical Letters, 2015 - Elsevier
Bedaquiline is a new medicine for pulmonary multi-drug resistant tuberculosis (MDR-TB),
which is a pure enantiomer with two chiral centers. The current industrial preparation …

贝达喹啉治疗耐多药结核病安全性与有效性的系统评价.

牛瑞青, 于珊珊, 付萌萌, 刘丽萍… - Evaluation & Analysis …, 2018 - search.ebscohost.com
摘要目的: 评价贝达喹啉治疗耐多药结核病的疗效与安全性. 方法: 计算机检索PubMed,
EMBase, the Cochrane Library, 维普数据库, 中国期刊全文数据库及万方数据库 …

Design, synthesis and biological evaluation of anti-tuberculosis agents based on bedaquiline structure

C Wu, J Luo, M Wu, F Meng, Z Cai, Y Chen… - Medicinal …, 2020 - ingentaconnect.com
Background: Bedaquiline is a novel anti-tuberculosis drug that inhibits Mycobacterial ATP
synthase. However, studies have found that bedaquiline has serious side effects due to high …