Structure via PubChem · Public domain (PubChem)
rentiapril
Sign in to saveRentiapril is an ACE inhibitor.
Chemical data
- Formula
- C13H15NO4S2
- Molecular weight
- 313.4 g/mol
- IUPAC name
- (2R,4R)-2-(2-hydroxyphenyl)-3-(3-sulfanylpropanoyl)-1,3-thiazolidine-4-carboxylic acid
- SMILES
- C1[C@H](N([C@H](S1)C2=CC=CC=C2O)C(=O)CCS)C(=O)O
- InChIKey
- BSHDUMDXSRLRBI-JOYOIKCWSA-N
- XLogP
- 1.3
- Polar surface area
- 104 Ų
- H-bond donors
- 3
- H-bond acceptors
- 6
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
50 papers- Reproductive toxicity studies of rentiapril.Arzneimittel-Forschung · 1987
- Toxicity study of the angiotensin converting enzyme inhibitor rentiapril in rats.Arzneimittel-Forschung · 1995
- Effects of the angiotensin converting enzyme inhibitors captopril, rentiapril, and alacepril in patients with essential and renovascular hypertension.Clinical therapeutics · 1989
- General pharmacological properties of the potent angiotensin converting enzyme inhibitor rentiapril.Arzneimittel-Forschung · 1987
- Kinetic and structural characterisation of domain-specific angiotensin I-converting enzyme inhibition by captopril, rentiapril and zofenoprilat.The FEBS journal · 2026
via PubMed
Wikidata facts
- Subclass of
- carboxylic acid
- Mass
- 313.044
Show 5 more facts
- chemical formula
- C₁₃H₁₅NO₄S₂
- isomeric SMILES
- C1[C@H](N([C@H](S1)C2=CC=CC=C2O)C(=O)CCS)C(=O)O
- canonical SMILES
- C1C(N(C(S1)C2=CC=CC=C2O)C(=O)CCS)C(=O)O
- subject has role
- ACE inhibitor
- Commons category
- Rentiapril
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
Rentiapril is an ACE inhibitor.
==References==
Excerpted from Wikipedia’s “rentiapril” article, available under the CC BY-SA 4.0 licence.
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via Wikidata sitelinks · CC0