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Details

Stereochemistry RACEMIC
Molecular Formula C16H23N3S
Molecular Weight 289.439
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GMC-1111 FREE BASE

SMILES

CCCN(CCC)C1CC2=CC3=C(C=C2C1)N=C(N)S3

InChI

InChIKey=REAPOTFJKWYQFW-UHFFFAOYSA-N
InChI=1S/C16H23N3S/c1-3-5-19(6-4-2)13-7-11-9-14-15(10-12(11)8-13)20-16(17)18-14/h9-10,13H,3-8H2,1-2H3,(H2,17,18)

HIDE SMILES / InChI

Molecular Formula C16H23N3S
Molecular Weight 289.439
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Motor effects of a dopamine stabilizer (GMC1111) in primate models of Parkinson and hemiparkinsonism.
2003-01-17
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:09:49 GMT 2025
Edited
by admin
on Mon Mar 31 22:09:49 GMT 2025
Record UNII
BT2QU919S1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
5H-INDENO(5,6-D)THIAZOLE-2,6-DIAMINE, 6,7-DIHYDRO-N6,N6-DIPROPYL-
Preferred Name English
GMC-1111 FREE BASE
Common Name English
Code System Code Type Description
CAS
254885-67-1
Created by admin on Mon Mar 31 22:09:49 GMT 2025 , Edited by admin on Mon Mar 31 22:09:49 GMT 2025
PRIMARY
FDA UNII
BT2QU919S1
Created by admin on Mon Mar 31 22:09:49 GMT 2025 , Edited by admin on Mon Mar 31 22:09:49 GMT 2025
PRIMARY
PUBCHEM
9904074
Created by admin on Mon Mar 31 22:09:49 GMT 2025 , Edited by admin on Mon Mar 31 22:09:49 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY