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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=C(O)C(=C2)[S+](C)[O-])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

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C20H27NO4S
Molecular Weight 377.498
Charge 0
Count
Stereochemistry MIXED
Additional Stereochemistry No
Defined Stereocenters 0 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

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 Feb
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:50 GMT 2023
Edited
by admin
on Fri Dec 15 15:23:50 GMT 2023
Record UNII
1E0AQI279F
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFINALOL HYDROCHLORIDE
MI   USAN  
USAN  
Official Name English
BENZENEMETHANOL, 4-HYDROXY-.ALPHA.-(((3-(4-METHOXYPHENYL)-1-METHYLPROPYL)AMINO)METHYL)-3-(METHYLSULFINYL)-, HYDROCHLORIDE
Systematic Name English
WIN 40808-7
Code 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 Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
Code System Code Type Description
MESH
C030225
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
NCI_THESAURUS
C152462
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
FDA UNII
1E0AQI279F
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
CAS
63251-39-8
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
ECHA (EC/EINECS)
264-046-5
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
EPA CompTox
DTXSID50979297
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
ChEMBL
CHEMBL424518
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
PUBCHEM
44438
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY
MERCK INDEX
m1258
Created by admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
PRIMARY Merck Index
Related Record Type Details
ACTIVE MOIETY