Antitubercular evaluation of dihydropyridine–triazole conjugates: design, synthesis, in vitro screening, SAR and in silico ADME predictions

Author:

Kushawaha Ajay Kishor1,Jaiswal Arvind Kumar1,Gupta Jay1,Katiyar Sarita12,Ansari Alisha12,Bhatt Hemlata12,Sharma Sandeep K.3,Choudhury Abhijit Deb4,Bhatta Rabi Sankar42ORCID,Singh Bhupendra N.32,Sashidhara Koneni V.152ORCID

Affiliation:

1. Medicinal and Process Chemistry Division, CSIR-Central Drug Research Institute, BS 10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India

2. Academy of Scientific and Innovative Research (AcSIR), Ghaziabad-201002, U.P, India

3. Molecular Microbiology & Immunology (MMI) Division, CSIR-Central Drug Research Institute, BS 10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, India

4. Pharmaceutics and Pharmacokinetics Division, CSIR- Central Drug Research Institute, Lucknow, India

5. Sophisticated Analytical Instrument Facility & Research, CSIR-Central Drug Research Institute, BS-10/1, Sector 10, Jankipuram Extension, Sitapur Road, Lucknow 226031, U.P, India

Abstract

The synthesis of a novel series of 32 dihydropyridine–triazole conjugates using click chemistry and their antitubercular activity, structure–activity relationship (SAR) analysis, and ADME predictions are discussed.

Funder

University Grants Commission

Department of Science and Technology, Ministry of Science and Technology, India

Publisher

Royal Society of Chemistry (RSC)

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