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Details

Stereochemistry RACEMIC
Molecular Formula C12H14N2O3
Molecular Weight 234.2512
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPROQUALONE

SMILES

CC1=NC2=CC=CC=C2C(=O)N1CC(O)CO

InChI

InChIKey=NTGLQWGMESPVBV-UHFFFAOYSA-N
InChI=1S/C12H14N2O3/c1-8-13-11-5-3-2-4-10(11)12(17)14(8)6-9(16)7-15/h2-5,9,15-16H,6-7H2,1H3

HIDE SMILES / InChI

Molecular Formula C12H14N2O3
Molecular Weight 234.2512
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Diproqualone was used primarily for the treatment of inflammatory pain associated with osteoarthritis. The analgesic activity of diproqualoneis synergistic with that of noramidopyrine. It also display anti-inflammatory action in the rat, inhibiting plantar edema with dextran or serotonin, atopic edema from ovalbumin, etc. It has spasmolytic, anticholinergic and antihistaminic action in higher doses. It is not hypnotic and has no anticonvulsant effects. The therapeutic symptoms for diproqualone are all types of pain: postoperative, posttraumatic, dental, neuritis, anti-inflammatory arthritis, etc.

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis of new 2,3-dihydroquinazolin-4(1H)-one derivatives for analgesic and anti-inflammatory evaluation.
2010 May
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:04:38 GMT 2023
Edited
by admin
on Fri Dec 15 16:04:38 GMT 2023
Record UNII
QY7HLH8V4L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIPROQUALONE
INN   MART.   WHO-DD  
INN  
Official Name English
Diproqualone [WHO-DD]
Common Name English
diproqualone [INN]
Common Name English
DIPROQUALONE [MART.]
Common Name English
4(3H)-QUINAZOLINONE, 3-(2,3-DIHYDROXYPROPYL)-2-METHYL-
Systematic Name English
3-(2,3-DIHYDROXYPROPYL)-2-METHYL-4(3H)-QUINAZOLINONE
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
Code System Code Type Description
EVMPD
SUB07226MIG
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
SMS_ID
100000082354
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
WIKIPEDIA
Diproqualone
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
CAS
36518-02-2
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
PUBCHEM
64112
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
INN
2737
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
ECHA (EC/EINECS)
253-081-1
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
ChEMBL
CHEMBL2106200
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
FDA UNII
QY7HLH8V4L
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
EPA CompTox
DTXSID30865821
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
NCI_THESAURUS
C65433
Created by admin on Fri Dec 15 16:04:38 GMT 2023 , Edited by admin on Fri Dec 15 16:04:38 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY