Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Suraj S. Kapale"'
Publikováno v:
Medicine in Drug Discovery, Vol 2, Iss , Pp - (2019)
The ligand library reporting anticancer activities was taken from literature containing forty-two 4-oxo-1,4-dihydroquinoline-3-carboxamides derivatives and was thoroughly investigated against cancer target (pdb id-5U6B) using docking protocol. In ord
Externí odkaz:
https://doaj.org/article/1b2b250a804446409e0852fbfcc1c86c
Present work reports an efficient and environmentally benign approach for the synthesis of isoxazole-5(4H)-ones derivatives using lipase as biocatalyst. The one-pot multicomponent reaction of aldehyde, ethyl acetoacetate, and hydroxylamine hydrochlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7cbf1d0c2db8785ceb6348d72273ba3
Publikováno v:
Journal of Asian natural products research. 23(7)
A green protocol for the synthesis of unsubstituted imidazoles has been demonstrated herein. The reaction is realized using commercially available lipase enzyme, porcine pancreas lipase (PPL) in water. The reaction conditions are selective and mild w
Publikováno v:
Journal of the Indian Chemical Society. 98:100262
Niclosamide is classified under World Health Organization's crucial medicines and it is categorized as an anthelmintic drug to target tapeworm infections. In recent findings it is successfully repurposed as a multifunctional drug effective against ma
A green protocol for the synthesis of unsubstituted imidazoles has been demonstrated herein. The reaction is realized using commercially available lipase enzyme, porcine pancreas lipase (PPL) in water. The reaction conditions are selective and mild w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be2c091bae81f4854ae0a702f00de18f
Publikováno v:
Medicine in Drug Discovery, Vol 2, Iss, Pp-(2019)
The ligand library reporting anticancer activities was taken from literature containing forty-two 4-oxo-1,4-dihydroquinoline-3-carboxamides derivatives and was thoroughly investigated against cancer target (pdb id-5U6B) using docking protocol. In ord