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Details

Stereochemistry ABSOLUTE
Molecular Formula C30H52O4
Molecular Weight 476.7315
Optical Activity UNSPECIFIED
Defined Stereocenters 11 / 11
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PANAXATRIOL

SMILES

[H][C@@]1(CC[C@]2(C)[C@]1([H])[C@H](O)C[C@]3([H])[C@@]4(C)CC[C@H](O)C(C)(C)[C@]4([H])[C@H](O)C[C@@]23C)[C@@]5(C)CCCC(C)(C)O5

InChI

InChIKey=QFJUYMMIBFBOJY-UXZRXANASA-N
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

HIDE SMILES / InChI
Panaxatriol is a triterpene sapogenin originally found in species of Panax (ginseng) that exhibits anti-inflammatory, hepatoprotective, anti-arrhythmic, and antioxidative activities. Panaxatriol increases expression of heme oxygenase 1 (HO-1) and activation of Nrf2 signaling in neurons in a PI3K/Akt-dependent manner. Panaxatriol also decreases acetaminophen-induced increases in ALT and TNF-α, preventing liver injury in vivo. Additionally, panaxatriol inhibits Ca2+ channels, decreasing channel open time and open state probability in vitro and displaying anti-arrhythmic potential. Panaxatriol is a tyrosine hydroxylase inducer. It shows neuroprotective and cardioprotective effects in vivo. Panaxatriol enhances antioxidant activity and inhibits mitochondria-mediated apoptosis. Pretreatment with ginseng total saponin, especially panaxatriol, ameliorates I/R-induced myocardial damage and this protection is caused by reducing oxidative stress. Panaxatriol can relieve myelosuppression induced by radiation injury. The abilities of regulating the expression of hemopoietic growth factor GM-CSF and promoting the maturation of bone marrow cells may be responsible for some of these beneficial effects.

CNS Activity

Curator's Comment: In mice Panaxatriol (Panaxatriol saponins (PTS)), an inducer of Trx-1, has pluripharmacological properties in the protection against Parkinson's disease (PD) including enhancing antioxidant activity, acting as neurotrophic factor, modulating inflammation and inhibiting mitochondria-mediated apoptosis.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Protective effects and its mechanism of panaxatriol saponins isolated from Panax notoginseng on cerebral ischemia].
2002 May
Effect of ginseng saponins on the recombinant serotonin type 3A receptor expressed in xenopus oocytes: implication of possible application as an antiemetic.
2003 Aug
Bioactivity-guided identification and cell signaling technology to delineate the immunomodulatory effects of Panax ginseng on human promonocytic U937 cells.
2009 May 14
Panaxatriol saponins extracted from Panax notoginseng induces thioredoxin-1 and prevents 1-methyl-4-phenylpyridinium ion-induced neurotoxicity.
2010 Feb 3
Circumvention of multi-drug resistance of cancer cells by Chinese herbal medicines.
2010 Jul 25
Pharmacology of ginsenosides: a literature review.
2010 Jun 11
Effects of American ginseng (Panax quinquefolius) on neurocognitive function: an acute, randomised, double-blind, placebo-controlled, crossover study.
2010 Oct
Patents

Patents

Sample Use Guides

Rats were orally administered once a day with total saponin (20 mg/kg), panaxadiol (5 mg/kg) and panaxatriol (5 mg/kg) for consecutive 7 days.
Route of Administration: Oral
HT1080 cell viability was impaired by about 60-70% of control for 3 or 6 d at 50 uM of Panaxatriol (PT). Treatment with 10 to 40/uM of PT for 3 or 6 d down-regulated the mRNA level of MMP-9 drastically.
Name Type Language
PANAXATRIOL
Common Name English
(20R)-20,25-EPOXYDAMMARANE-3.BETA.,6.BETA.,12.BETA.-TRIOL
Common Name English
(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
Common Name English
NSC-308880
Code English
Code System Code Type Description
EPA CompTox
DTXSID60954454
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
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PUBCHEM
73599
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
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FDA UNII
9F5B25FDDG
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
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CAS
32791-84-7
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
PRIMARY
NSC
308880
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
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WIKIPEDIA
PANAXATRIOL
Created by admin on Fri Dec 15 18:01:37 GMT 2023 , Edited by admin on Fri Dec 15 18:01:37 GMT 2023
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