Chlorotrianisene

CAS No. 569-57-3

Chlorotrianisene( Chlorotrianisene | Chlortrianisestrol | Chlortrianizen | Chlorotrianisine | Chlorestrolo | Chlorotrianizen | Khlortrianizen )

Catalog No. M15074 CAS No. 569-57-3

Chlorotrianisene is a powerful synthetic, non-steroidal estrogen.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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50MG 45 In Stock
100MG 59 In Stock
200MG 106 In Stock
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Biological Information

  • Product Name
    Chlorotrianisene
  • Note
    Research use only, not for human use.
  • Brief Description
    Chlorotrianisene is a powerful synthetic, non-steroidal estrogen.
  • Description
    Chlorotrianisene is a powerful synthetic, non-steroidal estrogen.(In Vitro):Comparison of intracellular estrogen receptor (ER) affinities of Chlorotrianisene with respective rat uterine cytosolic ER affinities has initially suggested the potential for activation of ER as a mechanism of growth stimulation. Chlorotrianisene exhibits concentration dependent cell growth stimulation with an EC50 of 28 nM and a Ki of 500 nM in MCF-7 cells.(In Vivo):The incubation of Chlorotrianisene with rat liver microsomes and NADPH generates a reactive intermediate which binds covalently to proteins. Intermediate may inactivate the uterine estrogen receptors (ER). The incubation of Chlorotrianisene with rat liver microsomes and NADPH in the presence of rat uteri, under conditions which generate intermediate, markedly decreased the binding capacity of the ER for [3H]estradiol (E2).
  • In Vitro
    Comparison of intracellularestrogen receptor (ER) affinities of Chlorotrianisene with respective rat uterine cytosolic ER affinities has initially suggested the potential for activation of ER as a mechanism of growth stimulation. Chlorotrianisene exhibits concentration dependent cell growth stimulation with an EC50 of 28 nM and a Ki of 500 nM in MCF-7 cells.
  • In Vivo
    The incubation of Chlorotrianisene with rat liver microsomes and NADPH generates a reactive intermediate which binds covalently to proteins. Intermediate may inactivate the uterine estrogen receptors (ER). The incubation of Chlorotrianisene with rat liver microsomes and NADPH in the presence of rat uteri, under conditions which generate intermediate, markedly decreased the binding capacity of the ER for [3H]estradiol (E2).
  • Synonyms
    Chlorotrianisene | Chlortrianisestrol | Chlortrianizen | Chlorotrianisine | Chlorestrolo | Chlorotrianizen | Khlortrianizen
  • Pathway
    Endocrinology/Hormones
  • Target
    Estrogen Receptor/ERR
  • Recptor
    ER
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    569-57-3
  • Formula Weight
    380.86
  • Molecular Formula
    C23H21ClO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 10 mM
  • SMILES
    COC1=CC=C(C=C1)C(=C(C2=CC=C(C=C2)OC)Cl)C3=CC=C(C=C3)OC
  • Chemical Name
    1-[1-chloro-2,2-bis(4-methoxyphenyl)ethenyl]-4-methoxybenzene

Shipping & Storage Information

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

Reference

1. Kupfer D, Bulger WH. FEBS Lett. 1990 Feb 12;261(1):59-62.
molnova catalog
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