Activators of voltage-dependent L-type calcium channels
For an excellent review, see the following. Rampe, D.; Kano, J. M. Activators of voltage-dependent L-type calcium channels. Drug Dev. Res. 1994, 33, 344-363.
The optical isomers of the 1,4-dihydropyridine Bay K 8644 show opposite effects on Ca channels
Franckowiak, G.; Bechem, M.; Schramm, M.; Thomas, G. The optical isomers of the 1,4-dihydropyridine Bay K 8644 show opposite effects on Ca channels. Eur. J. Pharmacol. 1985, 114, 223-226.
Pharmacologic and radioligand binding analysis of the action of 1,4-dihydropyridine activator-antagonist pairs in smooth muscle
Wei, X. Y.; Luckowski, E. M.; Rutledge, A.; Su, C. M.; Triggle, D. J. Pharmacologic and radioligand binding analysis of the action of 1,4-dihydropyridine activator-antagonist pairs in smooth muscle. J. Pharmacol. Exp. Ther. 1986, 239, 144-153.
Synthesis, calcium channel agonist-antagonist modulation activities, and voltage-clamp studies of isopropyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-pyridinylpyridine-5-carboxylate racemates and enantiomers
Vo, D.; Matowe, W. C.; Ramesh, M.; Iqbal, N.; Wolowyk, M. W.; Howlett, S. E.; Knaus, E. E. Synthesis, calcium channel agonist-antagonist modulation activities, and voltage-clamp studies of isopropyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-pyridinylpyridine-5-carboxylate racemates and enantiomers. J. Med. Chem. 1995, 38, 2851-2859.
Stereoselectivity at the calcium channel: Opposite action of the enantiomers of a 1,4-dihydropyridine
Hof, R. P.; Rüegg, U. T.; Hof, A.; Vogel, A. Stereoselectivity at the calcium channel: Opposite action of the enantiomers of a 1,4-dihydropyridine. J. Cardiovasc. Pharmacol. 1985, 7, 689-693.
Facile synthesis and NO-generating property of 4H-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-dione 1-oxides
Sako, M.; Oda, S.; Ohara, S.; Hirota, K.; Maki, Y. Facile synthesis and NO-generating property of 4H-[1,2,5]oxadiazolo[3,4-d]pyrimidine-5,7-dione 1-oxides. J. Org. Chem. 1998, 63, 6947-6951.
Nitric oxide donors: Chemical activities and biological applications
, 1091-1134; and references therein.
Wang, P. G.; Xian M.; Tang, X.; Wu, X.; Wen, Z.; Cai, T.; Janczuk, A. J. Nitric oxide donors: Chemical activities and biological applications. Chem. Rev. 2002, 102, 1091-1134; and references therein.
Synthesis and calcium channel modulating effects of modified Hantzsch nitrooxyalkyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(pyridinyl or 2-trifluoromethylphenyl)-5-pyridine-carboxylates
Miri, R.; McEwen, C.-A.; Knaus, E. E. Synthesis and calcium channel modulating effects of modified Hantzsch nitrooxyalkyl 1,4-dihydro-2,6-dimethyl-3-nitro-4-(pyridinyl or 2-trifluoromethylphenyl)-5-pyridine-carboxylates. Drug Dev. Res. 2000, 51, 225-232.
A low hazard procedure for the laboratory preparation of polynitrate esters
Marken, C. D.; Kristofferson, C. E.; Roland, M. M.; Manzara, A. P.; Barnes, M. W. A low hazard procedure for the laboratory preparation of polynitrate esters. Synthesis 1977, 484-485.
Preparation of metalated 2,1,3-benzoxa- or thiadiazole and their use in synthesis of dihydropyridine derivatives. Patentschrift, Switz. CH 661,728, 14 August 1987
Heitzmann, M. Preparation of metalated 2,1,3-benzoxa- or thiadiazole and their use in synthesis of dihydropyridine derivatives. Patentschrift, Switz. CH 661,728, 14 August 1987.
Hantzsch 1,4-dihydropyri dines containing a nitrooxyalkyl ester moiety to study calcium channel structure-activity relationships and nitric oxide release
Nguyen, J.-T.; McEwen, C.-A.; Knaus, E. E. Hantzsch 1,4-dihydropyri dines containing a nitrooxyalkyl ester moiety to study calcium channel structure-activity relationships and nitric oxide release. Drug Dev. Res. 2000, 51, 233-243.
Ethylene biosynthesis. 6. Synthesis and evaluation of methylaminocyclopropanocarboxylic acid
Pirrung, M. C.; McGeehan, G. M. Ethylene biosynthesis. 6. Synthesis and evaluation of methylaminocyclopropanocarboxylic acid. J. Org. Chem. 1986, 51, 2103-2106.