Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Prerna L. Tiwari"'
Autor:
Vaibhav S. Marde, Prerna L. Tiwari, Nitu L. Wankhede, Brijesh G. Taksande, Aman B. Upaganlawar, Milind J. Umekar, Mayur B. Kale
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-8 (2021)
Abstract Background Over the last decade, aggregating evidences suggested that there is a causative link between mutation in gene associated with mitochondrial dysfunction and development of several neurodegenerative disorders. Main text Recent struc
Externí odkaz:
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
Autor:
Pavitra S. Thacker, Prerna L. Tiwari, Andrea Angeli, Danaboina Srikanth, Baijayantimala Swain, Mohammed Arifuddin, Claudiu T. Supuran
Publikováno v:
Metabolites, Vol 11, Iss 4, p 225 (2021)
A series of coumarin-linked 4-anilinomethyl-1,2,3-triazoles (6a–t) was synthesized via a molecular hybridization approach, through carbon C-6 of the coumarin moiety. The synthesized compounds were evaluated for their inhibition of carbonic anhydras
Externí odkaz:
https://doaj.org/article/9cb8f55cf7294bf59c050f2eea9d143b
Autor:
Brijesh G. Taksande, Aman B. Upaganlawar, Milind J. Umekar, Nitu L. Wankhede, Mayur B. Kale, Vaibhav S. Marde, Prerna L. Tiwari
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-8 (2021)
Background Over the last decade, aggregating evidences suggested that there is a causative link between mutation in gene associated with mitochondrial dysfunction and development of several neurodegenerative disorders. Main text Recent structural and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6276525720a42210f737510bca665946
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
https://doaj.org/article/4e920affe7f1410b923a8b86d690d375
Autor:
Claudiu T. Supuran, Arifuddin Mohammed, Pavitra S. Thacker, Prerna L. Tiwari, Nerella S. Goud, Danaboina Srikanth, Andrea Angeli
Publikováno v:
Anti-cancer agents in medicinal chemistry. 22(14)
Background: Carbonic anhydrases (CAs, EC 4.2.1.1) catalyze the reversible hydration of carbon dioxide to bicarbonate and proton. Inhibition of isoforms IX and XII could aid in the amelioration of cancer. Objective: A series of coumarin carboxamides (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c48fb25db38ff2ba9998f5cbe3306e2
https://pubmed.ncbi.nlm.nih.gov/35249507
https://pubmed.ncbi.nlm.nih.gov/35249507
Autor:
Nitu L. Wankhede, Brijesh G. Taksande, Milind J. Umekar, Aman B. Upaganlawar, Saurabh P. Badole, Utkarsha A. Atkare, Vaibhav S. Marde, Mayur B. Kale, Prerna L. Tiwari, Shweta V. Gawali
Publikováno v:
Asian journal of psychiatry. 68
One of the comorbid conditions in an individual with Alzheimer’s disease is a sleep disorder. Clinical features of sleep disorders involve various sleep disturbances such as Obstructive Sleep Apnea (OSAS), Excessive Daytime Sleepiness (EDS), Rapid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad40dcc4e7bfaadb66f5b09ba3915bda
https://pubmed.ncbi.nlm.nih.gov/34890930
https://pubmed.ncbi.nlm.nih.gov/34890930
Autor:
Baijayantimala Swain, Andrea Angeli, Mohammed Arifuddin, Danaboina Srikanth, Pavitra S. Thacker, Claudiu T. Supuran, Prerna L. Tiwari
Publikováno v:
Metabolites
Volume 11
Issue 4
Metabolites, Vol 11, Iss 225, p 225 (2021)
Volume 11
Issue 4
Metabolites, Vol 11, Iss 225, p 225 (2021)
A series of coumarin-linked 4-anilinomethyl-1,2,3-triazoles (6a–t) was synthesized via a molecular hybridization approach, through carbon C-6 of the coumarin moiety. The synthesized compounds were evaluated for their inhibition of carbonic anhydras
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a995b4e409101fafb7985b30c5f7dca5
https://doi.org/10.3390/metabo11040225
https://doi.org/10.3390/metabo11040225
Autor:
Prerna L. Tiwari, Andrea Angeli, Omkar S. Argulwar, Pavitra S. Thacker, Claudiu T. Supuran, Mohammed Arifuddin
Publikováno v:
Bioorganic Chemistry. 98:103739
A series of coumarin linked 1,2,4-oxadiazoles were synthesized and the synthesized compounds were subjected for evaluation against the four physiologically and pharmacologically relevant hCA isoforms, hCA I, II, IX and XII. Upon evaluation of the res
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcbc0f28e3a6594a997e1a507cc65752
https://doi.org/10.1016/j.bioorg.2020.103739
https://doi.org/10.1016/j.bioorg.2020.103739