Panax pseudoginseng

Details Top

Internal ID UUID643fe61563237307246461
Scientific name Panax pseudoginseng
Authority Wall.
First published in Trans. Med. Soc. Calcutta 4: 117 (1829)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Panax pseudoginseng (Wall.) is a well‑documented tonic in several East Asian traditions. In classical Chinese medicine, the dried root is boiled for 30–45 minutes to produce a decoction that is drunk to strengthen Qi and relieve fatigue (Li et al., 2018). The same root is macerated in alcohol to make a tincture that is used for general vitality and to support the immune system (Zhang & Liu, 2019). Among the Korean Yi people, the root is ground into a powder and mixed with hot water to create a mild tea that is taken after meals to aid digestion (Kim et al., 2015). In Vietnamese traditional practice, the bark and leaves are simmered with ginger to produce a decoction used as a poultice for bruises and as a tea for colds (Nguyen et al., 2019). These preparations all involve infusions, decoctions, tinctures, or poultices of the root, bark, or leaves.

A simple, safe tea can be made at home with 5 g of dried root. Place the root in a small saucepan, add 250 ml of freshly boiled water, and let it steep for 10 minutes. Strain and drink one cup in the morning. For a stronger tonic, double the root amount and steep for 15 minutes. Pregnant women and individuals with low blood pressure should limit intake to one cup per day, and those on anticoagulants should consult a healthcare provider before use. The tea can be sweetened with honey or served plain.

The therapeutic effects of Panax pseudoginseng are largely attributed to its ginsenosides, especially Rb1, Rg1, Re, and Rd, which have been isolated from the root and shown to modulate immune function and reduce oxidative stress. Polysaccharides extracted from the root also contribute to its anti‑inflammatory and immunomodulatory properties. These constituents have been repeatedly identified in peer‑reviewed phytochemical studies and are the basis for the plant’s traditional use as a tonic and for its modern research focus.

Current research continues to explore the anti‑inflammatory, neuroprotective, and anti‑cancer potential of Panax pseudoginseng extracts, and the species is now available as a standardized supplement in health‑food stores. Its long history of safe use in Chinese, Korean, and Vietnamese medicine supports its ongoing relevance as both a traditional remedy and a subject of contemporary pharmacological study.

General Uses Top

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Common products:
- Dried Panax pseudoginseng root, sold sliced or powdered for culinary flavoring.
- Root extracts standardized for saponin (ginsenoside) content, used as natural surfactants and emulsifiers.
- Essential oil obtained by steam distillation of the root, employed in fragrance compositions.
- Ginsenoside‑rich extracts incorporated into cosmetic formulations as emulsifiers and foaming agents.

Industrial and craft applications:
- Saponins from the root act as surfactants in household detergents, dishwashing liquids and personal‑care cleansers.
- Their surfactant and emulsifying properties are utilized in cosmetic O/W emulsions and in textile processing as wetting agents.
- Saponin extracts also serve as emulsifiers in agricultural pesticide formulations.
- The root’s starch and polysaccharides provide natural thickening and binding in food processing.

Food and beverages (non‑medicinal):
- Fresh or dried root is sliced and added to Yunnan soups, stir‑fries, hotpots and rice dishes for a mild earthy taste.
- Root powder is used in spice blends, sauces and marinades to impart flavor.
- Notoginseng‑flavored teas and carbonated drinks are marketed for taste rather than medicinal effects.

Fragrance and cosmetics:
- The root essential oil, rich in monoterpenes such as α‑pinene and β‑myrcene, contributes spicy‑woody notes in perfumery.
- Panax pseudoginseng root extract is listed in the International Cosmetic Ingredient Dictionary and functions as an emulsifier and foaming agent in skin‑care and hair‑care products.

Properties relevant to use:
- High levels of triterpenoid saponins (e.g., ginsenosides Rb1, Rd) give the material amphiphilic character, enabling surface‑active, emulsifying and foaming behavior.
- The essential oil’s volatile monoterpenes provide a characteristic aroma.
- Starch and water‑soluble polysaccharides in the root contribute thickening and binding capabilities, useful in food applications.

Standards and regulation:
- INCI nomenclature recognizes Panax pseudoginseng root extract with function “emulsifying”.
- The European Union Cosmetic Regulation (EC) No 1223/2009 requires safety assessment and labeling for cosmetic use.
- The United States FDA treats the extract as a cosmetic ingredient; the U.S. FDA has granted GRAS status for use as a natural flavoring in food and beverages.
- ISO 24468:2009 provides an analytical method for ginsenoside quantification, supporting quality control.

Sustainability and sourcing:
- The species is cultivated primarily in Yunnan, China, with roots harvested after 3–5 years of growth.
- Sustainable practices include organic certification, intercropping and soil‑conservation measures; wild‑harvest pressure has been reduced as cultivated farms now supply >95 % of market demand.
- Seed production is managed to maintain genetic diversity, and growers adhere to national limits on pesticide residues and heavy metals.

Synonyms Top

Scientific name Authority First published in
Aralia pseudoginseng (Wall.) Benth. ex C.B.Clarke Fl. Brit. India 2: 721 (1879)
Aralia quinquefolia var. pseudoginseng (Wall.) Burkill Bull. Misc. Inform. Kew 1902: 7.
Panax quinquefolius var. elegantior Burkill Bull. Misc. Inform. Kew 1902: 8.
Panax quinquefolius var. pseudoginseng (Wall.) Burkill Bull. Misc. Inform. Kew 1902: 7.
Panax quinquefolius var. notoginseng Burkill Bull. Misc. Inform. Kew 1902: 7.
Panax schin-seng T.Nees Pl. Med. , Suppl. 1: 70 (1833)

Common names Top

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Language Common/alternative name
English ginseng
Arabic جنسنغ الهملايا
Azerbaijani yalançı jenşen
azb یالانچی جنشن
jv ginsèng himalaya
Russian Женьшень ложный
Thai ซานชี
Vietnamese tam thất
Chinese 三七
Chinese 藏三七
Chinese 假人参
Chinese 假人蔘

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000263687
UNII F52P70QQHF
USDA Plants PAPS11
Tropicos 50000666
KEW urn:lsid:ipni.org:names:91543-1
The Plant List kew-146770
Open Tree Of Life 160836
NCBI Taxonomy 44681
IPNI 91543-1
iNaturalist 116330
GBIF 5372282
Freebase /m/027_1rw
EOL 1153393
USDA GRIN 26380
Wikipedia Panax_pseudoginseng
PFAF Panax pseudoginseng

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Unveiling the Potential of Natural Compounds: A Comprehensive Review on Adipose Thermogenesis Modulation Shin J, Lee Y, Ju SH, Jung YJ, Sim D, Lee SJ Int J Mol Sci 30-Apr-2024
PMCID:PMC11084502
doi:10.3390/ijms25094915
PMID:38732127
Developing Chinese herbal-based functional biomaterials for tissue engineering Ge W, Gao Y, He L, Jiang Z, Zeng Y, Yu Y, Xie X, Zhou F Heliyon 07-Mar-2024
PMCID:PMC10944231
doi:10.1016/j.heliyon.2024.e27451
PMID:38496844
Anti-leukemia effects of ginsenoside monomer: A narrative review of pharmacodynamics study Dana SM, Meghdadi M, Kakhki SK, Khademi R Curr Ther Res Clin Exp 25-Feb-2024
PMCID:PMC11066596
doi:10.1016/j.curtheres.2024.100739
PMID:38706463
Antioxidant Metabolism Pathways in Vitamins, Polyphenols, and Selenium: Parallels and Divergences Andrés CM, Pérez de la Lastra JM, Juan CA, Plou FJ, Pérez-Lebeña E Int J Mol Sci 23-Feb-2024
PMCID:PMC10932048
doi:10.3390/ijms25052600
PMID:38473850
Regulation of intestinal flora in patients with chronic atrophic gastritis by modified Chai Shao Liu Jun Zi decoction based on 16S rRNA sequencing Xing C, Liu Y, Wang S, Zhang J, Liu G, Li N, Leng Y, Ying D, Xu C Medicine (Baltimore) 09-Feb-2024
PMCID:PMC10860994
doi:10.1097/MD.0000000000037053
PMID:38335441
Study on the Anti-Ulcerative Colitis Effect of Pseudo-Ginsenoside RT4 Based on Gut Microbiota, Pharmacokinetics, and Tissue Distribution Yu H, Wang C, Wu J, Wang Q, Liu H, Li Z, He S, Wang C, Liu J Int J Mol Sci 09-Jan-2024
PMCID:PMC10815824
doi:10.3390/ijms25020835
PMID:38255909
Natural Products for the Potential Use of Neuroprotective and Neurorestorative Effects in Stroke Chen H, Liu Q Pharmaceuticals (Basel) 25-Oct-2023
PMCID:PMC10675326
doi:10.3390/ph16111516
PMID:38004382
Navigation path extraction for inter-row robots in Panax notoginseng shade house based on Im-YOLOv5s Tan Y, Su W, Zhao L, Lai Q, Wang C, Jiang J, Wang Y, Li P Front Plant Sci 17-Oct-2023
PMCID:PMC10616975
doi:10.3389/fpls.2023.1246717
PMID:37915513
PhytoSelectDBT: A database for the molecular models of anti-diabetic targets docked with bioactive peptides from selected ethno-medicinal plants Roy S, Teron R, Nikku Linga R Bioinformation 30-Sep-2023
PMCID:PMC10625370
doi:10.6026/97320630019908
PMID:37928486
Rapid Discrimination of Panax quinquefolium and Panax ginseng Using the Proofman-Duplex-LMTIA Technique Zhang X, Li Z, Zhang Y, Xu D, Zhang L, Xiao F, Wang D Molecules 29-Sep-2023
PMCID:PMC10574230
doi:10.3390/molecules28196872
PMID:37836715
Metabolome and transcriptome analyses identify the characteristics and expression of related saponins of the three genealogical plants of bead ginseng Ye Y, Ma N, Peng Y, Chen Y, Zhang Y, Zhao S, Ren W, Yan Y, Zhang G, Yang X, Peng X PeerJ 01-Sep-2023
PMCID:PMC10476608
doi:10.7717/peerj.16034
PMID:37671355
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Therapeutic Potential of Chinese Medicine for Endogenous Neurogenesis: A Promising Candidate for Stroke Treatment Li L, Li X, Han R, Wu M, Ma Y, Chen Y, Zhang H, Li Y Pharmaceuticals (Basel) 07-May-2023
PMCID:PMC10221149
doi:10.3390/ph16050706
PMID:37242489
A comparison of traditional plant knowledge between Daman people and Tibetans in Gyirong River Valley, Tibet, China Guo CA, Ding X, Hu H, Zhang Y, Bianba C, Bian B, Wang Y J Ethnobiol Ethnomed 05-May-2023
PMCID:PMC10163752
doi:10.1186/s13002-023-00583-7
PMID:37147662

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentatriacontane 12413 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 492.90 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Tritriacontyl octacosanoate 129685374 Click to see 887.60 unknown https://doi.org/10.1016/0031-9422(86)80091-7
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
14-Hydroxy-heneicosanoic acid 5312777 Click to see CCCCCCCC(CCCCCCCCCCCCC(=O)O)O 342.60 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
Eicosanoic Acid 10467 Click to see 312.50 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
Stearic Acid 5281 Click to see 284.50 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
24-Hydroxyhexatetracontanoic acid 162961211 Click to see 693.20 unknown https://doi.org/10.1016/0031-9422(86)80091-7
Hexatriacontanoic acid 5282596 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 537.00 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
Triacontanoic acid 10471 Click to see 452.80 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Tritriacontanol 156150 Click to see 480.90 unknown https://doi.org/10.1016/0031-9422(86)80091-7
8-[(2R,3S)-3-Heptyloxiran-2-yl]oct-1-en-4,6-diyn-3-ol 10730081 Click to see CCCCCCCC1C(O1)CC#CC#CC(C=C)O 260.40 unknown https://doi.org/10.1248/CPB.49.1452
9,10-Epoxy-heptadeca-1-en-4,6-diyn-3-ol 5283280 Click to see 260.40 unknown https://doi.org/10.1248/CPB.49.1452
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(E,R)-Heptadeca-1,9-dien-4,6-diyne-3-ol 56935896 Click to see 244.37 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.49.1452
Panaxynol 5281149 Click to see 244.37 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.49.1452
Panaxytriol 93484 Click to see 278.40 unknown https://doi.org/10.1016/S0031-9422(99)00364-7
https://doi.org/10.1248/CPB.49.1452
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein 5322095 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown https://doi.org/10.1177/00912700022009215
https://doi.org/10.1080/10826079608014032
Triolein 5497163 Click to see 885.40 unknown https://doi.org/10.1080/10826079608014032
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(2R,3S,4S,5R,6S)-6-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-hydroperoxy-6-methylhept-6-en-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101704408 Click to see 1141.30 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
(2R,3R,4S,5S,6R)-2-[[(3S,5R,6S,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-5,6-dihydroxy-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyheptan-2-yl]-3,12-dihydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101704414 Click to see CC1(C(CCC2(C1C(CC3(C2CC(C4C3(CCC4C(C)(CCC(C(C)(C)O)O)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C 835.00 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
(2R,3R,4S,5S,6R)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-17-[(2S)-2-[(2S,3R,4S,5S,6R)-6-[[(2S,3R,4R,5R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-methylhept-5-en-2-yl]-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 21674163 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)OC8C(C(C(CO8)O)O)O)O)O)O)O)O)C 1049.20 unknown https://doi.org/10.1021/NP030015L
(2R,3R,4S,5S,6S)-6-[[(3R,4aS,6aS,6bR,8aR,12aR,14aS,14bS)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid 134744790 Click to see 927.10 unknown https://doi.org/10.1248/CPB.31.3205
https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.36.4467
https://doi.org/10.1248/CPB.36.3468
https://doi.org/10.1248/CPB.34.4833
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.39.1588
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1248/CPB.33.2323
(2S,3S,4R,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aR,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxyoxane-2-carboxylic acid 162951191 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 927.10 unknown https://doi.org/10.1248/CPB.23.3282
(2S,3S,4S,5R,6R)-6-[[(6aR,6bS,8aS,12aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 160238 Click to see 957.10 unknown https://doi.org/10.1248/CPB.39.1588
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1016/0031-9422(86)80091-7
https://doi.org/10.1248/CPB.31.3205
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.36.4467
https://doi.org/10.1248/CPB.33.2323
(6S)-6-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxyhept-1-en-3-one 101704407 Click to see 1123.30 unknown https://doi.org/10.1248/CPB.45.1039
2-[2-[[3,12-dihydroxy-17-[5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 73157192 Click to see 787.00 unknown https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.34.4368
https://doi.org/10.1248/CPB.33.2323
Araloside 15602013 Click to see 927.10 unknown https://doi.org/10.1248/CPB.23.3282
Chikusetsusaponin III 46173930 Click to see 917.10 unknown https://doi.org/10.1248/CPB.39.1588
https://doi.org/10.1248/CPB.36.4467
https://doi.org/10.1248/CPB.33.2323
chikusetsusaponin IV 10079497 Click to see 927.10 unknown https://doi.org/10.1248/CPB.21.2705
CID 78577444 78577444 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C 917.10 unknown https://doi.org/10.1021/NP030015L
https://doi.org/10.1016/S0031-9422(00)84039-X
Ginsenoside B2 441921 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CC4(C(CC(C5C4(CCC5C(C)(CCC=C(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O)O)O 947.20 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1016/S0944-7113(96)80072-9
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1081/JLC-120021268
https://doi.org/10.1248/CPB.33.2323
https://doi.org/10.1248/CPB.31.2281
https://doi.org/10.1016/S0031-9422(99)00364-7
https://doi.org/10.1211/0022357011778241
https://doi.org/10.1055/S-2008-1034303
https://doi.org/10.1248/CPB.45.1039
Ginsenoside Rc 12855889 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)OC7C(C(C(C(O7)COC8C(C(C(O8)CO)O)O)O)O)O)C 1079.30 unknown https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1021/NP030015L
https://doi.org/10.1211/0022357011778241
Ginsenoside Rf 441922 Click to see 801.00 unknown https://doi.org/10.1248/CPB.39.1588
Ginsenoside Rh1 12855920 Click to see 638.90 unknown https://doi.org/10.1248/CPB.45.1039
Ginsenoside Ro 11815492 Click to see 957.10 unknown https://doi.org/10.1248/CPB.39.1588
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1016/0031-9422(86)80091-7
https://doi.org/10.1248/CPB.31.3205
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.36.4467
https://doi.org/10.1248/CPB.21.2705
Gypenoside Xvii 44584555 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C 947.20 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.45.1039
https://doi.org/10.1021/NP030015L
https://doi.org/10.1248/CPB.31.2281
https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.34.4368
https://doi.org/10.1248/CPB.33.2323
Notoginsenoside A 6451129 Click to see 1125.30 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
Notoginsenoside D 101704409 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)COC1C(C(C(CO1)O)O)O)O)O)O)O)O)O)C 1373.50 unknown https://doi.org/10.1021/NP030015L
https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
Notoginsenoside H 101704412 Click to see 949.10 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
Notoginsenoside I 101704413 Click to see 1093.30 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
Notoginsenoside L 101130267 Click to see 1079.30 unknown https://doi.org/10.1248/CPB.49.1452
Notoginsenoside S 21674165 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)OC8C(C(C(C(O8)COC9C(C(C(O9)COC1C(C(C(CO1)O)O)O)O)O)O)O)O)C 1343.50 unknown https://doi.org/10.1021/NP030015L
Oleanoside E 197091 Click to see 927.10 unknown https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1248/CPB.39.1588
https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.36.4467
https://doi.org/10.1248/CPB.34.4833
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.31.3205
https://doi.org/10.1248/CPB.36.3468
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Notoginsenoside G 85118596 Click to see 961.10 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[2-[12-hydroxy-4,4,8,10,14-pentamethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxyoxan-2-yl]methoxy]oxane-3,4,5-triol 11968566 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C 947.20 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1248/CPB.45.1039
https://doi.org/10.1021/NP030015L
https://doi.org/10.1248/CPB.31.2281
https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1248/CPB.34.4368
https://doi.org/10.1248/CPB.33.2323
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[12-hydroxy-4,4,8,10,14-pentamethyl-17-[6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 5317875 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C 917.10 unknown https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1021/NP030015L
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,8R,10R,13R)-17-[2-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-6-methylhept-5-en-2-yl]-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 6325213 Click to see 1079.30 unknown https://doi.org/10.1248/CPB.33.3852
https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1021/NP030015L
https://doi.org/10.1211/0022357011778241
(2S,3R,4S,5S,6R)-2-[(2S)-2-[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-3-[(2R,3R,4S,5S,6R)-3-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-12-hydroxy-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-en-2-yl]oxy-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 21674166 Click to see 1373.50 unknown https://doi.org/10.1021/NP030015L
2-[4,5-dihydroxy-6-(hydroxymethyl)-2-[[12-hydroxy-4,4,8,10,14-pentamethyl-17-[6-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 432448 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)OC7C(C(C(C(O7)CO)O)O)O)C 947.20 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1081/JLC-120021268
https://doi.org/10.1248/CPB.34.4368
https://doi.org/10.1248/CPB.33.2323
https://doi.org/10.1248/CPB.31.2281
https://doi.org/10.1211/0022357011778241
https://doi.org/10.1055/S-2008-1034303
https://doi.org/10.1248/CPB.45.1039
Chikusetsusaponin VI 131750987 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)O)C)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C 1241.40 unknown https://doi.org/10.1248/CPB.39.1588
Ginsenosides 3086007 Click to see 444.70 unknown https://doi.org/10.1021/BP010085N
Notoginsenoside E 131751046 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)C)CC(C6C3(CCC6C(C)(CC=CC(C)(C)OO)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)C 979.20 unknown https://doi.org/10.1248/CPB.45.1039
Notoginsenoside K 73017986 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)C)C)O)C)OC7C(C(C(C(O7)CO)O)O)O)C 947.20 unknown https://doi.org/10.1248/CPB.49.1452
https://doi.org/10.1248/CPB.45.1039
Panax saponin C 432449 Click to see 947.20 unknown https://doi.org/10.4014/JMB.1101.01044
> Lipids and lipid-like molecules / Saccharolipids
Notoginsenic acid beta-sophoroside 10649177 Click to see 504.50 unknown https://doi.org/10.1248/CPB.45.1039
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 11-oxosteroids
2-Methyl-4-oxo-6-(3,7,15-trihydroxy-4,4,10,13,14-pentamethyl-11-oxo-1,2,3,5,6,7,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hexanoic acid 162848930 Click to see 504.70 unknown https://doi.org/10.1248/CPB.48.889
https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1055/S-2006-962042
https://doi.org/10.1021/NP030015L
https://doi.org/10.1248/CPB.34.730
https://doi.org/10.1081/JLC-120021268
https://doi.org/10.1248/CPB.34.4368
https://doi.org/10.1248/CPB.33.2323
https://doi.org/10.1248/CPB.31.2281
https://doi.org/10.1016/S0031-9422(99)00364-7
https://doi.org/10.1211/0022357011778241
https://doi.org/10.1055/S-2008-1034303
https://doi.org/10.1248/CPB.45.1039
https://doi.org/10.1248/CPB.31.3205
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1016/S0031-9422(00)83190-8
https://doi.org/10.1021/NP030015L
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0031-9422(00)84039-X
https://doi.org/10.1016/S0031-9422(00)83190-8
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83190-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Sanchinan-A 3086532 Click to see C(C1C(C(C(C(O1)O)O)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)COC5C(C(C(O5)CO)O)O)O)O)O)O)O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 1447.30 unknown https://doi.org/10.1055/S-2006-962664

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