Trachycarpus fortunei

Details Top

Internal ID UUID643fef8425902823828083
Scientific name Trachycarpus fortunei
Authority (Hook.) H.Wendl.
First published in Bull. Soc. Bot. France 8: 429 (1861)

Ethnobotanical Use Top

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General Uses Top

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Common products:
Leaf laminae are fabricated into hand fans and festival banners, with sheath fibers used to make brushes, brooms, cordage, and coarse textiles.

Industrial and craft applications:
Sheath fibers are processed into bast-fiber mats and, after retting and mechanical cleaning, supply fibers for coarse fabrics and paper pulps. Charcoal and fuelwood are produced from stems and pruning residues.

Food and beverages (non-medicinal):
The inflorescence sap is tapped to produce sugar or fermented into alcoholic beverages, notably in parts of China; sap yields are species- and climate-dependent.

Colorants and tanning:
High-lignin leaf laminae and fiber residues provide brown natural dyes for protein fibers and produce slow-tanning materials suitable for leather; the color intensity and fastness are attributed to condensed tannins and lignin-derived chromophores.

Wood and fiber:
Leaf sheaths yield durable, coarse bast fibers used for cordage and brushes. Stems are sometimes converted to charcoal; wood is generally not regarded as structural timber.

Fragrance and cosmetics:
No documented fragrance or essential oil uses specific to Trachycarpus fortunei.

Properties relevant to use:
Sheath fiber mechanical performance derives from high cellulose and lignin content; fiber coarseness and strength are consistent with bast-fiber applications. Leaf laminae are sufficiently rigid and flexible for fan fabrication. Sap sugar content (primarily sucrose) supports fermentation to ethanol; gum/resin composition in sap is low, minimizing microbial contamination and facilitating crystallization. Tanning efficacy stems from condensed tannins and lignin phenolics; brown dyes result from lignin and tannin-derived chromophores and mordanting on protein fibers.

Standards and regulation:
Fan and craft products fall under general consumer safety and materials standards (e.g., ISO/ASTM/EN material safety and labeling). Sugar and beverage products are subject to national food and alcohol regulations; sap tapping and transport must follow hygienic handling requirements. Import/export of fiber and wood products may require phytosanitary documentation per international plant health standards (e.g., IPPC). Environmental releases of byproducts and charcoal production are regulated under local air and waste rules.

Sustainability and sourcing:
Leaves and inflorescences are harvested without felling the palm, supporting regeneration. Sap tapping generally has low to moderate environmental impact when managed at sustainable intensity; over-tapping can stress trees. Plantation cultivation is expanding in temperate regions for ornamental fiber and craft use. Waste from leaf trimming is readily convertible to mulch or biomass, contributing to low-waste utilization.

Synonyms Top

Scientific name Authority First published in
Trachycarpus caespitosus Becc. Bull. Soc. Tosc. Ortic. , ser. 3, 20: 164 (1915)
Trachycarpus wagnerianus hort. ex Becc. Webbia 5: 70 (1921)
Chamaerops fortunei Hook. Bot. Mag. 86: t. 5221 (1860)

Common names Top

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Language Common/alternative name
English chusan palm
English chinese windmill palm
English windmill palm
English hemp palm
English chinese hemp palm
Spanish chamaerops fortunei
Spanish trachycarpus caespitosus
Spanish trachycarpus wagnerianus
Spanish palmito elevado
Spanish palmera excelsa
Spanish palmera de molino de viento
Spanish palmera china de abanico
Arabic نغبول
Arabic نخل مروحة
Arabic نخل دغل
Azerbaijani fortuna traxikarpusu
azb فورتونا تراخیکارپوسو
Bulgarian Китайска конопена палма
Bulgarian китайска конопена палма
Catalan palmera excelsa
cdo cĕ̤ng-chéu
Czech trachykarpus žíněný
Danish hørpalme
German tessiner palme
German chinesische hanfpalme
German trachycarpus wagnerianus
Esperanto ĉinia traĥikarpo
Esperanto treĉina palmo
Esperanto ĉinia kanabopalmo
Basque txinako palmondo
Persian نخل آسیابی
Finnish kuitupalmu
French chamaerops excelsa
French palmier de chine
French chamaerops chinensis
French palmier chanvre
French chamaerops fortunei
French palmier de chusan
French palmier-chanvre
Galician palmeira de abano
hak chûng-su
Upper Sorbian chinska konopjowa palma
Hungarian kínai kenderpálma
Italian palma di fortune
Japanese 椶櫚
Japanese 和棕櫚
Japanese シュロ
Japanese 棕櫚
Japanese 棕梠
Japanese ワジュロ
Korean 당종려
lzh
Macedonian кинеска конопна палма
Macedonian кинеска влакнеста палма
nan chang
Norwegian Bokmål vindmøllepalme
Polish szorstkowiec fortune'a
Polish szorstkowiec fortunego
Slovak trachycarpus wagnerianus
Slovak trachykarp konopný
Swedish väderkvarnspalm
Turkish telli palmiye
za go'gvang
Chinese 栟榈
Chinese 棕櫚
Chinese 棕榈花
Chinese 棕榈子
Chinese 棕榈叶
Chinese 棕树心
Chinese 棕榈根
Chinese 棕榈皮
Chinese 棕櫚樹
Chinese 棕果
Chinese 棕榈
Chinese 棕树

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
  • Europe
    • Middle Europe
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Italy

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000326529
UNII G77L97OMJO
USDA Plants TRFO3
Tropicos 2401392
INPN 126933
Flora of Italy 7845
KEW urn:lsid:ipni.org:names:670182-1
The Plant List kew-207159
Missouri Botanical Garden 276718
Open Tree Of Life 1003095
Observations.org 125675
NCBI Taxonomy 14027
NBN Atlas NHMSYS0000464504
IPNI 670182-1
iNaturalist 64323
GBIF 2739071
Freebase /m/04fwlt
EPPO TRRFO
EOL 1128696
USDA GRIN 36786
Wikipedia Trachycarpus_fortunei
CMAUP NPO12666

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 chromosome-level genome assembly of the spider mite Tetranychus piercei McGregor Chen L, Yu XY, Zhang F, Zhang HM, Guo LX, Ren L, Hong XY, Sun JT Sci Data 05-Apr-2024
PMCID:PMC10997676
doi:10.1038/s41597-024-03189-0
PMID:38580722
Pestalotiopsis jiangsuensis sp. nov. Causing Needle Blight on Pinus massoniana in China Li H, Peng BY, Xie JY, Bai YQ, Li DW, Zhu LH J Fungi (Basel) 21-Mar-2024
PMCID:PMC10970983
doi:10.3390/jof10030230
PMID:38535238
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Physiological responses to drought stress of three pine species and comparative transcriptome analysis of Pinus yunnanensis var. pygmaea Xiao F, Zhao Y, Wang X, Jian X, Yang Y BMC Genomics 16-Mar-2024
PMCID:PMC10944613
doi:10.1186/s12864-024-10205-5
PMID:38493093
First report of Rhabditis (Rhabditella) axei with the invasive palm borer Paysandisia archon Sciandra C, Amoriello S, Degli EI, Nicotera V, Barbieri F, Mazza G, Torrini G, Roversi PF, Strangi A J Nematol 14-Mar-2024
PMCID:PMC10940275
doi:10.2478/jofnem-2024-0005
PMID:38495930
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154
Morpho-Molecular Characterization Reveals a New Genus, Three Novel Species and Two New Host Records in Xylariomycetidae Li WL, Liang RR, Yang J, Liu JK J Fungi (Basel) 29-Feb-2024
PMCID:PMC10970796
doi:10.3390/jof10030189
PMID:38535198
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Phytoplasma: A plant pathogen that cannot be ignored in agricultural production—Research progress and outlook Wang R, Bai B, Li D, Wang J, Huang W, Wu Y, Zhao L Mol Plant Pathol 23-Feb-2024
PMCID:PMC10887288
doi:10.1111/mpp.13437
PMID:38393681
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review Rungjindamai N, Jones EB J Fungi (Basel) 15-Jan-2024
PMCID:PMC10820240
doi:10.3390/jof10010067
PMID:38248976
Commodity risk assessment of Corylus avellana plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 12-Jan-2024
PMCID:PMC10784871
doi:10.2903/j.efsa.2024.8495
PMID:38222930
Pest categorisation of Pestalotiopsis disseminata Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Dec-2023
PMCID:PMC10728885
doi:10.2903/j.efsa.2023.8494
PMID:38116101
Palm Fungi and Their Key Role in Biodiversity Surveys: A Review Pereira DS, Phillips AJ J Fungi (Basel) 19-Nov-2023
PMCID:PMC10672035
doi:10.3390/jof9111121
PMID:37998926
Taxonomic and Phylogenetic Updates on Apiospora: Introducing Four New Species from Wurfbainia villosa and Grasses in China Liao C, Senanayake IC, Dong W, Thilini Chethana KW, Tangtrakulwanich K, Zhang Y, Doilom M J Fungi (Basel) 06-Nov-2023
PMCID:PMC10671859
doi:10.3390/jof9111087
PMID:37998892

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
10-O-Methylprotosappanin B 5319768 Click to see 318.32 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne 5322029 Click to see CC#CC#CC#CC=CC=CC=C 166.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
methyl 4-[7,15-dihydroxy-4-(hydroxymethyl)-4,10,13,14-tetramethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]pentanoate 137796302 Click to see 490.60 unknown https://doi.org/10.1248/CPB.34.82
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12R,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162967412 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1248/CPB.32.295
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2R,4R,6R,7S,8R,9S,12R,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162920533 Click to see 1063.20 unknown https://doi.org/10.1248/CPB.32.295
(2S,3R,4R,5R,6S)-2-[(2R,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-16-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 131801368 Click to see 1031.20 unknown https://doi.org/10.1248/CPB.34.82
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(1S,2S,4S,8S,9S,12S,13R,16S)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-16-yl]oxy]oxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 102004848 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(OC(C(C3O)OC4C(C(C(C(O4)C)O)O)O)OC5CCC6(C7CCC8(C(C7CC=C6C5)CC9C8C(=C(O9)CCC(C)COC1C(C(C(C(O1)CO)O)O)O)C)C)C)CO)C)O)O)O 1177.30 unknown https://doi.org/10.1248/CPB.34.82
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12R,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162873040 Click to see 1015.20 unknown https://doi.org/10.1248/CPB.32.295
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1R,2R,4S,6S,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162982086 Click to see 1209.40 unknown https://doi.org/10.1248/CPB.32.295
(2S,3R,4R,5S,6S)-2-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-6-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 11968769 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)OC8C(C(C(C(O8)C)O)O)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)OC 1209.40 unknown via CMAUP database
(3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,7S,8R,9S,12S,13R,16S)-6-methoxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 123134748 Click to see 1063.20 unknown https://doi.org/10.1248/CPB.32.295
2-[4-Hydroxy-2-(hydroxymethyl)-6-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 271916 Click to see 869.00 unknown https://doi.org/10.1248/CPB.32.295
2-[4,5-Dihydroxy-6-[4-hydroxy-2-(hydroxymethyl)-6-(8-hydroxy-5',7,9,13-tetramethyl-spiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-tetrahydropyran]-16-yl)oxy-5-(3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl)oxy-tetrahydropyran-3-yl]oxy-2-methyl-tetrahydropyran-3-yl]oxy-6-methyl-tetrahydropyran-3,4,5-triol 12804743 Click to see 1031.20 unknown https://doi.org/10.1248/CPB.34.82
2-[4,5-Dihydroxy-6-[4-hydroxy-2-(hydroxymethyl)-6-[[6-methoxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-16-yl]oxy]-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-2-methyloxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73157218 Click to see 1209.40 unknown https://doi.org/10.1248/CPB.32.295
https://doi.org/10.1248/CPB.34.82
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1248/CPB.32.295
Npc269297 328441 Click to see 1015.20 unknown https://doi.org/10.1248/CPB.34.82
https://doi.org/10.1248/CPB.32.295
NSC-698790;Smilax saponin B 500376 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)OC 1063.20 unknown https://doi.org/10.1248/CPB.32.295
https://doi.org/10.1248/CPB.34.82
Pseduoprotodioscin 73817989 Click to see 1031.20 unknown https://doi.org/10.1248/CPB.34.82
Pseudoprotodioscin 21637110 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)C)O)O)O)OC4CCC5(C6CCC7(C(C6CC=C5C4)CC8C7C(=C(O8)CCC(C)COC9C(C(C(C(O9)CO)O)O)O)C)C)C)CO)O)O)O 1031.20 unknown https://doi.org/10.1248/CPB.34.82
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G97417CF 24802025 Click to see 342.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
1,8-dihydroxy-6-methyl-2,3-dihydro-1H-cyclopenta[b]chromen-9-one 10966363 Click to see 232.23 unknown https://doi.org/10.1248/CPB.34.82
> Organoheterocyclic compounds / Bi- and oligothiophenes
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Thioenol ethers
(7Z)-8-methylsulfanyltrideca-1,7-dien-3,5,9,11-tetrayne 101415640 Click to see 210.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-Dihydroxyphenyl)-5-hydroxy-7-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12315422 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.32.295
https://doi.org/10.1248/CPB.34.82
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.32.295
https://doi.org/10.1248/CPB.34.82
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/CPB.34.82
https://doi.org/10.1248/CPB.32.295
Scolymoside 10461109 Click to see 594.50 unknown https://doi.org/10.1248/CPB.34.82
https://doi.org/10.1248/CPB.32.295
Scolymoside 5282152 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.32.295
https://doi.org/10.1248/CPB.34.82
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Liquidambar styraciflua 16133892 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)OCC3C(C(C(C(O3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)OC(=O)C7=CC(=C(C(=C7)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)OC(=O)C9=CC(=C(C(=C9)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)OC(=O)C1=CC(=C(C(=C1)O)O)O)O)O 1701.20 unknown via CMAUP database

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