Estetrol-d4 (Major)

CAS: 15183-37-6

Ref. TR-E668452

Información del producto

• Nombre: Estetrol-d4 (Major)
• Sinónimos: (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, Estetrol

Descripción

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),

• Marca: TRC

Propiedades químicas

• Peso molecular: 308.41
• Fórmula: C₁₈H₂₀D₄O₄
• Color/Forma: White To Off-White
• InChI: 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
• Clave InChI: 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