Estriol-d3

• Description:

  Estriol-d3 is the deuterium labeled Estriol. Estriol is an antagonist of the G-protein coupled estrogen receptor in estrogen receptor-negative breast cancer cells.

• UNSPSC:

  12352005

• Hazard Statement:

  H351, H360, H362, H410

• Target:

  Endogenous Metabolite; Estrogen Receptor/ERR; Isotope-Labeled Compounds

• Type:

  Isotope-Labeled Compounds

• Related Pathways:

  Metabolic Enzyme/Protease; Others; Vitamin D Related/Nuclear Receptor

• Field of Research:

  Cancer

• Purity:

  97.57

• Solubility:

  DMSO : 250mg/mL (ultrasonic) |H2O : < 0.1 mg/mL

• Smiles:

  C[C@@]12[C@] (C[C@H] ([C@]2 ([2H]) O) O) ([H]) [C@@]3 ([H]) [C@@] (CC1) ([H]) C4=CC ([2H]) =C (O) C ([2H]) =C4CC3

• Molecular Formula:

  C18H21D3O3

• Molecular Weight:

  291.40

• Precautions:

  H351, H360, H362, H410

• References & Citations:

  [1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216. |[2]Morinaga, A., et al., Effects of sex hormones on Alzheimer's disease-associated beta-amyloid oligomer formation in vitro. Exp Neurol, 2011. 228 (2) : p. 298-302.|[3]Begum, M., et al., Neonatal estrogenic exposure suppresses PTEN-related endometrial carcinogenesis in recombinant mice. Lab Invest, 2006. 86 (3) : p. 286-96.|[4]Hewitt, S.C. and K.S. Korach, Estrogenic activity of bisphenol A and 2,2-bis (p-hydroxyphenyl) -1,1,1-trichloroethane (HPTE) demonstrated in mouse uterine gene profiles. Environ Health Perspect, 2011. 119 (1) : p. 63-70.

• Shipping Conditions:

  Room Temperature

• Storage Conditions:

  -20°C, 3 years; 4°C, 2 years (Powder)

• Scientific Category:

  Isotope-Labeled Compounds

• Clinical Information:

  No Development Reported

• CAS Number:

  79037-36-8