Repositioning Candidate Details

Candidate ID: R0760
Source ID: DB05295
Source Type: investigational
Compound Type: small molecule
Compound Name: Eldecalcitol
Synonyms: 1α,25-dihydroxy-2β-(3-hydroxypropoxy)cholecalciferol; Eldecalcitol
Molecular Formula: C30H50O5
SMILES: [H][C@@]1(CC[C@@]2([H])\C(CCC[C@]12C)=C\C=C1\C[C@@H](O)[C@@H](OCCCO)[C@H](O)C1=C)[C@H](C)CCCC(C)(C)O
Structure:
DrugBank Description: Eldecalcitol (ED-71), a vitamin D analog, is a more potent inhibitor of bone resorption than alfacalcidol in an estrogen-deficient rat model of osteoporosis. Eldecalcitol, effectively and safely increased lumbar and hip bone mineral density (BMD) in osteoporotic patients who also received vitamin D3 supplementation.
CAS Number: 104121-92-8
Molecular Weight: 490.725
DrugBank Indication: Investigated for use/treatment in osteoporosis.
DrugBank Pharmacology: --
DrugBank MoA: Eldecalcitol is an analog of 1a,25-dihydroxyvitamin D3 , bearing a hydroxypropoxy residue at the 2b position. Eldecalcitol is also effective in increasing bone mass and was able to enhance bone strength in rodents. It binds to the vitamin D receptor (VDR) with less affinity but binds to vitamin D-binding protein with higher affinity than 1,25(OH)2D, showing a long half-life in plasma.
Targets: Vitamin D3 receptor
Inclusion Criteria: Indication associated