Stemodene

Source: Wikipedia, the free encyclopedia.
Stemodene
Names
IUPAC name
(14S)-9,15:14,20-Dicyclo-8α-labd-13(16)-ene
Systematic IUPAC name
(4aS,6aS,8S,11aR,11bS)-4,4,11b-Trimethyl-9-methylidenetetradecahydro-8,11a-methanocyclohepta[a]naphthalene
Identifiers
3D model (
JSmol
)
10812290
ChEBI
ChemSpider
KEGG
UNII
  • InChI=1S/C20H32/c1-14-8-11-20-13-15(14)12-16(20)6-7-17-18(2,3)9-5-10-19(17,20)4/h15-17H,1,5-13H2,2-4H3/t15-,16-,17-,19-,20+/m0/s1
    Key: GNNRCBBKCVNPSC-VDWQKOAOSA-N
  • [H][C@@]12CC[C@@]3([H])C(C)(C)CCC[C@]3(C)[C@]1(CCC4=C)C[C@@H]4C2
Properties
C20H32
Molar mass 272.476 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Stemodene is a

olefin produced by each cyclase
shows structural similarities and is derived from the common precursor of syn-copalyl diphosphate.

References

  1. PMID 16256063. Archived from the original
    (PDF) on 2007-09-28. Retrieved 2006-11-07.


Stub icon

This article about an organic compound is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Stemodene&oldid=1185482228"