Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C24H34N2O5 |
| Molecular Weight | 430.5372 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(C)OC(=O)[C@H](CCC1=CC=CC=C1)N[C@@H](C)C(=O)N2[C@H]3CCC[C@H]3C[C@H]2C(O)=O
InChI
InChIKey=WJWHJJCWHNPKTH-MQBSTWLZSA-N
InChI=1S/C24H34N2O5/c1-15(2)31-24(30)19(13-12-17-8-5-4-6-9-17)25-16(3)22(27)26-20-11-7-10-18(20)14-21(26)23(28)29/h4-6,8-9,15-16,18-21,25H,7,10-14H2,1-3H3,(H,28,29)/t16-,18-,19-,20-,21-/m0/s1
| Molecular Formula | C24H34N2O5 |
| Molecular Weight | 430.5372 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/21429497
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21429497
Ramipril isopropyl ester is the proline-containing impurity of ramipril, labelled as ramipril Impurity B. Ramipril is an angiotensin-converting enzyme (ACE) inhibitor, used to treat high blood pressure (hypertension) and congestive heart failure.
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Quality by design approach: application of artificial intelligence techniques of tablets manufactured by direct compression. | 2012-12 |
|
| Development of a capillary electrophoresis method for the assay of ramipril and its impurities: an issue of cis-trans isomerization. | 2011-05-06 |
|
| Development and validation of a liquid chromatographic method for the determination of the related substances of ramipril in Altace capsules. | 2000-09 |
Patents
| Substance Class |
Chemical
Created
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Mon Mar 31 22:06:51 GMT 2025
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2S4N8A063C
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| Record Status |
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| Related Record | Type | Details | ||
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PARENT -> IMPURITY |