Pradigastat

drug
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Also known as Lcq-908LCQ-908NXAC0088797

Summary

Pradigastat (CHEMBL2364624) is a phase-3 clinical-stage small molecule; indicated across 6 conditions including metabolic dysfunction-associated steatotic liver disease and hepatitis c virus infection.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 6 conditions
  • Clinical trials: 2
  • Chemistry: 455.5 Da · C25H24F3N3O2

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL2364624
NamePradigastat
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID53387035
Molecular formulaC25H24F3N3O2
Molecular weight455.5
InChIKeyGXALXAKNHIROPE-UHFFFAOYSA-N

SMILES: C1CC(CCC1CC(=O)O)C2=CC=C(C=C2)C3=NC=C(C=C3)NC4=CN=C(C=C4)C(F)(F)F

IUPAC name: 2-[4-[4-[5-[[6-(trifluoromethyl)-3-pyridinyl]amino]-2-pyridinyl]phenyl]cyclohexyl]acetic acid

Also known as: Lcq-908, LCQ-908NXA, Pradigastat, PRADIGASTAT, pradigastat, C0088797

Parent form; salt/anhydrous children: CHEMBL2364625

Patent coverage: 102 distinct patent families (303 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 258 (85%) 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

Broader ChEMBL bioactivity targets: 2 (assay-derived). Sample: Diacylglycerol O-acyltransferase 1, Diacylglycerol O-acyltransferase 1.

Bioactivity

ChEMBL activities: 4 potent at pChembl ≥ 5 of 4 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
DGAT17.26IC5055nMCHEMBL_ACT_18855078
DGAT17.26IC5055nMCHEMBL_ACT_29118976
DGAT17.18IC5066nMCHEMBL_ACT_24842818
Q9Z2A77.15EC5071nMCHEMBL_ACT_18855088

Target pathways

No target-pathway data for this drug (no mapped target genes).

Indications & clinical

Indications

6 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.

Disease (in trials)PhaseMONDOEFO
metabolic dysfunction-associated steatotic liver disease2MONDO:0013209EFO:0003095
hepatitis C virus infection2MONDO:0005231EFO:0003047
constipation disorder2MONDO:0002203HP:0002019
liver disorder1MONDO:0005154EFO:0001421
kidney disorder1MONDO:0005240EFO:0003086
hyperlipoproteinemia1MONDO:0037748MONDO:0037748

Clinical trials

Total trials: 2.

Phase distribution

PhaseTrials
PHASE22

Top trials by phase / activity

NCTPhaseStatusTitle
NCT01474434PHASE2TERMINATEDEfficacy of LCQ908 on Cardiovascular Risk
NCT04620161PHASE2COMPLETEDA Proof of Concept Study of Pradigastat in Patients With Functional Constipation

Clinical evidence (CIViC)

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

Pharmacology

Pharmacogenomics

No PharmGKB pharmacogenomic data curated for this drug.

No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).