U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C19H32N2O5
Molecular Weight 368.4678
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3A-EPI-PERINDOPRIL, (3AR)-

SMILES

[H][C@@]12C[C@H](N(C(=O)[C@H](C)N[C@@H](CCC)C(=O)OCC)[C@@]1([H])CCCC2)C(O)=O

InChI

InChIKey=IPVQLZZIHOAWMC-QRJUGERDSA-N
InChI=1S/C19H32N2O5/c1-4-8-14(19(25)26-5-2)20-12(3)17(22)21-15-10-7-6-9-13(15)11-16(21)18(23)24/h12-16,20H,4-11H2,1-3H3,(H,23,24)/t12-,13+,14-,15-,16-/m0/s1

HIDE SMILES / InChI

Molecular Formula C19H32N2O5
Molecular Weight 368.4678
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 5 / 5
E/Z Centers 0
Optical Activity UNSPECIFIED

(3AR)-3A-epi-Perindopril is an epimer (S, RS, SS) of the drug perindopril which is commonly used to treat high blood pressure, hypertension, heart failure, or stable coronary artery disease. This epimer possesses equal activity with the parent compound, perindopril.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:30:43 GMT 2023
Edited
by admin
on Sat Dec 16 08:30:43 GMT 2023
Record UNII
E77W873JI7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3A-EPI-PERINDOPRIL, (3AR)-
Common Name English
1H-INDOLE-2-CARBOXYLIC ACID, 1-(2-((1-(ETHOXYCARBONYL)BUTYL)AMINO)-1-OXOPROPYL)OCTAHYDRO-, (2S-(1(R*(R*)),2.ALPHA.,3A.ALPHA.,7A.BETA.))-
Systematic Name English
Code System Code Type Description
PUBCHEM
58153637
Created by admin on Sat Dec 16 08:30:43 GMT 2023 , Edited by admin on Sat Dec 16 08:30:43 GMT 2023
PRIMARY
FDA UNII
E77W873JI7
Created by admin on Sat Dec 16 08:30:43 GMT 2023 , Edited by admin on Sat Dec 16 08:30:43 GMT 2023
PRIMARY
CAS
145513-31-1
Created by admin on Sat Dec 16 08:30:43 GMT 2023 , Edited by admin on Sat Dec 16 08:30:43 GMT 2023
PRIMARY