Tephrosin
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Tephrosin | ||
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IUPAC name 7a-Hydroxy-9,10-dimethoxy-3,3-dimethyl-13,13a-dihydro-3H,7aH-pyrano[2,3-c;6,5-f']dichromen-7-one | ||
Other names 12aβ-hydroxydeguelin[1] | ||
Identifiers | ||
CAS number | 76-80-2 | |
PubChem | 114909 | |
ChEBI | CHEBI:9442 | |
ChEMBL | CHEMBL241806 | |
Jmol-3D images | {{#if:CC1(C=CC2=C(O1)C=CC3=C2O[C@@H]4COC5=CC(=C(C=C5[C@@]4(C3=O)O)OC)OC)C|Image 1 | |
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Properties | ||
Molecular formula | C23H22O7 | |
Molar mass | 410.41658 g/mol | |
Related compounds | ||
Related compounds | Deguelin, toxicarol | |
(verify) (what is: / ?) Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | ||
Infobox references | ||
Tephrosin is rotenoid. It is a natural fish poison found in the leaves and seeds of Tephrosia purpurea[2] and T. vogelii.[3]
See also
- Cubé resin
References
- ↑ Cabizza, Maddalena; Alberto Angioni, Marinella Melis, Marco Cabras, Carlo V. Tuberoso, and Paolo Cabras (2004). "Rotenone and rotenoids in cubè resins, formulations, and residues on olives". Journal of Agriculture and Food Chemistry 52 (2): 288–293. doi:10.1021/jf034987a. PMID 14733510.
- ↑ Ahmad, V. U.; Z. Ali, S. R. Hussaini, F. Iqbal, M. Zahid, M. Abbas, and N. Saba (1999-08-01). "Flavonoids of Tephrosia purpurea". Fitoterapia 70 (4): 443–445. doi:10.1016/S0367-326X(99)00046-5.
- ↑ Production of rotenoids by heterotrophic and photomixotrophic cell cultures of tephrosia vogelii. Nadine Lambert, Marie-France Trouslot, Claudine Nef-Campa and Hervé Chrestin, Phytochemistry, Volume 34, Issue 6, December 1993, Pages 1515-1520, doi:10.1016/S0031-9422(00)90838-0
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