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Details

Stereochemistry RACEMIC
Molecular Formula C25H23ClN4O4
Molecular Weight 478.928
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAZINACLONE

SMILES

ClC1=NC2=NC(=CC=C2C=C1)N3C(CC(=O)N4CCC5(CC4)OCCO5)C6=CC=CC=C6C3=O

InChI

InChIKey=DPGKFACWOCLTCA-UHFFFAOYSA-N
InChI=1S/C25H23ClN4O4/c26-20-7-5-16-6-8-21(28-23(16)27-20)30-19(17-3-1-2-4-18(17)24(30)32)15-22(31)29-11-9-25(10-12-29)33-13-14-34-25/h1-8,19H,9-15H2

HIDE SMILES / InChI

Molecular Formula C25H23ClN4O4
Molecular Weight 478.928
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 18:44:17 UTC 2023
Edited
by admin
on Fri Dec 15 18:44:17 UTC 2023
Record UNII
MHK03047IJ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAZINACLONE
INN   MI   USAN   WHO-DD  
USAN   INN  
Official Name English
DN2327
Code English
PAZINACLONE [USAN]
Common Name English
DN-2327
Code English
1,4-DIOXA-8-AZASPIRO(4.5)DECANE, 8-((2-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-2,3-DIHYDRO-3-OXO-1H-ISOINDOL-1-YL)ACETYL)-
Common Name English
(±)-2-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-3-(((1,4-DIOXA-8-AZASPIRO(4.5)DEC-8-YL)CARBONYL)METHYL)-1-ISOINDOLINONE
Systematic Name English
Pazinaclone [WHO-DD]
Common Name English
A77000
Code English
(±)-8-((2-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-3-OXO-1-ISOINDOLINYL)ACETYL)-1,4-DIOXA-8-AZASPIRO(4.5)DECANE
Common Name English
A-77000
Code English
pazinaclone [INN]
Common Name English
PAZINACLONE [MI]
Common Name English
1H-ISOINDOL-1-ONE, 2-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-3-(2-(1,4-DIOXA-8-AZASPIRO(4.5)DEC-8-YL)-2-OXOETHYL)-2,3-DIHYDRO-
Systematic Name English
1,4-DIOXA-8-AZASPIRO(4.5)DECANE, 8-((2-(7-CHLORO-1,8-NAPHTHYRIDIN-2-YL)-2,3-DIHYDRO-3-OXO-1H-ISOINDOL-1-YL)ACETYL)-, (±)-
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C28197
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
Code System Code Type Description
EPA CompTox
DTXSID70869388
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
ChEMBL
CHEMBL2107504
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
CAS
103255-66-9
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
NCI_THESAURUS
C96874
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
FDA UNII
MHK03047IJ
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
USAN
EE-67
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
MESH
C060382
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
SMS_ID
100000083002
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
PUBCHEM
59743
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
WIKIPEDIA
PAZINACLONE
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
EVMPD
SUB09639MIG
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
INN
7190
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY
MERCK INDEX
m867
Created by admin on Fri Dec 15 18:44:17 UTC 2023 , Edited by admin on Fri Dec 15 18:44:17 UTC 2023
PRIMARY Merck Index
Related Record Type Details
TARGET->PARTIAL AGONIST
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY