| Weight | 285.815 g/mol |
|---|---|
| Formula | C15H24ClNO2 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 8 |
Alprenolol hydrochloride (13707-88-5)
Alprenolol · Aptin · Alpheprol
Score:
#2239 in Biochemistry
,
#4515 in Biology
,
#5716 in Chemistry
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- REDUCTION OF SUDDEN DEATHS AFTER MYOCARDIAL INFARCTION BY TREATMENT WITH ALPRENOLOL: Preliminary Results (The Lancet, 1974)
- Identification of beta-adrenergic receptors in human lymphocytes by (-) (3H) alprenolol binding. (Journal of Clinical Investigation, 1976)
- Rapid changes in rat pineal beta-adrenergic receptor: alterations in l-(3H)alprenolol binding and adenylate cyclase (Proceedings of the National Academy of Sciences of the United States of America, 1975)
- Stereospecific [3H]()-alprenolol binding sites, -adrenergic receptors and adenylate cyclase (Biochemical and Biophysical Research Communications, 1974)
- EFFECT OF ALPRENOLOL ON MORTALITY AMONG PATIENTS WITH DEFINITE OR SUSPECTED ACUTE MYOCARDIAL INFARCTION: Preliminary Results (The Lancet, 1979)
- -Blockers alprenolol and carvedilol stimulate -arrestin-mediated EGFR transactivation (Proceedings of the National Academy of Sciences of the United States of America, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Alprenolol
- Aptin
- Alpheprol
- Aptina
- H 56 28
- Aptine
- AptinDuriles
- Alfeprol
- 1-(o-Allylphenoxy)-3-(isopropylamino)-2-propanol
- H-56-28
- Aptin Duriles
- Aptin-Duriles
- H5628
-
SMILESCC(C)NCC(COC1=CC=CC=C1CC=C)O.Cl
-
InChIKeyRRCPAXJDDNWJBI-UHFFFAOYSA-N
Suppliers
Most-cited Publications
Areas of Application
Safety
Trends
Alternate Names
External Links
Synthesis
ISOPROPYLAMINE
+
Reactant
(Alkylation of primary amines)
Reactant
+
CID 5475562
(Chan-Lam coupling reaction)
2-ALLYLPHENOL
+
Reactant
(Williamson ether)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Alprenolol hydrochloride
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