Synthesis, Characterization, Molecular Docking Studies and Biological Evaluation of Some Conjugated Quinazoline‐Sulfonamide Scaffold. Issue 48 (21st December 2018)

• Record Type: Journal Article
• Authors: Kumar, A. Sunil; Kudva, Jyothi; Bharath, B. R.; Rai, Vaishali M; Kumar, S. Madan; Kumar, Vasantha; Sajankila, Shyama Prasad
• Is Part Of: ChemistrySelect. Volume 3:Issue 48(2018)
• Page Start: 13586
• Page End: 13595
• Publication Date: 2018-12-21
• Subjects: Antimicrobial -- antituberculosis -- antitumor -- docking -- quinazoline-sulfonamides.; Chemistry -- Periodicals; 540.5
• DOI: 10.1002/slct.201802402
• Languages: English
• ISSNs: 2365-6549

Abstract

Abstract: A series of sulfonamides containing 4‐aminoquinazoline scaffolds7 a‐7 l was synthesized, characterized and evaluated for their in vitro antitubercular, antimicrobial and anticancer activity. The compounds with 4‐nitrophenyl (7 c ), 3‐trifluoromethylphenyl (7 f ) and 5‐chloro‐pyridin‐2‐yl (7 h ) derivatives have shown potent antitubercular activity against Mycobacterium tuberculosi s H37Rv strain and the activity was two‐fold higher than the standard drug Ciprofloxacin. The compounds with 4‐chlorophenyl (7 a ), pyridin‐2‐yl (7 g ), 5‐chloro‐pyridin‐2‐yl (7 h ) and pyrimidin‐2‐yl (7 i, 7 j and7 k ) derivatives were observed as excellent antimicrobial agents. The preliminary toxicity of selected potent compounds was also tested on Red Blood Cells by hemolytic assay and found to be non‐toxic even at higher concentrations. Compounds with 4‐nitrophenyl (7 c) and 4‐fluorophenyl (7 e) substitutions emerged as potent molecules against MDA‐MB‐231 cell line. ADME (Absorption, Distribution, Metabolism and Excretion ) screening study revealed that the compounds are strong candidates for antitubercular activity with good ADME parameters. In addition, the structure and antitubercular activity relationship were further supported by molecular docking studies of the active compounds against the DNA topoisomerase II (5BTC) enzyme ofM. tuberculosis . Abstract : By combining the structural characteristics of quinazoline and sulfonamides, new hybrid compounds were synthesized using suitable method. Antitubercular activity screening of these compounds against M. tuberculosis strain identified phenylsulfonamide moieties as most potent candidates and the activity was further confirmed by docking studies against DNA topoisomerase II. The compounds have also shown antimicrobial activity against bacterial and fungal strains. The potent antitubercular compounds were further screened against cancer cell lines to find their dual inhibitions of cancer and tuberculosis.