Fosinopril

drug
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Also known as C09AA09Fosenopril

Summary

Fosinopril (CHEMBL3039598) is an approved small molecule (ATC C09AA09) targeting ACE; indicated across 4 conditions including cardiovascular disorder and diabetic kidney disease.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: C09AA09
  • Targets: 1 (ACE)
  • Indications: 4 conditions
  • Clinical trials: 7
  • Chemistry: 563.7 Da · C30H46NO7P

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3039598
NameFosinopril
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID9601226
ATCC09AA09
Molecular formulaC30H46NO7P
Molecular weight563.7
InChIKeyBIDNLKIUORFRQP-XYGFDPSESA-N

SMILES: CCC(=O)O[C@H](C(C)C)O[P@](=O)(CCCCC1=CC=CC=C1)CC(=O)N2C[C@@H](C[C@H]2C(=O)O)C3CCCCC3

IUPAC name: (2S,4S)-4-cyclohexyl-1-[2-[[(1S)-2-methyl-1-propanoyloxypropoxy]-(4-phenylbutyl)phosphoryl]acetyl]pyrrolidine-2-carboxylic acid

Also known as: C09AA09, Fosenopril, Fosinopril, fosinopril, FOSINOPRIL

Parent form; salt/anhydrous children: CHEMBL3039596

Patent coverage: 19 distinct patent families (61 SureChEMBL compound mentions), from 1 matched compound structure(s). Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
ACEAngiotensin-converting enzymeInhibition0.7%P12821

Broader ChEMBL bioactivity targets: 3 (assay-derived). Sample: Angiotensin-converting enzyme, D(1A) dopamine receptor, Bile salt export pump.

Bioactivity

ChEMBL activities: 1 potent at pChembl ≥ 5 of 3 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
ACE9IC501nMCHEMBL_ACT_660927

Target pathways

Aggregated over 1 target gene(s): ACE.

Top Reactome pathways

3 total, by targets touching each:

PathwayTargetsGenes
Metabolism of Angiotensinogen to Angiotensins1ACE
Peptide hormone metabolism1ACE
Metabolism of proteins1ACE

Dominant GO biological processes

GO termTargets
kidney development1
blood vessel remodeling1
angiotensin maturation1
regulation of renal output by angiotensin1
neutrophil mediated immunity1
antigen processing and presentation of peptide antigen via MHC class I1
regulation of systemic arterial blood pressure by renin-angiotensin1
positive regulation of systemic arterial blood pressure1
proteolysis1
spermatogenesis1
regulation of blood pressure1
male gonad development1
post-transcriptional regulation of gene expression1
negative regulation of gene expression1
substance P catabolic process1

Indications & clinical

Indications

4 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
cardiovascular disorder4MONDO:0004995EFO:0000319
diabetic kidney disease2MONDO:0005016EFO:0000401
hypertensive disorder2MONDO:0005044EFO:0000537
heart disorder2MONDO:0005267EFO:0003777

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE42
PHASE22
Not specified2
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01014338PHASE4COMPLETEDAngiotensin-converting Enzyme (ACE)-Inhibition and Mechanisms of Skeletal Muscle Weakness in Chronic Obstructive Pulmonary Disease (COPD)
NCT02646397PHASE4UNKNOWNBenidipine and Hydrochlorothiazide in Fosinopril Treated Chronic Kidney Disease Patients With Hypertension
NCT03073018PHASE3COMPLETEDPrevention of Renal and Vascular Endstage Disease Intervention Trial
NCT00051389PHASE2COMPLETEDACE Inhibition and Novel Cardiovascular Risk Factors
NCT00315016PHASE2COMPLETEDEplerenone, ACE Inhibition and Albuminuria
NCT00565396Not specifiedUNKNOWNEffectiveness Study on Fosinopril and/or Losartan in Patients With Chronic Kidney Disease Stage 3
NCT01342614Not specifiedCOMPLETEDThe Effect of Metformin on the Correlation Between Hyperinsulinemia and Hypertension

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

32 molecules share ≥1 primary target. Top 32 by shared-target count:

MoleculeSourceStatusShared targets
CAPTOPRILChEMBL + PubChemPhase 4 (approved)ACE
LOSARTANChEMBL + PubChemPhase 4 (approved)ACE
PERINDOPRILChEMBL + PubChemPhase 4 (approved)ACE
SITAGLIPTINChEMBL + PubChemPhase 4 (approved)ACE
BENAZEPRILChEMBLPhase 4 (approved)ACE
ENALAPRILChEMBLPhase 4 (approved)ACE
ENALAPRILATChEMBLPhase 4 (approved)ACE
IMIDAPRILChEMBLPhase 4 (approved)ACE
LISINOPRILChEMBLPhase 4 (approved)ACE
MOEXIPRILChEMBLPhase 4 (approved)ACE
QUINAPRILChEMBLPhase 4 (approved)ACE
RAMIPRILChEMBLPhase 4 (approved)ACE
TELMISARTANChEMBLPhase 4 (approved)ACE
TRANDOLAPRILChEMBLPhase 4 (approved)ACE
EDETIC ACIDChEMBLPhase 3ACE
QUINAPRILATChEMBL + PubChemPhase 2 (approved)ACE
BENAZEPRILATChEMBLPhase 2ACE
CERONAPRILChEMBLPhase 2ACE
FOSINOPRILATChEMBLPhase 2ACE
IMIDAPRILATChEMBLPhase 2ACE
LIBENZAPRILChEMBLPhase 2ACE
MOEXIPRILATChEMBLPhase 2ACE
OMAPATRILATChEMBLPhase 2ACE
PROLINEChEMBLPhase 2ACE
RENTIAPRILChEMBLPhase 2ACE
SAMPATRILATChEMBLPhase 2ACE
SPIRAPRILATChEMBLPhase 2ACE
TEPROTIDEChEMBLPhase 2ACE
ZOFENOPRILChEMBLPhase 2ACE
Gallic AcidPubChemApprovedACE
HydrochlorothiazidePubChemApprovedACE
PaclitaxelPubChemApprovedACE