Tephrosin

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Tephrosin
Tephrosin.png
Names
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
76-80-2 YesY
ChEBI CHEBI:9442 N
ChEMBL ChEMBL241806 N
ChemSpider 102858 N
Jmol 3D model Interactive image
KEGG C10535 N
PubChem 114909
  • InChI=1S/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1 N
    Key: AQBZCCQCDWNNJQ-AUSIDOKSSA-N N
  • InChI=1/C23H22O7/c1-22(2)8-7-12-15(30-22)6-5-13-20(12)29-19-11-28-16-10-18(27-4)17(26-3)9-14(16)23(19,25)21(13)24/h5-10,19,25H,11H2,1-4H3/t19-,23-/m1/s1
    Key: AQBZCCQCDWNNJQ-AUSIDOKSBD
  • CC1(C=CC2=C(O1)C=CC3=C2O[C@@H]4COC5=CC(=C(C=C5[C@@]4(C3=O)O)OC)OC)C
Properties
C23H22O7
Molar mass 410.41658 g/mol
Vapor pressure {{{value}}}
Related compounds
Related compounds
Deguelin, toxicarol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
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

References

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  3. 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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