ChemicalBook--->CAS DataBase List--->75659-07-3

75659-07-3

75659-07-3 Structure

75659-07-3 Structure
IdentificationBack Directory
[Name]

DILEVALOL
[CAS]

75659-07-3
[Synonyms]

Levadil
Unicard
Dilevaol
Dilevalon
DILEVALOL
Sch-19927
Dilevalolum
DILEVALOL HCL
(R,R)-Labetalol
Dilevalolum [latin]
2-Hydroxy-5-((R)-1-hydroxy-2-(((R)-4-phenylbutan-2-yl)aMino)ethyl)benzaMide
2-Hydroxy-5-[(R)-1-hydroxy-2-[[(R)-1-methyl-3-phenylpropyl]amino]ethyl]benzamide
2-Hydroxy-5-((1R)-1-hydroxy-2-(((1R)-1-methyl-3-phenylpropyl)amino)ethyl)benzamide
(-)-5-((1R)-1-Hydroxy-2-((1R)-1-methyl-3-phenylpropylamino)ethyl)salicylamid [iupac]
Benzamide, 2-hydroxy-5-((1R)-1-hydroxy-2-(((1R)-1-methyl-3-phenylpropyl)amino)ethyl)-
Benzamide, 2-hydroxy-5-(1-hydroxy-2-((1-methyl-3-phenylpropyl)amino)ethyl)-, (R-(R*,R*))-
[Molecular Formula]

C19H24N2O3
[MDL Number]

MFCD00072111
[MOL File]

75659-07-3.mol
[Molecular Weight]

328.41
Chemical PropertiesBack Directory
[Boiling point ]

552.7±50.0 °C(Predicted)
[density ]

1.200±0.06 g/cm3(Predicted)
[pka]

8.21±0.31(Predicted)
Hazard InformationBack Directory
[Description]

Dilevalol is a "dual-mechanism" antihypertensive reportedly suitable for a wide range of patients. Its partial beta2-agonist action is expected to induce vasodilation, whereas its beta1-antagonist component may protect against stress-induced hemodynamic charges without altering the cardiac output. Dilevalol is the R,R-isomer of labetalol.
[Originator]

Schering Plough (USA)
[Uses]

(R,R)-Labetalol is a specific competitive antagonist at both α-and β-adrenergic receptor sites. (R,R)-Labetalol is used as an antihypertensive.
[Uses]

Specific competitive antagonist at both α-and β-adrenergic receptor sites. Antihypertensive.
[Definition]

ChEBI: (R,R)-labetalol is a 2-hydroxy-5-{1-hydroxy-2-[(4-phenylbutan-2-yl)amino]ethyl}benzamide that has 1R,2R-configuration. It is a conjugate base of a dilevalol(1+).
[Brand name]

Levadil; Dilevalon
[World Health Organization (WHO)]

Dilevalol, a beta-adrenoreceptor antagonist, was introduced into medicine in 1989 for the treatment of hypertension. Shortly afterwards, its use became associated with isolated cases of hepatic toxicity. Although few cases were reported, the manufacturer discontinued sales in Japan and Portugal, the only countries where the drug was marketed, and withdrew applications for registration elsewhere.
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