Triazole derivatives and their anti-tubercular activity

S Zhang, Z Xu, C Gao, QC Ren, L Chang, ZS Lv… - European journal of …, 2017 - Elsevier
Tuberculosis (TB) remains one of the most widespread and leading deadliest diseases,
threats one-third of the world's population. Although numerous efforts have been undertaken …

Recent researches in triazole compounds as medicinal drugs

CH Zhou, Y Wang - Current medicinal chemistry, 2012 - ingentaconnect.com
Triazole compounds containing three nitrogen atoms in the five-membered aromatic azole
ring are readily able to bind with a variety of enzymes and receptors in biological system via …

Recent advances of imidazole-containing derivatives as anti-tubercular agents

YL Fan, XH Jin, ZP Huang, HF Yu, ZG Zeng… - European journal of …, 2018 - Elsevier
Tuberculosis still remains one of the most common, communicable, and leading deadliest
diseases known to mankind throughout the world. Drug-resistance in Mycobacterium …

Indole derivatives as anti-tubercular agents: An overview on their synthesis and biological activities

GS Reddy, M Pal - Current Medicinal Chemistry, 2021 - ingentaconnect.com
Background: The indole framework is considered as one of the privileged structures in the
area of medicinal chemistry and drug discovery because compounds containing this …

Indole-based hydrazide-hydrazones and 4-thiazolidinones: synthesis and evaluation as antitubercular and anticancer agents

G Cihan-Üstündağ, D Şatana, G Özhan… - Journal of Enzyme …, 2016 - Taylor & Francis
A new series of indolylhydrazones (6) and indole-based 4-thiazolidinones (7, 8) have been
designed, synthesized and screened for in vitro antitubercular activity against …

Contribution of N‐heterocycles towards anti‐tubercular drug discovery (2014–2019); predicted and reengineered molecular frameworks

D Atukuri, R Gunjal, N Holagundi… - Drug Development …, 2021 - Wiley Online Library
Tuberculosis is an infectious disease caused by Mycobacterium tuberculosis, responsible
for high death frequency every year all over the world. In this regard, efficient drug‐design …

Click chemistry based regioselective one‐pot synthesis of coumarin‐3‐yl‐methyl‐1,2,3‐triazolyl‐1,2,4‐triazol‐3(4H)‐ones as newer potent antitubercular agents

SM Somagond, RR Kamble… - Archiv der …, 2019 - Wiley Online Library
Abstract Coumarin‐3‐yl‐methyl‐1, 2, 3‐triazolyl‐1, 2, 4‐triazol‐3 (4H)‐ones (8k‐z) were
synthesized via copper (I)‐catalyzed azide‐alkyne cycloaddition click chemistry. The …

Recent advances in the design and synthesis of heterocycles as anti-tubercular agents

PMS Chauhan, N Sunduru… - Future Medicinal Chemistry, 2010 - Taylor & Francis
Due to the unusual structure and chemical composition of the mycobacterial cell wall,
effective tuberculosis (TB) treatment is difficult, making many antibiotics ineffective and …

Indole-fused spirochromenes as potential anti-tubercular agents: design, synthesis and in vitro evaluation

A Dogamanti, P Chiranjeevi, VK Aamate, SK Vagolu… - Molecular Diversity, 2021 - Springer
As part of an ongoing effort to develop new anti-tubercular agents, a series of novel indole-
fused spirochromene hybrids (7a–l) were efficiently synthesized in excellent yields by the …

Molecular docking study on the interaction between 2-substituted-4, 5-difuryl Imidazoles with different Protein Target for antileishmanial activity

JAR Vargas, AG Lopez, MC Piñol… - Journal of Applied …, 2018 - japsonline.com
Leishmaniasis is a disease which is caused by the protozoa Leishmania and is considered
the second-highest cause of death worldwide by parasitic infection. Looking for the right …