Phosphonium,tributyl[[4-[[(2S)-2-[[(cyclohexylamino)(cyclohexylimino)methyl]amino]-3-(2-naphthalenyl)-1-oxopropyl]amino]phenyl]methyl]-,chloride (1:1) (151039-63-3)

Identification
Name:	Phosphonium,tributyl[[4-[[(2S)-2-[[(cyclohexylamino)(cyclohexylimino)methyl]amino]-3-(2-naphthalenyl)-1-oxopropyl]amino]phenyl]methyl]-,chloride (1:1)
Synonyms:	Phosphonium,[[4-[[(2S)-2-[[bis(cyclohexylamino)methylene]amino]-3-(2-naphthalenyl)-1-oxopropyl]amino]phenyl]methyl]tributyl-,chloride (9CI); Phosphonium,[[4-[[2-[[bis(cyclohexylamino)methylene]amino]-3-(2-naphthalenyl)-1-oxopropyl]amino]phenyl]methyl]tributyl-,chloride, (S)-; Win 64338
CAS:	151039-63-3
Molecular Formula:	C45H68 N4 O P . Cl
Molecular Weight:	783.94
InChI:	InChI=1/C45H67N4OP.2ClH/c1-4-7-30-51(31-8-5-2,32-9-6-3)35-36-25-28-42(29-26-36)46-44(50)43(34-37-24-27-38-18-16-17-19-39(38)33-37)49-45(47-40-20-12-10-13-21-40)48-41-22-14-11-15-23-41;;/h16-19,24-29,33,40-41,43H,4-15,20-23,30-32,34-35H2,1-3H3,(H2-,46,47,48,49,50);2*1H/t43-;;/m1../s1
Molecular Structure:
Properties
Flash Point:	°C
Boiling Point:	°Cat760mmHg
Density:	g/cm³
Biological Activity:	The first potent, non-peptide, competitive bradykinin B 2 receptor antagonist. In organ bath studies, WIN 64338 inhibits [ 3 H]-bradykinin binding on guinea pig trachea with nanomolar affinity but is not active in the rabbit aorta (the classical bradykinin B 1 preparation).
Flash Point:	°C
Safety Data