BENAZEPRIL

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C24H28N2O5
Molecular Weight	424.4895
Optical Activity	UNSPECIFIED
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BENAZEPRIL

Structure Search

SMILES

CCOC(=O)[C@H](CCC1=CC=CC=C1)N[C@H]2CCC3=C(C=CC=C3)N(CC(O)=O)C2=O

InChI

InChIKey=XPCFTKFZXHTYIP-PMACEKPBSA-N

InChI=1S/C24H28N2O5/c1-2-31-24(30)20(14-12-17-8-4-3-5-9-17)25-19-15-13-18-10-6-7-11-21(18)26(23(19)29)16-22(27)28/h3-11,19-20,25H,2,12-16H2,1H3,(H,27,28)/t19-,20-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C24H28N2O5
Molecular Weight	424.4895
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	2 / 2
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:29:57 UTC 2023` Edited by `admin` on `Fri Dec 15 16:29:57 UTC 2023`
Record UNII	UDM7Q7QWP8
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

BENAZEPRIL

Official Name

English

benazepril [INN]

Common Name

English

CIBACEN WS

Common Name

English

BENAZEPRIL [MI]

Common Name

English

Benazepril [WHO-DD]

Common Name

English

1H-1-BENZAZEPINE-1-ACETIC ACID, 3-(((1S)-1-(ETHOXYCARBONYL)-3-PHENYLPROPYL)AMINO)-2,3,4,5-TETRAHYDRO-2-OXO-, (3S)-

Common Name

English

BENAZEPRIL SANDOZ

Brand Name

English

C09AA07

Code

English

BENAZEPRIL [VANDF]

Common Name

English

BRIEM

Common Name

English

BENAZEPRIL [EMA EPAR VETERINARY]

Common Name

English

((3S)-3-(((1S)-1-(ETHOXYCARBONYL)-3-PHENYLPROPYL)AMINO)-2-OXO-2,3,4,5-TETRAHYDRO-1H-1-BENZAZEPIN-1-YL)ACETIC ACID

Systematic Name

English

CGS-14824A

Code

English

CIBACENE

Common Name

English

FORTEEKOR

Brand Name

English

Classification Tree Code System Code

NDF-RT

N0000175562

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

EMA VETERINARY ASSESSMENT REPORTS

FORTEKOR PLUS [AUHTORIZED]

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

NDF-RT

N0000000181

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

WHO-ATC

C09AA07

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

NCI_THESAURUS

C247

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

WHO-VATC

QC09AA07

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

WHO-ATC

C09BA07

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

WHO-VATC

QC09BA07

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

LIVERTOX

NBK548659

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

Code System Code Type Description

INN

6129

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

WIKIPEDIA

BENAZEPRIL

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

RXCUI

18867

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

RxNorm

LACTMED

Benazepril

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

MESH

C044946

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

MERCK INDEX

m2303

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

Merck Index

EVMPD

SUB05700MIG

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

SMS_ID

100000090490

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

DRUG BANK

DB00542

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

PUBCHEM

5362124

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

ChEMBL

CHEMBL838

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

IUPHAR

6374

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

CHEBI

3012

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

EPA CompTox

DTXSID5022645

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

FDA UNII

UDM7Q7QWP8

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

DRUG CENTRAL

299

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

CHEBI

3011

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

CAS

86541-75-5

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

NCI_THESAURUS

C61645

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

DAILYMED

UDM7Q7QWP8

Created by admin on Fri Dec 15 16:29:57 UTC 2023 , Edited by admin on Fri Dec 15 16:29:57 UTC 2023

PRIMARY

Related Record Type Details


					N1SN99T69T

BENAZEPRIL HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:

Related Record Type Details


					JRM708L703

METABOLITE ACTIVE -> PRODRUG

Amount:


					37N77J2QK6

BEBAZEPRIL-GLUCURONIDE CONJUGATE

METABOLITE -> PARENT

Amount:

Related Record Type Details


					N1SN99T69T

BENAZEPRIL HYDROCHLORIDE

PARENT -> IMPURITY

Comments:

Impurity C: not more than 1.5 times the area of the principal peak in the chromatogram obtained with reference solution (c) (0.3 per cent)

Amount:

Related Record Type Details


					JRM708L703

ACTIVE MOIETY

Amount:

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Volume of Distribution	PHARMACOKINETIC

Biological Half-life	PHARMACOKINETIC