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Details

Stereochemistry MIXED
Molecular Formula C20H27NO4S.ClH
Molecular Weight 413.959
Optical Activity UNSPECIFIED
Defined Stereocenters 0 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SULFINALOL HYDROCHLORIDE

SMILES

Cl.COC1=CC=C(CCC(C)NCC(O)C2=CC([S+](C)[O-])=C(O)C=C2)C=C1

InChI

InChIKey=KJSMCQZGOIBBGM-UHFFFAOYSA-N
InChI=1S/C20H27NO4S.ClH/c1-14(4-5-15-6-9-17(25-2)10-7-15)21-13-19(23)16-8-11-18(22)20(12-16)26(3)24;/h6-12,14,19,21-23H,4-5,13H2,1-3H3;1H

HIDE SMILES / InChI
Sulfinalol is a hydroxyphenylalkanolamine derivative patented by Sterling Drug Inc. as the antiarrhythmic, antihypertensive, vasodilating, and adrenergic agent. Oral administration of sulfinalol reduces the pressure of conscious spontaneously hypertensive rats. Antihypertensive action of sulfinalol was inhibited by propranolol pretreatment. Sulfinalol demonstrates effective beta-adrenergic blockade at the antihypertensive dose tested as judged by inhibition of the chronotropic responses to sympathetic stimulation and isoproterenol in pithed rats. In the renal hypertensive dog. sulfinalol lowered both systolic and diastolic blood pressure to normal values with an only slight change in heart rate.

Approval Year

PubMed

PubMed

TitleDatePubMed
Antihypertensive actions of an isomer of labetalol and other vasodilator-beta-adrenoceptor blockers.
1983-02
Patents

Patents

Name Type Language
SULFINALOL HYDROCHLORIDE
MI   USAN  
USAN  
Official Name English
WIN 40808-7
Preferred Name English
BENZENEMETHANOL, 4-HYDROXY-.ALPHA.-(((3-(4-METHOXYPHENYL)-1-METHYLPROPYL)AMINO)METHYL)-3-(METHYLSULFINYL)-, HYDROCHLORIDE
Systematic Name English
WIN-40808-7
Code English
SULFINALOL HYDROCHLORIDE [USAN]
Common Name English
4-HYDROXY-.ALPHA.-(((3-(P-METHOXYPHENYL)-1-METHYLPROPYL)AMINO)METHYL)-3-(METHYLSULFINYL)BENZYL ALCOHOL HYDROCHLORIDE
Common Name English
SULFINALOL HYDROCHLORIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
Code System Code Type Description
MESH
C030225
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
PRIMARY
NCI_THESAURUS
C152462
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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FDA UNII
1E0AQI279F
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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CAS
63251-39-8
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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ECHA (EC/EINECS)
264-046-5
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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EPA CompTox
DTXSID50979297
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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SMS_ID
300000055249
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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ChEMBL
CHEMBL424518
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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PUBCHEM
44438
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
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MERCK INDEX
m1258
Created by admin on Mon Mar 31 17:56:20 GMT 2025 , Edited by admin on Mon Mar 31 17:56:20 GMT 2025
PRIMARY Merck Index