Chander S - Search Results

1

Biological evaluation and structure activity relationship of 9-methyl-1-phenyl-9H-pyrido[3,4-b]indole derivatives as anti-leishmanial agents.

Ashok P, Chander S, Smith TK, Prakash Singh R, Jha PN, Sankaranarayanan M. Ashok P, et al. Among authors: chander s. Bioorg Chem. 2019 Mar;84:98-105. doi: 10.1016/j.bioorg.2018.11.037. Epub 2018 Nov 22. Bioorg Chem. 2019. PMID: 30500524 Free PMC article.

2

Lead optimization studies towards the discovery of novel carbamates as potent AChE inhibitors for the potential treatment of Alzheimer's disease.

Roy KK, Tota S, Tripathi T, Chander S, Nath C, Saxena AK. Roy KK, et al. Among authors: chander s. Bioorg Med Chem. 2012 Nov 1;20(21):6313-20. doi: 10.1016/j.bmc.2012.09.005. Epub 2012 Sep 12. Bioorg Med Chem. 2012. PMID: 23026084

3

Design, Synthesis, and Biological Evaluation of 1-(thiophen-2-yl)-9H-pyrido[3,4-b]indole Derivatives as Anti-HIV-1 Agents.

Ashok P, Lu CL, Chander S, Zheng YT, Murugesan S. Ashok P, et al. Among authors: chander s. Chem Biol Drug Des. 2015 Jun;85(6):722-8. doi: 10.1111/cbdd.12456. Epub 2014 Nov 6. Chem Biol Drug Des. 2015. PMID: 25328020

4

Design, synthesis of new β-carboline derivatives and their selective anti-HIV-2 activity.

Ashok P, Chander S, Balzarini J, Pannecouque C, Murugesan S. Ashok P, et al. Among authors: chander s. Bioorg Med Chem Lett. 2015 Mar 15;25(6):1232-5. doi: 10.1016/j.bmcl.2015.01.058. Epub 2015 Jan 30. Bioorg Med Chem Lett. 2015. PMID: 25682562

5

De-novo design, synthesis and evaluation of novel 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline derivatives as HIV-1 reverse transcriptase inhibitors.

Chander S, Ashok P, Singh A, Murugesan S. Chander S, et al. Chem Cent J. 2015 Jun 9;9:33. doi: 10.1186/s13065-015-0111-6. eCollection 2015. Chem Cent J. 2015. PMID: 26075019 Free PMC article.

6

Synthesis, evaluation and molecular docking studies of amino acid derived N-glycoconjugates as antibacterial agents.

Baig N, Singh RP, Chander S, Jha PN, Murugesan S, Sah AK. Baig N, et al. Among authors: chander s. Bioorg Chem. 2015 Dec;63:110-5. doi: 10.1016/j.bioorg.2015.10.002. Epub 2015 Oct 9. Bioorg Chem. 2015. PMID: 26476390

7

Design, synthesis and in-vitro evaluation of novel tetrahydroquinoline carbamates as HIV-1 RT inhibitor and their antifungal activity.

Chander S, Ashok P, Zheng YT, Wang P, Raja KS, Taneja A, Murugesan S. Chander S, et al. Bioorg Chem. 2016 Feb;64:66-73. doi: 10.1016/j.bioorg.2015.12.005. Epub 2015 Dec 17. Bioorg Chem. 2016. PMID: 26717022

8

Design, synthesis and biological evaluation of novel quinoline-based carboxylic hydrazides as anti-tubercular agents.

Chander S, Ashok P, Cappoen D, Cos P, Murugesan S. Chander S, et al. Chem Biol Drug Des. 2016 Oct;88(4):585-91. doi: 10.1111/cbdd.12788. Epub 2016 Jun 24. Chem Biol Drug Des. 2016. PMID: 27203404

9

Rational design, synthesis, anti-HIV-1 RT and antimicrobial activity of novel 3-(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)-1-(piperazin-1-yl)propan-1-one derivatives.

Chander S, Wang P, Ashok P, Yang LM, Zheng YT, Murugesan S. Chander S, et al. Bioorg Chem. 2016 Aug;67:75-83. doi: 10.1016/j.bioorg.2016.05.009. Epub 2016 Jun 1. Bioorg Chem. 2016. PMID: 27288643

10

Synthesis and anti-leishmanial evaluation of 1-phenyl-2,3,4,9-tetrahydro-1H-β-carboline derivatives against Leishmania infantum.

Ashok P, Chander S, Tejería A, García-Calvo L, Balaña-Fouce R, Murugesan S. Ashok P, et al. Among authors: chander s. Eur J Med Chem. 2016 Nov 10;123:814-821. doi: 10.1016/j.ejmech.2016.08.014. Epub 2016 Aug 10. Eur J Med Chem. 2016. PMID: 27541264

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