Synthesis, Molecular Docking, and Evaluation of Triazole and Chalcone Conjugate as Antitubercular Agent

H Kaur, R Singh - 2021 - researchsquare.com
The aim of this work was to be combine two pharmocophoric nuclei viz, triazole and
chalcone and evaluate their antitubercular activity. Propargylated vanillin was condensed …

New quinoline linked chalcone and pyrazoline conjugates: Molecular properties prediction, antimicrobial and antitubercular activities

NS Rao, AB Shaik, SR Routhu, SMA Hussaini… - …, 2017 - Wiley Online Library
Two novel series comprising of forty two compounds have been synthesized by conjugating
quinoline scaffold with chalcone as well as pyrazoline motifs. All the synthesized conjugates …

Synthesis and biological evaluation of novel triazole-biscoumarin conjugates as potential antitubercular and anti-oxidant agents

AB Danne, AS Choudhari, D Sarkar… - Research on Chemical …, 2018 - Springer
The synthesis of a new series of triazole-biscoumarin conjugates by using a molecular
hybridization approach is described. The newly synthesized compounds 6a–k were …

Synthesis of coumarin-thioether conjugates as potential anti-tubercular agents: Their molecular docking and X-ray crystal studies

M Akki, DS Reddy, KS Katagi, A Kumar… - Journal of Molecular …, 2022 - Elsevier
In this work, we report a series of 4-(2, 6-dimethylphenyl) thio) methyl)-2H-chromen-2-one
conjugates as promising leads to treat tuberculosis. Spectroscopic and other analytical …

Synthesis, molecular docking, and antitubercular evaluation of triazole–chalcone conjugates

H Kaur, R Singh, Rishikant - Russian Journal of Organic Chemistry, 2022 - Springer
The condensation of propargylated vanillin with differently substituted acetophenones
produced the corresponding chalcones which were reacted with substituted benzyl azides …

Novel hybrid-pyrrole derivatives: their synthesis, antitubercular evaluation and docking studies

R Saha, MM Alam, M Akhter - RSC Advances, 2015 - pubs.rsc.org
Using novel hybrid molecules for the treatment of tuberculosis is one of the latest
approaches. Keeping this concept in mind, thirty two hybrid compounds were synthesized …

Pyrazole–coumarin and pyrazole–quinoline chalcones as potential antitubercular agents

G Kumar, V Siva Krishna, D Sriram… - Archiv der …, 2020 - Wiley Online Library
Pyrazole, coumarin, and quinoline are medicinally important moieties. In this study, two
series of novel pyrazole–coumarin chalcones and pyrazole–quinoline chalcones were …

A Chalcone Annulated Pyrazoline Conjugates as a Potent Antimycobacterial Agents: Synthesis and in Silico Molecular Modeling Studies

T Prabha, P Aishwaryah, E Manickavalli… - Research Journal of …, 2019 - indianjournals.com
Pyrazolines are well known and important nitrogen containing 5-membered heterocyclic
compounds could effective against diversity of biological issue in which the tuberculosis is …

Design, Synthesis and In vitro Antitubercular Effect of New Chalcone Derivatives Coupled with 1,2,3‐Triazoles: A Computational Docking Techniques

K Sadineni, S Reddy Basireddy… - Chemistry & …, 2024 - Wiley Online Library
A very interesting foundation for this study is the creation of new methods for modifying
compounds with a 1, 2, 3‐triazole and chalcone scaffolds, as these compounds are …

Thiazole–chalcone hybrids as prospective antitubercular and antiproliferative agents: Design, synthesis, biological, molecular docking studies and in silico ADME …

AB Kasetti, I Singhvi, R Nagasuri, RR Bhandare… - Molecules, 2021 - mdpi.com
Compounds bearing thiazole and chalcone pharmacophores have been reported to
possess excellent antitubercular and anticancer activities. In view of this, we designed …