U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C20H35NO2S.ClH
Molecular Weight 390.023
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIPROPIDIL HYDROCHLORIDE

SMILES

Cl.CCCCCCCCNCC(O)COC1=CC=C(SC(C)C)C=C1

InChI

InChIKey=QFKMDZYQWDSMPA-UHFFFAOYSA-N
InChI=1S/C20H35NO2S.ClH/c1-4-5-6-7-8-9-14-21-15-18(22)16-23-19-10-12-20(13-11-19)24-17(2)3;/h10-13,17-18,21-22H,4-9,14-16H2,1-3H3;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 C20H35NO2S
Molecular Weight 353.562
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Tipropidil designed for the treatment of cerebral and peripheral vascular diseases. Tipropidil has been investigated because of its expected antihyperviscosity properties. The increase in plasma free fatty acid levels and decrease in lipolytic response were found to be dependent on the amount of Tipropidil administered. Addition of Tipropidil to the in vitro lipolysis system inhibited norepinephrine- and theophylline-induced fatty acid release in a dose-dependent manner. These results suggest a potent inhibitory action for Tipropidyl on fatty acid mobilization in rat adipose tissue.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Effect of vasoactive agents on fatty acid metabolism: inhibition of lipolysis by tipropidil in rat epididymal adipose tissue.
1982 Jan
Action of drugs on the aggregation and deformability of red cells: effect of ABO blood groups.
1983

Sample Use Guides

Single dose - 50 mg/kg body wt
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:28 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:28 GMT 2023
Record UNII
34K00NS0TZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TIPROPIDIL HYDROCHLORIDE
USAN  
USAN  
Official Name English
2-PROPANOL, 1-(4-((1-METHYLETHYL)THIO)PHENOXY)-3-(OCTYLAMINO)-, HYDROCHLORIDE
Systematic Name English
TIPROPIDIL HYDROCHLORIDE [USAN]
Common Name English
TIPROPIDIL HCL
Common Name English
MJ 12,880-1
Code English
MJ-12880-1
Code English
1-(P-(ISOPROPYLTHIO)PHENOXY)-3-(OCTYLAMINO)-2-PROPANOL HYDROCHLORIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
Code System Code Type Description
CAS
70895-39-5
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
MESH
C033800
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
EPA CompTox
DTXSID40991185
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
FDA UNII
34K00NS0TZ
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
ChEMBL
CHEMBL2111005
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
NCI_THESAURUS
C77079
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
PUBCHEM
72175
Created by admin on Fri Dec 15 15:43:28 GMT 2023 , Edited by admin on Fri Dec 15 15:43:28 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
Related Record Type Details
ACTIVE MOIETY