Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Darbhamulla, Satyanarayana"'
Autor:
Shivalingrao NagabhushanMamle, Girish Bolakatti, Jennifer Fernandes, Manjunatha S. Katagi, Darbhamulla Satyanarayana
Publikováno v:
Rajiv Gandhi University of Health Sciences Journal of Pharmaceutical Sciences. 4:57-61
Organophosphate (OP) compounds exert inhibition of acetylcholinesterase (AChE) by irreversibly binding to catalytic site of an enzyme. Despite continued efforts to discover improved reactivators, there has been little success towards innovation of AC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ece630f90e0598e2dfde721a4cfae36c
https://doi.org/10.5530/rjps.2014.2.4
https://doi.org/10.5530/rjps.2014.2.4
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:
A. H. M. Vishwanathswamy, Pradeepkumar Ronad, Nista Ingale, Veeresh Maddi, Darbhamulla Satyanarayana, Shivalingrao Mamledesai, Mahesh B. Palkar
Publikováno v:
Medicinal Chemistry Research. 21:16-26
A novel series of 3-[(5-substituted-1,3,4-oxadiazol-2-yl-thio)acetyl]-2H-chromen-2-one (7a–i) were synthesized by the condensation between the appropriately substituted 5-substituted-1,3,4-oxadiazolyl-2-thione (4a–i) derived from various existing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4af50f6366b0d0931c9ec83c1a30bbeb
https://doi.org/10.1007/s00044-010-9494-z
https://doi.org/10.1007/s00044-010-9494-z
Autor:
Mahesh B. Palkar, Sandip Jaju, Shivalingarao Mamledesai, Darbhamulla Satyanarayana, Veeresh Maddi, Mangala Ghatole, Pradeepkumar Ronad
Publikováno v:
Archiv der Pharmazie. 342:723-731
A novel series of 14 new isonicotinyl hydrazide derivatives 2a-g, 3a-g containing a 4-thiazolidinone / 2-azetidinone nucleus were synthesized by reacting N'-substituted arylidene / heteroarylidene isonicotinyl hydrazide 1a-g with thioglycollic acid i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::638b598c8647657bffae31a7ce789a7f
https://doi.org/10.1002/ardp.200900001
https://doi.org/10.1002/ardp.200900001
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, Darbhamulla Satyanarayana, Sandip Jaju, Pradeepkumar Ronad, Mangala Ghatole, Mahesh B. Palkar, Veeresh Maddi
Publikováno v:
ChemInform. 41
A novel series of 14 new isonicotinyl hydrazide derivatives 2a-g, 3a-g containing a 4-thiazolidinone / 2-azetidinone nucleus were synthesized by reacting N'-substituted arylidene / heteroarylidene isonicotinyl hydrazide 1a-g with thioglycollic acid i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eddd21e9b4c007d6bf651cdfca5fc228
https://doi.org/10.1002/chin.201016031
https://doi.org/10.1002/chin.201016031
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