β-Estradiol-6-one 6-(O-carboxymethyloxime)

• CAT Number: R042514
• CAS Number: 35048-47-6
• Molecular Formula: C₂₀H₂₅NO₅
• Molecular Weight: 359.42
• Purity: ≥95%
• Synonyms: 2-[[[(17β)-3,17-Dihydroxyestra-1,3,5(10)-trien-6-ylidene]amino]oxy]acetic Acid; Estrane Acetic Acid Deriv.; 17β-Estradiol 6-(O-carboxymethyl)oxime; 6-Oxo-17β-estradiol 6-[O-(carboxymethyl)oxime]; 6-Oxoestradiol (carboxymethyl)oxime; Estradiol 6-(O-ca
• Storage: Desiccate at RT
• IUPAC Name: 2-[(Z)-[(8R,9S,13S,14S,17S)-3,17-dihydroxy-13-methyl-8,9,11,12,14,15,16,17-octahydro-7H-cyclopenta[a]phenanthren-6-ylidene]amino]oxyacetic acid
• InChI: InChI=1S/C20H25NO5/c1-20-7-6-13-12-3-2-11(22)8-15(12)17(21-26-10-19(24)25)9-14(13)16(20)4-5-18(20)23/h2-3,8,13-14,16,18,22-23H,4-7,9-10H2,1H3,(H,24,25)/b21-17-/t13-,14-,16+,18+,20+/m1/s1
• InChIKey: AWARIMYXKAIIGO-UYGYUSPXSA-N
• SMILES: CC12CCC3C(C1CCC2O)CC(=NOCC(=O)O)C4=C3C=CC(=C4)O

β-Estradiol-6-one 6-(O-carboxymethyloxime)(CAT: R042514) is a modified derivative of β-estradiol, a key estrogen hormone involved in various biological processes. The addition of a carboxymethyloxime group at the 6-position enhances its utility in biochemical and pharmaceutical research, particularly in studies focusing on hormone receptors, enzyme interactions, and metabolism. This compound is often used in conjugation reactions, enabling the formation of stable linkages with proteins or other molecules, making it valuable for assay development, immunology research, and drug discovery. Its unique structure allows for targeted exploration of estrogenic pathways and their role in human health and disease.