Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Shriram D. Ranade"'
Publikováno v:
European Journal of Medicinal Chemistry Reports, Vol 12, Iss , Pp 100213- (2024)
In search of new antidiabetic agents, heterocyclic compounds containing 3,5-Substituted thiazolidinedione moieties were synthesized through a concise three-step reaction process. The synthesis involved Knoevenagel condensation at the 5th position of
Externí odkaz:
https://doaj.org/article/7a0b07ff24814ad1a2122cfd9e0d03f4
Autor:
Shankar Gharge, Shankar G. Alegaon, Shriram D. Ranade, N.A. Khatib, Rohini S. Kavalapure, B.R. Prashantha Kumar, Vinod D, Nandkishor B. Bavage
Publikováno v:
European Journal of Medicinal Chemistry Reports, Vol 11, Iss , Pp 100151- (2024)
In this study, a series of nine novel heterocyclic compounds were synthesized through a concise three-step reaction process. The synthesis involved Knoevenagel condensation at the 5th position of the 2,4-thiazolidinedione or rhodanine ring-system. Co
Externí odkaz:
https://doaj.org/article/186c720a5e3449b8afc765e5bacb7b1a
Autor:
Shriram D. Ranade, Shankar G. Alegaon, U. Venkatasubramanian, A. Soundarya Priya, Rohini S. Kavalapure, Jagdish Chand, Sunil S. Jalalpure, D. Vinod
Publikováno v:
Computational Biology and Chemistry. 105:107881
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::868139676bd71538b68e891c018c7cdb
https://doi.org/10.1016/j.compbiolchem.2023.107881
https://doi.org/10.1016/j.compbiolchem.2023.107881
Autor:
K.R. Alagawadi, Shankar G. Alegaon, Soundarya Priya A, U. Venkatasubramanian, Sunil S. Jalalpure, Dushyant Kumar, Rohini S. Kavalapure, Shriram D. Ranade
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 40:6211-6227
New thiazole-thiazolidinedione hybrids (5a–k) were efficiently synthesized and evaluated for their in-vitro antimicrobial activity against four fungal and bacterial strains. The chemical structures of the compounds were elucidated by FTIR, 1H NMR,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1f2c7eca0b494361b48ec76cbdf4898
https://doi.org/10.1080/07391102.2021.1880479
https://doi.org/10.1080/07391102.2021.1880479
Autor:
Preeti S. Salve, Rohini S. Kavalapure, Shriram D. Ranade, Dhanashree Patil, Shankar G. Alegaon, A. Soundarya Priya, Sanjay Mishra, Sunil Jalalpure, Pukar Khanal, U. Venkatasubramanian
Publikováno v:
Bioorganic Chemistry. 116:105381
In Search of new microtubule-targeting compounds and to identify a promising Eg5 inhibitory agents, a series of 2-((7-chloroquinolin-4-yl) amino) benzohydrazide Schiff bases molecules (6 a-r) were synthesized using appropriate synthetic method. The s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22c59772c762f72b9e28a3be46ff9060
https://doi.org/10.1016/j.bioorg.2021.105381
https://doi.org/10.1016/j.bioorg.2021.105381