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 PERINDOPRIL

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-QXKUPLGCSA-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

Description

Perindoprilat is a metabolite of perindopril. Perindopril is a long-acting angiotensin converting enzyme (ACE) inhibitor and it is used to treat high blood pressure, heart failure or stable coronary artery disease. Perindopril is designed to allow oral administration as perindoprilat is poorly absorbed from the gastrointestinal tract.

CNS Activity

Curator's Comment: Known to be CNS active in rats. Human data not available.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
1.05 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ACEON

Approved Use

Perindopril erbumine tablets are indicated for treatment of patients with stable coronary artery disease to reduce the risk of cardiovascular mortality or nonfatal myocardial infarction. Perindopril erbumine tablets can be used with conventional treatment for management of coronary artery disease, such as antiplatelet, antihypertensive or lipid-lowering therapy.

Launch Date

1993
Primary
ACEON

Approved Use

Perindopril erbumine tablets are indicated for the treatment of patients with essential hypertension. Perindopril erbumine tablets may be used alone or given with other classes of antihypertensives, especially thiazide diuretics.

Launch Date

1993
Palliative
Unknown

Approved Use

Unknown
Cmax

Cmax

ValueDoseCo-administeredAnalytePopulation
83.83 ng/mL
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
3.54 ng/mL
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
130 ng × h/mL
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
170.61 ng × h/mL
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.05 h
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
38.01 h
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Funbound

Funbound

ValueDoseCo-administeredAnalytePopulation
40%
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRIL plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
80%
4 mg single, oral
dose: 4 mg
route of administration: Oral
experiment type: SINGLE
co-administered:
PERINDOPRILAT plasma
Homo sapiens
population: HEALTHY
age: ADULT
sex: FEMALE / MALE
food status: FASTED
Doses

Doses

DosePopulationAdverse events​
4 mg 1 times / day steady, oral
Recommended
Dose: 4 mg, 1 times / day
Route: oral
Route: steady
Dose: 4 mg, 1 times / day
Sources:
unhealthy, adult
n = 320
Health Status: unhealthy
Condition: hypertension
Age Group: adult
Sex: unknown
Population Size: 320
Sources:
Disc. AE: Cough...
AEs leading to
discontinuation/dose reduction:
Cough (2.8%)
Sources:
AEs

AEs

AESignificanceDosePopulation
Cough 2.8%
Disc. AE
4 mg 1 times / day steady, oral
Recommended
Dose: 4 mg, 1 times / day
Route: oral
Route: steady
Dose: 4 mg, 1 times / day
Sources:
unhealthy, adult
n = 320
Health Status: unhealthy
Condition: hypertension
Age Group: adult
Sex: unknown
Population Size: 320
Sources:
Overview

Overview

CYP3A4CYP2C9CYP2D6hERG

OverviewOther

Other InhibitorOther SubstrateOther Inducer




Drug as perpetrator​

Drug as perpetrator​

Drug as victim
PubMed

PubMed

TitleDatePubMed
Pharmacokinetics of perindopril and its metabolites in healthy volunteers.
1990
The initial hemodynamic response to newer antihypertensive agents at rest and during exercise: review of visacor, doxazosin, nisoldipine, tiapamil, perindoprilat, pinacidil, dilevalol, and carvedilol.
1990 Aug
ACE DD genotype is more susceptible than ACE II and ID genotypes to the antiproteinuric effect of ACE inhibitors in patients with proteinuric non-insulin-dependent diabetes mellitus.
2000 Oct
[Effects of angiotensin-converting enzyme inhibitors and cosaar on quality of life of patients with pulmonary tuberculosis and chronic heart failure].
2001
[Effects of perstarium on the systolic and diastolic functions of the myocardium in patients with chronic cardiac failure].
2001
Combination BP therapy cuts second stroke risk in half.
2001 Aug
Comparison of spectrophotometric and an LC method for the determination perindopril and indapamide in pharmaceutical formulations.
2001 Aug
Academic support for combination therapy in hypertension.
2001 Aug-Sep
Chronic ACE inhibition enhances the endothelial control of arterial mechanics and flow-dependent vasodilatation in heart failure.
2001 Dec 1
The lowering of blood pressure after stroke.
2001 Dec 8
The lowering of blood pressure after stroke.
2001 Dec 8
The lowering of blood pressure after stroke.
2001 Dec 8
Randomized placebo-controlled trial of perindopril in normotensive, normoalbuminuric patients with type 1 diabetes mellitus.
2001 Feb
Hyperoxia/normoxia-driven retinal angiogenesis in mice: a role for angiotensin II.
2001 Feb
Effect of perindopril on cerebral and renal perfusion in stroke patients with carotid disease.
2001 Feb
Coronary microvasculature alteration in hypertensive rats. Effect of treatment with a diuretic and an ACE inhibitor.
2001 Jan
Significance of endothelial prostacyclin and nitric oxide in peripheral and pulmonary circulation.
2001 Jan-Feb
Assessment of perindopril's efficacy on arterial distensibility in mild to moderate hypertension.
2001 Jul
Renoprotective and anti-hypertensive effects of combined valsartan and perindopril in progressive diabetic nephropathy in the transgenic (mRen-2)27 rat.
2001 Jul
The quantitative determination of several inhibitors of the angiotensin-converting enzyme by CE.
2001 Jul
Angiotensin converting enzyme inhibitor restrains inflammation-induced vascular injury in mice.
2001 Jun
What are 'tissue ACE inhibitors,' and should they be used instead of other ACE inhibitors?
2001 Mar
Effect of renin-angiotensin system blockade on the expression of the angiotensinogen gene and induction of hypertrophy in rat kidney proximal tubular cells.
2001 Mar-Apr
Antihypertensive efficacy and tolerability of low-dose perindopril/indapamide combination compared with losartan in the treatment of essential hypertension.
2001 May
Effect of angiotensin-converting enzyme inhibition on renal filtration surface area in hypertensive rats.
2001 Nov
Does ACE inhibition slow progression of glomerulopathy in patients with Type 2 diabetes mellitus?
2001 Nov
Angiotensin-converting enzyme gene insertion/deletion, not bradykinin B2 receptor -58T/C gene polymorphism, associated with angiotensin-converting enzyme inhibitor-related cough in Chinese female patients with non-insulin-dependent diabetes mellitus.
2001 Nov
Hypertension. Introduction.
2001 Oct 4
[Antihypertensive agents after cerebral stroke are more effective than expected].
2001 Sep-Oct
Detection of coronary microvascular disease by means of cardiac scintigraphy.
2002 Feb
Comparison of perindopril versus captopril for treatment of acute myocardial infarction.
2002 Jan 15
Combined therapy with indapamide and perindopril but not perindopril alone reduced the risk for recurrent stroke.
2002 Mar-Apr
Patents

Sample Use Guides

In Vivo Use Guide
In patients with essential hypertension, the recommended initial dose is 4 mg once a day. The dose may be titrated, as needed to a maximum of 16 mg per day. The usual maintenance dose range is 4 mg to 8 mg administered as a single daily dose or in two divided doses. In patients with stable coronary artery disease, Perindopril erbumine tablets should be given at an initial dose of 4 mg once daily for 2 weeks, and then increased as tolerated, to a maintenance dose of 8 mg once daily. In elderly patients (greater than 70 years), Perindopril erbumine tablets should be given as a 2 mg dose once daily in the first week, followed by 4 mg once daily in the second week and 8 mg once daily for maintenance dose if tolerated.
Route of Administration: Oral
In Vitro Use Guide
Perindoprilat (S-9780), the major metabolite of perindopril, inhibited guinea pig plasma angiotensin-converting enzyme (ACE) by 50% (IC50) at a concentration of 2.4 +/- 0.1 nM. A Ki of 1.2 nM was obtained for S-9780 (Dixon-Webb plot) with angiotensin I as a substrate.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:43:12 GMT 2023
Edited
by admin
on Fri Dec 15 15:43:12 GMT 2023
Record UNII
Y5GMK36KGY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PERINDOPRIL
INN   MART.   MI   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
Perindopril [WHO-DD]
Common Name English
(2S,3aS,7aS)-1-[(S)-N-[(S)-1-Carboxybutyl]alanyl]hexahydro-2-indolinecarboxylic acid, 1-ethyl ester
Common Name English
perindopril [INN]
Common Name English
1H-INDOLE-2-CARBOXYLIC ACID, 1-(2-((1-(ETHOXYCARBONYL)BUTYL)AMINO)-1-OXOPROPYL)OCTAHYDRO-, (2S-(1(R*(R*)),2.ALPHA.,3A.BETA.,7A.BETA.))-
Common Name English
S-9490
Code English
PERINDOPRIL [MART.]
Common Name English
PERINDOPRIL [VANDF]
Common Name English
MCN-A-2833
Code English
PERINDOPRIL [MI]
Common Name English
PERINDOPRIL [USAN]
Common Name English
Classification Tree Code System Code
WHO-VATC QC09AA04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C09BX01
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C10BX13
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C10BX11
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
NDF-RT N0000175562
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C10BX12
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C10BX14
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-VATC QC09BX01
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
LIVERTOX NBK547980
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
NDF-RT N0000000181
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-VATC QC09BB04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-VATC QC09BA04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C09AA04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
NCI_THESAURUS C247
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C09BX02
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C09BA04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C10BX15
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
WHO-ATC C09BB04
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
Code System Code Type Description
INN
5754
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
WIKIPEDIA
PERINDOPRIL
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
EPA CompTox
DTXSID6023440
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
DRUG BANK
DB00790
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
EVMPD
SUB09730MIG
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
CHEBI
8024
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
RXCUI
54552
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY RxNorm
NCI_THESAURUS
C72910
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
CAS
82834-16-0
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
ChEMBL
CHEMBL1581
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
USAN
AA-1
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
DAILYMED
Y5GMK36KGY
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
IUPHAR
6367
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
MERCK INDEX
m8555
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY Merck Index
DRUG CENTRAL
2108
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
FDA UNII
Y5GMK36KGY
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
SMS_ID
100000091461
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
MESH
D020913
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
PUBCHEM
107807
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
LACTMED
Perindopril
Created by admin on Fri Dec 15 15:43:12 GMT 2023 , Edited by admin on Fri Dec 15 15:43:12 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
BINDER->LIGAND
BINDING
Name Property Type Amount Referenced Substance Defining Parameters References
Biological Half-life PHARMACOKINETIC