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2517584-04-0

2517584-04-0 Structure

2517584-04-0 Structure
IdentificationBack Directory
[Name]

INDEX NAME NOT YET ASSIGNED
[CAS]

2517584-04-0
[Synonyms]

[Molecular Formula]

C11H18ClNO3
[MOL File]

2517584-04-0.mol
[Molecular Weight]

247.72
Chemical PropertiesBack Directory
[storage temp. ]

Store at -20°C
[solubility ]

DMSO: slightly soluble,Methanol: slightly soluble
[form ]

A solid
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P321-P362+P364-P332+P313-P337+P313-P403+P233-P405-P501
Hazard InformationBack Directory
[Uses]

Isoprenaline-d7 (hydrochloride) is a deuterated labeled Isoprenaline (hydrochloride)[1]. Isoprenaline (Isoproterenol) hydrochloride is a non-selective, orally active β-adrenergic receptor agonist. Isoprenaline has potent peripheral vasodilator, bronchodilator, and cardiac stimulating activities. Isoprenaline can be used for the research of bradycardia and bronchial asthma[2][3][4][5][6][7].
[Biological Activity]

Isoproterenol-d7 is intended for use as an internal standard for the quantification of isoproterenol by GC- or LC-MS. Isoproterenol is an agonist of β1- and β2-adrenergic receptors (β1- and β2-ARs; Kis = 224 and 458 nM, respectively).1 It is selective for β1- and β2-ARs over β3-ARs (Ki = 1,570 nM). Isoproterenol inhibits contractions in isolated field-stimulated rat vas deferens (EC50 = 45.6 nM).2 In vivo, isoproterenol (0.33 mg/kg) decreases blood pressure and increases water intake in nephrectomized rats.3 It reduces blood pressure and increases heart rate in renal hypertensive rabbits.4 Isoproterenol inhibits histamine-induced bronchospasms in anesthetized dogs.5 Formulations containing isoproterenol have been used in the treatment of bradydysrhythmias and to improve breathing during anesthesia.
[in vivo]

Isoprenaline (Isoproterenol) hydrochloride (oral, 0.27-0. 64 μg/kg) is extensively metabolizes by a relatively small number of reactions in dogs[7].

[References]

1.Hoffmann, C., Leitz, M.R., Oberdorf-Maass, S., et al.Comparative pharmacology of human β-adrenergic receptor subtypes—characterization of stably transfected receptors in CHO cellsNaunyn Schmiedebergs Arch. Pharmacol.369(2)151-159(2004) 2.Lotti, V.J., Cerino, D., and Kling, P.Characterization of the adrenoreceptor activities of isoprenaline in the field stimulated rat vas deferens: Selective supersensitivity to β2-mediated responses following reserpine treatmentJ. Auton. Pharmacol.2(3)169-174(1982) 3.Hosutt, J.A., Rowland, N., and Stricker, E.M.Hypotension and thirst in rats after isoproterenol treatmentPhysiol. Behav.21(4)593-598(1978) 4.van Boom, M., and Saxena, P.R.Systemic and regional haemodynamic responses to isoprenaline in conscious renal hypertensive rabbitsClin. Exp. Pharmacol. Physiol.8(3)227-239(1981) 5.Wasserman, M.A., and Levy, B.Cardiovascular and bronchomotor responses to selective beta adrenergic receptor agonists in the anesthetized dogJ. Pharmacol. Exp. Ther.189(2)445-455(1974)
2517584-04-0 suppliers list
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Company Name: Cayman Chemical Company  
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Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Website: www.caymanchem.com
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