BMY 20064

structure given in first source

Also Known As:

3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-, 3-(4-(2-methoxyphenyl)-1-piperazinyl)propyl methyl ester; BMY-20064

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

1.	Ganglion Cysts (Ganglion) 04/01/1988 - "It was less active than nifedipine in antagonizing Ca2+-induced contractions of isolated guinea pig papillary muscles paced at 0.2, 1.0, or 2 Hz. BMY 20064 was a potent (0.1-0.2 X prazosin) and selective alpha 1-adrenoceptor antagonist in radioligand binding assays and in ganglion-blocked anesthetized rats challenged with phenylephrine. "

1.	Prazosin (Minipress)
2.	Phenylephrine (Neo-Synephrine)
3.	Nifedipine (Adalat)