Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Saurabh C. Khadse"'
Autor:
Saurabh C. Khadse, Nikhil D. Amnerkar, Manasi U. Dave, Deepak K. Lokwani, Ravindra R. Patil, Vinod G. Ugale, Nitin B. Charbe, Vivekanand A. Chatpalliwar
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 5, Iss 1, Pp 1-14 (2019)
Abstract Background A small library of quinazolin-4-one clubbed thiazole acetates/acetamides lacking toxicity-producing functionalities was designed, synthesized, and evaluated for antidiabetic potential as glucokinase activators (GKA). Molecular doc
Externí odkaz:
https://doaj.org/article/4c7e4c94458a48c6932d72c802b12f5b
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 3, Iss 1, Pp 18-22 (2017)
HPTLC method was developed for estimating the content of desonide in bulk and pharmaceutical formulation. Desonide is a topically applied low potency anti-inflammatory corticosteroid. In the proposed method pre-coated HPTLC aluminum plates with silic
Externí odkaz:
https://doaj.org/article/7b911440544647f59974bd7a86e0fbfc
Publikováno v:
Arabian Journal of Chemistry, Vol 10, Iss S1, Pp S859-S863 (2017)
This paper presents the synthesis of some benzamide compounds (B1–B10) by microwave-assisted ring opening of 4-(4-dimethylaminobenzylidene)-2-phenyl-5-oxazolone (AZ4). By conventional synthesis involving heating, it was found difficult to obtain ri
Externí odkaz:
https://doaj.org/article/048e5a825c38436f932135494186312b
Autor:
Vikas R. Patil, Ashish M. Dhote, Rina Patil, Nikhil D. Amnerkar, Deepak K. Lokwani, Vinod G. Ugale, Nitin B. Charbe, Sandip D. Firke, Prashant Chaudhari, Sapan K. Shah, Chetan H. Mehta, Usha Y. Nayak, Saurabh C. Khadse
Publikováno v:
Journal of Biomolecular Structure and Dynamics. :1-12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86cc8c81533737474ca1dc6ce50a796f
https://doi.org/10.1080/07391102.2023.2175377
https://doi.org/10.1080/07391102.2023.2175377
Autor:
Prashant J. Chaudhari, Sanjaykumar B. Bari, Sanjay J. Surana, Atul A. Shirkhedkar, Chandrakant G. Bonde, Saurabh C. Khadse, Vinod G. Ugale, Akhil A. Nagar, Rameshwar S. Cheke
Publikováno v:
ACS Omega. 7:17270-17294
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1f96717fa06f0b2271aa6e627b2d86c6
https://doi.org/10.1021/acsomega.2c01198
https://doi.org/10.1021/acsomega.2c01198
Autor:
Nitin B Charbe, Vinod G. Ugale, Bhoomendra A. Bhongade, Deepak K. Lokwani, Vikas R. Patil, Saurabh C. Khadse, Nikhil D. Amnerkar, Ashish M Dhote
Publikováno v:
Journal of Biomolecular Structure and Dynamics. 40:11914-11931
Severe acute respiratory syndrome coronavirus (SARS-CoV-2), a novel member of the betacoronavirus family is a single-stranded RNA virus that has spread worldwide prompting the World Health Organization to declare a global pandemic. This creates an al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c662888835ccb63cbaeacae8967b3ad0
https://doi.org/10.1080/07391102.2021.1965912
https://doi.org/10.1080/07391102.2021.1965912
Autor:
Atul A. Shirkhedkar, Aditya Joshi, Akhil Nagar, Dipali Bagal, Aishwarya Chachare, Saurabh C. Khadse
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 7, Iss 1, Pp 1-7 (2021)
Background In the current study, a simple, improved, precise, rapid, and accurate reverse phase liquid chromatographic method was produced for the estimation of dalfampridine in bulk and tablet dosage form which is a potassium channel blocker used fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a7254a2073f41d07c3e6fb5d48e3117
https://doaj.org/article/0f0522dbc90249da97a3719d53358d79
https://doaj.org/article/0f0522dbc90249da97a3719d53358d79
Autor:
Akshay D. Umale, Harshal Ramkrishna Baviskar, Sandip D. Firke, Shailesh S. Chalikwar, Saurabh C. Khadse
Publikováno v:
Journal of Drug Delivery and Therapeutics. 10:175-182
Apremilast is used for treatment of psoriasis and psoriatic arthritis. It may also be beneficial for other inflammatory diseases relevant to the immune system. The drug functions as a selective enzyme phosphodiesterase 4 (PDE4) inhibitor and avoids t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::acbd7280d9992647604bb29aaf48e34d
https://doi.org/10.22270/jddt.v10i2-s.4012
https://doi.org/10.22270/jddt.v10i2-s.4012
Autor:
Prashant Jagannath Chaudhari, Sanjay B. Bari, Saurabh C. Khadse, Chandrakant G. Bonde, Pedavenkatagari Narayana Reddy, Vinod G. Ugale
Publikováno v:
ChemistrySelect. 5:2902-2912
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45a8cc37c95ef19b0f7c8b20dc670da5
https://doi.org/10.1002/slct.201904776
https://doi.org/10.1002/slct.201904776
Autor:
Vivekanand A. Chatpalliwar, Manasi U. Dave, Ravindra R. Patil, Deepak K. Lokwani, Nitin Charbe, Nikhil D. Amnerkar, Saurabh C. Khadse, Vinod G. Ugale
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 5, Iss 1, Pp 1-14 (2019)
Background A small library of quinazolin-4-one clubbed thiazole acetates/acetamides lacking toxicity-producing functionalities was designed, synthesized, and evaluated for antidiabetic potential as glucokinase activators (GKA). Molecular docking stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::360becbc82e69ef64c1cc826663808a7
https://doaj.org/article/4c7e4c94458a48c6932d72c802b12f5b
https://doaj.org/article/4c7e4c94458a48c6932d72c802b12f5b