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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
Structure of TIPRENOLOL HYDROCHLORIDE

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

HIDE SMILES / InChI

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

PubMed

PubMed

TitleDatePubMed
Effects of tiprenolol, practolol and propranolol on experimental ventricular tachyarrhythmias.
1974 Jun
[Drug effects on blood pressure and heart rate in unanesthetized animals. (1). Effects of beta-blocking agents (author's transl)].
1977 May
Patents

Patents

Sample Use Guides

Single dose - 2 mg
Route of Administration: Intravenous
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:24:01 GMT 2023
Edited
by admin
on Fri Dec 15 15:24:01 GMT 2023
Record UNII
23XED8VNVE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIPRENOLOL HYDROCHLORIDE
USAN  
USAN  
Official Name English
TIPRENOLOL HYDROCHLORIDE [USAN]
Common Name English
(±)-1-(ISOPROPYLAMINO)-3-(O-(METHYLTHIO)PHENOXY)-2-PROPANOL HYDROCHLORIDE
Common Name English
DU-21445
Code English
PROPANOL, 1-((1-METHYLETHYL)AMINO)-3-(2-(METHYLTHIO)PHENOXY)-, HYDROCHLORIDE, (±)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29576
Created by admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
Code System Code Type Description
FDA UNII
23XED8VNVE
Created by admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
PRIMARY
NCI_THESAURUS
C152652
Created by admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
PRIMARY
CAS
39832-43-4
Created by admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111163
Created by admin on Fri Dec 15 15:24:01 GMT 2023 , Edited by admin on Fri Dec 15 15:24:01 GMT 2023
PRIMARY
PUBCHEM
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
PRIMARY
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