Labdane

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Labdane
150px
Names
IUPAC name
(4aR,5S,6S,8aS)- 1,1,4a,6-tetramethyl-5- [(3R)-3-methylpentyl]decalin
Identifiers
561-90-0 YesY
ChEBI CHEBI:36505 YesY
ChEMBL ChEMBL1087749 YesY
ChemSpider 7827634 YesY
Jmol 3D model Interactive image
PubChem 9548711
  • InChI=1S/C20H38/c1-7-15(2)9-11-17-16(3)10-12-18-19(4,5)13-8-14-20(17,18)6/h15-18H,7-14H2,1-6H3/t15-,16+,17+,18+,20-/m1/s1 YesY
    Key: LEWJAHURGICVRE-AISVETHESA-N YesY
  • InChI=1/C20H38/c1-7-15(2)9-11-17-16(3)10-12-18-19(4,5)13-8-14-20(17,18)6/h15-18H,7-14H2,1-6H3/t15-,16+,17+,18+,20-/m1/s1
    Key: LEWJAHURGICVRE-AISVETHEBV
  • C2CC([C@@H]1CC[C@@H]([C@@H]([C@@]1(C)C2)CC[C@H](C)CC)C)(C)C
Properties
C20H38
Molar mass 278.516
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Labdane is a natural bicyclic diterpene. It forms the structural core for a wide variety of natural products collectively known as labdanes or labdane diterpenes. The labdanes were so named because the first members of the class were originally obtained from labdanum, a resin derived from rockrose plants.[1][2]

A variety of biological activities have been determined for labdane diterpenes including antibacterial, antifungal, antiprotozoal, and anti-inflammatory activities.[3]

Examples

See also

References

  1. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  2. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ Studies in Natural Product Chemistry : Bioactive Natural Products, Part F, Atta-Ur-Rahman (Editor), ISBN 978-0-08-044001-9
  4. ↑ Isocupressic acid, an abortifacient component of Cupressus macrocarpa. K. Parton, D. Gardner and N.B. Williamson, New Zealand Veterinary Journal, 1996, Volume 44, Issue 3, doi:10.1080/00480169.1996.35946
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