Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Prashant Aragade"'
Publikováno v:
Medicinal Chemistry Research. 22:2279-2283
The purpose of this study was to evaluate the antimycobacterial activity of various pyrazole derivatives derived from the isoniazid pharmacophore along with coumarin scaffold. The synthesized title compounds (4a–4k) were investigated for their in v
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e585ccb867982de7d89c510bb846fdf
https://doi.org/10.1007/s00044-012-0222-8
https://doi.org/10.1007/s00044-012-0222-8
Autor:
Mohan Agrawal, Pankaj Patil, Prashant Aragade, Prashant Shinde, Veeresh Maddi, R. Venkat Narayanan
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 27:849-853
A series of 3-[3-(substituted phenyl)-1-phenyl-1H-pyrazol-5-yl]-2H-chromen-2-one (4a-k) were synthesized by reaction of 3-[2,3-dibromo-3-(substituted phenyl)propanoyl]-2H-chromen-2-one (3 a-k) with phenyl hydrazine in presence of triethylamine in abs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b02e0dba8b64fbba7f210d75b75c5e9
https://doi.org/10.3109/14756366.2011.622270
https://doi.org/10.3109/14756366.2011.622270
Autor:
Shivalingarao Mamledesai, Mahesh B. Palkar, Darbhamulla Satyanarayana, Suresh Khode, Pradeepkumar Ronad, Prashant Aragade, Veeresh Maddi
Publikováno v:
Archiv der Pharmazie. 342:361-366
A novel series of 3-[3-(substituted phenyl)-1-isonicotinoyl-1H-pyrazol-5-yl]-2H-chromen-2-one derivatives 4a-k have been synthesized by the reaction of 3-[2,3-dibromo-3-(substituted phenyl) propanoyl]-2H-chromen-2-one 3a-k and isonicotinic acid hydra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::45272dfbd15c18237a1a4ff8d8744a8a
https://doi.org/10.1002/ardp.200800156
https://doi.org/10.1002/ardp.200800156
Autor:
Prashant Aragade, Veeresh Maddi, Suresh Khode, A. H. M. Thippeswamy, Mahesh B. Palkar, Darbhamulla Satyanarayana, Shivalingarao Mamledesai, Pradeep Kumar Ronad
Publikováno v:
European Journal of Medicinal Chemistry. 44:1682-1688
A novel series of 5-(substituted)aryl-3-(3-coumarinyl)-1-phenyl-2-pyrazolines (3a-l) were synthesized by reacting various substituted 3-aryl-1-(3-coumarinyl)propan-1-ones (2a-l) with phenylhydrazine in the presence of hot pyridine. Structures of all
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63149352ba2c77c9df2e0f83c3a24606
https://doi.org/10.1016/j.ejmech.2008.09.020
https://doi.org/10.1016/j.ejmech.2008.09.020
Autor:
Shivalingarao Mamledesai, Prashant Aragade, Mahesh B. Palkar, Darbhamulla Satyanarayana, Veeresh Maddi, Pradeepkumar Ronad, Suresh Khode
Publikováno v:
ChemInform. 40
A novel series of 3-[3-(substituted phenyl)-1-isonicotinoyl-1H-pyrazol-5-yl]-2H-chromen-2-one derivatives 4a-k have been synthesized by the reaction of 3-[2,3-dibromo-3-(substituted phenyl) propanoyl]-2H-chromen-2-one 3a-k and isonicotinic acid hydra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01f3fc089d18691d77e02e9989171fc5
https://doi.org/10.1002/chin.200942144
https://doi.org/10.1002/chin.200942144
Autor:
A. H. M. Thippeswamy, Pradeep Kumar Ronad, Shivalingarao Mamledesai, Prashant Aragade, Suresh Khode, Darbhamulla Satyanarayana, Mahesh B. Palkar, Veeresh Maddi
Publikováno v:
ChemInform. 40
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc287a24e7b0a94c7c4725ce52188d68
https://doi.org/10.1002/chin.200931112
https://doi.org/10.1002/chin.200931112
Autor:
Prashant, Aragade, Veeresh, Maddi, Suresh, Khode, Mahesh, Palkar, Pradeepkumar, Ronad, Shivalingarao, Mamledesai, Darbhamulla, Satyanarayana
Publikováno v:
Archiv der Pharmazie. 342(6)
A novel series of 3-[3-(substituted phenyl)-1-isonicotinoyl-1H-pyrazol-5-yl]-2H-chromen-2-one derivatives 4a-k have been synthesized by the reaction of 3-[2,3-dibromo-3-(substituted phenyl) propanoyl]-2H-chromen-2-one 3a-k and isonicotinic acid hydra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0f7be891a27b92934d812215afac38dd
https://pubmed.ncbi.nlm.nih.gov/19475595
https://pubmed.ncbi.nlm.nih.gov/19475595