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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H21N3S
Molecular Weight 347.477
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TIOMERGINE

SMILES

CN1C[C@H](CSC2=CC=CC=N2)C=C3[C@H]1CC4=CNC5=C4C3=CC=C5

InChI

InChIKey=VCRAKEDGLIINLR-AUUYWEPGSA-N
InChI=1S/C21H21N3S/c1-24-12-14(13-25-20-7-2-3-8-22-20)9-17-16-5-4-6-18-21(16)15(11-23-18)10-19(17)24/h2-9,11,14,19,23H,10,12-13H2,1H3/t14-,19-/m1/s1

HIDE SMILES / InChI

Molecular Formula C21H21N3S
Molecular Weight 347.477
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Tiomergine is an ergot alkaloid derivative. It is the agonist of the postulated presynaptic dopamine receptor. Tiomergine is the antiparkinsonian agent. Tiomergine modified brain glucose metabolism in a way similar to the neuroleptics but different from postsynaptic agonists. It was ineffective in the treatment of tardive dyskinesia.

Approval Year

PubMed

PubMed

TitleDatePubMed
Treatment of dyskinetic and dystonic disorders with CF 25-397: clinical and pharmacological aspects.
1980
Bromocriptine and CF 25-397 in the treatment of tardive dyskinesia.
1980 Apr
Presynaptic dopaminergic agonists modify brain glucose metabolism in a way similar to the neuroleptics.
1984 Sep 7
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 17:54:31 GMT 2025
Edited
by admin
on Mon Mar 31 17:54:31 GMT 2025
Record UNII
85J22V47HN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
9,10-DIDEHYDRO-6-METHYL-8B-((2-PYRIDYLTHIO)METHYL)ERGOLINE
Preferred Name English
TIOMERGINE
INN  
INN  
Official Name English
tiomergine [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66884
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
Code System Code Type Description
SMS_ID
100000077231
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
EPA CompTox
DTXSID901024153
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104731
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
NCI_THESAURUS
C152639
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
INN
4640
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
EVMPD
SUB11085MIG
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
CAS
57935-49-6
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
FDA UNII
85J22V47HN
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
PUBCHEM
9884658
Created by admin on Mon Mar 31 17:54:31 GMT 2025 , Edited by admin on Mon Mar 31 17:54:31 GMT 2025
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY