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Pteridium esculentum

Pteridium esculentum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405a4d36ea1838752293
Scientific name Pteridium esculentum
Authority (G.Forst.) Cockayne
First published in Rep. Bot. Surv. Tongariro Natl. Park : 34 (1908)

Description Top

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Pteridium esculentum, also known as bracken fern, is a species of fern found in the Southern Hemisphere. Its name, esculentum, means edible, and it has been used as a food source by indigenous peoples such as the Eora people in Australia and the Māori in New Zealand. It is a quick-growing plant that can outcompete other species and is often considered a weed. However, it also provides shelter and food for native insects. The rhizomes of Pteridium esculentum were traditionally used as a staple food by the Māori and Aborigines, and were prepared by pounding and roasting. It is important to note that Pteridium esculentum contains a carcinogen, ptaquiloside, which can be found in varying concentrations in different areas.

Synonyms Top

Scientific name Authority First published in
Allosorus esculentus (G.Forst.) C.Presl Tent. Pterid. 154 (1836)
Cincinalis esculenta Trevis. Syll. Sporoph. Ital. 1: 31 (1874)
Ornithopteris esculenta J.Sm. Hist. Fil. 298. 1875
Pteris esculenta Forst. Pl. Esc. : 74 (1786)
Pteris aquilina f. esculenta (G.Forst.) Christ Monsunia (1900)
Pteridium aquilinum subsp. esculentum (G.Forst.) C.Chr. Index Filicum 1857
Pteridium aquilinum var. aequipinnulum Domin Biblioth. Bot. 22(89): (1928)
Pteridium aquilinum var. esculentum (G.Forst.) Kuhn Die Gruppe de Chaetopterides unter der Polypodiaceen (1882) 27 [in Festschrift zu 50 j?hr. Jubil. d. kgl. Realschule zu Berlin 1882
Pteris aquilina var. esculenta (G.Forst.) Hook.f. Fl. Nov.-Zel. (1854)

Common names Top

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Language Common/alternative name
Persian سرخس اسکولنتوم
Chinese 蕨根
Chinese 食蕨

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Pteridium esculentum subsp. arachnoideum (Kaulf.) J.A.Thomson Telopea 14: 45 (2012)
Pteridium esculentum subsp. campestre (Schrad.) Schwartsb. & J.Prado Phytotaxa 333(1): 32. 2018

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
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Queensland
      • South Australia
      • Tasmania
      • Victoria
      • Western Australia
    • New Zealand
      • Antipodean Islands
      • Chatham Islands
      • Kermadec Islands
      • New Zealand North
      • New Zealand South
  • Pacific
    • South-central Pacific
      • Society Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Tonga
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001284721
Tropicos 50324886
INPN 672331
KEW urn:lsid:ipni.org:names:17415070-1
The Plant List tro-50324886
Open Tree Of Life 195647
NCBI Taxonomy 32102
IPNI 17415070-1
iNaturalist 194768
GBIF 5532455
Freebase /m/0cc9bc8
EPPO PTEES
USDA GRIN 418444
Wikipedia Pteridium_esculentum
CMAUP NPO18866

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
Small mammals reduce activity during high moon illumination under risk of predation by introduced predators Taylor P, Swan M, Sitters H, Smith A, Di Stefano J Sci Rep 29-Jun-2023
PMCID:PMC10310734
doi:10.1038/s41598-023-37166-1
PMID:37386037
The effect of seabird presence and seasonality on ground‐active spider communities across temperate islands Pascoe P, Houghton M, Jones HP, Weldrick C, Trebilco R, Shaw J Ecol Evol 03-Dec-2022
PMCID:PMC9719043
doi:10.1002/ece3.9570
PMID:36479030
Review of the Foundational Knowledge Required for Assessing Horse Welfare Harvey AM, Ramp D, Mellor DJ Animals (Basel) 01-Dec-2022
PMCID:PMC9736110
doi:10.3390/ani12233385
PMID:36496906
Untying the Gordian knot of plastid phylogenomic conflict: A case from ferns Wang T, Li TZ, Chen SS, Yang T, Shu JP, Mu YN, Wang KL, Chen JB, Xiang JY, Yan YH Front Plant Sci 24-Nov-2022
PMCID:PMC9730426
doi:10.3389/fpls.2022.918155
PMID:36507421
Using eDNA metabarcoding to understand the effect of fire on the diet of small mammals in a woodland ecosystem Wanniarachchi S, Swan M, Nevil P, York A Ecol Evol 08-Nov-2022
PMCID:PMC9643072
doi:10.1002/ece3.9457
PMID:36381390
Identity, Prevalence, and Pathogenicity of Entomopathogenic Fungi Infecting Invasive Polistes (Vespidae: Polistinae) Paper Wasps in New Zealand Reason A, Bulgarella M, Lester PJ Insects 12-Oct-2022
PMCID:PMC9604194
doi:10.3390/insects13100922
PMID:36292870
Plant rarity in fire-prone dry sclerophyll communities Sritharan MS, Scheele BC, Blanchard W, Foster CN, Werner PA, Lindenmayer DB Sci Rep 14-Jul-2022
PMCID:PMC9283327
doi:10.1038/s41598-022-15927-8
PMID:35835789
Applying early divergent characters in higher rank taxonomy of Melampsorineae (Basidiomycota, Pucciniales) Zhao P, Li Y, Li Y, Liu F, Liang J, Zhou X, Cai L Mycology 11-Jul-2022
PMCID:PMC9930778
doi:10.1080/21501203.2022.2089262
PMID:36816773
Post-disturbance reorganization of forest ecosystems in a changing world Seidl R, Turner MG Proc Natl Acad Sci U S A 05-Jul-2022
PMCID:PMC9282434
doi:10.1073/pnas.2202190119
PMID:35787053
Differential effects of ecosystem engineering by the superb lyrebird Menura novaehollandiae and herbivory by large mammals on floristic regeneration and structure in wet eucalypt forests Maisey AC, Haslem A, Leonard SW, Bennett AF Ecol Evol 02-Jun-2022
PMCID:PMC9163197
doi:10.1002/ece3.8956
PMID:35784040
Post‐fire pickings: Large herbivores alter understory vegetation communities in a coastal eucalypt forest Chard M, Foster CN, Lindenmayer DB, Cary GJ, MacGregor CI, Blanchard W Ecol Evol 23-Apr-2022
PMCID:PMC9034452
doi:10.1002/ece3.8828
PMID:35475176
First Multi-Organ Full-Length Transcriptome of Tree Fern Alsophila spinulosa Highlights the Stress-Resistant and Light-Adapted Genes Hong Y, Wang Z, Li M, Su Y, Wang T Front Genet 04-Feb-2022
PMCID:PMC8854977
doi:10.3389/fgene.2021.784546
PMID:35186007
Spatial associations between plants and vegetation community characteristics provide insights into the processes influencing plant rarity Sritharan MS, Scheele BC, Blanchard W, Lindenmayer DB PLoS One 20-Dec-2021
PMCID:PMC8687526
doi:10.1371/journal.pone.0260215
PMID:34928957
Phylogenetic relationships among fern rust fungi and Desmella lygodii comb. nov. Okane I, Ono Y, Ohmachi K, Aime MC, Yamaoka Y Mycoscience 20-Nov-2021
PMCID:PMC9721508
doi:10.47371/mycosci.2021.06.006
PMID:37090176
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia Lebel T, Douch J, Tegart L, Vaughan L, Cooper JA, Nuytinck J Persoonia 03-Aug-2021
PMCID:PMC10486632
doi:10.3767/persoonia.2021.47.01
PMID:37693797

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
Thermospine 638234 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
N-Methylcytisine 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 unknown via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 21586634 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown via CMAUP database
(1R,2R,9R,17R)-9-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 15385686 Click to see C1CC2C3CC=CC(=O)N3CC4(C2N(C1)CCC4)O 262.35 unknown via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 21763818 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
5,9-Dihydroxymatrine 14274649 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown via CMAUP database
Allomatrine 7000681 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Isomatrine 5271984 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Matrine 91466 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Sophoranol 12442899 Click to see C1CC2C3CCCN4C3C(CCC4)(CN2C(=O)C1)O 264.36 unknown via CMAUP database
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Lupanine 91471 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
4-Vinylphenol 62453 Click to see C=CC1=CC=C(C=C1)O 120.15 unknown https://doi.org/10.1016/0031-9422(93)85251-L
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(4aR,5S,8S,8aS)-3-(hydroxymethyl)-8-methyl-5-prop-1-en-2-yl-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one 163014021 Click to see CC1CCC(C2C1CC(=O)C(=C2)CO)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(93)85251-L
3-(hydroxymethyl)-8-methyl-5-prop-1-en-2-yl-4a,5,6,7,8,8a-hexahydro-1H-naphthalen-2-one 163014020 Click to see CC1CCC(C2C1CC(=O)C(=C2)CO)C(=C)C 234.33 unknown https://doi.org/10.1016/0031-9422(93)85251-L
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3aR,7S,7aR)-7-hydroxy-2-(hydroxymethyl)-2,5,7-trimethyl-3a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,7a-dihydroindene-6,1'-cyclopropane]-1-one 162848659 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)(C)CO)OC4C(C(C(C(O4)CO)O)O)O 428.50 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
7-Hydroxy-2-(hydroxymethyl)-2,5,7-trimethyl-3a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,7a-dihydroindene-6,1'-cyclopropane]-1-one 162848658 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)(C)CO)OC4C(C(C(C(O4)CO)O)O)O 428.50 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 21636205 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 1251.40 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
7-hydroxy-2-(hydroxymethyl)-5,7-dimethyl-3a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[3,7a-dihydro-2H-indene-6,1'-cyclopropane]-1-one 163091870 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)CO)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
Aquilide A 160303 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
Braxin C 53297436 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown https://doi.org/10.1016/0031-9422(93)85251-L
https://doi.org/10.1016/S0021-9673(01)88870-1
Ptaquiloside 13962857 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
Ptesculentoside 101502412 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)CO)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown https://doi.org/10.1016/J.TETLET.2010.02.032
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(4-ethenylphenoxy)-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 162960657 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 414.40 unknown https://doi.org/10.1016/0031-9422(93)85251-L
4-Ethenylphenyl beta-D-glucopyranoside 182338 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 282.29 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Glucopyranoside, p-vinylphenyl 13964527 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 282.29 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Ptelatoside A 13964506 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 414.40 unknown https://doi.org/10.1016/0031-9422(93)85251-L
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see CC1=CN=C(N1)C 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see CC1=CN=CN1 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10831417 Click to see COC1C2C(C3(CCC(=O)C=C3O1)OC)OC4=CC5=C(C=C24)OCO5 346.30 unknown via CMAUP database
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10496772 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=CC5=C(C=C24)OCO5 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=C2C=CC(=C4)OC 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Sophoramine 169014 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 244.33 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Isokuraramine 101665417 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran 15953774 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C 338.40 unknown via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran 44260109 Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
3,4-Dihydroxy cinnamic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone 118975901 Click to see CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 38351420 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O)C 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one 44584091 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 11351168 Click to see CC1(CCC2=CC(=C(C=C2O1)O)C3C(C(=O)C4=C(O3)C5=C(C=C4O)OC(CC5)(C)C)O)C 440.50 unknown via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one 102004822 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 26209050 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
(2S)-2'-methoxykurarinone 11982641 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C 370.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one 44563122 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O 426.50 unknown via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 60039901 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-Euchrenone A7 44593508 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C 354.40 unknown via CMAUP database
7,2',4'-Trihydroxy-8-lavandulyl-5-methoxyflavanone 11982640 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown via CMAUP database
CID 102004745 102004745 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C 492.60 unknown via CMAUP database
Isobavachin 193679 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 456.50 unknown via CMAUP database
Kushenol A 44563121 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown via CMAUP database
Kushenol I 20832634 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown via CMAUP database
Kushenol L 21721878 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C 440.50 unknown via CMAUP database
Kushenol M 180948 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown via CMAUP database
Kushenol R 42607847 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 422.50 unknown via CMAUP database
Kushenol S 10854625 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C 340.40 unknown via CMAUP database
Kushenol U 42608062 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C)C)C 422.50 unknown via CMAUP database
KushenolK 44428630 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
Leachianone A 44593449 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C 356.40 unknown via CMAUP database
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol 5481964 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 11451469 Click to see CC1(CCC2=C3C(=C(C=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)C 368.40 unknown via CMAUP database
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Flavenochromane B 11327657 Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=C(O3)C5=CC=C(C=C5)O)O)C 422.50 unknown via CMAUP database
Isoanhydroicaritin 5322079 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 368.40 unknown via CMAUP database
Kushenol C 5481237 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 438.50 unknown via CMAUP database
Kushenol G 44259516 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O 456.50 unknown via CMAUP database
Sophoflavescenol 9929189 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 57369598 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(93)85251-L
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Leucoside 44566720 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Rustoside 74977996 Click to see C1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 580.50 unknown https://doi.org/10.1016/0031-9422(93)85251-L
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 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 via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5318902 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain-3-O-glucosyl-6''-O-malonate 23724669 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6 532.40 unknown via CMAUP database
(-)-Variabilin 442828 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
(+)-Maackiain 161298 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 6326060 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol 361910 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC(=C(C=C4O3)O)O 286.28 unknown via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 21676223 Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown via CMAUP database
(6aS,12aS)-6abeta,12abeta-Dihydro-3-methoxy-6H-[1,3]dioxolo[5,6]benzofuro[3,2-c][1]benzopyran 373519 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown via CMAUP database
CID 44428627 44428627 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
Pterocarpin 1715306 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone 5284648 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101238023 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one 101238024 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 382.40 unknown via CMAUP database
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
Lupalbigenin 10001388 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 406.50 unknown via CMAUP database
Luteone 5281797 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 73603979 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
3'-Hydroxy-4'-methoxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 73603978 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
3'-Hydroxydaidzin 68607439 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131642 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
3',4'-(Epoxymethanoxy)-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131643 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O 576.50 unknown via CMAUP database
Calycosin 7-O-xylosylglucoside 73603980 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O 548.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 284.26 unknown via CMAUP database
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridine 44428631 Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C 438.50 unknown via CMAUP database
Xanthohumol 639665 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione 73603972 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(C(CO4)O)O)O)O)O)O)O)O 582.50 unknown via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione 73603983 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 582.50 unknown via CMAUP database

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