Levobunolol (l-Bunolol) hydrochloride is a strong and non-selective beta-adrenergic receptor antagonist with an IC50 of 48μM.

 

Brand: BCM

 

Melting Point: 209-211°C

 

Specific Rotation: 24589 -19.6±0.7° (c = 2.90 in methanol)

 

Signaling Pathways: GPCR/G Protein; Neuroscience

 

Solubility: Soluble in DMSO; soluble in Ethanol; soluble in Water.

 

Stability: Light Sensitive

 

Isomeric SMILES: CC(C)(C)NC[C@@H](COC1=CC=CC2=C1CCCC2=O)O.Cl  

 

InChIKey: DNTDOBSIBZKFCP-YDALLXLXSA-N  

 

InChI: InChI=1S/C17H25NO3.ClH/c1-17(2,3)18-10-12(19)11-21-16-9-5-6-13-14(16)7-4-8-15(13)20;/h5-6,9,12,18-19H,4,7-8,10-11H2,1-3H3;1H/t12-;/m0./s1

 

Attribute
[Chem Name]	5-[(2S)-3-(tert-butylamino)-2-hydroxypropoxy]-3,4-dihydro-2H-naphthalen-1-one;hydrochloride
[Synonym]	Levobunolol hydrochloride; l-Bunolol hydrochloride
[CAS No.]	27912-14-7
[EINECS]	248-725-3
[MDL No.]	MFCD03425587
[Formula]	C17H26ClNO3
[Molecular]	327.85
[Form]	White to off-white solid
[Storage]	Amber Vial. Refrigerator. Under inert atmosphere

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