Details
Stereochemistry | RACEMIC |
Molecular Formula | C13H21NO2S.ClH |
Molecular Weight | 291.837 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CSC1=C(OCC(O)CNC(C)C)C=CC=C1
InChI
InChIKey=PZWMMXHCUXTDQM-UHFFFAOYSA-N
InChI=1S/C13H21NO2S.ClH/c1-10(2)14-8-11(15)9-16-12-6-4-5-7-13(12)17-3;/h4-7,10-11,14-15H,8-9H2,1-3H3;1H
Molecular Formula | C13H21NO2S |
Molecular Weight | 255.376 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
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 |
Tiprenolol (DU21445) has been shown by both in vitro and in vivo animal experiments, to possess strong beta-adrenergic blocking but a relatively less strong negative inotropic activity. The same report also demonstrated by its inhibiting influence on spontaneous mobility of rat uterus, an intrinsic beta-sympathomimetic activity. Tiprenolol reveals effects similar to propranolol. Tiprenolol was shown to have significantly less heart rate slowing effect at rest than propranolol. However, all other measurements failed to show any difference of statistical significance between the two drugs with respect to any negative inotropic or beta‐blocking activity. The administration of tiprenolol or propranolol depressed the arterial pressure and caused the deaths of some dogs in which a coronary artery had been ligated.
Approval Year
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4149632
Single dose - 2 mg
Route of Administration:
Intravenous
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:24:01 GMT 2023
by
admin
on
Fri Dec 15 15:24:01 GMT 2023
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Record UNII |
23XED8VNVE
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Record Status |
Validated (UNII)
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Record Version |
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-
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NCI_THESAURUS |
C29576
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23XED8VNVE
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C152652
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39832-43-4
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CHEMBL2111163
Created by
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3014729
Created by
admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
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Related Record | Type | Details | ||
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PARENT -> SALT/SOLVATE |
Related Record | Type | Details | ||
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ACTIVE MOIETY |