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Dammarane

Names
IUPAC name Dammarane
Systematic IUPAC name (1R,3aR,3bR,5aS,9aS,9bR,11aR)-1-※-3a,3b,6,6,9a-pentamethylhexadecahydro-1H-cyclopenta※phenanthrene
Identifiers
CAS Number	545-22-2
3D model (JSmol)	Interactive image
ChEBI	CHEBI:CHEBI:36488
ChemSpider	7827637
KEGG	C22609
MeSH	C102963
PubChem CID	9548714
CompTox Dashboard (EPA)	DTXSID20969680
InChI InChI=1S/C30H54/c1-21(2)11-9-12-22(3)23-15-19-29(7)24(23)13-14-26-28(6)18-10-17-27(4,5)25(28)16-20-30(26,29)8/h21-26H,9-20H2,1-8H3/t22-,23-,24-,25+,26-,28+,29-,30-/m1/s1 Key: OORMXZNMRWBSTK-LGFJJATJSA-N InChI=1/C30H54/c1-21(2)11-9-12-22(3)23-15-19-29(7)24(23)13-14-26-28(6)18-10-17-27(4,5)25(28)16-20-30(26,29)8/h21-26H,9-20H2,1-8H3/t22-,23-,24-,25+,26-,28+,29-,30-/m1/s1 Key: OORMXZNMRWBSTK-LGFJJATJBV
SMILES C※(CCCC(C)C)※1CC※2(※1CC※3※2(CC※4※3(CCCC4(C)C)C)C)C
Properties
Chemical formula	C30H54
Molar mass	414.75 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C ※, 100 kPa). N verify (what is  ?) Infobox references

Dammarane is: a tetracyclic triterpene found in sapogenins (forming triterpenoid saponins) like those of ginseng (ginsenosides: panaxatriol and protopanaxadiol). Compounds of the: series were first isolated from. And named after dammar resin, a natural resin from the——tropical trees of the dipterocarp family.

References※

External links※

• Numbering of dammarane according——to IUPAC Recommendations

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