CAS 40957-83-3|Glycitein
| Common Name | Glycitein | ||
|---|---|---|---|
| CAS Number | 40957-83-3 | Molecular Weight | 284.263 |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 547.4±50.0 °C at 760 mmHg |
| Molecular Formula | C16H12O5 | Melting Point | >300ºC |
| MSDS | ChineseUSA | Flash Point | 210.1±23.6 °C |
Names
| Name | glycitein |
|---|---|
| Synonym | More Synonyms |
Glycitein BiologicalActivity
| Description | Glycitein is a soybean (yellow cultivar) isoflavonoid; used in combination with other isoflavonoids such as genistein and daidzein to study apoptosis and anti-oxidation processes. |
|---|---|
| Related Catalog | Signaling Pathways >>Others >>OthersNatural Products >>FlavonoidsResearch Areas >>Others |
| References | [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. |
Chemical & Physical Properties
| Density | 1.4±0.1 g/cm3 |
|---|---|
| Boiling Point | 547.4±50.0 °C at 760 mmHg |
| Melting Point | >300ºC |
| Molecular Formula | C16H12O5 |
| Molecular Weight | 284.263 |
| Flash Point | 210.1±23.6 °C |
| Exact Mass | 284.068481 |
| PSA | 79.90000 |
| LogP | 2.57 |
| Vapour Pressure | 0.0±1.5 mmHg at 25°C |
| Index of Refraction | 1.669 |
| InChIKey | DXYUAIFZCFRPTH-UHFFFAOYSA-N |
| SMILES | COc1cc2c(=O)c(-c3ccc(O)cc3)coc2cc1O |
| Storage condition | −20°C |
Safety Information
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| Hazard Codes | Xi |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2914509090 |
Customs
| HS Code | 2914509090 |
|---|---|
| Summary | HS:2914509090 other ketones with other oxygen function VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
Articles27
More Articles| Isoflavone pharmacokinetics and metabolism after consumption of a standardized soy and soy-almond bread in men with asymptomatic prostate cancer. Cancer Prev. Res. (Phila.) 8 , 1045-54, (2015) Epidemiologic associations suggest that populations consuming substantial amounts of dietary soy exhibit a lower risk of prostate cancer. A 20-week randomized, phase II, crossover trial was conducted ... | |
| Amino acid, mineral, and polyphenolic profiles of black vinegar, and its lipid lowering and antioxidant effects in vivo. Food Chem. 168 , 63-9, (2014) Black vinegar (BV) contains abundant essential and hydrophobic amino acids, and polyphenolic contents, especially catechin and chlorogenic acid via chemical analyses. K and Mg are the major minerals i... | |
| Isoflavone extraction from okara using water as extractant. Food Chem. 160 , 371-8, (2014) We here report on the use of water as a 'green' extraction solvent for the isolation of isoflavones from okara, a by-product of soymilk production. At a low liquid-to-solid ratio of 20 to 1 and 20 °C,... |
Synonyms
| 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxychromen-4-one |
| 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4-chromenone |
| MFCD00016679 |
| Glycitein |
| Glycetein |
| 4',7-Dihydroxy-6-methoxyisoflavone |
| 7,4'-Dihydroxy-6-methoxyisoflavone |
| 4’,7-dihydroxy-6-methoxyisoflavone |
| 4,7-Dihydroxy-6-methoxyisoflavone |
| 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-chromen-4-one |
| 4H-1-Benzopyran-4-one, 7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy- |
| 7-Hydroxy-3-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one |
| 4H-1-Benzopyran-4-one,7-hydroxy-3-(4-hydroxyphenyl)-6-methoxy |
