Esuberaprost

drug
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Also known as Aps-314d free acidAps-314dBPS-314d

Summary

Esuberaprost (CHEMBL3137314) is a phase-3 clinical-stage small molecule targeting PTGIR; indicated across 1 condition including pulmonary arterial hypertension.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Targets: 1 (PTGIR)
  • Indications: 1 condition
  • Clinical trials: 1
  • Chemistry: 398.5 Da · C24H30O5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL3137314
NameEsuberaprost
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID10501053
Molecular formulaC24H30O5
Molecular weight398.5
InChIKeyCTPOHARTNNSRSR-NOQAJONNSA-N

SMILES: CC#CC[C@H](C)[C@@H](/C=C/[C@H]1[C@@H](C[C@H]2[C@@H]1C3=CC=CC(=C3O2)CCCC(=O)O)O)O

IUPAC name: 4-[(1R,2R,3aS,8bS)-2-hydroxy-1-[(E,3S,4S)-3-hydroxy-4-methyloct-1-en-6-ynyl]-2,3,3a,8b-tetrahydro-1H-cyclopenta[b][1]benzofuran-5-yl]butanoic acid

Also known as: Aps-314d free acid, Aps-314d, BPS-314d, Esuberaprost, ESUBERAPROST

Parent form; salt/anhydrous children: CHEMBL3137337, CHEMBL4298145

Patent coverage: 39 distinct patent families (120 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 75 (62%) of the total. 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
PTGIRIP receptorAgonist7.890.2%P43119

Bioactivity

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

Target pathways

Aggregated over 1 target gene(s): PTGIR.

Top Reactome pathways

3 total, by targets touching each:

PathwayTargetsGenes
Prostanoid ligand receptors1PTGIR
Prostacyclin signalling through prostacyclin receptor1PTGIR
G alpha (s) signalling events1PTGIR

Dominant GO biological processes

GO termTargets
inflammatory response1
G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger1
adenylate cyclase-activating G protein-coupled receptor signaling pathway1
positive regulation of cytosolic calcium ion concentration1
cell-cell signaling1
negative regulation of platelet-derived growth factor receptor signaling pathway1
response to lipopolysaccharide1
negative regulation of smooth muscle cell proliferation1
signal transduction1
G protein-coupled receptor signaling pathway1

Indications & clinical

Indications

1 indication (0 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
pulmonary arterial hypertension3MONDO:0015924EFO:0001361

Clinical trials

Total trials: 1.

Phase distribution

PhaseTrials
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT03657095PHASE3TERMINATEDA Study With BPS-314d-MR-PAH-303 in Participants With Pulmonary Arterial 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.

16 molecules share ≥1 primary target. Top 16 by shared-target count:

MoleculeSourceStatusShared targets
ALPROSTADILChEMBL + PubChemPhase 4 (approved)PTGIR
DINOPROSTONEChEMBL + PubChemPhase 4 (approved)PTGIR
ILOPROSTChEMBL + PubChemPhase 4 (approved)PTGIR
TREPROSTINILChEMBL + PubChemPhase 4 (approved)PTGIR
LAROPIPRANTChEMBLPhase 4 (approved)PTGIR
SELEXIPAGChEMBLPhase 4 (approved)PTGIR
RALINEPAGChEMBLPhase 3PTGIR
TIMAPIPRANTChEMBLPhase 3PTGIR
BUTAPROSTChEMBLPhase 2PTGIR
LASELIPAGChEMBLPhase 2PTGIR
BelzutifanPubChemApprovedPTGIR
DinoprostPubChemApprovedPTGIR
epoprostenolPubChemApprovedPTGIR
GrapiprantPubChemApprovedPTGIR
IndomethacinPubChemApprovedPTGIR
YohimbinePubChemApprovedPTGIR