Glycitein

• CAT Number: I003490
• CAS Number: 40957-83-3
• Molecular Formula: C16H12O5
• Molecular Weight: 284.3
• Purity: ≥95%
• Synonyms: 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one
• Target: Apoptosis
• Solubility: 10 mM in DMSO
• Storage: -20°C
• IUPAC Name: 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one
• InChI: InChI=1S/C16H12O5/c1-20-15-6-11-14(7-13(15)18)21-8-12(16(11)19)9-2-4-10(17)5-3-9/h2-8,17-18H,1H3
• InChIKey: DXYUAIFZCFRPTH-UHFFFAOYSA-N
• SMILES: COC1=C(C=C2C(=C1)C(=O)C(=CO2)C3=CC=C(C=C3)O)O

Glycitein（Cat No.:I003490） is an isoflavonoid found in yellow cultivar soybeans. It is often used in combination with other isoflavonoids like genistein and daidzein to study processes such as apoptosis (programmed cell death) and anti-oxidation. By combining these isoflavonoids, researchers can investigate their potential synergistic effects and explore their roles in various cellular processes. Glycitein offers a valuable tool for studying the bioactive properties of soy isoflavonoids and their potential applications in areas such as cancer research and oxidative stress.

Reference

[1]. Song TT, et al. Estrogenic activity of glycitein, a soy isoflavone. J Agric Food Chem. 1999 Apr;47(4):1607-10.

[2]. Yoshida H, et al. Glycitein effect on suppressing the proliferation and stimulating the differentiation of osteoblastic MC3T3-E1 cells. Biosci Biotechnol Biochem. 2001 May;65(5):1211-3.

[3]. Pan W, et al. Genistein, daidzein and glycitein inhibit growth and DNA synthesis of aortic smooth muscle cells from stroke-prone spontaneously hypertensive rats. J Nutr. 2001 Apr;131(4):1154-8.