Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Preeti S. Salve"'
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
Autor:
Aparna Inamdar, Shweta Pote, Suraj Sawant, Preeti S Salve, Shailendra S. Suryawanshi, Mahesh Palled
Cardiovascular (CVS) drugs are medications whose primary effects are experienced by the heart and blood vessels to treat cardiovascular disorders such as coronary artery disease, arrhythmias, high blood-pressure, heart failure and stroke. Evaluation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc6f11a052369c4606181748ee061ec3
https://doi.org/10.21203/rs.3.rs-2653667/v1
https://doi.org/10.21203/rs.3.rs-2653667/v1
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
The renin angiotensin system (RAS) provides the most powerful regulation of blood pressure and angiotensin II is the primary mediator in this system. The binding of angiotensin II to AT1 receptors produces a number of potentially harmful effects that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95aa34712f3368573cc4d84decb56e6e
https://doi.org/10.9734/bpi/nfmmr/v3/10844d
https://doi.org/10.9734/bpi/nfmmr/v3/10844d
Autor:
Shankar G. Alegaon, Preeti S. Salve, Kamlesh Kashniyal, Sanket Kuncolienkar, Shailendra S Suryawanshi, Mahesh S Palled, Sunil Jalalpure, Rohini S. Kavalapure
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 6, Iss 1, Pp 1-1 (2020)
Following publication of the original article [1], the authors reported an error in one of the authors’ names.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7b739dd68d6b899f63e7a24ca0d9ee1
https://doi.org/10.1186/s43094-020-0019-4
https://doi.org/10.1186/s43094-020-0019-4
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
Autor:
Shankar G. Alegaon, Preeti S. Salve
Publikováno v:
Medicinal Chemistry Research. 27:1-14
Molecular hybridization is a developing approach to design novel compounds by merger of two or more biological subunits of known medicinal agents. In the present study, new series of 7-chloro-4-phenoxyquinoline analogs were synthesized, characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1006dacf673aa74d9d51b26b1601917a
https://doi.org/10.1007/s00044-017-1970-2
https://doi.org/10.1007/s00044-017-1970-2
Autor:
Preeti S. Salve, K.R. Alagawadi, L.D. Araujo, Sunil S. Jalalpure, V. M. Kumbar, Shankar G. Alegaon, P. Parchure
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 27:1566-1571
In search of new heterocyclic anticancer agents, a new quinoline-azetidinone hybrid template have been designed, synthesized and screened for their cytotoxic activity against human cancer cell lines such as Hep G2, and Hep 3B by the MTT assay and res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a9782df01ee3f1806776112663b2888
https://doi.org/10.1016/j.bmcl.2017.02.043
https://doi.org/10.1016/j.bmcl.2017.02.043
Autor:
Shankar G. Alegaon, K.R. Alagawadi, V. M. Kumbar, V. P. Rasal, Sunil S. Jalalpure, Mita B. Hirpara, Preeti S. Salve
Publikováno v:
Medicinal Chemistry Research. 26:1127-1138
A series of 1,3,4-trisubstituted pyrazole derivatives (3a–f), (4a–r), (5a–f) and (6a–f) have been synthesized and evaluated for their Mycobacterium tuberculosis (MTB) (H37Rv) inhibitory activity. The structures of newly synthesized compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8bc4e1c24a1014fe29f0f142ea07f1d6
https://doi.org/10.1007/s00044-017-1821-1
https://doi.org/10.1007/s00044-017-1821-1