Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C23H22N8O |
| Molecular Weight | 426.4738 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCC1=C(CC2=CC=C(C=C2)C3=CC=CC=C3C4=NN=NN4)C5=NC(=O)NN5C(C)=N1
InChI
InChIKey=OLJAPHMBAMBVKL-UHFFFAOYSA-N
InChI=1S/C23H22N8O/c1-3-6-20-19(22-25-23(32)28-31(22)14(2)24-20)13-15-9-11-16(12-10-15)17-7-4-5-8-18(17)21-26-29-30-27-21/h4-5,7-12H,3,6,13H2,1-2H3,(H,28,32)(H,26,27,29,30)
| Molecular Formula | C23H22N8O |
| Molecular Weight | 426.4738 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Ripisartan (UP-269-6) is a specific nonpeptide angiotensin II receptor antagonist. Oral administration of ripisartan in rats and dogs resulted in a dose-dependent and long-lasting inhibition of the angiotensin II-induced pressor response. It did not show agonistic properties in animals. In vitro, ripisartan was found to bind selectively to AT1 receptors. In humans, it showed high biliary excretion and reabsorption. Canine studies have suggested it might have cardioprotective properties after acute ischemia-reperfusion.
Approval Year
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:01:14 GMT 2025
by
admin
on
Mon Mar 31 18:01:14 GMT 2025
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| Record UNII |
7LQ7OQP653
|
| Record Status |
Validated (UNII)
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| Record Version |
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Download
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Code | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C66930
Created by
admin on Mon Mar 31 18:01:14 GMT 2025 , Edited by admin on Mon Mar 31 18:01:14 GMT 2025
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| Code System | Code | Type | Description | ||
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SUB10329MIG
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100000080589
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DTXSID10164001
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7LQ7OQP653
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C90658
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CHEMBL312104
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132840
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148504-51-2
Created by
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7365
Created by
admin on Mon Mar 31 18:01:14 GMT 2025 , Edited by admin on Mon Mar 31 18:01:14 GMT 2025
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PRIMARY |
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