Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Rohini S. Kavalapure"'
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:
Preeti S. Salve, Prajakta Parchure, Lisel Araujo, Rohini S. Kavalapure, Sunil S. Jalalpure, Dharmarajan Sriram, Vagolu Siva Krishna, Madhu Rekha Estharla, Shankar G. Alegaon
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-10 (2021)
Abstract Background Tuberculosis is evidently a major health threat among human populations worldwide. The current study presents the synthesis of new 3-((7-chloroquinolin-4-yl)amino)thiazolidin-4-one analogs (4a–o) as potential Mycobacterium tuber
Externí odkaz:
https://doaj.org/article/3a6e0533143a4486ba50230062ef6e60
Publikováno v:
Chemistry Africa. 6:367-373
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4e6c6f172e434b5d9a01334214f9b50
https://doi.org/10.1007/s42250-022-00516-z
https://doi.org/10.1007/s42250-022-00516-z
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:
Prajakta Parchure, Preeti S. Salve, Madhu Rekha Estharla, Shankar G. Alegaon, Sunil S. Jalalpure, Vagolu Siva Krishna, Dharmarajan Sriram, Rohini S. Kavalapure, Lisel Araujo
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-10 (2021)
Background Tuberculosis is evidently a major health threat among human populations worldwide. The current study presents the synthesis of new 3-((7-chloroquinolin-4-yl)amino)thiazolidin-4-one analogs (4a–o) as potential Mycobacterium tuberculosis D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc714bdba54e5008df9d4809606d99d6
https://doaj.org/article/3a6e0533143a4486ba50230062ef6e60
https://doaj.org/article/3a6e0533143a4486ba50230062ef6e60
Autor:
Shailendra S Suryawanshi, Shankar G. Alegaon, Kamlesh Kashniyal, Sunil S. Jalalpure, Sanket Kuncolienkar, Mahesh S Palled, Preeti S. Salve, Rohini S. Kavalapure
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 6, Iss 1, Pp 1-12 (2020)
Background Based on bioisosteric similarities with thiacetazone, a series of 7-chloro-4-aminoquinoline derivatives have been designed and synthesized. The target compounds were elucidated by NMR, mass, and FTIR spectral data. All synthesized compound
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7a3b9711ac69778bb3521510b157671
https://doaj.org/article/f469e3e59308495b98ff5eb711e8f95f
https://doaj.org/article/f469e3e59308495b98ff5eb711e8f95f
Autor:
Ismail Pasha, Sharad Chand, Pukar Khanal, Taaza Duyu, B. M. Patil, Rohini S. Kavalapure, Shailendra S. Gurav, Yadu Nandan Dey
Publikováno v:
3 Biotech
The majority of the bioactives under investigation were predicted to target TNF receptor-associated factor 5 in the Janus kinase/signal transducers and activators of the transcription pathway. Similarly, druglikeness prediction identified vitexilacto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9f65088d2225b39fdcf2bac03af76eb
Aim. The present study was aimed to identify the lead hits from reported anti-viral Indian medicinal plants to modulate the proteins through the JAK-STAT pathway and to identify the proteins that share the domain with coronavirus (COVID19) associated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9b59333e41d3c820e64ec1ed5041176
https://doi.org/10.21203/rs.3.rs-32233/v1
https://doi.org/10.21203/rs.3.rs-32233/v1
