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=C(C=CC=C3)C4=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
Fri Dec 15 15:33:43 GMT 2023
by
admin
on
Fri Dec 15 15:33:43 GMT 2023
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Record UNII |
7LQ7OQP653
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Record Status |
Validated (UNII)
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Record Version |
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Code | English |
Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C66930
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admin on Fri Dec 15 15:33:43 GMT 2023 , Edited by admin on Fri Dec 15 15:33:43 GMT 2023
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SUB10329MIG
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100000080589
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DTXSID10164001
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7LQ7OQP653
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admin on Fri Dec 15 15:33:43 GMT 2023 , Edited by admin on Fri Dec 15 15:33:43 GMT 2023
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C90658
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CHEMBL312104
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132840
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148504-51-2
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7365
Created by
admin on Fri Dec 15 15:33:43 GMT 2023 , Edited by admin on Fri Dec 15 15:33:43 GMT 2023
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PRIMARY |
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