Aprotinin

drug
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Also known as Aprotinin (bovine)Aprotinin (synthetic)Aprotinin biosyntheticAprotinin bovineAprotinin concentrated solutionAprotininaAprotinineBAYER A 128BAYER-A-128BAYERA-128Bovine aprotininFibrinolysis inhibitorRIKER 52GRIKER-52GRP 9921RP-9921Trasylol

Summary

Aprotinin (CHEMBL1201619) is an approved unknown (ATC B02AB01) targeting PLG; indicated across 3 conditions including pancreatitis and breast neoplasm.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Unknown
  • ATC class: B02AB01
  • Targets: 1 (PLG)
  • Indications: 3 conditions
  • Clinical trials: 7

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL1201619
NameAprotinin
TypeUnknown
Max phase4
ATCB02AB01

Also known as: Aprotinin, Aprotinin (bovine), Aprotinin (synthetic), Aprotinin biosynthetic, Aprotinin bovine, Aprotinin concentrated solution, Aprotinina, Aprotinine, BAYER A 128, BAYER-A-128, BAYERA-128, Bovine aprotinin

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
PLGplasminogenBinding6.84.6%P00747

Bioactivity

No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).

Target pathways

Aggregated over 1 target gene(s): PLG.

Top Reactome pathways

6 total, by targets touching each:

PathwayTargetsGenes
Platelet degranulation1PLG
Degradation of the extracellular matrix1PLG
Activation of Matrix Metalloproteinases1PLG
Signaling by PDGF1PLG
Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs)1PLG
Dissolution of Fibrin Clot1PLG

Dominant GO biological processes

GO termTargets
proteolysis1
blood coagulation1
negative regulation of cell population proliferation1
negative regulation of cell-substrate adhesion1
protein processing1
extracellular matrix disassembly1
tissue regeneration1
fibrinolysis1
positive regulation of blood vessel endothelial cell migration1
myoblast differentiation1
muscle cell cellular homeostasis1
tissue remodeling1
biological process involved in interaction with symbiont1
negative regulation of fibrinolysis1
positive regulation of fibrinolysis1

Indications & clinical

Indications

3 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
pancreatitis1MONDO:0004982EFO:0000278
breast neoplasm1MONDO:0021100MONDO:0007254

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
Not specified4
PHASE12
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT07317050PHASE3NOT_YET_RECRUITINGClinical Trial With Aprotinin in the Acute Respiratory Distress Syndrome Treatment
NCT00354900PHASE1TERMINATEDPhase I Study of Aprotinin in Advanced Breast Cancer
NCT00357851PHASE1COMPLETEDCan Aprotinin Reduce Pancreatitis After Scoliosis Surgery
NCT00131040Not specifiedCOMPLETEDInvestigation of Leukocyte Trafficking Into Skin Blisters During Cardiopulmonary Bypass
NCT00257751Not specifiedCOMPLETEDDifferent Regimen of Aprotinine(Trasylol) Administration in Patients Receiving Antiplatelet Therapy With Clopidogrel (Plavix)
NCT00617955Not specifiedCOMPLETEDEffects of Aprotinin During Cardiac Surgery/Long Term Death Rates
NCT04527133Not specifiedUNKNOWNAn Open Non-comparative Study of the Efficacy and Safety of Aprotinin in Patients Hospitalized With COVID-19

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.

11 molecules share ≥1 primary target. Top 11 by shared-target count:

MoleculeSourceStatusShared targets
AMINOCAPROIC ACIDChEMBLPhase 4 (approved)PLG
BEROTRALSTATChEMBLPhase 4 (approved)PLG
MELAGATRANChEMBLPhase 4 (approved)PLG
PENTAMIDINEChEMBLPhase 4 (approved)PLG
TELAPREVIRChEMBLPhase 4 (approved)PLG
TRANEXAMIC ACIDChEMBLPhase 4 (approved)PLG
DABIGATRANChEMBLPhase 3PLG
GABEXATEChEMBLPhase 3PLG
MILVEXIANChEMBLPhase 3PLG
NAFAMOSTATChEMBLPhase 3PLG
EFEGATRANChEMBLPhase 2PLG