Bicyclol

drug
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Summary

Bicyclol (CHEMBL482035) is a phase-3 clinical-stage small molecule; indicated across 1 condition including injury.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 1 condition
  • Clinical trials: 1
  • Chemistry: 390.3 Da · C19H18O9

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL482035
NameBicyclol
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID9821754
Molecular formulaC19H18O9
Molecular weight390.3
InChIKeyKXMTXZACPVCDMH-UHFFFAOYSA-N

SMILES: COC1=C2C(=C(C(=C1)CO)C3=C4C(=C(C=C3C(=O)OC)OC)OCO4)OCO2

IUPAC name: methyl 4-[5-(hydroxymethyl)-7-methoxy-1,3-benzodioxol-4-yl]-7-methoxy-1,3-benzodioxole-5-carboxylate

Also known as: Bicyclol, bicyclol, BICYCLOL

Patent coverage: 266 distinct patent families (413 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 397 (96%) 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

No target linkage available.

Bioactivity

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

Target pathways

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

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
injury3MONDO:0021178EFO:0000546

Clinical trials

Total trials: 1.

Phase distribution

PhaseTrials
Not specified1

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05711459Not specifiedUNKNOWNBicyclol in the Treatment of Antineoplastic Drug-induced Liver Injury.

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).