Hexestrol

CAS No. 84-16-2

Hexestrol( Cycloestrol | Erythrohexestrol | Hexoestrol | HSDB 2149 )

Catalog No. M19165 CAS No. 84-16-2

Hexestrol binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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50MG 34 In Stock
100MG 42 In Stock
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Biological Information

  • Product Name
    Hexestrol
  • Note
    Research use only, not for human use.
  • Brief Description
    Hexestrol binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.
  • Description
    Hexestrol is a synthetic ER agonist, microtubule polymerization inhibitor, and potential carcinogen. It induces mitotic arrest, aneuploidy, and DNA adduct formation.(In Vivo):Hexestrol (3 and 6 mg/kg; i.p. once daily for 30 days) has a not significant influence in the ovaries from mice at the dose of 3 mg/kg.
  • In Vitro
    ——
  • In Vivo
    Hexestrol (3 and 6 mg/kg; i.p. once daily for 30 days) has a not significant influence in the ovaries from mice at the dose of 3 mg/kg. Animal Model:Mus musculus (90-120 days, 25-50 g)Dosage:3, 6 mg/kg (adopted the same dose used to increase weight gain in cattle)Administration:I.p. once daily for 30 days Result:Numerous follicles in different stages of development were found at the dose of 3 mg/kg in the ovaries.Not detected the corpora lutea (CL) at the dose of 6 mg/kg.
  • Synonyms
    Cycloestrol | Erythrohexestrol | Hexoestrol | HSDB 2149
  • Pathway
    Cytoskeleton/Cell Adhesion Molecules
  • Target
    Glucokinase
  • Recptor
    ERα| ERβ
  • Research Area
    Endocrinology
  • Indication
    ——

Chemical Information

  • CAS Number
    84-16-2
  • Formula Weight
    270.37
  • Molecular Formula
    C18H22O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (369.86 mM)
  • SMILES
    CC[C@@H]([C@@H](CC)C1=CC=C(O)C=C1)C1=CC=C(O)C=C1
  • Chemical Name
    4,4'-((3R,4S)-hexane-3,4-diyl)diphenol

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Waibel M, et al. Eur J Med Chem, 2009, 44(9), 3412-3424.
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