Estetrol-d4 (Major)

CAS: 15183-37-6

Ref. TR-E668452

Informação sobre produto

• Nome: 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

Descrição

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

Propriedades químicas

• Peso molecular: 308.41
• Fórmula: C₁₈H₂₀D₄O₄
• Cor/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
• Chave 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