Eleutherococcus nodiflorus

Details Top

Internal ID UUID6440390ec2d9c425239138
Scientific name Eleutherococcus nodiflorus
Authority (Dunn) S.Y.Hu
First published in J. Arnold Arbor. 61: 109 (1980)

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.

In traditional Chinese materia medica the dried root bark of Eleutherococcus nodiflorus, called Wu Jia Pi, is prepared as a decoction, a short infusion, an alcoholic tincture, or applied fresh as a poultice. The decoction is made by simmering sliced bark in water for several tens of minutes; the infusion is produced by steeping a few grams of dried bark in hot water for ten to fifteen minutes; the tincture is obtained by macerating the bark in a moderate‑strength ethanol solution for several weeks; and a poultice is created by crushing fresh bark with a little warm water and applying the mash directly to bruised or painful joints. Each of these preparations uses the same plant organ – the root bark – and the dosage is kept modest to avoid gastrointestinal irritation.

Among the Han Chinese of central and southern provinces, Wu Jia Pi decoction is recorded as a remedy for wind‑dampness, joint pain, and lower‑back weakness in the classic materia medica of Bensky et al., 2004 and in the historic Bencao Gangmu (Li Shizhen, 1596). In the Dai communities of Xishuangbanna, Yunnan, ethnobotanical fieldwork documented the same decoction being taken in the evenings to alleviate rheumatic aches (Zhang et al., 2013). Tibetan practitioners of Qinghai use a brief infusion of the bark to “warm the meridians” and to relieve stiff joints, a practice reported by Wang et al., 2015. The tincture of Wu Jia Pi appears in the Chinese Pharmacopoeia (2020) as a standardized preparation for circulatory support, while the fresh‑bark poultice is mentioned in a regional ethnobotanical survey of the Miao people of Guizhou (Liu et al., 2017).

To prepare a mild therapeutic tea, place 6 g of dried root bark in a saucepan with 500 mL of cold water, bring to a gentle boil, and simmer for 20 minutes. Remove from heat, strain, and drink the warm liquid in 100‑mL portions no more than twice daily for up to ten days. This decoction should not be used by pregnant women; patients on anticoagulant medication or with gastric ulcer disease should seek professional advice before taking it.

Phytochemical investigations of Eleutherococcus nodiflorus have identified the lignan glycosides eleutheroside B (syringin) and eleutheroside E, as well as flavonoid glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside, together with phenolic acids like caffeic acid (Zhao et al., 2005; Li et al., 2020). These compounds are known for anti‑inflammatory and antioxidant activity, which provides a logical biochemical basis for the traditional analgesic actions. Modern research continues to examine standardized Wu Jia Pi extracts for arthritis relief, and both dried bark powders and alcohol tinctures are widely sold in Chinese herbal markets today.

General Uses Top

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Wood and fiber:
The species is documented to provide wood utilized for tool handles and small implements, particularly in regions like China where its synonym *Acanthopanax gracilistylus* is recognized. This application leverages the physical characteristics of the wood, such as hardness and grain structure, suitable for crafting functional hand tools.

Synonyms Top

Scientific name Authority First published in
Aralia scandens Poir. Encycl. , Suppl. 1: 419 (1811)
Acanthopanax gracilistylus W.W.Sm. Notes Roy. Bot. Gard. Edinburgh 5: 6 (1917)
Acanthopanax gracilistylus var. major G.Hoo Acta Phytotax. Sin., Addit. 1: 159 1965
Acanthopanax gracilistylus var. pubescens (Pamp.) H.L.Li Sargentia 2: 85. 1942
Acanthopanax gracilistylus var. trifoliolatus C.B.Shang J. Nanjing Inst. Forest. 1985(2): 22 (1985)
Acanthopanax hondae Matsuda Bot. Mag. (Tokyo) 31: 333 (1917)
Acanthopanax hondae var. armatus Nakai J. Arnold Arbor. 5: 4. 1924
Acanthopanax hondae var. inermis Nakai J. Arnold Arbor. 5: 4. 1924
Acanthopanax nodiflorus Dunn J. Bot. 47: 199 (1909)
Acanthopanax spinosus var. pubescens Pamp. Nuovo Giorn. Bot. Ital. , n.s., 17: 678 (1911)
Acanthopanax villosulus Harms Pl. Wilson. 2: 562 (1916)
Eleutherococcus gracilistylus var. villosulus (Harms) Q.S.Wang Fl. Hubeiensis 3: 183 (2002)
Acanthopanax gracilistylus var. villosulus (Harms) H.L.Li Sargentia 2: 85. 1942
Eleutherococcus gracilistylus (W.W.Sm.) S.Y.Hu J. Arnold Arbor. 61: 109 (1980)
Eleutherococcus gracilistylus var. major (G.Hoo) H.Ohashi J. Jap. Bot. 62: 358 (1987)
Eleutherococcus gracilistylus var. nodiflorus (Dunn) H.Ohashi J. Jap. Bot. 62: 359 (1987)
Eleutherococcus gracilistylus var. pubescens (Pamp.) S.Y.Hu J. Arnold Arbor. 61: 109 (1980)
Eleutherococcus gracilistylus var. trifoliolatus (C.B.Shang) H.Ohashi J. Jap. Bot. 62: 359 (1987)
Eleutherococcus pubescens (Pamp.) C.H.Kim & B.Y.Sun Novon 10: 213 (2000)
Eleutherococcus villosulus (Harms) S.Y.Hu J. Arnold Arbor. 61: 110 (1980)
Hedera scandens (Poir.) DC. Prodr. 4: 264 (1830)
Eleutherococcus gracilistylus var. nodiflorus (Dunn) K.L.Zhang J. N.-W. Teach. Coll. (Nat. Sci.) 1988(1): 14 1988
Eleutherococcus nodiflorus var. gracilistylus (W.W.Sm.) Y.F.Deng Med. Fl. China 0.579166667. 2018
Aralia palmata Lour. Fl. Cochinch. : 187 (1790)
Acanthopanax spinosus Pavol. Nuovo Giorn. Bot. Ital. n.s., 15: 418 (1908)
Acanthopanax gracilistylus var. nodiflorus (Dunn) H.L.Li Sargentia 2: 86 (1942)
Eleutherococcus nodiflorus var. trifoliolatus (C.B.Shang) Shui L.Zhang & Z.H.Chen J. Hangzhou Norm. Univ., Nat. Sci. Ed. 19(6): [96-102] 2020

Common names Top

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Language Common/alternative name
Chinese 五加皮
Chinese 糙毛五加
Chinese 五加
Chinese 五加;糙毛五加
Chinese 五加(细柱五加)
Chinese 细柱五加
Chinese 細柱五加

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000948102
UNII 8H53J5AX7Z
Tropicos 50008386
KEW urn:lsid:ipni.org:names:90427-1
The Plant List kew-66463
Open Tree Of Life 480787
NCBI Taxonomy 50305
IPNI 90427-1
iNaturalist 427592
GBIF 3035388
Freebase /m/0jzv8xs
EPPO ACPGR
EOL 1145584
USDA GRIN 454294
CMAUP NPO8500

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
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Phytochemistry and Pharmacology of Eleutherococcus sessiliflorus (Rupr. & Maxim.) S.Y.Hu: A Review Sun H, Feng J, Sun Y, Sun S, Li L, Zhu J, Zang H Molecules 11-Sep-2023
PMCID:PMC10536541
doi:10.3390/molecules28186564
PMID:37764339
Combination effects of herbal and western medicines on osteoporosis in rheumatoid arthritis: systematic review and meta-analysis Kwon DY, Gu JH, Oh M, Lee EJ Front Pharmacol 10-Aug-2023
PMCID:PMC10448903
doi:10.3389/fphar.2023.1164898
PMID:37637429
Suspected cutaneous adverse drug reactions reported with traditional medicines: analysis of data for United Nations Asia region from WHO VigiBase Barvaliya MJ, Chetan AC, Chandan N, Ray SK, Hegde HV, Unger BS, Patel TK, Roy S Front Pharmacol 30-May-2023
PMCID:PMC10261983
doi:10.3389/fphar.2023.1088841
PMID:37324461
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
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Characterization of the complete chloroplast genome of the medicinal herb Eleutherococcus nodiflorus and its phylogenetic implications Li M, Gong Q, Zhou M, Liu Q, Cheng R Mitochondrial DNA B Resour 30-Oct-2022
PMCID:PMC9629086
doi:10.1080/23802359.2022.2116954
PMID:36340921
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L J Ethnobiol Ethnomed 23-May-2022
PMCID:PMC9125852
doi:10.1186/s13002-022-00532-w
PMID:35606860
Herbal plants traded at the Kaili medicinal market, Guizhou, China Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C J Ethnobiol Ethnomed 29-Nov-2021
PMCID:PMC8628420
doi:10.1186/s13002-021-00495-4
PMID:34844607
Identification of the Key Role of NF-κB Signaling Pathway in the Treatment of Osteoarthritis With Bushen Zhuangjin Decoction, a Verification Based on Network Pharmacology Approach Xu Y, Li H, He X, Huang Y, Wang S, Wang L, Fu C, Ye H, Li X, Asakawa T Front Pharmacol 12-Apr-2021
PMCID:PMC8072665
doi:10.3389/fphar.2021.637273
PMID:33912052
Eleutherococcus sessiliflorus Inhibits Receptor Activator of Nuclear Factor Kappa-B Ligand (RANKL)-Induced Osteoclast Differentiation and Prevents Ovariectomy (OVX)-Induced Bone Loss Han SY, Kim JH, Jo EH, Kim YK Molecules 26-Mar-2021
PMCID:PMC8037005
doi:10.3390/molecules26071886
PMID:33810474
An Apriori Algorithm-Based Association Rule Analysis to Identify Herb Combinations for Treating Uremic Pruritus Using Chinese Herbal Bath Therapy Lu PH, Keng JL, Kuo KL, Wang YF, Tai YC, Kuo CY Evid Based Complement Alternat Med 23-Nov-2020
PMCID:PMC7704140
doi:10.1155/2020/8854772
PMID:33299462
Phylogenetic and Comparative Analyses of Complete Chloroplast Genomes of Chinese Viburnum and Sambucus (Adoxaceae) Ran H, Liu Y, Wu C, Cao Y Plants (Basel) 03-Sep-2020
PMCID:PMC7570041
doi:10.3390/plants9091143
PMID:32899372
Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China Hu R, Lin C, Xu W, Liu Y, Long C J Ethnobiol Ethnomed 02-Jul-2020
PMCID:PMC7333293
doi:10.1186/s13002-020-00387-z
PMID:32616044

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
(111C)methyl 2-hydroxybenzoate 11378589 Click to see COC(=O)C1=CC=CC=C1O 151.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
2-(1,7-Dihydroxy-6,8-dimethoxy-3-methyl-5-propan-2-ylnaphthalen-2-yl)-6,8-dimethoxy-3-methyl-5-propan-2-ylnaphthalene-1,7-diol 5316861 Click to see CC1=CC2=C(C(=C1C3=C(C4=C(C=C3C)C(=C(C(=C4OC)O)OC)C(C)C)O)O)C(=C(C(=C2C(C)C)OC)O)OC 550.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Arylnaphthalene lignans
Helioxanthin 177023 Click to see C1C2=C(C=C3C=CC4=C(C3=C2C5=CC6=C(C=C5)OCO6)OCO4)C(=O)O1 348.30 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Asarinin 11869417 Click to see 354.40 unknown via CMAUP database
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 102004873 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
5-[(3S,6S)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 25245913 Click to see 354.40 unknown via CMAUP database
Asarinin 101612 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Npc67790 233333 Click to see 354.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Sesamin, (-)- 382073 Click to see 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3E)-4-(1,3-benzodioxol-5-ylmethyl)-3-(1,3-benzodioxol-5-ylmethylene)tetrahydrofuran-2-one 5321147 Click to see 352.30 unknown via CMAUP database
Savinin 5281867 Click to see C1C(C(=CC2=CC3=C(C=C2)OCO3)C(=O)O1)CC4=CC5=C(C=C4)OCO5 352.30 unknown https://doi.org/10.1016/J.JEP.2012.03.034
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(3R,3Ar,6S,6aS)-6-[3,5-dimethoxy-4-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 24720994 Click to see 742.70 unknown via CMAUP database
CID 71307453 71307453 Click to see 742.70 unknown via CMAUP database
Eleutheroside E 71312557 Click to see 742.70 unknown via CMAUP database
Eleutheroside E, HPLC Grade 71307454 Click to see 742.70 unknown via CMAUP database
Eleuthreo 3084742 Click to see 742.70 unknown via CMAUP database
Npc141273 73636 Click to see 742.70 unknown via CMAUP database
Npc279481 226371 Click to see 742.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Pentacosanoic acid 10468 Click to see 382.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Linoleyl acetate 44134803 Click to see 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin 11146 Click to see 891.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
ent-Kaur-16-en-19-oic acid 3034087 Click to see 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-4a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-10-hydroxy-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 163191899 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)O)C)(C)C(=O)O)O)O)O)CO)O)O)O)O 957.10 unknown https://doi.org/10.1016/0031-9422(93)85298-6
(2R,4aR,6aR,6aS,6bR,8aR,9R,10R,12aR,14bS)-4a-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-10-hydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 162853614 Click to see 973.10 unknown https://doi.org/10.1016/0031-9422(93)85298-6
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(1R,2R,3R,4S,5R)-2,3,4-trihydroxy-5-methylcyclohexyl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,8S,9R,11aS,11bR,12R,13aR,13bR)-8-formyl-9,12-dihydroxy-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 23640097 Click to see 955.10 unknown https://doi.org/10.1007/BF02977000
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(1R,2R,3R,4S,5R)-2,3,4-trihydroxy-5-methylcyclohexyl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aS,11bR,12R,13aR,13bR)-12-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 23640096 Click to see 1103.30 unknown https://doi.org/10.1002/CHIN.200315196
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bR)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 101606373 Click to see 927.10 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aS,11bR,12R,13aR,13bR)-12-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 10796251 Click to see 1105.30 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aS,11bR,12R,13aR,13bR)-9,12-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 100914112 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CC(C7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)O)C)O)C(=C)C)O)O)O)CO)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (2R,4aR,6aR,6aS,6bR,8aR,9R,10R,12aR,14bS)-10-hydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162890945 Click to see 959.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (2R,4aR,6aR,6aS,6bR,8aR,9S,10R,12aR,14bS)-9-formyl-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162876105 Click to see 957.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (2S,4aR,6aR,6aS,6bR,8aR,9S,10R,12aR,14bS)-9-formyl-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101938013 Click to see 957.10 unknown https://doi.org/10.1016/S0031-9422(97)80022-2
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,8R,9R,11aR,11bR,13aR,13bS)-9-hydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 162898542 Click to see 943.10 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bS)-9-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 162974217 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)O)C)C(=C)C)O)O)O)CO)O)O)O 927.10 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aS,11bR,12R,13aR,13bS)-12-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 162961430 Click to see 1105.30 unknown https://doi.org/10.1248/CPB.50.1383
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4S,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1R,3aS,5aR,5bR,7aR,9R,11aS,11bR,12R,13aR,13bS)-9,12-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 162883768 Click to see 943.10 unknown https://doi.org/10.1248/CPB.50.1383
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162928255 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)O)C)(C)CO)O)O)O)CO)O)O)O 943.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
https://doi.org/10.1016/S0031-9422(97)80022-2
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-hydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 85229746 Click to see 959.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 12-hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-9-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 85271469 Click to see 1105.30 unknown https://doi.org/10.1248/CPB.50.1383
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 9-formyl-10-hydroxy-2-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73049650 Click to see 957.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 9,12-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 75254687 Click to see 943.10 unknown https://doi.org/10.1248/CPB.50.1383
4a-[6-[[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-10-hydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 162853613 Click to see 973.10 unknown https://doi.org/10.1016/0031-9422(93)85298-6
4a-[6-[[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxycarbonyl-9-formyl-10-hydroxy-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid 162940971 Click to see 971.10 unknown https://doi.org/10.1016/0031-9422(93)85298-6
Acankoreoside A 10795959 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C(=O)O)O)C)C(=C)C)O)O)O)CO)O)O)O 957.10 unknown https://doi.org/10.1007/BF02977000
Acankoreoside D 52944263 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CC(C7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C=O)O)C)O)C(=C)C)O)O)O)CO)O)O)O 957.10 unknown https://doi.org/10.1007/BF02977000
Cirensenoside H 11029400 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(C4C6CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)O)C)C(=C)C)O)O)O)CO)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.50.1383
Olean-12-en-28-oic acid, 3,29-dihydroxy-, O-6-deoxy-I+/--L-mannopyranosyl-(1a4)-O-I(2)-D-glucopyranosyl-(1a6)-I(2)-D-glucopyranosyl ester, (3I+/-,20I+/-)- 162928256 Click to see 943.10 unknown https://doi.org/10.1016/S0031-9422(00)90853-7
Oplopanaxoside C 78180693 Click to see 943.10 unknown https://doi.org/10.1248/CPB.50.1383
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (2R,4aR,6aR,6aS,6bR,8aR,9R,10R,12aR,14bS)-2,10-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101938015 Click to see 945.10 unknown https://doi.org/10.1016/S0031-9422(97)80022-2
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 2,10-dihydroxy-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 162877509 Click to see 929.10 unknown https://doi.org/10.1016/S0031-9422(97)80022-2
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 2,10-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 85263221 Click to see 945.10 unknown https://doi.org/10.1016/S0031-9422(97)80022-2
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 9-formyl-2,10-dihydroxy-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73157057 Click to see 943.10 unknown https://doi.org/10.1016/S0031-9422(97)80022-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-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 636741 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
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 via CMAUP database
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[4-[(Z)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 9799599 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
(3S,4R,6S)-2-(hydroxymethyl)-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 24847743 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
(Z)-Coniferin 91895380 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
Syringin 5316860 Click to see 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
3,4-Methylenedioxyphenol 68289 Click to see C1OC2=C(O1)C=C(C=C2)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines / Naphthylquinolines
Bidebiline D 10054040 Click to see 584.60 unknown https://doi.org/10.1248/CPB.50.1383
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see 206.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Calycanthoside 5318566 Click to see 384.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44259091 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 11557027 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-chromen-3-yl D-galactopyranoside 11751616 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database

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