Euphane

Euphane
Names
	IUPAC name 13α,14β-Lanostane
	Systematic IUPAC name (1S,3aR,3bR,5aS,9aR,9bS,11aS)-3a,6,6,9a,11a-Pentamethyl-1-[(2R)-6-methylheptan-2-yl]hexadecahydro-1H-cyclopenta[a]phenanthrene
Identifiers
CAS Number	516-29-0 ;
3D model (JSmol)	Interactive image;
ChemSpider	25942061;
PubChem CID	12312921;
CompTox Dashboard (EPA)	DTXSID401337036 ;
	InChI InChI=1S/C30H54/c1-21(2)11-9-12-22(3)23-15-19-30(8)25-13-14-26-27(4,5)17-10-18-28(26,6)24(25)16-20-29(23,30)7/h21-26H,9-20H2,1-8H3/t22-,23+,24+,25-,26+,28-,29+,30-/m1/s1 Key: ZQIOPEXWVBIZAV-RRKMEGOCSA-N;
	SMILES C[C@H](CCCC(C)C)[C@@H]1CC[C@]2([C@]1(CC[C@H]3[C@H]2CC[C@@H]4[C@@]3(CCCC4(C)C)C)C)C;
Properties
Chemical formula	C30H54
Molar mass	414.762 g·mol−1
Density	0.897 g/cm3
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Euphane is a tetracyclic triterpene that is the 13α,14β-stereoisomer of lanostane. Its derivatives are widely distributed in many plants.^[2]^[3]

References

^ Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (© 1994-2019 ACD/Labs). Retrieved from SciFinder. [2019-10-19]
^ Hou Y, Cao S, Brodie PJ, Miller JS, Birkinshaw C, Andrianjafy MN, Andriantsiferana R, Rasamison VE, TenDyke K, Shen Y, Suh EM, Kingston DG (2010). "Euphane triterpenoids of Cassipourea lanceolata from the Madagascar rainforest". Phytochemistry. 71 (5–6): 669–674. Bibcode:2010PChem..71..669H. doi:10.1016/j.phytochem.2009.12.009. PMC 2847016. PMID 20074760.
^ Wang LY, Wang NL, Yao XS, Miyata S, Kitanaka S (2003). "Euphane and tirucallane triterpenes from the roots of Euphorbia kansui and their in vitro effects on the cell division of Xenopus". J Nat Prod. 66 (5): 660–663. doi:10.1021/np0205396. PMID 12762796.