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
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
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
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:23:50 GMT 2023
by
admin
on
Fri Dec 15 15:23:50 GMT 2023
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Record UNII |
1E0AQI279F
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Record Status |
Validated (UNII)
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Record Version |
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-
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Official Name | English | ||
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Systematic Name | English | ||
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Code | English | ||
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Common Name | English | ||
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Common Name | English |
Classification Tree | Code System | Code | ||
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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
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Code System | Code | Type | Description | ||
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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
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C152462
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admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
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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
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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
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264-046-5
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admin on Fri Dec 15 15:23:50 GMT 2023 , Edited by admin on Fri Dec 15 15:23:50 GMT 2023
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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
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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
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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
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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
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PRIMARY | Merck Index |
Related Record | Type | Details | ||
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ACTIVE MOIETY |