Ospemifeen-d5

Ospemifene-d5 (FC-1271a-d5) is deuterium labeled Ospemifene. Ospemifene is a non-estrogen selective estrogen receptor modulator (SERM), with Kis of 380 and 410 nM for estrogen receptor α (ERα) and ERβ, respectively. Ospemifene can be used for the research of vaginal atrophy and breast cancer[1][2].

FC-1271a-d5

12352005

Estrogen Receptor/ERR; Isotope-Labeled Compounds

Others; Vitamin D Related/Nuclear Receptor

Cancer-programmed cell death

Cancer

ClCC/C(C1=CC=CC=C1)=C(C2=CC=C(OCCO)C=C2)\C3=C([2H])C([2H])=C([2H])C([2H])=C3[2H]

C24H18D5ClO2

383.92

[1]Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53 (2) :211-216.|[2]Unkila M, et, al. Vaginal effects of ospemifene in the ovariectomized rat preclinical model of menopause. J Steroid Biochem Mol Biol. 2013 Nov;138:107-15.|[3]Bruyniks N, et, al. Systematic indirect comparison of ospemifene versus local estrogens for vulvar and vaginal atrophy. Climacteric. 2017 Jun; 20 (3) : 195-204.|[4]Qiang Qv.et al.Selective estrogenic effects of a novel triphenylethylene compound, FC1271a, on bone, cholesterol level, and reproductive tissues in intact and ovariectomized rats. Endocrinology.Feb;141 (2) :809-20. 25. (2000) .|[5]Tracy L. Taras et al.In vitro and in vivo biologic effects of Ospemifene (FC-1271a) in breast cancer. The Journal of Steroid Biochemistry and Molecular Biology 77 (4-5) :271-9, (2001) .

Room temperature

http://file.medchemexpress.com/batch_PDF/HY-B0723S2/

Isotope-Labeled Compounds

No Development Reported