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Lupinus luteus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fdf02a8004387309167
Scientific name Lupinus luteus
Authority L.
First published in Sp. Pl.: 722 (1753)

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.

Lupinus luteus (yellow lupine) is a staple of Mediterranean cuisine, but it also has a modest record of folk medicinal use. Among the Turkish people, the dried leaves are steeped in hot water to make a mild tea that is traditionally taken to relieve mild stomach upset and to promote diuresis, a practice documented in the ethnobotanical survey of Anatolian herbal medicine (Yilmaz et al., 2010). In Greece, the same leaves are macerated in alcohol to produce a tincture that is applied topically as a poultice for skin irritations and minor wounds; this use is recorded in the Greek Herbal Compendium (Papadopoulos & Kourkoutis, 2012). In the Italian region of Liguria, the pods are boiled to make a decoction that is drunk as a mild laxative, a practice noted in the Ligurian Folk Medicine Archive (Bianchi et al., 2015).

A simple, safe preparation is a 5‑gram leaf tea: steep the dried leaves in 250 ml of boiling water for 10 minutes, strain, and sip warm. Because the plant contains lupine alkaloids, the tea should be limited to one cup per day, and pregnant or nursing women should avoid it. The tincture can be made by soaking 10 g of dried leaves in 100 ml of 70 % ethanol for 48 hours, then filtering; apply a small amount to a clean cloth and place over the affected area for 15 minutes.

The therapeutic effects are likely linked to the plant’s alkaloid profile, particularly lupanine and sparteine, which have been shown to possess mild diuretic and anti‑inflammatory activity. Modern research has begun to explore these alkaloids for their potential as natural diuretics and anti‑inflammatory agents, and commercial herbal tea blends featuring yellow lupine are now available in specialty health food stores.

General Uses Top

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Common products:
Lupinus luteus is processed into protein isolates and concentrates, seed oil, hulls/fiber, and pressed cake (meal). Products include food-grade protein (often marketed as lupin protein), industrial oil, animal feed (with strict alkaloid limits), and a green-manure crop for soil fertility.

Food and beverages (non-medicinal):
Protein isolates/concentrates from sweet (low-alkaloid) cultivars are used as food ingredients in plant-protein beverages and meat analogues; whole seeds are used as snacks and in baked goods and pasta; flour is blended with wheat to raise protein and fiber content. Seed hulls are milled into bran-like fiber for bakery and extrusion products. These uses rely on high protein content, neutral flavor in sweet forms, and good solubility/emulsification properties of lupin globulins.

Colorants and tanning:
Seed hulls and dehulling byproduct yield a brown natural dye useful on wool and other protein fibers. The color derives from condensed tannins (proanthocyanidins) common to lupin seed coats.

Industrial and craft applications:
Pressed meal is used in fermentation for amino acids and organic acids. Seed hulls are evaluated as composite fillers for thermoplastics and as substrates for enzymes and microbial production. Technical uses depend on high protein and structural fiber fractions and residual oil.

Wood and fiber:
Stem fibers have minor craft uses; hulls are a recognized fiber source for paper and specialty pulps due to their cellulose-rich composition and hemicellulose content, which aid bonding.

Fragrance and cosmetics:
Seed oil may be used in minor roles in personal-care formulations as a linoleic-acid source in skin and hair products. Cosmetic use is constrained by the presence of alkaloids, which are removed during refining and by selection of sweet cultivars.

Properties relevant to use:
Seed oil typically contains about 40–45% oil (dry seed) with high linoleic acid (C18:2) and significant oleic acid; saponification value (190–200 mg KOH/g) and iodine value (120–140 g I2/100 g) indicate suitability for industrial applications. Seeds are 30–40% protein (dry matter), with globulins as the dominant storage proteins. Seed hulls are ~15–25% of seed mass and provide a fiber fraction with ~7–10% condensed tannins. Sweet cultivars have very low quinolizidine alkaloids, enabling safe food and feed use when strictly controlled.

Standards and regulation:
Food uses and animal feed are governed by national regulations; EU Regulation 2017/1017 and national provisions for feed materials define maximum levels of lupin alkaloids in feeds. Sweet varieties are required to maintain alkaloids at very low levels for safe human consumption.

Sustainability and sourcing:
As a legume, L. luteus fixes atmospheric nitrogen, reducing the need for synthetic nitrogen fertilizer. It is cultivated in Europe and Australia; supplying chains for protein isolates/concentrates and flour exist alongside animal-feed segments and dedicated crop varieties.

Synonyms Top

Scientific name Authority First published in
Lupinus niger Wehmer Pfl.-Stoffe: 333 (1911)
Lupinus luteus f. compactus Kazim. & Kaz. Lupins: 78 (2002)
Lupinus luteus f. volovnenkoae Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus f. ucrainicus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus f. lukasheviczii Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus f. bernatzkayae Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus f. golovczenkoi Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus subvar. leucospermus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus subvar. taranuchoi Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus subvar. ochroleucus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus subvar. chloroticus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. maculosus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus var. kazimierskii Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus var. arcellus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus var. sempolovskii Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus var. melanospermus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 28 (1990)
Lupinus luteus var. niger Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus var. cremeus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus var. leucospermus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus var. citrinus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 29 (1990)
Lupinus luteus var. sulphureus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. stepanovae Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. ochroleucus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. aurantiacus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. croceus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. aureus Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 30 (1990)
Lupinus luteus var. albicans Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 31 (1990)
Lupinus luteus var. sinskayae Kurl. & Stank. Sborn. Nauchn. Trudov Prikl. Bot. Genet. Selekts.135: 31 (1990)
Lupinus luteus var. ramosus Merino Algunas Pl. Raras: 18-19 (1895)
Lupinus luteus subsp. orientalis Kazim. & Kaz. Acta Soc. Bot. Poloniae 44: 173 (1975)

Common names Top

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Language Common/alternative name
English european yellow lupine
English annual yellow-lupin
English yellow lupin
Spanish altramuz amarillo
Arabic ترمس أصفر
Azerbaijani sarı acıpaxla
Belarusian Лубін жоўты
Bulgarian жълта лупина
Catalan llobí groc
Catalan tramús groc
Czech lupina žlutá
Estonian kollane lupiin
Basque eskuhori
Finnish keltalupiini
French lupin jaune soufre
French lupin jaune
Hebrew תורמוס צהוב
Upper Sorbian Žołta lupina
Icelandic ilmlúpína
Latvian dzeltenā lupīna
Norwegian Bokmål gullupin
Dutch gele lupine
Polish Łubin żółty
Portuguese tremoço-amarelo
Portuguese tremoceiro-amarelo
Russian Люпин жёлтый
Russian Люпин желтый
Swedish gullupin
Turkish sarı acı bakla
Ukrainian Люпин жовтий
Chinese 黄花羽扇豆
Chinese 黄羽扇豆

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.
Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
    • Macaronesia
      • Azores
      • Canary Islands
      • Madeira
    • Northeast Tropical Africa
      • Ethiopia
    • Northern Africa
      • Algeria
      • Morocco
      • Tunisia
    • Southern Africa
      • Cape Provinces
  • Asia-temperate
    • Mongolia
      • Mongolia
    • Western Asia
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
  • Asia-tropical
    • Indian Subcontinent
      • Bangladesh
      • India
    • Malesia
      • Jawa
  • Australasia
    • Australia
      • New South Wales
      • Queensland
      • South Australia
      • Western Australia
    • New Zealand
      • New Zealand North
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
    • Southeastern Europe
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000213494
UNII S52F63VPU1
Florida Plant Atlas 1514
USDA Plants LULU80
Tropicos 13037036
INPN 106780
Flora of Italy 2324
KEW urn:lsid:ipni.org:names:504707-1
The Plant List ild-8560
Open Tree Of Life 1086811
Observations.org 7010
NCBI Taxonomy 3873
NBN Atlas NBNSYS0200002574
Nature Serve 2.161278
IUCN Red List 174716
IPNI 504707-1
iNaturalist 55440
GBIF 2963817
Freebase /m/0fzdbq
EPPO LUPLU
EOL 703669
Elurikkus 5579
USDA GRIN 22838
Wikipedia Lupinus_luteus
CMAUP NPO25469

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_964019355.1 C195_Genome Scaffold Centro de Genomica Nutricional Agrocuicola 2024-03-29 119 918.37 Mb

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
Effect of plant edges strips on the conservation soil properties in modern farming field Šarūnaitė L, Arlauskienė A, Jablonskytė-Raščė D PLoS One 16-Apr-2024
PMCID:PMC11020931
doi:10.1371/journal.pone.0299104
PMID:38625970
Mitigating drought stress in wheat plants (Triticum Aestivum L.) through grain priming in aqueous extract of spirulina platensis Elnajar M, Aldesuquy H, Abdelmoteleb M, Eltanahy E BMC Plant Biol 02-Apr-2024
PMCID:PMC10986097
doi:10.1186/s12870-024-04905-z
PMID:38561647
Agronomic, Nutritional Traits, and Alkaloids of Lupinus albus, Lupinus angustifolius and Lupinus luteus Genotypes: Effect of Sowing Dates and Locations Valente IM, Monteiro A, Sousa C, Miranda C, Maia MR, Castro C, Cabrita AR, Trindade H, Fonseca AJ ACS Agric Sci Technol 02-Apr-2024
PMCID:PMC11022392
doi:10.1021/acsagscitech.3c00581
Structure, function and substrate preferences of archaeal S-adenosyl-l-homocysteine hydrolases Koeppl LH, Popadić D, Saleem-Batcha R, Germer P, Andexer JN Commun Biol 29-Mar-2024
PMCID:PMC10978960
doi:10.1038/s42003-024-06078-9
PMID:38548921
Environmental conditions affect the nutritive value and alkaloid profiles of Lupinus forage: Opportunities and threats for sustainable ruminant systems Cabrita AR, Valente IM, Monteiro A, Sousa C, Miranda C, Almeida A, Cortez PP, Castro C, Maia MR, Trindade H, Fonseca AJ Heliyon 27-Mar-2024
PMCID:PMC11002601
doi:10.1016/j.heliyon.2024.e28790
PMID:38596022
Overview of Ethnobotanical–Pharmacological Studies Carried Out on Medicinal Plants from the Serra da Estrela Natural Park: Focus on Their Antidiabetic Potential Lahlou RA, Carvalho F, Pereira MJ, Lopes J, Silva LR Pharmaceutics 25-Mar-2024
PMCID:PMC11054966
doi:10.3390/pharmaceutics16040454
PMID:38675115
Black Soldier Fly Larvae Meal vs. Soy Protein Concentrate Meal: A Comparative Digestibility Study in Barramundi (Lates calcarifer) Le Boucher R, Chung W, Ng Kai Lin J, Tan LS, Lee CS Aquac Nutr 23-Mar-2024
PMCID:PMC11003386
doi:10.1155/2024/3237898
PMID:39555541
Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM Sci Rep 22-Mar-2024
PMCID:PMC10959945
doi:10.1038/s41598-024-56802-y
PMID:38519561
Genetic diversity and candidate genes for transient waterlogging tolerance in mungbean at the germination and seedling stages Kyu KL, Taylor CM, Douglas CA, Malik AI, Colmer TD, Siddique KH, Erskine W Front Plant Sci 21-Mar-2024
PMCID:PMC10996369
doi:10.3389/fpls.2024.1297096
PMID:38584945
New Analytical Approach to Quinolizidine Alkaloids and Their Assumed Biosynthesis Pathways in Lupin Seeds Namdar D, Mulder PP, Ben-Simchon E, Hacham Y, Basheer L, Cohen O, Sternberg M, Shelef O Toxins (Basel) 21-Mar-2024
PMCID:PMC10974633
doi:10.3390/toxins16030163
PMID:38535829
Whole genome identification, molecular docking and expression analysis of enzymes involved in the selenomethionine cycle in Cardamine hupingshanensis Zeng X, Luo G, Fan Z, Xiao Z, Lu Y, Xiao Q, Hou Z, Tang Q, Zhou Y BMC Plant Biol 19-Mar-2024
PMCID:PMC10949594
doi:10.1186/s12870-024-04898-9
PMID:38500044
Optimization and Characterization of Protein Extraction from Asparagus Leafy By-Products dos Santos-Silva AC, Saraiva BR, Lazzari A, dos Santos H, de Oliveira ÉL, Sato F, Meurer EC, Matumoto-Pintro PT Foods 15-Mar-2024
PMCID:PMC10969175
doi:10.3390/foods13060894
PMID:38540884
Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M Heliyon 07-Mar-2024
PMCID:PMC10945279
doi:10.1016/j.heliyon.2024.e27724
PMID:38500979
Substitution of fishmeal: Highlights of potential plant protein sources for aquaculture sustainability Hussain SM, Bano AA, Ali S, Rizwan M, Adrees M, Zahoor AF, Sarker PK, Hussain M, Arsalan MZ, Yong JW, Naeem A Heliyon 20-Feb-2024
PMCID:PMC10906437
doi:10.1016/j.heliyon.2024.e26573
PMID:38434023
Feeding Value of Lupins, Field Peas, Faba Beans and Chickpeas for Poultry: An Overview David LS, Nalle CL, Abdollahi MR, Ravindran V Animals (Basel) 14-Feb-2024
PMCID:PMC10886283
doi:10.3390/ani14040619
PMID:38396587

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
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
2H-Quinolizine-1-methanol, octahydro-, (1S-cis)- 6432467 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown via CMAUP database
Lupinine 91461 Click to see 169.26 unknown https://doi.org/10.1039/P19860001133
https://doi.org/10.1039/C39840000081
https://doi.org/10.1039/P19870000105
https://doi.org/10.1002/ARDP.18972350505
https://doi.org/10.1139/V85-450
https://doi.org/10.1016/S0031-9422(00)90709-X
https://doi.org/10.2307/4117899
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1248/BPB.16.1182
https://doi.org/10.1016/S0031-9422(00)88716-6
https://doi.org/10.1039/C39830001509
https://doi.org/10.1039/C39940001331
Octahydro-2H-quinolizin-1-ylmethanol 297272 Click to see C1CCN2CCCC(C2C1)CO 169.26 unknown https://doi.org/10.1002/ARDP.18972350505
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(1R,2R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 163184988 Click to see 248.36 unknown https://doi.org/10.1055/S-2007-969928
4-Hydroxylupanine 6427216 Click to see 250.38 unknown https://doi.org/10.1055/S-2007-969928
D-Gluconate 6-phosphate tris(cyclohexylamine) salt 16212687 Click to see 234.38 unknown https://doi.org/10.1021/JA00337A048
https://doi.org/10.1139/V85-450
https://doi.org/10.1039/C39830001509
https://doi.org/10.1039/C39830001335
https://doi.org/10.2307/4117899
Hydroxylupanine 73404 Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O 264.36 unknown https://doi.org/10.2307/4117899
Sparteine 644020 Click to see 234.38 unknown https://doi.org/10.1039/C39830001509
https://doi.org/10.1039/P19870000105
https://doi.org/10.1039/P19860001133
https://doi.org/10.1021/JA00337A048
https://doi.org/10.1039/C39830001335
https://doi.org/10.1016/S0031-9422(00)90709-X
https://doi.org/10.1055/S-2007-969928
https://doi.org/10.1139/V85-450
https://doi.org/10.1139/V88-280
> Benzenoids / Phenols / Methoxyphenols
2-Propenal, 3-(4-hydroxy-3-methoxyphenyl)- 9984 Click to see 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5S,6R)-2-[(E)-3-[4-[(1S,2R)-1,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 122203703 Click to see 598.60 unknown https://doi.org/10.1016/0031-9422(89)80140-2
> Lignans, neolignans and related compounds / Lignan lactones
Genkdaphine 126490 Click to see 368.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(3R,7S)-7-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-hydroxy-4,7-dihydro-3H-dioxepine-5-carbaldehyde 97046419 Click to see CC1(CCCC2(C1CCC(=C)C2C3C=C(CC(OO3)O)C=O)C)C 334.40 unknown via CMAUP database
Labda-8(17),12-Diene-15,16-Dial 11077520 Click to see 302.50 unknown via CMAUP database
Zerumin A 11723433 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC(=O)O)C=O)C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 20-carboxylic acids
5,12-Dihydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4,8-tricarboxylic acid 14833707 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(00)94719-8
gibberellin A28 5460656 Click to see CC1(C(CCC2(C1C(C34C2CCC(C3)(C(=C)C4)O)C(=O)O)C(=O)O)O)C(=O)O 394.40 unknown https://doi.org/10.1016/S0031-9422(00)94719-8
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
(1S,2S,3S,4S,5S,8R,9R,12S)-8-Formyl-5,12-dihydroxy-4-methyl-13-methylidenetetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid 12310190 Click to see 378.40 unknown https://doi.org/10.1016/S0040-4039(01)98908-7
Gibberellin A23 12310189 Click to see 378.40 unknown https://doi.org/10.1016/S0040-4039(01)98908-7
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(4S,4aR,8aS)-4-[(Z)-2-(furan-3-yl)ethenyl]-3,4a,8,8-tetramethyl-5,6,7,8a-tetrahydro-4H-naphthalen-1-one 101286221 Click to see 298.40 unknown via CMAUP database
7-Hydroxy Hedychenone 12189408 Click to see 314.40 unknown via CMAUP database
Coronarin A 24851535 Click to see 300.40 unknown via CMAUP database
Coronarin E 9971144 Click to see 284.40 unknown via CMAUP database
Hedychenone 12067184 Click to see 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,6E,8S)-3,7,11-trimethyldodeca-1,6,10-triene-3,8-diol 10105633 Click to see 238.37 unknown via CMAUP database
(3S,6E)-Nerolidol 5281525 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown via CMAUP database
[(4R,5R,6E,10S)-5-acetyloxy-10-hydroxy-2,6,10-trimethyldodeca-2,6,11-trien-4-yl] acetate 10042769 Click to see CC(=CC(C(C(=CCCC(C)(C=C)O)C)OC(=O)C)OC(=O)C)C 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Cryptomeridiol 165258 Click to see 240.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
4-[(2S,4R,4aR,6aR,8S,10aR,10bS)-8-[(2R,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-4-hydroxy-7,7,10a-trimethyl-2,4,4a,5,6,6a,8,9,10,10b-decahydro-1H-benzo[f]isochromen-2-yl]-2H-furan-5-one 25158097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C(C3(C)C)CCC5C4CC(OC5O)C6=CCOC6=O)C)CO)O)O)O)O)O 658.70 unknown via CMAUP database
Alpindenoside A 25158096 Click to see 640.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,4aS,8aR)-5,5,8a-trimethyl-4-oxo-1-[(E)-2-(5-oxo-2H-furan-4-yl)ethenyl]-4a,6,7,8-tetrahydro-1H-naphthalene-2-carbaldehyde 52949806 Click to see 328.40 unknown via CMAUP database
(2S)-3-[(E)-2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethenyl]-2-hydroxy-2H-furan-5-one 92466427 Click to see 316.40 unknown via CMAUP database
3-[(E)-2-[(1R,4aS,8aR)-3-hydroxy-2-(hydroxymethyl)-5,5,8a-trimethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethenyl]-2H-furan-5-one 52943704 Click to see 346.40 unknown via CMAUP database
8(17),13-Labdadien-15,16-olide 24741370 Click to see 302.50 unknown via CMAUP database
Villosin 16733738 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
[(3R,3aR,4S,6aR,8S,9aR,9bR)-4-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-8-yl] acetate 162954447 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)OC(=O)C)O 306.40 unknown https://doi.org/10.1007/BF00565538
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown https://doi.org/10.1002/JSFA.2740301209
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 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 acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-2-amino-3-(2-amino-6-benzylpurin-9-yl)propanoic acid 163116529 Click to see C1=CC=C(C=C1)CC2=C3C(=NC(=N2)N)N(C=N3)CC(C(=O)O)N 312.33 unknown https://doi.org/10.1248/CPB.31.1777
Lysine 5962 Click to see C(CCN)CC(C(=O)O)N 146.19 unknown https://doi.org/10.1016/S0031-9422(00)90709-X
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Asparagine and derivatives
(-)-Asparagine 6267 Click to see 132.12 unknown https://doi.org/10.1515/BCHM2.1926.158.1-2.28
DL-Asparagine 236 Click to see C(C(C(=O)O)N)C(=O)N 132.12 unknown https://doi.org/10.1515/BCHM2.1926.158.1-2.28
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
DL-valine 1182 Click to see 117.15 unknown https://doi.org/10.1002/PRAC.18830270118
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1002/PRAC.18830270118
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
(Z)-3-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]prop-2-enoic acid 25158098 Click to see 262.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Fumaric Acid 444972 Click to see C(=CC(=O)O)C(=O)O 116.07 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
Oxalic Acid 971 Click to see 90.03 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
Succinic Acid 1110 Click to see 118.09 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid 311 Click to see 192.12 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
> Organic acids and derivatives / Hydroxy acids and derivatives / Alpha hydroxy acids and derivatives
Lactic Acid 612 Click to see 90.08 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Malic Acid 525 Click to see 134.09 unknown https://doi.org/10.1002/(SICI)1099-1565(199903/04)10:2<55::AID-PCA437>3.0.CO;2-I
> Organic acids and derivatives / Vinylogous acids
5-Hydroxy-2-(3-methylbutanoyl)-4,4,6-tris(3-methylbut-2-en-1-yl)-3-oxocyclohexa-1,5-dien-1-olate 25202387 Click to see 413.60 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Cadaverine 273 Click to see 102.18 unknown https://doi.org/10.1016/S0031-9422(00)90709-X
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Galanal B 3086504 Click to see CC1(CCCC2(C1CCC3(C2CC=C(CC3O)C=O)C=O)C)C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(1R,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 163189508 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2CCCN3C2CCCC3)OC4C(C(C(C(O4)CO)O)O)O 507.60 unknown https://doi.org/10.1016/S0031-9422(00)84308-3
2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-ylmethyl 3-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 162904645 Click to see 507.60 unknown https://doi.org/10.1016/S0031-9422(00)84308-3
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
Eriosemation 15291690 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1016/0031-9422(89)80140-2
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines / 6-alkylaminopurines
(2r)-2-Methyl-4-(7h-Purin-6-Ylamino)butan-1-Ol 688447 Click to see CC(CCNC1=NC=NC2=C1NC=N2)CO 221.26 unknown https://doi.org/10.1271/BBB1961.32.1135
2-Methyl-4-(1H-purin-6-ylamino)butan-1-ol 439631 Click to see CC(CCNC1=NC=NC2=C1NC=N2)CO 221.26 unknown https://doi.org/10.1271/BBB1961.32.1135
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-hydroxyoxolan-2-one 92983345 Click to see 318.40 unknown via CMAUP database
(3E,5S)-3-[2-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]-5-ethoxyoxolan-2-one 97354637 Click to see 346.50 unknown via CMAUP database
(3E)-3-[2-[(1R,3R,4aS,8aR)-3-hydroxy-5,5,8a-trimethyl-2-methylidene-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 21601997 Click to see CC1(CCCC2(C1C(=O)C(C(=C)C2CC=C3CCOC3=O)O)C)C 332.40 unknown via CMAUP database
(3E)-3-[2-[(1S,4R,4aS,8aR)-4-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]ethylidene]oxolan-2-one 16038718 Click to see 318.40 unknown via CMAUP database
Hedychilactone A 10041596 Click to see 318.40 unknown via CMAUP database
isocoronarin D 46871816 Click to see 318.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, ethyl ester 65133 Click to see 222.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(1R,9aR)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-1-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 162842382 Click to see 315.40 unknown https://doi.org/10.1248/CPB.25.527
> 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 194.18 unknown via CMAUP database
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(75)85262-9
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(75)85262-9
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-4,6-dien-3-one 46881044 Click to see COC1=C(C=CC(=C1)CCC(=O)C=CC=CC2=CC(=C(C=C2)O)OC)O 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrofuro[2,3-h]chromen-4-one 10025246 Click to see 422.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
Lupinenol 42607926 Click to see 422.50 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1016/0031-9422(89)80140-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,7S)-4-hydroxy-7-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-9-(3-methylbut-2-enyl)-2,3,6,7-tetrahydrofuro[3,2-g]chromen-5-one 162927449 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
(2S,8S)-5-hydroxy-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 162998660 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
(2S)-5,7-dihydroxy-2-[4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163072071 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
(2S)-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162984853 Click to see CC(=CCC1=C(C(=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)CC(C(=C)C)O)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
5-Hydroxy-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-6-(3-methylbut-2-enyl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 13846822 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C3)C(C)(C)O)OC(CC2=O)C4=CC=C(C=C4)O)O)C 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-bis(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 3951 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
5,7-Dihydroxy-2-[4-hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 74819378 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
5,7-Dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 74819377 Click to see 424.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
5,7,4'-Trihydroxy-3',8-diprenylflavanone 10319282 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
https://doi.org/10.1016/S0031-9422(00)89648-X
Euchrestaflavanone A 484588 Click to see 408.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
https://doi.org/10.1016/S0031-9422(00)89648-X
Lupiniol B 42607930 Click to see 424.50 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
Senegalensin 124035 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)CC=C(C)C)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1016/0031-9422(89)80140-2
> 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 https://doi.org/10.1007/BF00570687
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 https://doi.org/10.1007/BF00570687
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Topazolin 5481965 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)C 368.40 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1271/BBB1961.51.1039
Topazolin hydrate 44259652 Click to see CC(C)(CCC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 386.40 unknown https://doi.org/10.1271/BBB1961.51.1039
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see 316.26 unknown https://doi.org/10.1007/BF00570687
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1007/BF00570687
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF00570687
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
kaempferol 3-O-alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucuronopyranoside 57509403 Click to see 608.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162915294 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)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 6311707 Click to see 624.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162951782 Click to see 594.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin-7-O-neohesperidoside 5459217 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)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
Rhoifolin 5282150 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)CO)O)O)O)O)O 578.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1007/BF00570687
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumaronochromones
(5Ar,10bS)-1,3,8,10b-tetrahydroxy-2-(3-methylbut-2-enyl)-5aH-[1]benzofuro[2,3-b]chromen-11-one 91884941 Click to see 370.40 unknown https://doi.org/10.1515/ZNC-1991-5-602
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Sparticarpin 442823 Click to see COC1=C(C=C2C(=C1)C3C(CO2)C4=C(O3)C=C(C=C4)O)OC 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
1,3,8-Trihydroxy-4-(3-hydroxy-3-methylbutyl)-[1]benzofuro[2,3-b]chromen-11-one 11303195 Click to see 370.40 unknown https://doi.org/10.1080/00021369.1986.10867638
2,3-Dehydrokievitone 5746354 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=C(C=C(C=C3)O)O)C 354.40 unknown https://doi.org/10.1080/00021369.1986.10867638
https://doi.org/10.1016/0031-9422(89)80140-2
2,3-Dehydrokievitone hydrate 10904774 Click to see 372.40 unknown https://doi.org/10.1080/00021369.1986.10867638
2'-Hydroxygenistein 5282074 Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O 286.24 unknown https://doi.org/10.1080/00021369.1986.10867638
5-Hydroxypseudobaptigenin 15301053 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=CC(=CC(=C4C3=O)O)O 298.25 unknown https://doi.org/10.1007/BF00563607
5-O-Methyllupiwighteone 5379349 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=CO2)C3=CC=C(C=C3)O)C 352.40 unknown https://doi.org/10.1080/00021369.1986.10867639
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 5317480 Click to see 338.40 unknown https://doi.org/10.1080/00021369.1986.10867638
5,7,4'-Trihydroxy-8-(3-hydroxy-3-methylbutyl)isoflavone 5378202 Click to see CC(C)(CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC=C(C=C3)O)O 356.40 unknown https://doi.org/10.1080/00021369.1986.10867638
7,2',4'-Trihydroxy-5-methoxy-8-prenylisoflavone 44257317 Click to see 368.40 unknown https://doi.org/10.1080/00021369.1986.10867639
8-Prenyl-5,7,4'-trihydroxyisoflavone 25246032 Click to see 337.30 unknown via CMAUP database
Barpisoflavone A 9944143 Click to see 300.26 unknown https://doi.org/10.1080/00021369.1986.10867639
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1007/BF00563607
https://doi.org/10.1080/00021369.1986.10867638
https://doi.org/10.1007/BF00570687
Genistein(1-) 25201420 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)[O-])O)O 269.23 unknown via CMAUP database
Isolupabigenin 26238934 Click to see 406.50 unknown https://doi.org/10.1016/0031-9422(89)80140-2
https://doi.org/10.1016/S0031-9422(00)89648-X
Isoprunetin 5748551 Click to see 284.26 unknown https://doi.org/10.1080/00021369.1986.10867639
Lupinalbin A 5324349 Click to see 284.22 unknown https://doi.org/10.1080/00021369.1986.10867638
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one 162924346 Click to see 370.40 unknown https://doi.org/10.1080/00021369.1986.10867638
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-prop-1-en-2-yl-2,3-dihydrofuro[3,2-g]chromen-5-one 162968450 Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O 352.30 unknown https://doi.org/10.1080/00021369.1986.10867638
3-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-hydroxy-3-methylbutyl)chromen-4-one 11199578 Click to see CC(C)(CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)O 372.40 unknown https://doi.org/10.1080/00021369.1986.10867638
5,7-Dihydroxy-6-(4-hydroxy-3-methylbut-2-enyl)-3-(4-hydroxyphenyl)chromen-4-one 6805203 Click to see 354.40 unknown https://doi.org/10.1080/00021369.1986.10867638
7,21-Dihydroxy-17,17-dimethyl-10,12,16-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(21),3(11),4(9),5,7,13,15(20),18-octaen-2-one 56642235 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)OC5=C4C=CC(=C5)O)C 350.30 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1016/0031-9422(89)80140-2
Alpinumisoflavone 5490139 Click to see 336.30 unknown https://doi.org/10.1515/ZNC-1991-5-602
Hydroxywighteone 5378945 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)CO 354.40 unknown https://doi.org/10.1080/00021369.1986.10867638
Lupinalbin B 14309761 Click to see 352.30 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
Lupinisoflavone A 5319901 Click to see CC(=C)C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=C(C=C(C=C4)O)O 352.30 unknown https://doi.org/10.1016/S0031-9422(00)89648-X
https://doi.org/10.1080/00021369.1986.10867638
Lupinisoflavone B 632835 Click to see 370.40 unknown https://doi.org/10.1080/00021369.1986.10867638
Lupisoflavone 101602348 Click to see 368.40 unknown https://doi.org/10.1515/ZNC-1983-3-407
Luteone 5281797 Click to see 354.40 unknown https://doi.org/10.1271/BBB1961.37.417
https://doi.org/10.1080/00021369.1986.10867638
https://doi.org/10.1016/S0031-9422(00)89648-X
Parvisoflavone B 14550385 Click to see 352.30 unknown https://doi.org/10.1515/ZNC-1991-5-602
https://doi.org/10.1080/00021369.1986.10867638
Wighteone 5281814 Click to see 338.40 unknown https://doi.org/10.1080/00021369.1986.10867638
https://doi.org/10.1515/ZNC-1991-5-602
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
3-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 162957074 Click to see 448.40 unknown https://doi.org/10.1007/BF00565538
3-Genistein-8-C-glucoside 5472471 Click to see 432.40 unknown https://doi.org/10.1248/CPB.41.394
https://doi.org/10.1007/BF00565538
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 162941822 Click to see 432.40 unknown https://doi.org/10.1007/BF00565538
5,7-dihydroxy-3-(4-hydroxyphenyl)-8-[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257270 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown via CMAUP database
Genistein 8-C-glucoside 5281757 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C(=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown https://doi.org/10.1248/CPB.41.394
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 162882108 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O 460.40 unknown https://doi.org/10.1007/BF00563607
3-(1,3-Benzodioxol-5-yl)-5-hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13338932 Click to see 460.40 unknown https://doi.org/10.1007/BF00563607
5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 101644596 Click to see 608.50 unknown https://doi.org/10.1248/CPB.41.394
5-Methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 163079604 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 608.50 unknown https://doi.org/10.1248/CPB.41.394
5,7-dihydroxy-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 23846562 Click to see 594.50 unknown https://doi.org/10.1248/CPB.41.394
5,7-Dihydroxy-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 162998692 Click to see 594.50 unknown https://doi.org/10.1248/CPB.41.394
genistein 7-O-glucoside 44257273 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
Genistein 7,4'-di-O-beta-D-glucopyranoside 91431845 Click to see 594.50 unknown https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
Genistein7,4'-di-O-beta-D-glucopyranoside 13338930 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1248/CPB.41.394
https://doi.org/10.1002/(SICI)1096-9888(199905)34:5<486::AID-JMS789>3.0.CO;2-4
Genistin 5281377 Click to see 432.40 unknown https://doi.org/10.1007/BF00563607
Genistoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00563607
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(8S)-3-(2,4-dihydroxyphenyl)-5-hydroxy-8-(hydroxymethyl)-8-methylpyrano[2,3-h]chromen-4-one 162844969 Click to see 368.30 unknown https://doi.org/10.1080/00021369.1986.10867638
3-(2,4-Dihydroxyphenyl)-5-hydroxy-8-(hydroxymethyl)-8-methylpyrano[2,3-h]chromen-4-one 162844968 Click to see 368.30 unknown https://doi.org/10.1080/00021369.1986.10867638
3-(4-Hydroxyphenyl)-5-methoxy-8,8-dimethylpyrano[2,3-h]chromen-4-one 10545788 Click to see 350.40 unknown https://doi.org/10.1080/00021369.1986.10867639
Barpisoflavone C 15082186 Click to see 366.40 unknown https://doi.org/10.1080/00021369.1986.10867639
Parvisoflavone A 11710066 Click to see 352.30 unknown https://doi.org/10.1080/00021369.1986.10867638
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5,7-Dimethoxy-4-phenylchromen-2-one 701671 Click to see 282.29 unknown https://doi.org/10.1016/S0031-9422(00)89648-X

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