Genistein-2’,3’,5’,6’-d4 (Major)

• CAT Number: R001593
• CAS Number: 187960-08-3
• Molecular Formula: C15H10O5
• Molecular Weight: 274.264
• Purity: ≥95%
• Synonyms: 5,7-Dihydroxy-3-(4-hydroxyphenyl)-4H-1-benzopyran-4-one-d4; Baichanin A-d4; Bonistein-d4; ?4’,5,7-Trihydroxyisoflavone-d4; GeniVida-d4; Genisteol-d4; NSC 36586-d4; Prunetol-d4; Sophoricol-d4
• Target: JAK/STAT Signaling
• Storage: -20°C
• IUPAC Name: 5,7-dihydroxy-3-(2,3,5,6-tetradeuterio-4-hydroxyphenyl)chromen-4-one
• InChI: InChI=1S/C15H10O5/c16-9-3-1-8(2-4-9)11-7-20-13-6-10(17)5-12(18)14(13)15(11)19/h1-7,16-18H/i1D,2D,3D,4D
• InChIKey: TZBJGXHYKVUXJN-RHQRLBAQSA-N
• SMILES: [2H]C1=C(C(=C(C(=C1C2=COC3=CC(=CC(=C3C2=O)O)O)[2H])[2H])O)[2H]

Genistein-2′,3′,5′,6′-d4 is a deuterated form of genistein, an isoflavone found in soy products with known antioxidant and estrogenic properties. The deuterium labeling enhances the stability of genistein, facilitating its use in detailed pharmacokinetic and metabolic studies through techniques like NMR and mass spectrometry. In pharmaceutical research, Genistein-2′,3′,5′,6′-d4 is valuable for studying its potential benefits in cancer prevention, cardiovascular health, and bone density improvement. In organic chemistry, it aids in understanding biosynthetic pathways and reaction mechanisms. This compound also supports nutritional and biomedical research by enabling precise tracking of genistein’s biological effects.