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ICONC16267 Labetalone hydrochloride (96441-14-4)
 
 
Catalog No.: C16267
CAS No.: 96441-14-4
Synonym: 2-Hydroxy-5-(2-(4-phenylbutan-2-ylamino)acetyl)benzamide hydrochloride;5-{2[(1-methyl-3-phenyl)propyl]amido}ethyl-1-one salicylamide hydrochloride
Chemical Name:
2-Hydroxy-5-(2-(4-phenylbutan-2-ylamino)acetyl)benzamide hydrochloride;5-{2[(1-methyl-3-phenyl)propyl]amido}ethyl-1-one salicylamide hydrochloride
Molecular Formula: C19H23ClN2O3
Molecular Weight: 362.85
 
Technical Data:
Appearance: off-white powder
Solubility: Soluble in Water
Purity: ≥99%
Storage: at -20℃ 2 years
Original QC Data:
Shipping Conditions: Ambient Temp.
 
Price and Availability of Labetalone hydrochloride:

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Biological Activity:
Labetalone hydrochloride combines both selective, competitive, alpha-1-adrenergic blocking and nonselective, competitive, beta-adrenergic blocking activity in a single substance. In man, the ratios of alpha- to beta- blockade have been estimated to be approximately 1:3 and 1:7 following oral and intravenous (IV) administration, respectively. The principal physiologic action of labetalol is to competitively block adrenergic stimulation of β-receptors within the myocardium (β1-receptors) and within bronchial and vascular smooth muscle (β2-receptors), and α1-receptors within vascular smooth muscle. This causes a decrease in systemic arterial blood pressure and systemic vascular resistance without a substantial reduction in resting heart rate, cardiac output, or stroke volume, apparently because of its combined α- and β-adrenergic blocking activity.
 
References:

1. Katzung, Bertram G. (2006). Basic and clinical pharmacology. New York: McGraw-Hill Medical. p. 170. ISBN 0-07-145153-6.

2. Shiohara T, Kano Y (2007). "Lichen planus and lichenoid dermatoses". In Bolognia JL.Dermatology. St. Louis: Mosby. p. 161. ISBN 1-4160-2999-0.

 
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