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Details

Stereochemistry ACHIRAL
Molecular Formula C19H19Cl2N3O3
Molecular Weight 408.278
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PINADOLINE

SMILES

ClCCCCC(=O)NNC(=O)N1CC2=CC=CC=C2OC3=CC=C(Cl)C=C13

InChI

InChIKey=OUNSOXPSCMCFHX-UHFFFAOYSA-N
InChI=1S/C19H19Cl2N3O3/c20-10-4-3-7-18(25)22-23-19(26)24-12-13-5-1-2-6-16(13)27-17-9-8-14(21)11-15(17)24/h1-2,5-6,8-9,11H,3-4,7,10,12H2,(H,22,25)(H,23,26)

HIDE SMILES / InChI

Molecular Formula C19H19Cl2N3O3
Molecular Weight 408.278
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Pinadoline is a competitive PGE2 antagonist. It is an analgesic agent. Pinadoline demonstrated the antinociceptive activity in the rat using the writhing and the formalin tests. In the writhing test, pinadoline was significantly more potent than inhibitors of PG synthesis, but less potent than opiate analgesics. In the formalin test, pinadoline appeared less active than aspirin and ibuprofen and more active than acetaminophen. Pinadoline does not possess the antiinflammatory activity of aspirin and ibuprofen and may be more like acetaminophen, which had diminished antiinflammatory activity. At high concentrations, pinadoline is a non-competitive antagonist of serotonin in guinea-pig ileum.

Approval Year

PubMed

PubMed

TitleDatePubMed
N-substituted dibenzoxazepines as analgesic PGE2 antagonists.
1993-10-29
The antinociceptive effects of prostaglandin antagonists in the rat.
1987-01-20

Sample Use Guides

In Vivo Use Guide
Curator's Comment: Rat data
150 and 300 mg/kg in a volume of 2 ml/kg
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Wed Apr 02 09:16:51 GMT 2025
Edited
by admin
on Wed Apr 02 09:16:51 GMT 2025
Record UNII
KUO32K2TRD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SC-25469
Preferred Name English
PINADOLINE
INN   USAN  
INN   USAN  
Official Name English
DIBENZ(B,F)(1,4)OXAZEPINE-10(11H)-CARBOXYLIC ACID, 8-CHLORO-, 2-(5-CHLORO-1-OXOPENTYL)HYDRAZIDE
Common Name English
1-((8-CHLORODIBENZ(B,F)(1,4)OXAZEPIN-10(11H-YL)CARBONYL)-2-(5-CHLOROVALERYL)HYDRAZINE
Common Name English
PINADOLINE [USAN]
Common Name English
pinadoline [INN]
Common Name English
8-CHLORODIBENZ(B,F) (1,4)OXAZEPINE-10(11H)-CARBOXYLIC ACID,-2-(5-CHLORO-1-OXOPENTYL)HYDRAZIDE
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C241
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
Code System Code Type Description
PUBCHEM
38191
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
SMS_ID
100000081976
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
NCI_THESAURUS
C82227
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
USAN
U-4
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
CAS
38955-22-5
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
FDA UNII
KUO32K2TRD
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
EVMPD
SUB09849MIG
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
EPA CompTox
DTXSID40192251
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
INN
5404
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
ChEMBL
CHEMBL114395
Created by admin on Wed Apr 02 09:16:51 GMT 2025 , Edited by admin on Wed Apr 02 09:16:51 GMT 2025
PRIMARY
Related Record Type Details
ACTIVE MOIETY