Zobrazeno 1 - 10 of 17 pro vyhledávání: '"P. L. Kole"'
1
Transport studies through liquid membranes of ciprofloxacin and norfloxacin
Autor: A N, Nagappa, P L, Kole, P V, Pandi, R T, Patil, K, Zeeyauddin, I, Shanmukha
Publikováno v: Indian journal of biochemistrybiophysics. 41(1)
Ciprofloxacin and norfloxacin, the widely used drugs have been shown to generate liquid membranes in series with a supporting membrane (Sartorius celluose acetate microfiltration membrane). Transport of dextrose and ions, such as NH4+, Mg2+, Ca2+, K+
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2f79758c31203d0dedbe4baa4b403e04
https://pubmed.ncbi.nlm.nih.gov/22896909
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3
Synthesis and tumor-initiating activity in mouse skin of dibenzo[a,l]pyrene syn- and anti-fjord-region diolepoxides
Autor: J. C. Wiley, Kai Ming Li, P. L. Kole, Ercole L. Cavalieri, Sheila Higginbotham, Harpal S. Gill, Eleanor G. Rogan
Publikováno v: Carcinogenesis. 15(11)
Dibenzo[a,l]pyrene (DB[a,l]P) is the most potent carcinogen among polycyclic aromatic hydrocarbons. Because the fjord-region diolepoxide (DE) pathway is one of the mechanisms of activation, (+/)-trans-DB[a,l]P-11,12-dihydrodiol, (+/-)-anti-DB[a,l]PDE
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb815f1b394c5e363b2f20db1c756a6c
https://pubmed.ncbi.nlm.nih.gov/7955091
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4
Seco-oestradiols and some non-steroidal oestrogens: Structural correlates of oestrogenic action
Autor: B.S. Setty, S. Durani, Suprabhat Ray, P. L. Kole, Nitya Anand, A.K. Agarwal, Reena Saxena, R. C. Gupta
Publikováno v: Journal of Steroid Biochemistry. 11:67-77
Oestrogens can be grouped into two classes, based on their structural characteristics and biological activities; the typical oestrogens exemplified by the steroidal and the stilbene types, and the atypical oestrogens by the triaryl-ethylene types. In
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bde2d527a4f4cb4e0d4ea4047dcdb6b9
https://doi.org/10.1016/0022-4731(79)90278-4
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5
Centchroman: In vitro metabolism by rat liver homogenate
Autor: K. P. Sircar, Suprabhat Ray, M. Salman, Nitya Anand, K. P. Madhusudan, P. L. Kole, Sanjeev Ratna, S. K. Roy
Publikováno v: Drug Development Research. 7:173-178
Centchroman (trans-2,2-dimethyl-3-phenyl-4-(p-(β-pyrrolidinoethoxy) phenyl)-7-methoxy chroman) (I), a postcoital antifertility agent under clinical development was extensively metabolized by rat liver homogenate in vitro. Employing field desorption
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::09a1587b9a42889f57124d6f0d39198b
https://doi.org/10.1002/ddr.430070208
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6
Synthesis of trans-2,2-Dimethyl-3-phenyl-4-(p-β-pyrrolidinoethoxy)phenyl-7-methoxy-[2-14C]chroman
Autor: Suprabhat Ray, P. L. Kole
Publikováno v: Journal of Labelled Compounds and Radiopharmaceuticals. 16:373-375
The synthesis of trans-2,2-dimethyl-3-phenyl-4-(p-β-pyrrolidinoethoxy) phenyl-7-methoxy-[2-14C]chroman (Centchroman), a post-coital antifertility agent from [1-14C]phenylacetic acid is reported.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e59d721e9042765e5f9ebea71e32ceb7
https://doi.org/10.1002/jlcr.2580160220
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