Tuberculosis drug discovery: A decade of hit assessment for defined targets

S Oh, L Trifonov, VD Yadav, CE Barry III… - Frontiers in Cellular …, 2021 - frontiersin.org
More than two decades have elapsed since the publication of the first genome sequence of
Mycobacterium tuberculosis (Mtb) which, shortly thereafter, enabled methods to determine …

Drug-resistance in Mycobacterium tuberculosis: where we stand

A Mabhula, V Singh - Medchemcomm, 2019 - pubs.rsc.org
Tuberculosis (TB), an infectious disease caused by the bacterium Mycobacterium
tuberculosis (Mtb), has burdened vulnerable populations in modern day societies for …

Ullmann‐Ma Reaction: Development, Scope and Applications in Organic Synthesis

Q Cai, W Zhou - Chinese Journal of Chemistry, 2020 - Wiley Online Library
Copper‐catalyzed cross‐couplings of aryl halides and nucleophiles, traditionally called
Ullmann‐type coupling reactions, were initially reported by Ullmann et al. from 1901—1929 …

Recent advancements and developments in search of anti-tuberculosis agents: a quinquennial update and future directions

TM Dhameliya, KA Bhakhar, ND Gajjar, KA Patel… - Journal of Molecular …, 2022 - Elsevier
Tuberculosis (TB) has been considered as the highly chronic, contagious and infectious
disorder caused by Mycobacterium tuberculosis (Mtb). Every year more than 10 million …

A novel reversible oxazole-based NIR fluorescent probe for Cu2+ and S2− ions detection

H Mei, C Yang, X Yang, Z Huang, P Cheng… - Journal of Molecular …, 2022 - Elsevier
In this study, we reported a novel oxazole-based NIR probe for the detection of Cu 2+ and S
2− ions sequentially in buffer solution. The probe showed a" turn-off" fluorescent response …

[HTML][HTML] An insight into the discovery, clinical studies, compositions, and patents of macozinone: A drug targeting the DprE1 enzyme of Mycobacterium tuberculosis

M Imran, SA Khan, SMB Asdaq, M Almehmadi… - Journal of Infection and …, 2022 - Elsevier
Abstract Decaprenyl-phosphoryl-ribose 2′-epimerase (DprE1) inhibitors are an innovative
and futuristic orally active group of antituberculosis agents. A few DprE1 inhibitors are in the …

Discovery of GuaB inhibitors with efficacy against Acinetobacter baumannii infection

EM Kofoed, I Aliagas, T Crawford, J Mao, SF Harris… - MBio, 2024 - journals.asm.org
Guanine nucleotides are required for growth and viability of cells due to their structural role
in DNA and RNA, and their regulatory roles in translation, signal transduction, and cell …

Evaluation of activity of some 2, 5-disubstituted benzoxazole derivatives against acetylcholinesterase, butyrylcholinesterase and tyrosinase: ADME prediction, DFT …

I Celik, M Erol, O Temiz Arpaci… - Polycyclic Aromatic …, 2022 - Taylor & Francis
In this study, p-tert-butyl at position 2 and acetamide bridged 4-substituted
piperazine/piperidine at position 5 bearing benzoxazole derivatives were evaluated for their …

Deciphering the allosteric regulation of mycobacterial inosine-5′-monophosphate dehydrogenase

O Bulvas, Z Knejzlík, J Sýs, A Filimoněnko… - Nature …, 2024 - nature.com
Allosteric regulation of inosine 5′-monophosphate dehydrogenase (IMPDH), an essential
enzyme of purine metabolism, contributes to the homeostasis of adenine and guanine …

Identification of nitrofuranylchalcone tethered benzoxazole-2-amines as potent inhibitors of drug resistant Mycobacterium tuberculosis demonstrating bactericidal …

SK Sahoo, S Maddipatla, SNR Gajula… - Bioorganic & Medicinal …, 2022 - Elsevier
Ever increasing drug resistance has become an impeding threat that continues to hamper
effective tackling of otherwise treatable tuberculosis (TB). Such dismal situation necessitates …