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Elocalcitol

Base Information
  • Chemical Name:Elocalcitol
  • CAS No.:199798-84-0
  • Molecular Formula:C29H43FO2
  • Molecular Weight:442.658
  • Hs Code.:
  • UNII:2WDS5F2V6Q
  • Metabolomics Workbench ID:149666
  • NCI Thesaurus Code:C166600
  • Nikkaji Number:J3.510.012A
  • Pharos Ligand ID:8ZGHMGCXRDWT
  • Wikidata:Q27077174
  • Mol file:199798-84-0.mol
Elocalcitol

Synonyms:BXL-628;BXL628;Elocalcitol

Suppliers and Price of Elocalcitol
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Medical Isotopes, Inc.
  • Elocalcitol
  • 5 mg
  • $ 690.00
  • DC Chemicals
  • Elocalcitol >99%
  • 250 mg
  • $ 4000.00
  • DC Chemicals
  • Elocalcitol >99%
  • 100 mg
  • $ 2000.00
  • Cayman Chemical
  • BXL-628 ≥98%
  • 5mg
  • $ 435.00
  • Cayman Chemical
  • BXL-628 ≥98%
  • 1mg
  • $ 145.00
  • American Custom Chemicals Corporation
  • ELOCALCITOL 95.00%
  • 5MG
  • $ 502.91
  • AK Scientific
  • Elocalcitol
  • 5mg
  • $ 687.00
Total 42 raw suppliers
Chemical Property of Elocalcitol
Chemical Property:
  • PSA:40.46000 
  • LogP:7.15820 
  • XLogP3:5.7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:7
  • Exact Mass:442.32470877
  • Heavy Atom Count:32
  • Complexity:813
Purity/Quality:

99% *data from raw suppliers

Elocalcitol *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC(CC)(C=CCC(C)C1=CCC2C1(CCCC2=CC=C3CC(CC(C3=C)F)O)C)O
  • Isomeric SMILES:CCC(CC)(/C=C/C[C@H](C)C1=CC[C@@H]\2[C@@]1(CCC/C2=C\C=C/3\C[C@H](C[C@@H](C3=C)F)O)C)O
  • Recent EU Clinical Trials:A randomized, double blind, placebo controlled, parallel group study to determine the effect of Elocalcitol on sperm parameters in infertile male patients
  • Description BXL-628 is an analog of vitamin D3 that has diverse biological activities. It increases death of androgen-stimulated human benign prostatic hyperplasia (BPH) cells via induction of apoptosis in a dose-dependent manner. In vivo, BXL-628 completely inhibits androgen-stimulated prostate overgrowth in a rat model of BPH. It reduces expression of IL-13 and IgE/mast cell-derived protease 1 (MMCP1) and decreases edema and leukocyte infiltration in the bladder wall in a mouse model of allergen-induced interstitial cystitis. BXL-628 also reduces the number of adherent endometrial stromal cells and decreases the total weight of endometrial lesions in a mouse model of endometriosis. Formulations containing BXL-628 are under clinical investigation for the treatment of BPH.
Technology Process of Elocalcitol

There total 40 articles about Elocalcitol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
<3S-(1Z,3α,5β)>-<2-<3-Fluoro-5-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-methylenecyclohexylidene>ethyl>diphenylphosphine Oxide; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.0833333h;
(3aR,7aS)-1-((S,E)-6-ethyl-6-(trimethylsilyloxy)oct-4-en-2-yl)-7a-methyl-3,3a,5,6,7,7a-hexahydro-3H-inden-4-one; In tetrahydrofuran; hexane; at -78 - -20 ℃; for 3.16667h;
With tetrabutyl ammonium fluoride; water; potassium hydrogencarbonate; rochelle salt; more than 3 stages; Product distribution / selectivity;
Guidance literature:
(3aR,7aS)-1-((S,E)-6-ethyl-6-(trimethylsilyloxy)oct-4-en-2-yl)-7a-methyl-3,3a,5,6,7,7a-hexahydro-3H-inden-4-one; <3S-(1Z,3α,5β)>-<2-<3-Fluoro-5-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-methylenecyclohexylidene>ethyl>diphenylphosphine Oxide; With lithium hexamethyldisilazane; In tetrahydrofuran; at -55 - 25 ℃; for 1.58333h;
With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃;
With potassium hydrogencarbonate; In tetrahydrofuran; Product distribution / selectivity;
Guidance literature:
<3S-(1Z,3α,5β)>-<2-<3-Fluoro-5-<<(1,1-dimethylethyl)dimethylsilyl>oxy>-2-methylenecyclohexylidene>ethyl>diphenylphosphine Oxide; With n-butyllithium; In tetrahydrofuran; hexane; at -75 - -50 ℃; for 0.333333h;
(3aR,4S,7aR)-1-((S,E)-5-ethyl-5-hydroxy-1-methyl-hept-3-enyl)-7a-methyl-3a,4,5,6,7,7a-hexahydro-3H-inden-4-one; In tetrahydrofuran; hexane; at -50 - -10 ℃; for 2.08333h; Product distribution / selectivity;
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