Edotecarin

drug
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Also known as EdotecarinaEdotecarineJ-107088PF-804950NB-506 Analogue

Summary

Edotecarin (CHEMBL435191) is a phase-3 clinical-stage small molecule; indicated across 3 conditions including glioblastoma and gastric neoplasm.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Indications: 3 conditions
  • Clinical trials: 5
  • Chemistry: 608.6 Da · C29H28N4O11

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL435191
NameEdotecarin
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID9808998
Molecular formulaC29H28N4O11
Molecular weight608.6
InChIKeyQMVPQBFHUJZJCS-NTKFZFFISA-N

SMILES: C1=CC2=C(C=C1O)NC3=C4C(=C5C(=C23)C(=O)N(C5=O)NC(CO)CO)C6=C(N4[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)C=C(C=C6)O

IUPAC name: 13-(1,3-dihydroxypropan-2-ylamino)-6,20-dihydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,13,23-triazahexacyclo[14.7.0.02,10.04,9.011,15.017,22]tricosa-1,4(9),5,7,10,15,17(22),18,20-nonaene-12,14-dione

Also known as: Edotecarin, Edotecarina, Edotecarine, J-107088, PF-804950, NB-506 Analogue, edotecarin, EDOTECARIN

Patent coverage: 458 distinct patent families (1,181 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 1,098 (93%) 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: DNA topoisomerase 1, DNA topoisomerase 1.

Bioactivity

ChEMBL activities: 4 potent at pChembl ≥ 5 of 4 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
Q047508.82EC501.5nMCHEMBL_ACT_2511675
TOP17.29EC5051nMCHEMBL_ACT_19439596
TOP17.29EC5051nMCHEMBL_ACT_447732
TOP17EC50100nMCHEMBL_ACT_2511770

Target pathways

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

Indications & clinical

Indications

3 indications (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
glioblastoma3MONDO:0018177EFO:0000519
gastric neoplasm2MONDO:0021085EFO:0003897
breast neoplasm2MONDO:0021100MONDO:0007254

Clinical trials

Total trials: 5.

Phase distribution

PhaseTrials
PHASE23
PHASE31
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00068952PHASE3COMPLETEDStudy of IV Edotecarin Vs Temozolomide or Carmustine (BCNU) or Lomustine (CCNU) in Patients With Glioblastoma Multiforme
NCT00067314PHASE2COMPLETEDStudy in Women With Metastatic Breast Cancer Whose Cancer Has Gotten Worse After Anthracycline and Taxane Therapy
NCT00070031PHASE2COMPLETEDEdotecarin in Treating Women With Locally Advanced or Metastatic Breast Cancer That Has Not Responded to Chemotherapy
NCT00087503PHASE2COMPLETEDIntravenous Edotecarin in Patients With Advanced Gastric Cancer That Has Progressed or Recurred After Chemotherapy
NCT00072332PHASE1COMPLETEDEdotecarin and Cisplatin in Treating Patients With Advanced or Metastatic Solid Tumors

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).