Specific Target Organ Toxicity – Single exposure, category 3
Storage Temperature
2-8°C
Physical Property
Optical Rotation
[α]25/D -25.5°, c = 1.0 in ethanol(lit.)
Solubility
45% (w/v) aq 2-hydroxypropyl-β-cyclodextrin: soluble8.0 mg/mL
H2O: soluble50 mg/mL (With heat. Aqueous solutions are most stable at pH 3.0 and decompose rapidly at basic pH. Decomposition is accompanied by discoloration of the solution.)
DMSO: <14.5 mg/mL
ethanol: soluble10 mg/mL
Melting Point
193-195 °C(lit.)
Apperance
powder
Pharmacology Properties
Gene Information
human ... ADRB1(153), ADRB2(154), ADRB3(155), HTR1A(3350), HTR1B(3351), HTR1D(3352), HTR1E(3354), HTR1F(3355)
Product Information
Purity
≥98% (TLC)
Molecule Details
包装 100, 500 mg in glass bottle Biochem/physiol Actions Active β-adrenoceptor blocking enantiomer, as measured by inhibition of isoprenaline-induced tachycardia; Propranolol is also non-specific 5-HT1A, 5-HT1B and 5-HT1C serotonin receptor antagonist. The stereoselective association of mianserin and propranolol with the 5HT1A, 5HT1B and 5HT1C sites may prove useful in the characterization of these sites