Barnidipine hydrochloride is a dihydropyridine calcium channel blocker with a selective effect on CaA receptors. It is an antihypertensive drug that works by reducing peripheral vascular resistance secondary to its vasodilating effect.

 

Brand: BCM

 

Melting Point: 223-226°C

 

Target: Calcium Channel

 

Signaling Pathways: Metabolism; Membrane transporter/Ion channel

 

Specific Rotation: D20 +116.4° (c = 1 in methanol)

 

Solubility: Soluble in DMSO.

 

GHS: GHS07

 

Isomeric SMILES: CC1=C([C@@H](C(=C(N1)C)C(=O)O[C@H]2CCN(C2)CC3=CC=CC=C3)C4=CC(=CC=C4)[N+](=O)[O-])C(=O)OC.Cl  

 

InChIKey: XEMPUKIZUCIZEY-YSCHMLPRSA-N  

 

InChI: InChI=1S/C27H29N3O6.ClH/c1-17-23(26(31)35-3)25(20-10-7-11-21(14-20)30(33)34)24(18(2)28-17)27(32)36-22-12-13-29(16-22)15-19-8-5-4-6-9-19;/h4-11,14,22,25,28H,12-13,15-16H2,1-3H3;1H/t22-,25-;/m0./s1

 

Attribute
[CAS No.]	104757-53-1
[Formula]	C27H30ClN3O6
[Molecular]	528
[Chem Name]	5-O-[(3S)-1-benzylpyrrolidin-3-yl] 3-O-methyl (4S)-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3,5-dicarboxylate;hydrochloride
[Synonym]	Barnidipine hydrochloride
[Storage]	Sealed in dry. Room Temperature
[MDL No.]	MFCD00915772
[Form]	A crystalline solid

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