Zobrazeno 1 - 6 of 6 pro vyhledávání: '"Venkat M. Shinde"'
1
Design, Synthesis of Some Innovative Indolo[3,2-c]Isoquinoline-5-One Analogs and Associated Bioactivities, Pharmacophore, Molecular Docking, MEP, and Conceptual DFT Studies
Autor: Vaijinath A. Verma, Venkat M. Shinde, Anand R. Saundane, Rajkumar S. Meti, Dushyanth R. Vennapu
Publikováno v: Polycyclic Aromatic Compounds. :1-18
A series of novel triazolothiadiazolethione and triazolothiadiazine appended indolo[3,2-c]isoquinoline-5-one were designed, synthesized, and validated by IR, 1H, 13C NMR, and mass spectroscopy strategies. All compounds are determined by their DFT inv
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbe31edb1add0e7b3672c69446027012
https://doi.org/10.1080/10406638.2022.2149573
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3
Novel indolo [3,2-c]isoquinoline-5-one-6-yl [1,2,4]triazolo [3,4-b] [1,3,4]thiadiazole analogues: Design, synthesis, anticancer activity, docking with SARS-CoV-2 Omicron protease and MESP/TD-DFT approaches
Autor: Vaijinath A. Verma, Anand R. Saundane, Raju Shamrao, Rajkumar S. Meti, Venkat M. Shinde
Publikováno v: Journal of molecular structure. 1264
Indoloisoquinoline derivatives are associated with varieties of biological and pharmacological properties. Therefore, we herein reported the synthesis of novel series of indolo [3,2-c]isoquinoline incorporated with [1,2,4]triazolo [3,4-b] [1,3,4]thia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::10f4933cfaf1a1823b61f71f43dbed1f
https://pubmed.ncbi.nlm.nih.gov/36532891
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4
Synthesis, E-pharmacophore, Molecular Docking Studies with SARS-CoV-2 Protease, Their Biological Properties and DFT Calculation of Some New Indolo[3,2-c]Isoquinoiline Hybrids
Autor: Venkat M. Shinde, Ramesh L Londonkar, Dushyanth R. Vennapu, Anand R. Saundane, Vaijinath A. Verma, Raju Shamrao, Rajkumar S. Meti
A series of novel indolo[3,2-c]isoquinoline hybrids derivatives were synthesized. On the basis of spectroscopic and analytical data, the structures of newly synthesized compounds were determined. They were further evaluated for their in vitro antimic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9307d2dc9d8682a0661eb1db25304b4
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