Panaxatriol

Panaxatriol

Names
IUPAC name (3S,5R,6R,8R,9R,10R,12R,13R,14R,17S)-4,4,8,10,14-pentamethyl-17-[(2R)-2,6,6-trimethyloxan-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,6,12-triol
Other names (20R)-20,25-Epoxydammarane-3β,6β,12β-triol
Identifiers
CAS Number	32791-84-7
ChemSpider	66270
Jmol interactive 3D	Image
PubChem	73599
InChI InChI=1S/C30H52O4/c1-25(2)12-9-13-30(8,34-25)18-10-15-28(6)23(18)19(31)16-21-27(5)14-11-22(33)26(3,4)24(27)20(32)17-29(21,28)7/h18-24,31-33H,9-17H2,1-8H3/t18-,19+,20+,21+,22-,23-,24-,27+,28+,29+,30+/m0/s1 Key: QFJUYMMIBFBOJY-UXZRXANASA-N InChI=1/C30H52O4/c1-25(2)12-9-13-30(8,34-25)18-10-15-28(6)23(18)19(31)16-21-27(5)14-11-22(33)26(3,4)24(27)20(32)17-29(21,28)7/h18-24,31-33H,9-17H2,1-8H3/t18-,19+,20+,21+,22-,23-,24-,27+,28+,29+,30+/m0/s1 Key: QFJUYMMIBFBOJY-UXZRXANABD
SMILES C[C@@]1(CCCC(O1)(C)C)[C@H]2CC[C@@]3([C@@H]2[C@@H](C[C@H]4[C@]3(C[C@H]([C@@H]5[C@@]4(CC[C@@H](C5(C)C)O)C)O)C)O)C
Properties
Chemical formula	C30H52O4
Molar mass	476.73 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Panaxatriol is an organic coumpound characterizing a group of ginsenosides.^[1] It is a dammarane-type tetracyclic triterpene sapogenin found in ginseng (Panax ginseng) and in notoginseng (Panax pseudoginseng). It is formed by the dehydration of protopanaxatriol.

See also

• Protopanaxadiol

References

1. Ginsenosides of the protopanaxatriol group cause endothelium-dependent relaxation in the rat aorta

External links

• Panaxatriol on www.chemblink.com