Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C13H15NO4S2 |
| Molecular Weight | 313.393 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 2 / 2 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
OC(=O)[C@@H]1CS[C@@H](N1C(=O)CCS)C2=CC=CC=C2O
InChI
InChIKey=BSHDUMDXSRLRBI-JOYOIKCWSA-N
InChI=1S/C13H15NO4S2/c15-10-4-2-1-3-8(10)12-14(11(16)5-6-19)9(7-20-12)13(17)18/h1-4,9,12,15,19H,5-7H2,(H,17,18)/t9-,12+/m0/s1
Rentiapril (SA-446) is an angiotensin-converting-enzyme (ACE) inhibitor that has antihypertensive activity. This compound binds to ACE and blocks the conversion of angtiotensin I to angtiontensin II. Angiotensin II has vasoconstrictive activity, which rentiapril prevents, leading to vasodilation. Rentiapril has been shown to inhibit ADE activity more strongly and for longer periods than two other ACE inhibitors (captopril, and alacepril), and reduces blood pressure more quickly and for a longer time in patients with renovascular hypertension. Because rentiapril also decreases angiotensin II-induced aldosterone secretion by the adrenal cortex, it increases sodium excretion and (subsequently) water outflow.
Approval Year
| Name | Type | Language | ||
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Official Name | English | ||
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Preferred Name | English | ||
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Common Name | English |
| Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C247
Created by
admin on Wed Apr 02 07:33:19 GMT 2025 , Edited by admin on Wed Apr 02 07:33:19 GMT 2025
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| Code System | Code | Type | Description | ||
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RENTIAPRIL
Created by
admin on Wed Apr 02 07:33:19 GMT 2025 , Edited by admin on Wed Apr 02 07:33:19 GMT 2025
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D0TAM1017B
Created by
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C033437
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DTXSID80230646
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CHEMBL309962
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100000080827
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80830-42-8
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C72912
Created by
admin on Wed Apr 02 07:33:19 GMT 2025 , Edited by admin on Wed Apr 02 07:33:19 GMT 2025
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SUB10277MIG
Created by
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71244
Created by
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5931
Created by
admin on Wed Apr 02 07:33:19 GMT 2025 , Edited by admin on Wed Apr 02 07:33:19 GMT 2025
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PRIMARY |
ACTIVE MOIETY