Glycitin

• CAT Number: I003461
• CAS Number: 40246-10-4
• Molecular Formula: C22H22O10
• Molecular Weight: 446.40
• Purity: ≥95%
• Synonyms: Glycitein-7-β-O-glucoside
• Target: Bacterial
• Solubility: 10 mM in DMSO
• Storage: Store at -20°C
• IUPAC Name: 3-(4-hydroxyphenyl)-6-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
• InChI: InChI=1S/C22H22O10/c1-29-15-6-12-14(30-9-13(18(12)25)10-2-4-11(24)5-3-10)7-16(15)31-22-21(28)20(27)19(26)17(8-23)32-22/h2-7,9,17,19-24,26-28H,8H2,1H3/t17-,19-,20+,21-,22-/m1/s1
• InChIKey: OZBAVEKZGSOMOJ-MIUGBVLSSA-N
• SMILES: COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O

Glycitin（Cat No.:I003461）is an isoflavone glycoside found in soybeans and other legumes, recognized for its antioxidant and estrogenic properties. As a phytoestrogen, it mimics estrogenic activity in the body, making it valuable in research on hormone-related health benefits, including potential applications in managing menopausal symptoms and supporting bone health. Glycitin is also studied for its role in protecting against oxidative stress, cardiovascular health, and anti-inflammatory effects. Its bioactive profile makes it a focal compound in studies exploring natural alternatives for hormone modulation and disease prevention.

Reference

[1]. Uesugi T, et al. Comparative study on reduction of bone loss and lipid metabolism abnormality in ovariectomized rats by soy isoflavones, daidzin, genistin, and glycitin. Biol Pharm Bull. 2001 Apr;24(4):368-72.

[2]. Li XH, et al. Effect of daidzin, genistin, and glycitin on osteogenic and adipogenic differentiation of bone marrow stromal cells and adipocytic transdifferentiation of osteoblasts. Acta Pharmacol Sin. 2005 Sep;26(9):1081-6.