Labdane

Labdane

File:Labdane.svg
Names
IUPAC name Labdane
Systematic IUPAC name (4aR,5S,6S,8aS)-1,1,4a,6-Tetramethyl-5-[(3R)-3-methylpentyl]decahydronaphthalene
Identifiers
CAS Number	561-90-0 checkY
3D model (JSmol)	Interactive image
ChEBI	CHEBI:36505 checkY
ChEMBL	ChEMBL1087749 checkY
ChemSpider	7827634 checkY
ECHA InfoCard
E number
PubChem CID	9548711
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI 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 checkY Key: LEWJAHURGICVRE-AISVETHESA-N checkY 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
SMILES C2CC([C@@H]1CC[C@@H]([C@@H]([C@@]1(C)C2)CC[C@H](C)CC)C)(C)C
Properties
Chemical formula	C20H38
Molar mass	278.524 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). checkY verify (what is checkY☒N ?) 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 the gum rockrose.

A variety of biological activities have been determined for labdane diterpenes including antibacterial, antifungal, antiprotozoal, and anti-inflammatory activities. Natural labdanes in tree resin are believed to be the precursors of amber, which polymerise under great pressure.

Example labdane derivatives

• Forskolin
• Galanolactone
• Isocupressic acid - is an abortifacient component of Cupressus macrocarpa.
• Medigenin
• Sclareol
• Stemodene

See also

• Abietane