| Weight | 270.24 g/mol |
|---|---|
| Formula | C15H10O5 |
| Hydrogen Acceptors | 5 |
| Hydrogen Donors | 3 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
Genistein (446-72-0, 690224-00-1)
Genestein
Score:
#101 in Biochemistry
,
#439 in Biology
,
#457 in Chemistry
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- Genistein, a specific inhibitor of tyrosine-specific protein kinases. (Journal of Biological Chemistry, 1987)
- Genistein, daidzein, and their .beta.-glycoside conjugates: antitumor isoflavones in soybean foods from American and Asian diets (Journal of Agricultural and Food Chemistry, 1993)
- Maternal genistein alters coat color and protects Avy mouse offspring from obesity by modifying the fetal epigenome. (Environmental Health Perspectives, 2006)
- Genistein, a dietary-derived inhibitor of in vitro angiogenesis (Proceedings of the National Academy of Sciences of the United States of America, 1993)
- Inhibitory Effects of the Tyrosine Kinase Inhibitor Genistein on Mammalian DNA Topoisomerase II (Cancer Research, 1989)
- Estrogenic Effects of Genistein on the Growth of Estrogen Receptor-positive Human Breast Cancer (MCF-7) Cells in Vitro and in Vivo (Cancer Research, 1998)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Genestein
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SMILESC1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O
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InChIKeyTZBJGXHYKVUXJN-UHFFFAOYSA-N
- Pubchem - Genistein
- Wikipedia - genistein
Genistein is an isoflavone that is described as an angiogenesis inhibitor and a phytoestrogen. It was first isolated in 1899 from the dyer's broom, Genista tinctoria; hence, the chemical name. The compound structure was established in 1926, when it was found to be identical with that of prunetol.
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Genistein
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