Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Carol-Anne McEwen"'
Publikováno v:
ARKIVOC, Vol 2001, Iss 6, Pp 42-62 (2001)
Externí odkaz:
https://doaj.org/article/cddb2077c59941babd23dcec882fb2e1
Publikováno v:
Drug Development Research. 56:1-16
A group of racemic 1,4-dihydro-2,6-dimethyl-5-nitro-3-pyridinecarboxylates possessing either a C-4 2-trifluoromethylphenyl (22–24), benzofurazan-4-yl (42–44), 2-pyridyl (45–47), 3-pyridyl (48–50), or 4-pyridyl (51–53), substituent in conjun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6a3a13f2218002f6c07e4a00c5778e0
https://doi.org/10.1002/ddr.10050
https://doi.org/10.1002/ddr.10050
Publikováno v:
Drug Development Research. 51:233-243
A group of 3-nitrooxyalkyl 5-alkyl 1,4-dihydro-2,6-dimethyl-4-(pyridyl)-3,5-pyridinedicarboxylates were prepared using a modified Hantzsch reaction that involved the condensation of a nitrooxyalkyl acetoacetate with an alkyl 3-aminocrotonate and a py
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::971c3adc45c74366ef512d7ac85a26d7
https://doi.org/10.1002/ddr.4
https://doi.org/10.1002/ddr.4
Publikováno v:
Drug Development Research. 51:225-232
A group of racemic nitrooxyalkyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(pyridinyl or 2-trifluoromethylphenyl)-5-pyridinecarboxylates 8a-o were synthesized using modified Hantzsch reactions. In vitro calcium channel antagonist activities, determined usin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5cd77138574d67ec046ed4d1843bafe4
https://doi.org/10.1002/ddr.3
https://doi.org/10.1002/ddr.3
Publikováno v:
Drug Development Research. 51:177-186
A group of isopropyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-phenylpyridine-5-carboxylates (13–15) possessing ortho-, meta-, and para-CH2S(O)nMe and –S(O)nMe (n = 0–2) phenyl substituents were synthesized using a modified Hantzsch reaction. Calcium
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c4fc50136bdefa226b6d505bf5835b1
https://doi.org/10.1002/1098-2299(200011)51:3<177::aid-ddr6>3.0.co
https://doi.org/10.1002/1098-2299(200011)51:3<177::aid-ddr6>3.0.co
Autor:
Murthy R. Akula, Michael W. Wolowyk, Dean Vo, Nadeem Iqbal, Carol Anne McEwen, Edward E. Knaus, Wandikayi C. Matowe
Publikováno v:
Journal of medicinal chemistry. 41(11)
A group of racemic alkyl and 2-phenethyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(3- or 6-substituted-2-pyridyl)-5-pyridinecarboxylates (13a-q) was prepared using a modified Hantzsch reaction that involved the condensation of a 3- or 6-substituted-2-pyrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fdba5e7154a79d552b2beb7110f0d7ec
https://pubmed.ncbi.nlm.nih.gov/9599233
https://pubmed.ncbi.nlm.nih.gov/9599233
Publikováno v:
Chirality. 6(7)
The (+)- and (−)-enantiomers of 3-isopropyl 5-(4-methylphenethyl) 1,4-dihydro-2,6-dimethyl-4-(2-pyridyl)-3,5-pyridinedicarboxylate were synthesized using an efficient highly enantioselective (ee ≥ 96%) variant of the Hantzsch dihydropyridine synt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0f5e90a7e2598ae3b90349ceace2ce85
https://pubmed.ncbi.nlm.nih.gov/7986665
https://pubmed.ncbi.nlm.nih.gov/7986665
Publikováno v:
ResearcherID
A group of alkane and alkanoic acid compounds of general formula MeS(O) m (CH 2 ) n R [m = 0-2; n = 1, 5, 13; R = Me, CO 2 H(Na)] were synthesized for evaluation as cardiac inotropic and antifungal agents. Inotropic activity was determined as the abi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e7d81b195786fa874656007f84111c65
https://www.ncbi.nlm.nih.gov/pubmed/11039185
https://www.ncbi.nlm.nih.gov/pubmed/11039185
