Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Ramesh L. Sawant"'
Publikováno v:
Pharmaceutical Sciences, Vol 27, Iss 4, Pp 453-471 (2021)
Polo-like kinase 1(Plk1) plays an important role in the inhibition of cell proliferation and which is come under the family of serine/threonine-protein kinase. Which is a highly specific target for cancer therapy. In some clinical studies, Plk1 has b
Externí odkaz:
https://doaj.org/article/0a9f7fde490847278b7fe11ff030ad94
Autor:
Ramesh L. Sawant, Manish S. Bhatia
Publikováno v:
Bulletin of the Chemical Society of Ethiopia, Vol 22, Iss 3, Pp 391-402 (2008)
The purpose of this study was to synthesize several 3-benzoyl-5-acyl-6-methyl-4-substituted-2-oxo/thioxo-1,2,3,4-tetrahydropyrimidines, evaluate them for their antibacterial activity and to establish correlation between the activity and physicochemic
Externí odkaz:
https://doaj.org/article/0afb6b3bec4a4a05bfcd913e05e6e4e2
Publikováno v:
Journal of Chemistry, Vol 2013 (2013)
In continuation with our research program, in search of potent enzyme tyrosinase inhibitor, a series of synthesized 2,5-disubstituted 1,3,4-oxadiazoles have been evaluated for enzyme tyrosinase inhibitory activity. Subsequently, 3D QSAR and docking s
Externí odkaz:
https://doaj.org/article/19e4403f84e04cc880247d5a4b5b0702
A new, rapid, sensitive and specific liquid chromatographic method with UV detection for the simultaneous estimation of quinine and ciprofloxacin was developed. Separation was achieved with HibarR 250-4.6 HPLC column PurosphensR STAR RP-18 and mobile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::46528bca3137d3e97df88e577eddab0e
Autor:
Pravin S. Tajane, Ramesh L. Sawant
Publikováno v:
International journal of health sciences. :7169-7179
A growing number of researchers in the field of medicinal chemistry are focused on nitrogenous heterocyclic compounds. Benzimidazole scaffolds appear often in this group of heterocyclic compounds. Benzimidazole derivatives are important chemotherapeu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::745a68a105307da26ea737b9c1840c48
https://doi.org/10.53730/ijhs.v6ns1.6543
https://doi.org/10.53730/ijhs.v6ns1.6543
Publikováno v:
Research Journal of Pharmacy and Technology. :6369-6373
Benzimidazole derivatives of substituted 2 [2-(3-nitrophenyl)-1H-benzimidazole-1-yl] acetamide analogues were synthesized and studied for antihelminthic activity. Compounds 3a–o were obtained in three steps, starting with the Oxidative Condensation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8625ad8da559c21e5f01079b493ebc27
https://doi.org/10.52711/0974-360x.2021.01101
https://doi.org/10.52711/0974-360x.2021.01101
Publikováno v:
Pharmaceutical Sciences, Vol 27, Iss 3, Pp 345-352 (2021)
Background: Cancer is a major cause of death all over the globe. Controlling cell division byinhibition of mitosis is the most successful clinical strategy for cancer treatment. The developmentof novel anticancer agents is the most important area in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d0bf55a72cac9a6300dd9d7694cb93
https://ps.tbzmed.ac.ir/PDF/ps-27-345.pdf
https://ps.tbzmed.ac.ir/PDF/ps-27-345.pdf
Publikováno v:
INTERNATIONAL JOURNAL OF PHARMACEUTICAL QUALITY ASSURANCE. 11:334-337
Racecodotril (RCT), (N-[2-[(acetylthio) methyl]-1- oxo- 3- phenyl propyl] -glycine phenylmethyl ester) is an enkephalinase inhibitor. A rapid, specific, and economic UV spectrophotometric two methods have been developed using a solvent composed of me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d741bf6ad12bacdba5aad3b642372600
https://doi.org/10.25258/ijpqa.11.3.5
https://doi.org/10.25258/ijpqa.11.3.5
Publikováno v:
International Research Journal of Pharmacy. 11:56-65
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93c8b154703d5a00f49ea1442d4db42a
https://doi.org/10.7897/2230-8407.110442
https://doi.org/10.7897/2230-8407.110442
Autor:
Anjali S. Rajbhoj, Rushikesh D. Ukirde, Ganesh D. Barkade, Manisha R. Sawant, Jyoti B. Wadekar, Ramesh L. Sawant
Background: Cancer is a leading cause of death worldwide. Inhibiting mitosis is the most effective clinical technique for cancer treatment. The most critical field of medicinal chemistry and drug development research is the discovery of innovative an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::63ca3c6f19afd3eb63dd16c021a2233d
https://doi.org/10.21203/rs.3.rs-872668/v1
https://doi.org/10.21203/rs.3.rs-872668/v1