Ghosh B - Search Results

1

Structure-activity relationship of human carbonic anhydrase-II inhibitors: Detailed insight for future development as anti-glaucoma agents.

Ghorai S, Pulya S, Ghosh K, Panda P, Ghosh B, Gayen S. Ghorai S, et al. Among authors: ghosh k, ghosh b. Bioorg Chem. 2020 Jan;95:103557. doi: 10.1016/j.bioorg.2019.103557. Epub 2019 Dec 27. Bioorg Chem. 2020. PMID: 31911296 Review.

2

Synthesis, screening and quantitative structure-activity relationship (QSAR) studies of some glutamine analogues for possible anticancer activity.

Srikanth K, Kumar ChA, Ghosh B, Jha T. Srikanth K, et al. Among authors: ghosh b. Bioorg Med Chem. 2002 Jul;10(7):2119-31. doi: 10.1016/s0968-0896(02)00079-2. Bioorg Med Chem. 2002. PMID: 11983508

3

Quantitative structure-activity relationship study using refractotopological state atom index on some neonicotinoid insecticides.

Debnath B, Gayen S, Basu A, Ghosh B, Srikanth K, Jha T. Debnath B, et al. Among authors: ghosh b. Bioorg Med Chem. 2004 Dec 1;12(23):6137-45. doi: 10.1016/j.bmc.2004.09.003. Bioorg Med Chem. 2004. PMID: 15519158

4

QSAR modeling on dopamine D2 receptor binding affinity of 6-methoxy benzamides.

Samanta S, Debnath B, Gayen S, Ghosh B, Basu A, Srikanth K, Jha T. Samanta S, et al. Among authors: ghosh b. Farmaco. 2005 Oct;60(10):818-25. doi: 10.1016/j.farmac.2005.06.018. Epub 2005 Aug 1. Farmaco. 2005. PMID: 16055122

5

Design, synthesis and biological evaluation of 2-(3,4-dimethoxyphenyl)-6 (1,2,3,6-tetrahydropyridin-4-yl)imidazo[1,2-a]pyridine analogues as antiproliferative agents.

Chitti S, Singireddi S, Santosh Kumar Reddy P, Trivedi P, Bobde Y, Kumar C, Rangan K, Ghosh B, Sekhar KVGC. Chitti S, et al. Among authors: ghosh b. Bioorg Med Chem Lett. 2019 Sep 15;29(18):2551-2558. doi: 10.1016/j.bmcl.2019.08.013. Epub 2019 Aug 7. Bioorg Med Chem Lett. 2019. PMID: 31420269

6

Discovery of 1,2,3-triazole based quinoxaline-1,4-di-N-oxide derivatives as potential anti-tubercular agents.

Srinivasarao S, Nandikolla A, Suresh A, Ewa AK, Głogowska A, Ghosh B, Kumar BK, Murugesan S, Pulya S, Aggarwal H, Sekhar KVGC. Srinivasarao S, et al. Among authors: ghosh b. Bioorg Chem. 2020 Jul;100:103955. doi: 10.1016/j.bioorg.2020.103955. Epub 2020 May 20. Bioorg Chem. 2020. PMID: 32464405

7

HDAC6 as privileged target in drug discovery: A perspective.

Pulya S, Amin SA, Adhikari N, Biswas S, Jha T, Ghosh B. Pulya S, et al. Among authors: ghosh b. Pharmacol Res. 2021 Jan;163:105274. doi: 10.1016/j.phrs.2020.105274. Epub 2020 Nov 7. Pharmacol Res. 2021. PMID: 33171304 Review.

8

PT3: A Novel Benzamide Class Histone Deacetylase 3 Inhibitor Improves Learning and Memory in Novel Object Recognition Mouse Model.

Pulya S, Mahale A, Bobde Y, Routholla G, Patel T, Swati, Biswas S, Sharma V, Kulkarni OP, Ghosh B. Pulya S, et al. Among authors: ghosh b. ACS Chem Neurosci. 2021 Mar 3;12(5):883-892. doi: 10.1021/acschemneuro.0c00721. Epub 2021 Feb 12. ACS Chem Neurosci. 2021. PMID: 33577290

9

Design, synthesis and biological evaluation of 7-(5-((substituted - amino)-methyl)-thiophen-2-yl)-spiro-[chroman-2,4'-piperidin]-4-one hydrochloride analogues as anticancer agents.

Chitti S, Pulya S, Nandikolla A, Patel TK, Karan Kumar B, Murugesan S, Ghosh B, Sekhar KVGC. Chitti S, et al. Among authors: ghosh b. Bioorg Chem. 2021 Jul;112:104865. doi: 10.1016/j.bioorg.2021.104865. Epub 2021 Mar 26. Bioorg Chem. 2021. PMID: 33812269

10

Synthesis, biological evaluation, and molecular docking analysis of novel linker-less benzamide based potent and selective HDAC3 inhibitors.

Routholla G, Pulya S, Patel T, Abdul Amin S, Adhikari N, Biswas S, Jha T, Ghosh B. Routholla G, et al. Among authors: ghosh b. Bioorg Chem. 2021 Sep;114:105050. doi: 10.1016/j.bioorg.2021.105050. Epub 2021 Jun 4. Bioorg Chem. 2021. PMID: 34120025

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