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Details

Stereochemistry ACHIRAL
Molecular Formula C9H8N2O
Molecular Weight 160.1726
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MEDORINONE

SMILES

CC1=NC=CC2=C1C=CC(=O)N2

InChI

InChIKey=OCCZJXAHSUCJSA-UHFFFAOYSA-N
InChI=1S/C9H8N2O/c1-6-7-2-3-9(12)11-8(7)4-5-10-6/h2-5H,1H3,(H,11,12)

HIDE SMILES / InChI

Molecular Formula C9H8N2O
Molecular Weight 160.1726
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Medorinone is an inhibitor of cAMP phosphodiesterase activity. Inhibition of cAMP phosphodiesterase by medorinone in cardiac and vascular smooth muscle is a mechanism by which this agent produces both positive cardiac inotropy and vascular smooth muscle relaxation. It inhibits platelet aggregation.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
0.55 µM [IC50]
PubMed

PubMed

TitleDatePubMed
Novel cAMP PDE III inhibitors: 1,6-naphthyridin-2(1H)-ones.
1992 Dec 25
Electric field mapping and structure-activity relationship for cardiotonic activities of medorinone and some of its analogs.
1997 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:55:19 GMT 2023
Edited
by admin
on Fri Dec 15 15:55:19 GMT 2023
Record UNII
80X61Y4X0B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MEDORINONE
INN   USAN  
USAN   INN  
Official Name English
1,6-NAPHTHYRIDIN-2(1H)-ONE, 5-METHYL-
Systematic Name English
WIN-49016
Code English
WIN 49,016
Code English
WIN-49,016
Code English
MEDORINONE [USAN]
Common Name English
medorinone [INN]
Common Name English
5-Methyl-1,6-naphthyridin-2(1H)-one
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C744
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
Code System Code Type Description
SMS_ID
100000081971
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
ChEMBL
CHEMBL144399
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
FDA UNII
80X61Y4X0B
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
PUBCHEM
5362132
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID50236938
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
CAS
88296-61-1
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
MESH
C064867
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
USAN
W-65
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
INN
5779
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
NCI_THESAURUS
C74352
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
EVMPD
SUB08694MIG
Created by admin on Fri Dec 15 15:55:19 GMT 2023 , Edited by admin on Fri Dec 15 15:55:19 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY