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
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)
| 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
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2094125 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8381357 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/3816919
1 to 10 mg as a single dose
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:30:50 GMT 2025
by
admin
on
Mon Mar 31 18:30:50 GMT 2025
|
| Record UNII |
C4A61P8A37
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Official Name | English | ||
|
Preferred Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
NCI_THESAURUS |
C744
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
C4A61P8A37
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
C66205
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
5659
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
65819
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
SUB09075MIG
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
90697-57-7
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
CHEMBL2104670
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
C051270
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
100000080393
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
DTXSID30869061
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
PRIMARY | |||
|
93749-03-2
Created by
admin on Mon Mar 31 18:30:50 GMT 2025 , Edited by admin on Mon Mar 31 18:30:50 GMT 2025
|
SUPERSEDED |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ENANTIOMER -> RACEMATE |
|
||
|
|
ENANTIOMER -> RACEMATE |
|
||
|
|
TARGET -> INHIBITOR |
IC50
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|