Estetrol-d4 (Major)

CAS: 15183-37-6

Ref. TR-E668452

Produktinformation

• Name: Estetrol-d4 (Major)
• Synonyme: (15a,16a,17ß)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol-d4, Estra-1,3,5(10)-triene-3,15a,16a,17ß-tetrol-d4, 15a-Hydroxyestriol-d4, 3,15a,16a,17ß-Tetrahydroxyestra-1,3,5(10)-triene-d4, (15Alpha,16Alpha,17Beta)-Estra-1,3,5(10)-Triene-3,15,16,17-Tetrol, (15a,16a,17)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol, (15α,16α,17β)-Estra-1,3,5(10)-triene-3,15,16,17-tetrol, 1,3,5(10)-Estratrien-3,15-Alpha, 16-Alpha, 17-Beta-Tetrol, 15-Alpha-Hydroxyestriol, 15a-Hydroxyestriol, 3,15a,16a,17-Tetrahydroxyestra-1,3,5(10)-triene, 3,15α,16α,17β-Tetrahydroxyestra-1,3,5(10)-triene, E 4, Enb 39R14Vf, Estra-1,3,5(10)-trien-3,15α,16α,17β-tetraol, Estra-1,3,5(10)-triene-3,15,16,17-tetrol, (15α,16α,17β)-, Estra-1,3,5(10)-triene-3,15a,16a,17-tetrol, Estra-1,3,5(10)-triene-3,15α,16α,17β-tetrol
• CAS: 15183-37-6

Beschreibung

Applications A labelled metabolite of Estradiol. It is an estrogenic steroid synthesized exclusively by the fetal liver during human pregnancy and reaching the maternal circulation through the placenta.
References Gurpide, E., et al.: J. Clin. Endocrinol., 26, 1355 (1966), Hagen, A., et al.: J. Clin. Endocrinol., 30, 763 (1970), Schollberg, K., et al.: Exp. Clin. Endocrinol., 85, 204 (1985), Coelingh Bennink, H., et al.: Contraception, 77, 186 (2008),

• Marke: TRC

Chemische Eigenschaften

• Molekulargewicht: 308.41
• Formel: C₁₈H₂₀D₄O₄
• Farbe/Form: White To Off-White
• InChl: InChI=1S/C18H24O4/c1-18-7-6-12-11-5-3-10(19)8-9(11)2-4-13(12)14(18)15(20)16(21)17(18)22/h3,5,8,12-17,19-22H,2,4,6-7H2,1H3/t12-,13-,14-,15-,16-,17+,18+/m1/s1/i2D2,3D,8D
• InChI Key: InChIKey=AJIPIJNNOJSSQC-SCCHASIWSA-N
• SMILES: [2H]c1cc2c(c([2H])c1O)C([2H])([2H])C[C@@H]1[C@@H]2CC[C@@]2(C)[C@H]1[C@@H](O)[C@@H](O)[C@@H]2O