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Details

Stereochemistry RACEMIC
Molecular Formula C12H12N4OS
Molecular Weight 260.315
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of MOTAPIZONE

SMILES

CC1CC(=O)NN=C1C2=CC(=CS2)N3C=CN=C3

InChI

InChIKey=NPFVRBCDMFKOPY-UHFFFAOYSA-N
InChI=1S/C12H12N4OS/c1-8-4-11(17)14-15-12(8)10-5-9(6-18-10)16-3-2-13-7-16/h2-3,5-8H,4H2,1H3,(H,14,17)

HIDE SMILES / InChI

Molecular Formula C12H12N4OS
Molecular Weight 260.315
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Motapizone is a pyridazinone derivative patented by pharmaceutical company Nattermann, A., und Cie. G.m.b.H. as an antithrombotic and hypotensive agent. Motapizone ats as a potent inhibitor of the isoenzyme phophodiesterase type III. In preclinical studies potent antithrombotic and hypotensive properties of motapizone has been shown in rats, cats, and dogs. In normal human volunteers, single oral doses of motapizone up to 10 mg produced significant inhibition of platelet aggregation measured by the ex vivo method. These effects were dependent upon the dose of motapizone and associated with an increase in heart rate and a reduction in diastolic blood pressure.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
PubMed

PubMed

TitleDatePubMed
Hypotensive and antiplatelet actions of motapizone depend on dose and time after ingestion.
1986
Patents

Patents

Sample Use Guides

1 to 10 mg as a single dose
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:32:31 UTC 2023
Edited
by admin
on Fri Dec 15 16:32:31 UTC 2023
Record UNII
C4A61P8A37
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
MOTAPIZONE
INN  
INN  
Official Name English
MOTAPIZON
Common Name English
(±)-4,5-DIHYDRO-6-(4-IMIDAZOL-1-YL-2-THIENYL)-5-METHYL-3(2H)-PYRIDAZINONE
Systematic Name English
3(2H)-PYRIDAZINONE, 4,5-DIHYDRO-6-(4-(1H-IMIDAZOL-1-YL)-2-THIENYL)-5-METHYL-, (±)-
Systematic Name English
3(2H)-PYRIDAZINONE, 4,5-DIHYDRO-6-(4-(1H-IMIDAZOL-1-YL)-2-THIENYL)-5-METHYL-
Systematic Name English
motapizone [INN]
Common Name English
NAT-05-239
Code English
Classification Tree Code System Code
NCI_THESAURUS C744
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
Code System Code Type Description
FDA UNII
C4A61P8A37
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
NCI_THESAURUS
C66205
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
INN
5659
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
PUBCHEM
65819
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
EVMPD
SUB09075MIG
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
CAS
90697-57-7
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
ChEMBL
CHEMBL2104670
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
MESH
C051270
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
SMS_ID
100000080393
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
EPA CompTox
DTXSID30869061
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
PRIMARY
CAS
93749-03-2
Created by admin on Fri Dec 15 16:32:31 UTC 2023 , Edited by admin on Fri Dec 15 16:32:31 UTC 2023
SUPERSEDED
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
TARGET -> INHIBITOR
IC50
Related Record Type Details
ACTIVE MOIETY