Estramustine phosphate

CAT:
804-HY-13627A
Size:
1 Each

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
Estramustine phosphate - image 1

Estramustine phosphate

  • Description:

    Estramustine phosphate, an estradiol analog, is an orally active antimicrotubule chemotherapy agent. Estramustine phosphate depolymerises microtubules by binding to microtubule associated proteins (MAPs) and/or to tubulin. Estramustine phosphate can interfere mitosis, trigger cell death and induce apoptosis, which can be used for the research of cancer like prostate cancer[1][2][3].
  • UNSPSC:

    12352005
  • Hazard Statement:

    H301-H311-H331-H341
  • Target:

    Apoptosis; Microtubule/Tubulin; Mitosis
  • Type:

    Reference compound
  • Related Pathways:

    Apoptosis; Cell Cycle/DNA Damage; Cytoskeleton
  • Applications:

    Metabolism-protein/nucleotide metabolism
  • Field of Research:

    Cancer; Endocrinology; Inflammation/Immunology
  • Assay Protocol:

    https://www.medchemexpress.com/estramustine-phosphate.html
  • Solubility:

    10 mM in DMSO
  • Smiles:

    O=C(OC1=CC=C2[C@@]3([H])CC[C@]4(C)[C@@H](OP(O)(O)=O)CC[C@@]4([H])[C@]3([H])CCC2=C1)N(CCCl)CCCl
  • Molecular Formula:

    C23H32Cl2NO6P
  • Molecular Weight:

    520.38
  • Precautions:

    P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P403+P233-P405-P501
  • References & Citations:

    [1]C Wei, et al. Estramustine phosphate induces prostate cancer cell line PC3 apoptosis by down-regulating miR-31 levels. Eur Rev Med Pharmacol Sci. 2018 Jan;22 (1) :40-45. |[2]Sonja S Mojsilovic, et al. Estramustine Phosphate Inhibits TGF- β-Induced Mouse Macrophage Migration and Urokinase-Type Plasminogen Activator Production. Anal Cell Pathol (Amst) . 2018 Sep 2;2018:3134102. |[3]Stephane Oudard, et al. Activity of docetaxel with or without estramustine phosphate versus mitoxantrone in androgen dependent and independent human prostate cancer xenografts. J Urol. 2003 May;169 (5) :1729-34.
  • Shipping Conditions:

    Room temperature
  • Scientific Category:

    Reference compound1
  • Clinical Information:

    Launched
  • CAS Number:

    [4891-15-0]