Hexacyclinol

Hexacyclinol
(1) The structure for hexacyclinol proposed by Rychnovsky and synthesized by Porco, Jr.
Names
IUPAC name
(2aS,3R,5aR,6aS,7R,8R,8aS,10R)-7-hydroxy-3-(1-methoxy-1-methylethyl)-10-(2-methylprop-1-en-1-yl)-1a,5a,6a,7,7a,7b,8,8a-octahydro-2H-8,2a-(epoxymethano)phenanthro[2,3-b:6,7-b']bisoxirene-2,5(3H)-dione
Identifiers
3D model (JSmol)
ChemSpider
MeSH C469535
UNII
  • InChI=1S/C23H28O7/c1-8(2)6-11-23-10(22(3,4)27-5)7-9-12(15(25)18-17(29-18)14(9)24)13(23)16(28-11)19-20(30-19)21(23)26/h6-7,10-13,15-20,25H,1-5H3/t10-,11-,12-,13-,15-,16-,17-,18+,19+,20+,23+/m1/s1 Y
    Key: PFZFRWWDGXFULQ-NHFKQXEKSA-N Y
  • O=C5[C@]34[C@H](\C=C2\C(=O)[C@H]1O[C@H]1[C@H](O)[C@H]2[C@@H]3[C@@H](O[C@@H]4\C=C(/C)C)[C@@H]6O[C@H]56)C(OC)(C)C
Properties
C23H28O7
Molar mass 416.470 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

Hexacyclinol is a natural metabolite of a fungus, Panus rudis. Significant controversy surrounded its proposed structure until its total synthesis by John Porco, Jr. in 2006.

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