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Details

Stereochemistry RACEMIC
Molecular Formula C12H20N2O4S.ClH
Molecular Weight 324.824
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOTERENOL HYDROCHLORIDE

SMILES

Cl.CC(C)NCC(O)C1=CC=C(O)C(NS(C)(=O)=O)=C1

InChI

InChIKey=LTQWQTNRIBKUMN-UHFFFAOYSA-N
InChI=1S/C12H20N2O4S.ClH/c1-8(2)13-7-12(16)9-4-5-11(15)10(6-9)14-19(3,17)18;/h4-6,8,12-16H,7H2,1-3H3;1H

HIDE SMILES / InChI
Soterenol [(+)-1-(3-methanesulphonamido, 4-hydroxyphenyl)-2-isopropylaminoethanol, MJ 1992] is a directly acting sympathomimetic amine which has been shown to display Beta2-adrenoceptor selectivity. Soterenol, a methanesulfonamido-phenethanolamine related structurally to isoproterenol, was a highly effective bronchodilator agent in several animal species by various routes of administration. The bronchodilator potency of soterenol was equivalent to, or greater than, that of isoproterenol. Soterenol also had potent stimulant action on the alpha-receptor of the smooth muscle.

Approval Year

PubMed

PubMed

TitleDatePubMed
Application of trihydroxyindole reaction to methanesulfonanilides: fluorometric analysis for soterenol and mesuprine.
1976 May
Patents

Sample Use Guides

In Vivo Use Guide
Treatment with soterenol (0.3-300 ug/kg, i.v.) increased the mean arterial blood pressure and decreased heart rate in rabbits.
Route of Administration: Intravenous
In Vitro Use Guide
Soterenol (0.02-0.5 ug/ml) inhibited responses of the isolated guinea-pig trachea to transmural electrical stimulation. Increases in the force of contraction of guinea-pig left atria which were isolated and electrically driven were obtained with soterenol (5-100 ug/ml)
Name Type Language
SOTERENOL HYDROCHLORIDE
USAN  
USAN  
Official Name English
METHANESULFONAMIDE, N-(2-HYDROXY-5-(1-HYDROXY-2-((1-METHYLETHYL)AMINO)ETHYL)PHENYL)-, MONOHYDROCHLORIDE
Common Name English
SOTERENOL MONOHYDROCHLORIDE [MI]
Common Name English
DL-SOTERENOL HYDROCHLORIDE
Common Name English
2'-HYDROXY-5'-(1-HYDROXY-2-(ISOPROPYLAMINO)ETHYL)METHANESULFONAMIDE MONOHYDROCHLORIDE
Common Name English
SOTERENOL HYDROCHLORIDE [USAN]
Common Name English
METHANESULFONAMIDE, N-(2-HYDROXY-5-(1-HYDROXY-2-((1-METHYLETHYL)AMINO)ETHYL)PHENYL)-, HYDROCHLORIDE (1:1)
Systematic Name English
(±)-SOTERENOL HYDROCHLORIDE
Common Name English
SOTERENOL HCL
Common Name English
(±)-2'-HYDROXY-5'-(1-HYDROXY-2-(ISOPROPYLAMINO)ETHYL)METHANESULFONAMIDE MONOHYDROCHLORIDE
Common Name English
MJ 1992
Code English
MJ-1992
Code English
SOTERENOL MONOHYDROCHLORIDE
MI  
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C319
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID60933320
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
PRIMARY
NCI_THESAURUS
C152410
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
PRIMARY
PUBCHEM
66375
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
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FDA UNII
YNR17WO88K
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
PRIMARY
CAS
14816-67-2
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
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ChEMBL
CHEMBL30746
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
PRIMARY
ECHA (EC/EINECS)
238-889-4
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
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MERCK INDEX
m10125
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
PRIMARY Merck Index
CAS
28418-29-3
Created by admin on Fri Dec 15 18:57:26 GMT 2023 , Edited by admin on Fri Dec 15 18:57:26 GMT 2023
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