CHEBI:32315 - zopiclone

ChEBI IDCHEBI:32315
ChEBI Namezopiclone
Stars
DefinitionA pyrrolo[3,4-b]pyrazine compound having a 4-methylpiperazine-1-carboxyl group at the 5-position, a 5-chloropyridin-2-yl group at the 6-position and an oxo-substituent at the 7-position.
Last Modified9 July 2025
DownloadsMolfile
FormulaC17H17ClN6O3
Net Charge0
Average Mass388.815
Monoisotopic Mass388.10507
SMILESCN1CCN(C(=O)OC2c3nccnc3C(=O)N2c2ccc(Cl)cn2)CC1
InChIInChI=1S/C17H17ClN6O3/c1-22-6-8-23(9-7-22)17(26)27-16-14-13(19-4-5-20-14)15(25)24(16)12-3-2-11(18)10-21-12/h2-5,10,16H,6-9H2,1H3
InChIKeyGBBSUAFBMRNDJC-UHFFFAOYSA-N
Wikipedia
Roles Classification
Applications:
central nervous system depressant  A loosely defined group of drugs that tend to reduce the activity of the central nervous system.
sedative  A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.
ChEBI Ontology
Outgoing Relation(s)
zopiclone (CHEBI:32315) has role central nervous system depressant (CHEBI:35488)
zopiclone (CHEBI:32315) has role sedative (CHEBI:35717)
zopiclone (CHEBI:32315) is a monochloropyridine (CHEBI:39172)
zopiclone (CHEBI:32315) is a pyrrolopyrazine (CHEBI:48337)
Incoming Relation(s)
(5R)-zopiclone (CHEBI:53762) is a zopiclone (CHEBI:32315)
eszopiclone (CHEBI:53760) is a zopiclone (CHEBI:32315)
IUPAC Name 
6-(5-chloropyridin-2-yl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl 4-methylpiperazine-1-carboxylate
INNs  Source
zopicloneWHO MedNet
zopicloneWHO MedNet
zopiclonaWHO MedNet
zopiclonumWHO MedNet
Synonyms  Source
(±)-zopicloneDrugBank
6-(5-chloro-2-pyridinyl)-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazin-5-yl 4-methyl-1-piperazinecarboxylateNIST Chemistry WebBook
Brand Names  Source
AmobanKEGG DRUG
ImovaneDrugCentral
ZimovaneDrugCentral
Manual XrefsDatabases
D01372KEGG DRUG
DB01198DrugBank
DE2300491Patent
US3862149Patent
ZopicloneWikipedia
LSM-4408LINCS
2873DrugCentral
HMDB0015329HMDB
Registry NumbersSources
Beilstein:768704Beilstein
CAS:43200-80-2KEGG DRUG
CAS:43200-80-2DrugBank
CAS:43200-80-2ChemIDplus
Citations