Toremifene

CAT:
804-HY-B0005A-01
Size:
10 mg

For Laboratory Research Only. Not for Clinical or Personal Use.

  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
Toremifene - image 1

Toremifene

  • Description :

    Toremifene (Z-Toremifene) is a second-generation selective estrogen-receptor modulator (SERM) in development for the prevention of osteoporosis. Toremifene also potent inhibits infectious EBOV Zaire and Marburg (MARV) with IC50 of 0.07 μM and 2.6 μM, respectively[1][2].
  • Product Name Alternative :

    Z-Toremifene; NK 622 (free base) ; FC-1157a (free base)
  • UNSPSC :

    12352005
  • Hazard Statement :

    H301, H311, H331, H341
  • Target :

    Estrogen Receptor/ERR
  • Type :

    Reference compound
  • Related Pathways :

    Vitamin D Related/Nuclear Receptor
  • Applications :

    Cancer-programmed cell death
  • Field of Research :

    Cancer; Infection
  • Assay Protocol :

    https://www.medchemexpress.com/toremifene.html
  • Concentration :

    10mM
  • Purity :

    99.86
  • Solubility :

    DMSO : 62.5 mg/mL (ultrasonic; warming; heat to 60°C)
  • Smiles :

    ClCC/C(C1=CC=CC=C1)=C(C2=CC=C(OCCN(C)C)C=C2)\C3=CC=CC=C3
  • Molecular Formula :

    C26H28ClNO
  • Molecular Weight :

    405.96
  • Precautions :

    H301, H311, H331, H341
  • References & Citations :

    [1]Matthew R Smith, Selective Estrogen Receptor Modulators to Prevent Treatment-Related Osteoporosis.Rev Urol. 2005; 7 (Suppl 3) : S30-S35.|[2]Gauri J Sabnis, Luciana Macedo, Olga Goloubeva, Toremifene - Atamestane; Alone or In Combination: Predictions from the Preclinical Intratumoral Aromatase Model. J Steroid Biochem Mol Biol. 2008 January; 108 (1-2) : 1-7.|[3]Taneja SS, Morton R, Barnette G, Prostate cancer diagnosis among men with isolated high-grade intraepithelial neoplasia enrolled onto a 3-year prospective phase III clinical trial of oral toremifene. J Clin Oncol. 2013 Feb 10;31 (5) :523-9.|[4]Laura Cooper, et al. Screening and Reverse-Engineering of Estrogen Receptor Ligands as Potent Pan-Filovirus Inhibitors. J Med Chem. 2020 Sep 4.
  • Shipping Conditions :

    Room Temperature
  • Storage Conditions :

    -20°C, 3 years; 4°C, 2 years (Powder)
  • Scientific Category :

    Reference compound1
  • Clinical Information :

    Launched
  • Citation 01 :

    BioRxiv. 2020 May.|J Pharm Biomed Anal. 2021 Feb 20:195:113870.|Patent. US11696914.|Res Sq. 2020 Dec 31:rs.3.rs-100914.|Cell Rep Methods. 2023 Oct 23;3 (10) :100599.|J Med Chem. 2020 Oct 8;63 (19) :11085-11099.|Viruses. 2021 Jun 28;13 (7) :1255.
  • CAS Number :

    [89778-26-7]

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