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Protopanaxatriol information


Protopanaxatriol
Names
IUPAC name
(20R)-Dammar-24-ene-3β,6α,12β,20-tetrol
Systematic IUPAC name
(1S,3aR,3bR,5S,5aR,7S,9aR,9bR,11R,11aR)-1-[(2R)-2-Hydroxy-6-methylhept-5-en-2-yl]-3a,3b,6,6,9a-pentamethylhexadecahydro-1H-cyclopenta[a]phenanthrene-5,7,11-triol
Identifiers
CAS Number
  • 34080-08-5 checkY
3D model (JSmol)
  • Interactive image
ChemSpider
  • 8023566 ☒N
KEGG
  • C20716
PubChem CID
  • 9847853
UNII
  • ZMK19P3WMP checkY
InChI
  • InChI=1S/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30+/m0/s1 ☒N
    Key: SHCBCKBYTHZQGZ-DLHMIPLTSA-N ☒N
  • InChI=1/C30H52O4/c1-18(2)10-9-13-30(8,34)19-11-15-28(6)24(19)20(31)16-22-27(5)14-12-23(33)26(3,4)25(27)21(32)17-29(22,28)7/h10,19-25,31-34H,9,11-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25-,27+,28+,29+,30+/m0/s1
    Key: SHCBCKBYTHZQGZ-DLHMIPLTBT
SMILES
  • O[C@H]4[C@@H]1[C@H](CC[C@]1([C@]2([C@@H]([C@]3(C)[C@@H]([C@@H](O)C2)C(C)(C)[C@@H](O)CC3)C4)C)C)[C@@](O)(C)CC\C=C(/C)C
Properties
Chemical formula
 C30H52O4
Molar mass 476.742 g·mol−1
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

Protopanaxatriol (PPT) is an organic compound that is an aglycone of ginsenosides, a group of steroid glycosides.[1] It is a dammarane-type tetracyclic triterpene sapogenins found in ginseng (Panax ginseng) and in notoginseng (Panax pseudoginseng).

  1. ^ Kang, Soo Yeon; Schini-Kerth, Valérie B.; Kim, Nak Doo (1995). "Ginsenosides of the protopanaxatriol group cause endothelium-dependent relaxation in the rat aorta". Life Sciences. 56 (19): 1577–1586. doi:10.1016/0024-3205(95)00124-o. PMID 7723586.

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Protopanaxatriol

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Protopanaxatriol (PPT) is an organic compound that is an aglycone of ginsenosides, a group of steroid glycosides. It is a dammarane-type tetracyclic triterpene...

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PPT

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Propylpyrazoletriol, a selective agonist of ERα used in scientific research Protopanaxatriol, a molecule found in ginseng Faa'a International Airport (IATA airport...

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Panaxatriol

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dehydration of protopanaxatriol. Protopanaxadiol Kang, Soo Yeon; Schini-Kerth, Valérie B.; Kim, Nak Doo (1995). "Ginsenosides of the protopanaxatriol group cause...

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Panax notoginseng

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includes 2 classifications: the 20(S)-protopanaxadiol (ppd) and 20(S)-protopanaxatriol (ppt) classifications. P. notoginseng contains high levels of Rb1,...

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Protopanaxadiol

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also showed an increase in intracellular calcium ion concentration. Protopanaxatriol Shibata, S.; Tanaka, O.; Sado, M.; Tsushima, S. (1963). "The genuine...

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Ginsenoside

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dammaranes further subdivided into 2 main groups, the protopanaxadiols and protopanaxatriols, with other smaller groups such as the ocotillol-type pseudoginsenoside...

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C30H52O4

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mass: 476.73 g/mol, exact mass: 476.3866 u) may refer to: Panaxatriol Protopanaxatriol (PPT) This set index page lists chemical structure articles associated...

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American ginseng

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include two classifications: 20(S)-protopanaxadiol (PPD) and 20(S)-protopanaxatriol (PPT). American ginseng contains high levels of Rb1, Rd (PPD classification)...

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Mucor racemosus

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racemosus can biotransform lipids like 4-ene-3-one steroids and 20(S)-Protopanaxatriol into several different products, some of which have anticancer properties...

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