Tetrazolylmethyl quinolines: design, docking studies, synthesis, anticancer and antifungal analyses

Shaikh, Saba Kauser J. and Kamble, Ravindra R. and Shilpa, M. S. and Devarajegowda, H. C. and Dixit, Sheshagiri R. and Joshi, Shrinivas D. (2017) Tetrazolylmethyl quinolines: design, docking studies, synthesis, anticancer and antifungal analyses. European Journal of Medicinal Chemistry, 128. 258 - 273. ISSN 0223-5234

[img] Text (Full Text)
Tetrazolylmethyl quinoline Designdocking studiessynthesisanticancer and antifungal analyses.pdf - Published Version
Download (3MB)
Official URL: https://doi.org/10.1016/j.ejmech.2017.01.043

Abstract

A new series of 2,5 and 1,5-regioisomers of the tetrazolyl group viz., 3-(5-benzyl/benzylthio-2H-tetrazol-2-yl) methyl-2-chloro-6-substituted quinoline 6h-q and 3-(5-benzyl/benzylthio-1H-tetrazol-1-yl) methyl-2-chloro-6-substituted quinolines 7h-q were synthesized. Docking studies of all these compounds with DNA as target using PDB: 1AU5 and 453D revealed that the compounds 6h and 6i act as covalent cross linker on the DNA helix of the former and intercalate the latter both with higher C score values. Another set of docking studies in the active pocket of dihydrofolate reductase and N-myristoyl transferase as targets to assess antifungal activity revealed that compounds 6k, 6l, 6p and 7q (with bromo and fluro substituents) showcases different binding modes and hydrogen bonding. Further, the compounds were screened for anticancer activity (primary cytotoxicity) against NCI-60 Human tumor cell line at a single high dose (10−5 M) concentration assay. Among the tested compounds, 6h has shown 99.28% of GI against Melanoma (SK-MEL-5) and compound 6i has shown 97.56% of GI against Breast Cancer (T-47D). Further, in vitro antifungal assay against A. fumigatus and C. albicans for these compounds 6h-q and 7h-q revealed potential to moderate activities as compared to the standard.

Item Type: Article
Uncontrolled Keywords: Quinoline, Tetrazole, Regioisomer, Molecular docking, DNA, -Myristoyl transferase, Dihydrofolate reductase, Anticancer activity, Antifungal screening
Subjects: D Physical Science > Physics
Divisions: Yuvaraj college > Physics
Depositing User: C Swapna Library Assistant
Date Deposited: 25 Jun 2019 05:43
Last Modified: 29 Jun 2019 09:22
URI: http://eprints.uni-mysore.ac.in/id/eprint/3792

Actions (login required)

View Item View Item
uomeprints is powered by EPrints 3 which is developed by the School of Electronics and Computer Science at the University of Southampton. More information and software credits.