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Erteberel (LY500307)

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Company Name: Henan Fengda Chemical Co., Ltd
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Products Intro: Product Name:Erteberel (LY500307)
CAS:533884-09-2
Purity:99% Package:1kg;32USD|1000kg;1.3USD
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CAS:533884-09-2
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CAS:533884-09-2
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Products Intro: Product Name:Erteberel (LY500307)
CAS:533884-09-2
Purity:99.9% Package:25kgs/Drum;200kgs/Drum Remarks:FDA GMP CEP Approved Manufacturer

Erteberel (LY500307) manufacturers

  • Erteberel (LY500307)
  • Erteberel (LY500307) pictures
  • $32.00 / 1kg
  • 2024-03-29
  • CAS:533884-09-2
  • Min. Order: 1kg
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
  • Erteberel (LY500307)
  • Erteberel (LY500307) pictures
  • $1.00 / 1g
  • 2020-01-14
  • CAS:533884-09-2
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 200kg
  • Erteberel (LY500307)
  • Erteberel (LY500307) pictures
  • $1.00 / 1g
  • 2020-01-14
  • CAS:533884-09-2
  • Min. Order: 1g
  • Purity: 99%
  • Supply Ability: 200kg
Erteberel (LY500307) Basic information
Product Name:Erteberel (LY500307)
Synonyms:LY500307;(3aS,4R,9bR)-1,2,3,3a,4,9b-Hexahydro-4-(4-hydroxyphenyl)cyclopenta[c][1]benzopyran-8-ol;LY500307 (Erteberel);(3aS,4R,9bR)-4-(4-hydroxyphenyl)-1,2,3,3a,4,9b-hexahydrocyclopenta[c]chromen-8-ol;Erteberel (LY500307);Erteberel (LY500307) USP/EP/BP;CS-897;SERBA-1
CAS:533884-09-2
MF:C18H18O3
MW:282.33
EINECS:
Product Categories:Inhibitors
Mol File:533884-09-2.mol
Erteberel (LY500307) Structure
Erteberel (LY500307) Chemical Properties
Boiling point 485.2±45.0 °C(Predicted)
density 1.268
storage temp. Store at -20°C
solubility insoluble in H2O; ≥14.1 mg/mL in DMSO; ≥48.3 mg/mL in EtOH
form solid
pka9.79±0.30(Predicted)
Safety Information
MSDS Information
Erteberel (LY500307) Usage And Synthesis
UsesErteberel is a highly selective estrogen receptor β (ERβ) agonist.
Biological Activityerteberel (ly500307) is a potent and selective erβ (estrogen receptor beta) agonist (ec50 = 0.66 nm). [1]estrogen receptors are nuclear hormone receptors that act as a ligand-activated transcription factor. it regulates gene expression, cell proliferation and differentiation in target tissues and involved in breast cancer, endometrial cancer and osteoporosis etc. [1]in transcription assay of cotransfected human prostate cancer cell line, erteberel showed potency (ec50 = 0.66 nm), selectivity (32-fold) and full agonist function (>90% relative efficacy) to erβ than to erα. [1]in mouse model, prostate wet weight of cd-1 mice were measured following oral daily doses of erteberel for 7 days. results showed reduction on prostate weight in a dose-dependent manner (0.01 mg/kg – 0.05 mg/kg), and no effect on testes/seminal vesicle weight and androgens testosterone/dihydrotestosterone circulating level. [1]
references[1] norman bh, dodge ja, richardson ti, borromeo ps, lugar cw, jones sa, chen k, wang y, durst gl, barr rj, montrose-rafizadeh c, osborne he, amos rm, guo s, boodhoo a, krishnan v. benzopyrans are selective estrogen receptor beta agonists with novel activity in models of benign prostatic hyperplasia. j med chem. 2006 oct 19;49(21):6155-7.
Erteberel (LY500307) Preparation Products And Raw materials
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