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

Details

Stereochemistry ABSOLUTE
Molecular Formula C17H17ClN6O3
Molecular Weight 388.808
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ESZOPICLONE

SMILES

CN1CCN(CC1)C(=O)O[C@@H]2N(C(=O)C3=C2N=CC=N3)C4=CC=C(Cl)C=N4

InChI

InChIKey=GBBSUAFBMRNDJC-INIZCTEOSA-N
InChI=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/t16-/m0/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
ESZOPICLONE
HSDB   INN   JAN   MART.   ORANGE BOOK   USAN   VANDF   WHO-DD  
INN   USAN  
Official Name English
ESZOPICLONE [USAN]
Common Name English
Eszopiclone [WHO-DD]
Common Name English
1-PIPERAZINECARBOXYLIC ACID, 4-METHYL-, (5S)-6-(5-CHLORO-2-PYRIDINYL)-6,7-DIHYDRO-7-OXO-5H-PYRROLO(3,4-B)PYRAZIN-5-YL ESTER
Common Name English
ESZOPICLONE [JAN]
Common Name English
(+)-(5S)-6-(5-CHLOROPYRIDIN-2-YL)-7-OXO-6,7-DIHYDRO-5H-PYRROLO(3,4-B)PYRAZIN-5-YL 4-METHYLPIPERAZINE-1-CARBOXYLATE
Systematic Name English
ESZOPICLONE [VANDF]
Common Name English
ESZOPICLONE CIV [USP-RS]
Common Name English
LUNESTA
Brand Name English
ESZOPICLONE [MART.]
Common Name English
GSK-1755165
Code English
ZOPICLONE S-FORM [MI]
Common Name English
ESZOPICLONE [USP MONOGRAPH]
Common Name English
ESZOPICLONE [HSDB]
Common Name English
ZOPICLONE S-FORM
MI  
Common Name English
ESZOPICLON
Common Name English
ESZOPICLONE [ORANGE BOOK]
Common Name English
ESZOPICLONE CIV
USP-RS  
Common Name English
eszopiclone [INN]
Common Name English
(S)-ZOPICLONE
Common Name English
ESTORRA
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C29756
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
WHO-VATC QN05CF04
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
WHO-ATC N05CF04
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
LIVERTOX NBK548047
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
Code System Code Type Description
MESH
C515051
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
RXCUI
461016
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY RxNorm
USAN
NN-76
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
NCI_THESAURUS
C65545
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
LACTMED
Eszopiclone
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
DRUG CENTRAL
1068
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
RS_ITEM_NUM
1255850
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
MERCK INDEX
m11663
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY Merck Index
PUBCHEM
969472
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
IUPHAR
7429
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
SMS_ID
100000092238
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
CAS
138729-47-2
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
FDA UNII
UZX80K71OE
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
ChEMBL
CHEMBL1522
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
DRUG BANK
DB00402
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
EVMPD
SUB21373
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
DAILYMED
UZX80K71OE
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
INN
8258
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
WIKIPEDIA
ESZOPICLONE
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
HSDB
7472
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
CHEBI
53760
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
EPA CompTox
DTXSID8046086
Created by admin on Fri Dec 15 15:55:44 UTC 2023 , Edited by admin on Fri Dec 15 15:55:44 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of ESZOPICLONE
METABOLITE (PARENT)
Structure of SEP-174559
METABOLITE INACTIVE (PARENT)
Structure of ESZOPICLONE N-OXIDE
METABOLITE INACTIVE (PARENT)
Structure of (S)-N-OXIDEZOPICLONE
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966