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
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
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
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20951784
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
Targets
Primary Target | Pharmacology | Condition | Potency |
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Target ID: WP173 Sources: https://www.ncbi.nlm.nih.gov/pubmed/20353807 |
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Target ID: CHEMBL1969 |
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Target ID: GO:0005245 Sources: https://www.ncbi.nlm.nih.gov/pubmed/7516611 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
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Preventing | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
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Primary | Unknown Approved UseUnknown |
PubMed
Title | Date | PubMed |
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[Protective effects and its mechanism of panaxatriol saponins isolated from Panax notoginseng on cerebral ischemia]. | 2002 May |
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Effect of ginseng saponins on the recombinant serotonin type 3A receptor expressed in xenopus oocytes: implication of possible application as an antiemetic. | 2003 Aug |
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Bioactivity-guided identification and cell signaling technology to delineate the immunomodulatory effects of Panax ginseng on human promonocytic U937 cells. | 2009 May 14 |
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Panaxatriol saponins extracted from Panax notoginseng induces thioredoxin-1 and prevents 1-methyl-4-phenylpyridinium ion-induced neurotoxicity. | 2010 Feb 3 |
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Circumvention of multi-drug resistance of cancer cells by Chinese herbal medicines. | 2010 Jul 25 |
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Pharmacology of ginsenosides: a literature review. | 2010 Jun 11 |
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Effects of American ginseng (Panax quinquefolius) on neurocognitive function: an acute, randomised, double-blind, placebo-controlled, crossover study. | 2010 Oct |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20353807
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
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10597035
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.
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DTXSID60954454
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73599
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308880
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PANAXATRIOL
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SUBSTANCE RECORD