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| | artocarpin Basic information |
| Product Name: | artocarpin | | Synonyms: | artocarpin;2',4',5-Trihydroxy-6-(3-methyl-1-butenyl)-3-(3-methyl-2-butenyl)-7-methoxyflavone;NSC 241010;2',4',5-Trihydroxy-7-methoxy-6-(3-methyl-1-butenyl)-3-(3-methyl-2-butenyl)flavone;4H-1-Benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-6-(3-methyl-1-buten-1-yl)-3-(3-methyl-2-buten-1-yl)-;2-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-6-[(1E)-3-methyl-1-buten-1-yl]-3-(3-methyl-2-buten-1-yl)-4H-chromen-4-one | | CAS: | 7608-44-8 | | MF: | C26H28O6 | | MW: | 436.5 | | EINECS: | | | Product Categories: | | | Mol File: | 7608-44-8.mol |  |
| | artocarpin Chemical Properties |
| Boiling point | 667.1±55.0 °C(Predicted) | | density | 1.242±0.06 g/cm3(Predicted) | | pka | 6.38±0.40(Predicted) |
| | artocarpin Usage And Synthesis |
| Uses | Artocarpin can be used in combination with other agents for treating various diseases. It can also be used to activate the Nrf2-mediated defense system, SAR, and inhibit intracellular oxidative insults. | | Definition | ChEBI: A trihydroxyflavone that is flavone substituted by hydroxy groups at positions 5, 2', and 4', a methoxy group at position 7, a prenyl group at position 3 and a (1E)-3-methylbut-1-enyl group at position 6. Isolated from Artocarpus het
rophyllus and Artocarpus integrifolia, it exhibits antineoplastic activity. |
| | artocarpin Preparation Products And Raw materials |
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