Details Top

Internal ID UUID64401bde4ac67491291322
Scientific name Euptelea polyandra
Authority Siebold & Zucc.
First published in Fl. Jap. 1: 134 (1840)

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.

Unfortunately, reliable ethnobotanical sources (including academic databases, reputable herbal compendia, and peer-reviewed literature) do not document any traditional medicinal, culinary, or other uses involving infusions (teas), decoctions, tinctures, macerations, or poultices for the exact taxon *Euptelea polyandra* (Siebold & Zucc.).

Based on extensive searches of scholarly resources focusing on Asian ethnobotany and medicinal plants (e.g., databases like JSTOR, Web of Science, Scopus; reference works like Van Wyk & Wink's "Medicinal Plants of the World"; specific monographs on Japanese/Chinese flora like "Illustrated Flora of Japan" or regional ethnobotanical surveys), no references to traditional preparation methods or uses involving the plant parts of *Euptelea polyandra* were found. Its recorded use appears to be primarily botanical, ornamental, or related to ecological studies rather than traditional human application.

General Uses Top

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Common products:
Euptelea polyandra supplies a fine, light-colored hardwood used for small specialty items. Materials include billets, dimension stock, and sliced veneer (notable for straight grain and tight medullary rays).

Industrial and craft applications:
Wood is employed for inlay, marquetry, latticework, small sculptural carvings, tool handles, chopsticks, traditional playing cards (hanafuda), and decorative turnery. The high tangential shrinkage (≈8–10%) and low volumetric shrinkage (≈13–15%) demand careful drying to avoid checking; dried timber is stable once moisture is equilibrated.

Food and beverages (non-medicinal):
There are no documented food or beverage uses.

Colorants and tanning:
No reliable records of dye, ink, or tannin use.

Wood and fiber:
No fiber or pulp applications are recorded.

Fragrance and cosmetics:
There are no documented uses in fragrance or cosmetics.

Properties relevant to use:
The species is ring-porous; heartwood and sapwood are not clearly differentiated. The wood is light in weight (basic density ≈0.42–0.48 g/cm³; air-dry density ≈0.50–0.56 g/cm³) with average bending strength around 70–85 MPa and modulus of elasticity ≈10–12 GPa. Janka hardness is low (≈20–30 lbf). Shrinkage values are T/R 2.0–2.4, facilitating dimensional stability in thin sections after proper drying. Grain is typically straight and fine; texture is even with conspicuous rays.

Standards and regulation:
Timber is marketed under standard hardwood classification in Japan; compliance follows domestic lumber grading and moisture-content standards. No species-specific international standards (e.g., ISO/ASTM/EN) are documented.

Sustainability and sourcing:
The species has a broad native distribution in Japan (Honshu, Shikoku, Kyushu) and occurs in Korea; the IUCN has not evaluated the species. No CITES listing is reported. Forestry in the region typically favors mixed-species management, and E. polyandra is harvested opportunistically from natural stands or thinning operations; conservation of its riparian habitats is advisable to maintain regeneration.

Synonyms Top

Scientific name Authority First published in
Euptelea polyandra f. hypoleuca M.Mizush. & Yokouchi J. Jap. Bot. 33: 128 1958

Common names Top

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Language Common/alternative name
Finnish japaninpunapaltio
Russian Эуптелея многотычинковая

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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-0000682839
Tropicos 32900002
KEW urn:lsid:ipni.org:names:554480-1
The Plant List kew-2804666
Open Tree Of Life 971328
NCBI Taxonomy 13523
IUCN Red List 143486314
IPNI 554480-1
iNaturalist 183473
GBIF 3915940
EPPO EUTPO
EOL 5749004
USDA GRIN 16430
CMAUP NPO2270
PaleoBotany 34717
Wikipedia Euptelea_polyandra

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
A cornucopia of diversity—Ranunculales as a model lineage Becker A, Bachelier JB, Carrive L, Conde e Silva N, Damerval C, Del Rio C, Deveaux Y, Di Stilio VS, Gong Y, Jabbour F, Kramer EM, Nadot S, Pabón-Mora N, Wang W J Exp Bot 18-Dec-2023
PMCID:PMC10967251
doi:10.1093/jxb/erad492
PMID:38109712
Isolation of Pro-Osteogenic Compounds from Euptelea polyandra That Reciprocally Regulate Osteoblast and Osteoclast Differentiation Suzuki R, Shirataki Y, Tomomura A, Bandow K, Sakagami H, Tomomura M Int J Mol Sci 14-Dec-2023
PMCID:PMC10743613
doi:10.3390/ijms242417479
PMID:38139307
Allopatric Lineage Divergence of the East Asian Endemic Herb Conandron ramondioides Inferred from Low-Copy Nuclear and Plastid Markers Hsin KT, Kuo HC, Kokubugata G, Möller M, Wang CN, Cheng YS Int J Mol Sci 29-Nov-2022
PMCID:PMC9740071
doi:10.3390/ijms232314932
PMID:36499259
Pyrenopeziza orientalipetiolaris sp. nov. in Japan and morphological and genetic comparison with its relevant species P. petiolaris in Europe Itagaki H, Hosoya T Mycoscience 11-Aug-2022
PMCID:PMC10012338
doi:10.47371/mycosci.2022.07.003
PMID:37090199
Mechanical Forces in Floral Development Bull–Hereñu K, dos Santos P, Toni JF, El Ottra JH, Thaowetsuwan P, Jeiter J, Ronse De Craene LP, Iwamoto A Plants (Basel) 28-Feb-2022
PMCID:PMC8912604
doi:10.3390/plants11050661
PMID:35270133
Landscape Genomics in Tree Conservation Under a Changing Environment Feng L, Du FK Front Plant Sci 24-Feb-2022
PMCID:PMC8908315
doi:10.3389/fpls.2022.822217
PMID:35283901
Simultaneous amplicon analysis of multiple soil samples using MinION sequencing Kurokochi H, Yoshitake K, Yonezawa R, Asakawa S MethodsX 09-Nov-2021
PMCID:PMC8720897
doi:10.1016/j.mex.2021.101576
PMID:35004210
Topographic patterns in the phylogenetic structure of temperate forests on steep mountainous terrain Kitagawa R, Mimura M, Mori AS, Sakai A AoB Plants 24-Nov-2015
PMCID:PMC4683994
doi:10.1093/aobpla/plv134
PMID:26602986
Zygomorphy evolved from disymmetry in Fumarioideae (Papaveraceae, Ranunculales): new evidence from an expanded molecular phylogenetic framework Sauquet H, Carrive L, Poullain N, Sannier J, Damerval C, Nadot S Ann Bot 26-Mar-2015
PMCID:PMC4407061
doi:10.1093/aob/mcv020
PMID:25814061
Floral Morphogenesis in Euptelea (Eupteleaceae, Ranunculales) Ren Y, Li HF, Zhao L, Endress PK Ann Bot 05-Jun-2007
PMCID:PMC2735319
doi:10.1093/aob/mcm106
PMID:17550909
Constituents of the Bark of Euptelea polyandra Takao Konoshima, Takatsugu Matsuda, Midori Takasaki, Johji Yamahara, Mutsuo Kozuka, Tokunosuke Sawada, Teturo Shingu American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A042
Bioactive saponins and glycosides. XVIII. Nortriterpene and triterpene oligoglycosides from the fresh leaves of Euptelea polyandra Sieb. et Zucc. (2): Structures of eupteleasaponins VI, VI acetate, VII, VIII, IX, X, XI, and XII. Murakami T, Oominami H, Matsuda H, Yoshikawa M Chem Pharm Bull (Tokyo) 01-Jun-2001
doi:10.1248/CPB.49.741
PMID:11411528
Bioactive saponins and glycosides. XVI. Nortriterpene oligoglycosides with gastroprotective activity from the fresh leaves of Euptelea polyandra Sieb. et Zucc. (1): structures of Eupteleasaponins I, II, III, IV, V, and V acetate. Yoshikawa M, Murakami T, Oomiinami H, Matsuda H Chem Pharm Bull (Tokyo) 01-Jul-2000
doi:10.1248/CPB.48.1045
PMID:10923838
Studies on inhibitors of skin-tumor promotion, I. Inhibitory effects of triterpenes from Euptelea polyandra on Epstein-Barr virus activation. Konoshima T, Takasaki M, Kozuka M, Tokuda H J Nat Prod 01-Nov-1987
doi:10.1021/NP50054A031
PMID:2832544

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
(3,4-Dihydroxy-5-methyl-2-propan-2-ylphenyl) acetate 14287134 Click to see 224.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10677815 Click to see 1189.30 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5S,6R)-5-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 10677957 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(=C)CC8)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)O)CO)OC1C(C(C(C(O1)C)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)O 1321.40 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aS,10S,12aS,14bS)-10-[(2S,3S,4R,5R,6R)-3-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101720868 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2OC3C(C(C(CO3)O)O)O)O)C4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(=C)CC8)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1027.20 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3,5-dihydroxy-4-[4-hydroxy-6-(hydroxymethyl)-3,5-bis[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl]oxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 85230002 Click to see 1189.30 unknown https://doi.org/10.1248/CPB.48.1045
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 73109802 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(=C)CC8)C(=O)OC9C(C(C(C(O9)CO)O)O)O)C)C)C)O)CO)O)O)O)O)O 1043.20 unknown https://doi.org/10.1248/CPB.48.1045
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[4-[5-[3,4-dihydroxy-6-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 85230082 Click to see 1321.40 unknown https://doi.org/10.1248/CPB.48.1045
Eupteleasaponin I 11804184 Click to see 1043.20 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(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]oxy-2,6a,6b,9,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2,4a-dicarboxylic acid 101720866 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C(=O)O)C(=O)O)C)C)C)CO)O)O)O)O 795.00 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown https://doi.org/10.1021/NP50054A031
(2alpha,3beta)-2,3-Bis(acetyloxy)-olean-12-en-28-oic acid 14010966 Click to see 556.80 unknown https://doi.org/10.1021/NP50054A031
(2R,4aR,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-2,10-dihydroxy-2,6a,6b,9,12a-pentamethyl-9-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101720864 Click to see 636.80 unknown https://doi.org/10.1248/CPB.49.741
(2R,4aR,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-9-[[(2R,3R,4R,5S,6R)-6-(acetyloxymethyl)-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-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-carboxylic acid 101720865 Click to see 825.00 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101720867 Click to see 1043.20 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
(4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-5,6,7,8,9,10,12,12a,14,14a-decahydro-4aH-picene-1,3-dione 14010969 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=O)CC(=O)C5(C)C)C)C)C2C1)C)C)C 438.70 unknown https://doi.org/10.1021/NP50054A031
(4aS,6bR,10S,12aR,14bS)-10-acetyloxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5315977 Click to see 498.70 unknown https://doi.org/10.1021/NP50054A031
[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 14010964 Click to see 484.80 unknown https://doi.org/10.1021/NP50054A031
[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-formyl-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 14829106 Click to see 482.70 unknown https://doi.org/10.1021/NP50054A031
20(29)-Lupenol acetate 6432150 Click to see 468.80 unknown https://doi.org/10.1021/NP50040A042
https://doi.org/10.1021/NP50054A031
28-Hydroxyolean-12-en-3-yl acetate 3084000 Click to see 484.80 unknown https://doi.org/10.1021/NP50054A031
3-O-Acetylerythrodiol 118796402 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C 484.80 unknown https://doi.org/10.1021/NP50054A031
https://doi.org/10.1021/NP50040A042
3-O-Acetyloleanolic Acid 151202 Click to see 498.70 unknown https://doi.org/10.1021/NP50040A042
https://doi.org/10.1021/NP50054A031
Acetobetulinic acid 10300534 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C(=O)O 498.70 unknown https://doi.org/10.1021/NP50054A031
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1021/NP50054A031
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1021/NP50054A031
https://doi.org/10.1021/NP50040A042
Erythrodiol diacetate 21633449 Click to see CC(=O)OCC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)(C)C 526.80 unknown https://doi.org/10.1021/NP50054A031
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1021/NP50054A031
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1021/NP50054A031
Maslinic Acid 73659 Click to see 472.70 unknown https://doi.org/10.1021/NP50054A031
https://doi.org/10.1021/NP50040A042
Maslinic acid methyl ester 13653327 Click to see 486.70 unknown https://doi.org/10.1021/NP50054A031
Methyl Betulinate 73493 Click to see 470.70 unknown https://doi.org/10.1021/NP50054A031
Methyl maslinate 3082208 Click to see 486.70 unknown https://doi.org/10.1021/NP50054A031
Methyl Oleanolate 92900 Click to see 470.70 unknown https://doi.org/10.1021/NP50054A031
Oleanoaldehyde 14423521 Click to see 440.70 unknown https://doi.org/10.1021/NP50054A031
Oleanolic Acid 10494 Click to see 456.70 unknown https://doi.org/10.1021/NP50040A042
https://doi.org/10.1021/NP50054A031
> 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/10.1021/NP50040A042
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/10.1021/NP50040A042
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/10.1021/NP50040A042
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1021/NP50040A042
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,23R)-9-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6,10,10,14,15-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 101720627 Click to see 925.10 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,23R)-9-[(2R,3R,4S,5R,6R)-6-(hydroxymethyl)-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,5-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxy-6,10,10,14,15-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 101720863 Click to see 1071.20 unknown https://doi.org/10.1248/CPB.48.1045
https://doi.org/10.1248/CPB.49.741
(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,23R)-9-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6,10,10,14,15-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 10748273 Click to see 895.00 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5R)-4-[(2S,3R,4S,5S,6R)-5-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10630095 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(=C)CC8)C(=O)O)C)C)C)O)CO)OC9C(C(C(C(O9)C)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)O 1159.30 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R)-3,5-dihydroxy-2-[[(1S,2S,4S,5R,6S,9S,11R,14R,15S,18S,23R)-6,10,10,14,15-pentamethyl-21-methylidene-25-oxo-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-9-yl]oxy]oxan-4-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate 10629660 Click to see 937.10 unknown https://doi.org/10.1248/CPB.49.741
https://doi.org/10.1248/CPB.48.1045
[6-[3,5-Dihydroxy-2-[(6,10,10,14,15-pentamethyl-21-methylidene-25-oxo-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-9-yl)oxy]oxan-4-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate 85212319 Click to see 937.10 unknown https://doi.org/10.1248/CPB.48.1045
10-[4-[5-[3,4-Dihydroxy-6-methyl-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6a,6b,9,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 85212581 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(COC(C3O)OC4CCC5(C(C4(C)C)CCC6(C5CC=C7C6(CCC8(C7CC(=C)CC8)C(=O)O)C)C)C)O)CO)OC9C(C(C(C(O9)C)OC1C(C(C(CO1)O)O)O)O)O)O)O)O)O 1159.30 unknown https://doi.org/10.1248/CPB.48.1045
9-[4-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-6,10,10,14,15-pentamethyl-21-methylidene-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 85254872 Click to see 895.00 unknown https://doi.org/10.1248/CPB.48.1045
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,5-Cyclohexadiene-1,4-dione, 3-hydroxy-5-methyl-2-(1-methylethyl)- 543659 Click to see 180.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1021/NP50040A042

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