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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H22N4O2
Molecular Weight 350.4143
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ROMERGOLINE

SMILES

CN1C[C@H](CN2CC(=O)NC(=O)C2)C=C3[C@H]1CC4=CNC5=C4C3=CC=C5

InChI

InChIKey=RJCXNCSJGRUWRW-SJKOYZFVSA-N
InChI=1S/C20H22N4O2/c1-23-8-12(9-24-10-18(25)22-19(26)11-24)5-15-14-3-2-4-16-20(14)13(7-21-16)6-17(15)23/h2-5,7,12,17,21H,6,8-11H2,1H3,(H,22,25,26)/t12-,17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H22N4O2
Molecular Weight 350.4143
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Romergoline (FCE 23884) is an ergoline derivative and a dopamine receptor agonist and antagonist. Its action depends on the functional state of the biological substrate, mostly related to the presence or absence of dopamine. In healthy animals, it behaves as a full dopamine antagonist, but in denervated models it behaves as an agonist. Therefore, romergoline was suggested to be potentially useful in both psychotic states and extrapyramidal diseases. In Parkinson patients, the degree of dopamine receptor stimulation was found to be insufficient to improve symptoms. Information about further development of romergoline is not available.

Approval Year

PubMed

PubMed

TitleDatePubMed
Effect of the putative dopamine D1 agonist and D2 antagonist FCE 23884 on Parkinson's disease.
1996-05
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 18:21:59 GMT 2025
Edited
by admin
on Mon Mar 31 18:21:59 GMT 2025
Record UNII
I4880ZI08R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-((9,10-DIDEHYDRO-6-METHYLERGOLIN-8B-YL)METHYL)-2,6-PIPERAZINEDIONE
Preferred Name English
ROMERGOLINE
INN  
INN  
Official Name English
romergoline [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C66884
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
Code System Code Type Description
EVMPD
SUB10372MIG
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
INN
6859
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
PUBCHEM
65898
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
CAS
107052-56-2
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
EPA CompTox
DTXSID60147889
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
SMS_ID
100000084374
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
FDA UNII
I4880ZI08R
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
NCI_THESAURUS
C90839
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
ChEMBL
CHEMBL2104885
Created by admin on Mon Mar 31 18:21:59 GMT 2025 , Edited by admin on Mon Mar 31 18:21:59 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY