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

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H21NOS2
Molecular Weight 355.517
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TINOFEDRINE

SMILES

C[C@H](NCC=C(C1=CSC=C1)C2=CSC=C2)[C@H](O)C3=CC=CC=C3

InChI

InChIKey=JQSHEDRVRBSFCZ-YWZLYKJASA-N
InChI=1S/C20H21NOS2/c1-15(20(22)16-5-3-2-4-6-16)21-10-7-19(17-8-11-23-13-17)18-9-12-24-14-18/h2-9,11-15,20-22H,10H2,1H3/t15-,20-/m0/s1

HIDE SMILES / InChI
Tinofedrine is a dithienylamine derivative patented by Deutsche Gold- und Silber-Scheideanstalt vorm. Roessler for improvement of cerebral and peripheral blood flow. In anesthetized dogs, Tinofedrine causes a remarkable increase of cardiac output by positive inotropic and chronotropic stimulation of the heart and simultaneous reduction of peripheral vascular resistance. In comparison with typical beta-agonists Tinofedrine at isotropically equieffective doses, has a much weaker effect on the heart rate. In coronary circulation, Tinofedrine causes vasodilation so that in a therapeutic dose range increased workload is equalized by sufficient myocardial supply.

Approval Year

PubMed

PubMed

TitleDatePubMed
[The effect of tinofedrine on the EEG].
1978
Patents

Patents

Sample Use Guides

0.12 to 0.17 mg​/kg
Route of Administration: Intravenous
Name Type Language
TINOFEDRINE
INN   MI  
INN  
Official Name English
(+)-(R)-.ALPHA.-((S)-1-((3,3-DI-3-THIENYLALLYL)AMINO)ETHYL)BENZYL ALCOHOL
Systematic Name English
TINOFEDRINE [MI]
Common Name English
tinofedrine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C87053
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
Code System Code Type Description
DRUG CENTRAL
3843
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
PRIMARY
CAS
66788-41-8
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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ChEMBL
CHEMBL2105422
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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EPA CompTox
DTXSID00216907
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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ECHA (EC/EINECS)
266-477-4
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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SMS_ID
100000077208
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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FDA UNII
OVJ0W8F17T
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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MESH
C018159
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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MERCK INDEX
m498
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
PRIMARY Merck Index
INN
3666
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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NCI_THESAURUS
C90634
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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EVMPD
SUB11076MIG
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
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PUBCHEM
3033341
Created by admin on Fri Dec 15 15:46:38 GMT 2023 , Edited by admin on Fri Dec 15 15:46:38 GMT 2023
PRIMARY