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Details

Stereochemistry ABSOLUTE
Molecular Formula C15H19NO3S2
Molecular Weight 325.446
Optical Activity UNSPECIFIED
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ZOFENOPRILAT

SMILES

C[C@H](CS)C(=O)N1C[C@H](C[C@H]1C(O)=O)SC2=CC=CC=C2

InChI

InChIKey=UQWLOWFDKAFKAP-WXHSDQCUSA-N
InChI=1S/C15H19NO3S2/c1-10(9-20)14(17)16-8-12(7-13(16)15(18)19)21-11-5-3-2-4-6-11/h2-6,10,12-13,20H,7-9H2,1H3,(H,18,19)/t10-,12+,13+/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H19NO3S2
Molecular Weight 325.446
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Zofenopril is an inhibitor of Angiotensin Converting Enzyme (ACE), which is approved in Europe for the treatment of hypertension and acute myocardial infarction.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P12821
Gene ID: 1636.0
Gene Symbol: ACE
Target Organism: Homo sapiens (Human)
10.9 nM [IC50]
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
ZOPRANOL

Approved Use

ZOPRANOL is indicated for the treatment of mild to moderate essential hypertension.

Launch Date

9.6465597E11
Primary
ZOPRANOL

Approved Use

ZOPRANOL is indicated for the treatment initiated within the first 24 hours of patients with acute myocardial infarction with or without signs and symptoms of heart failure.

Launch Date

9.6465597E11
PubMed

PubMed

TitleDatePubMed
Effect of Zofenopril on regeneration of sciatic nerve crush injury in a rat model.
2009 Jun 9
Randomised comparison of zofenopril and ramipril plus acetylsalicylic acid in postmyocardial infarction patients with left ventricular systolic dysfunction: a post hoc analysis of the SMILE-4 Study in patients according to levels of left ventricular ejection fraction at entry.
2015
Efficacy of Zofenopril Compared With Placebo and Other Angiotensin-converting Enzyme Inhibitors in Patients With Acute Myocardial Infarction and Previous Cardiovascular Risk Factors: A Pooled Individual Data Analysis of 4 Randomized, Double-blind, Controlled, Prospective Studies.
2017 Jan
Patents

Sample Use Guides

The usual effective dose in hypertension is 30 mg/day (in patients without volume or salt depletion) and the starting dose is 7.5 or 15 mg/day (in patients with volume or salt depletion). In acute myocardial infarction the treatment scheme is the following: 7.5 mg every 12 h (1st and 2nd day); 15 mg every 12 h (3rd and 4th day); 30 mg every 12 h (from 5th day).
Route of Administration: Oral
Zofenopril (36 uM) significantly increased coronary flow after 5 min of incubation with isolated rat hearts.
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:15:16 UTC 2023
Edited
by admin
on Fri Dec 15 17:15:16 UTC 2023
Record UNII
4G4WDK2YBS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ZOFENOPRILAT
INN  
INN  
Official Name English
L-PROLINE, 1-(3-MERCAPTO-2-METHYL-1-OXOPROPYL)-4-(PHENYLTHIO)-, (1(R*),2ALPHA,4ALPHA)-
Systematic Name English
zofenoprilat [INN]
Common Name English
L-PROLINE, 1-(3-MERCAPTO-2-METHYL-1-OXOPROPYL)-4-(PHENYLTHIO)-, (1(R*),2.ALPHA.,4.ALPHA.)-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C247
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
Code System Code Type Description
CHEBI
82602
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
CAS
75176-37-3
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
MESH
C065520
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
DRUG BANK
DB08766
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
IUPHAR
6463
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
WIKIPEDIA
ZOFENOPRILAT
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
PUBCHEM
3034048
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
INN
6599
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
FDA UNII
4G4WDK2YBS
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID50231443
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
EVMPD
SUB00171MIG
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
NCI_THESAURUS
C95293
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
SMS_ID
100000078772
Created by admin on Fri Dec 15 17:15:16 UTC 2023 , Edited by admin on Fri Dec 15 17:15:16 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE
Related Record Type Details
ACTIVE MOIETY