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Details

Stereochemistry RACEMIC
Molecular Formula C13H16N2O4
Molecular Weight 264.2771
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DOMIPIZONE

SMILES

COC1=CC=C(C=C1OC)C2=NNC(=O)CC2CO

InChI

InChIKey=ZJWVOYSMOZCLEV-UHFFFAOYSA-N
InChI=1S/C13H16N2O4/c1-18-10-4-3-8(5-11(10)19-2)13-9(7-16)6-12(17)14-15-13/h3-5,9,16H,6-7H2,1-2H3,(H,14,17)

HIDE SMILES / InChI

Molecular Formula C13H16N2O4
Molecular Weight 264.2771
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Domipizone is a platelet aggregation inhibitor, cardiotonic and vasodilator.

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:01:12 GMT 2023
Edited
by admin
on Fri Dec 15 16:01:12 GMT 2023
Record UNII
AV4229D6CH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DOMIPIZONE
INN  
INN  
Official Name English
domipizone [INN]
Common Name English
(±)-6-(3,4-DIMETHOXYPHENYL)-4,5-DIHYDRO-5-(HYDROXYMETHYL)-3(2H)-PYRIDAZINONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
Code System Code Type Description
PUBCHEM
208852
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
CAS
95355-10-5
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
SMS_ID
100000080759
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
NCI_THESAURUS
C65462
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
EVMPD
SUB06357MIG
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
FDA UNII
AV4229D6CH
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106229
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
INN
5917
Created by admin on Fri Dec 15 16:01:12 GMT 2023 , Edited by admin on Fri Dec 15 16:01:12 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY