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| | 5-Hydroxydequelin Basic information |
| Product Name: | 5-Hydroxydequelin | | Synonyms: | TOXICAROL;(7aS)-13,13aα-Dihydro-6-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aαH)-one;(7aS,13aS)-13,13a-Dihydro-6-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one;alpha-Toxicarol;Α-TOXICAROL;3H-Bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one, 13,13a-dihydro-6-hydroxy-9,10-dimethoxy-3,3-dimethyl-, (7aS,13aS)-;α-Toxicarol;5-Hydroxydequelin | | CAS: | 82-09-7 | | MF: | C23H22O7 | | MW: | 410.42 | | EINECS: | | | Product Categories: | Miscellaneous Natural Products | | Mol File: | 82-09-7.mol |  |
| | 5-Hydroxydequelin Chemical Properties |
| Melting point | 222℃ | | Boiling point | 607.2±55.0 °C(Predicted) | | density | 1.312±0.06 g/cm3(Predicted) | | refractive index | >1.768 | | pka | 7.06±0.40(Predicted) |
| | 5-Hydroxydequelin Usage And Synthesis |
| Uses | α-Toxicarol is a potent inhibitor of EBV.α-Toxicarol significantly inhibits mouse skin tumor in vivo. α-Toxicarol inhibits the TPA-induced EBV-EA activation[1]. | | Definition | ChEBI: Toxicarol is a member of isoflavanones. | | References | [1] Ito, C., et al. Cancer Chemopreventive Activity of Rotenoids fromDerris trifoliata . Planta Medica, 70(6), 585–588. |
| | 5-Hydroxydequelin Preparation Products And Raw materials |
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