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
[H][C@@]12CCC[C@]1([H])N([C@@H](C2)C(O)=O)C(=O)[C@H](C)N[C@@H](CCC3=CC=CC=C3)C(=O)OC(C)C
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
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 |
---|---|---|
Development and validation of a liquid chromatographic method for the determination of the related substances of ramipril in Altace capsules. | 2000 Sep |
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Development of a capillary electrophoresis method for the assay of ramipril and its impurities: an issue of cis-trans isomerization. | 2011 May 6 |
Patents
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11669166
Created by
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295328-72-2
Created by
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1598323
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2S4N8A063C
Created by
admin on Sat Dec 16 08:29:24 GMT 2023 , Edited by admin on Sat Dec 16 08:29:24 GMT 2023
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SUBSTANCE RECORD