Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ghate Anil Vasantrao"'
Autor:
Narayan S. Punekar, Anil K. Mishra, Palakodety Subbarayan, Ghate Anil Vasantrao, Anjali V. Kulkarni, Swati Bal-Tembe, Ramanujam Rajagopalan, Dilip N. Bhedi
Publikováno v:
Bioorganic & Medicinal Chemistry. 5:1381-1387
Ester analogues of methyl-2-(4-(2-piperidinoethoxy)benzoyl)-benzoate hydrochloride (pitofenone) (2) were prepared with an aim to find a more potent and metabolically stable antispasmodic compound. The compounds were evaluated for their in vitro and i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4596ff1f47abd00ee0f5af172500e811
https://doi.org/10.1016/s0968-0896(97)00067-9
https://doi.org/10.1016/s0968-0896(97)00067-9
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::311005aeef47ca952aff12361662083e
https://doi.org/10.1002/chin.199918176
https://doi.org/10.1002/chin.199918176
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::35f03e47fd152fa7e7a67acbb96a9e46
https://doi.org/10.1002/chin.199941096
https://doi.org/10.1002/chin.199941096
Autor:
Ghate Anil Vasantrao, Ramesh M. Gidwani, Bansi Lal, Ramanujam Rajagopalan, Ashok Kumar Gangopadhyay
Publikováno v:
ChemInform. 37
The coupling of ω-halo acid or acrylic acid with 6β-2-hydroxyacyl forskolin 1 in the presence of DCC and DMAP gives 6β-ω-haloacyloxy or acryloxy derivatives 10-12. These derivatives undergo halogen displacement or Michael addition reaction with a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90d9ea36e87ec23238412db39bb5fa73
https://doi.org/10.1002/chin.200619180
https://doi.org/10.1002/chin.200619180
Publikováno v:
ChemInform. 37
This paper describes the design and synthesis of water soluble forskolin and some of its novel 2-hydroxyl acyl derivatives (A and B) based on the approach adopted by Bundgaard el al. using a number of 3-or 4-substituted amino benzoate esters. I lowev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1508bcaf493c81809caa658993bba448
https://doi.org/10.1002/chin.200610183
https://doi.org/10.1002/chin.200610183
Publikováno v:
Bioorganicmedicinal chemistry. 6(11)
Using appropriate protection and deprotection sequence novel hydroxyacyl chains of the type CO(CH 2 ) n OH are synthesized and are utilized to develop new analogues of forskolin. Several compounds showed good positive inotropic activity. Compound 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b5cab38d28ac52da83fd0c9998828cc
https://pubmed.ncbi.nlm.nih.gov/9881097
https://pubmed.ncbi.nlm.nih.gov/9881097
Publikováno v:
ChemInform; May1999, Vol. 30 Issue 18, pno-no, 1p
Autor:
Lal, Bansi a, *, Gangopadhyay, Ashok Kumar a, Gidwani, Ramesh M. a, Fernandes, Magno a, Rajagopalan, Ramanujam b, c, Ghate, Anil Vasantrao b
Publikováno v:
In Bioorganic & Medicinal Chemistry 1998 6(11):2075-2083