Eldecalcitol

drug
On this page

Also known as Ed-71

Summary

Eldecalcitol (CHEMBL4297608) is a phase-3 clinical-stage small molecule targeting VDR; indicated across 1 condition including osteoporosis.

At a glance

  • Status: Max clinical phase 3 (not approved)
  • Modality: Small molecule
  • Targets: 1 (VDR)
  • Indications: 1 condition
  • Clinical trials: 7
  • Chemistry: 490.7 Da · C30H50O5

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL4297608
NameEldecalcitol
TypeSmall molecule
Max phase3
FDA approvedno
PubChem CID6918141
ChEBICHEBI:73927
Molecular formulaC30H50O5
Molecular weight490.7
InChIKeyFZEXGDDBXLBRTD-AYIMTCTASA-N

SMILES: C[C@H](CCCC(C)(C)O)[C@H]1CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H]([C@H]([C@@H](C3=C)O)OCCCO)O)C

IUPAC name: (1R,2R,3R,5Z)-5-[(2E)-2-[(1R,3aS,7aR)-1-[(2R)-6-hydroxy-6-methylheptan-2-yl]-7a-methyl-2,3,3a,5,6,7-hexahydro-1H-inden-4-ylidene]ethylidene]-2-(3-hydroxypropoxy)-4-methylidenecyclohexane-1,3-diol

ChEBI definition: A hydroxycalciol that is calcitriol with a 3-hydroxypropoxy group at position 2.

Other ChEBI roles (chemical / environmental): metabolite.

Also known as: Ed-71, Eldecalcitol, ELDECALCITOL

Patent coverage: 106 distinct patent families (197 SureChEMBL compound mentions), from 1 matched compound structure(s). 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
VDRVitamin D receptorAgonist80.2%P11473

Bioactivity

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

Target pathways

Aggregated over 1 target gene(s): VDR.

Top Reactome pathways

3 total, by targets touching each:

PathwayTargetsGenes
Vitamin D (calciferol) metabolism1VDR
Nuclear Receptor transcription pathway1VDR
SUMOylation of intracellular receptors1VDR

Dominant GO biological processes

GO termTargets
negative regulation of transcription by RNA polymerase II1
cell morphogenesis1
skeletal system development1
calcium ion transport1
intracellular calcium ion homeostasis1
lactation1
negative regulation of cell population proliferation1
positive regulation of gene expression1
negative regulation of keratinocyte proliferation1
cell differentiation1
positive regulation of bone mineralization1
intracellular receptor signaling pathway1
phosphate ion transmembrane transport1
nuclear receptor-mediated bile acid signaling pathway1
mRNA transcription by RNA polymerase II1

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
osteoporosis3MONDO:0005298EFO:0003882

Clinical trials

Total trials: 7.

Phase distribution

PhaseTrials
PHASE44
Not specified2
PHASE31

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05902078PHASE4RECRUITINGEldecalcitol and Calcitriol in Postmenopausal Women With Low Bone Mineral Density or Mild Osteoporosis
NCT06537115PHASE4RECRUITINGClinical Intervention of Idecalcitol Combined With Whey Protein Powder and Exercise for Sarcopenia
NCT05884372PHASE4COMPLETEDEfficacy and Safety of Combination Denosumab With Eldecalcitol for Postmenopausal Women With Osteoporosis.(ESCORT)
NCT06385093PHASE4UNKNOWNA Study on the Prevention and Treatment of GIOP With Eldecalcitol
NCT00144456PHASE3COMPLETEDA New Active Vitamin D, ED-71 for Osteoporosis
NCT01974167Not specifiedUNKNOWNEldecalcitol for GLucocorticoid Induced OsteopoRosIs Versus Alfacalcidol
NCT05433207Not specifiedUNKNOWNPost-Marketing Drug Intensive Monitoring Surveillance of EDIROL in Patients With Postmenopausal Osteoporosis

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.

10 molecules share ≥1 primary target. Top 10 by shared-target count:

MoleculeSourceStatusShared targets
CALCIPOTRIENEChEMBLPhase 4 (approved)VDR
CALCITRIOLChEMBLPhase 4 (approved)VDR
CHOLECALCIFEROLChEMBLPhase 4 (approved)VDR
DOXERCALCIFEROLChEMBLPhase 4 (approved)VDR
TACALCITOLChEMBLPhase 4 (approved)VDR
CURCUMINChEMBLPhase 3VDR
MAXACALCITOLChEMBLPhase 3VDR
SEOCALCITOLChEMBLPhase 3VDR
TAUROLITHOCHOLIC ACIDChEMBLPhase 3VDR
chenodiolPubChemApprovedVDR