Details Top

Internal ID UUID643fd861e27a2291615861
Scientific name Cajanus cajan
Authority (L.) Millsp.

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.

Cajanus cajan, commonly known as pigeon pea, is used in several traditional medicinal systems for its soothing and antimicrobial properties. Among the people of Karnataka in southern India, the fresh leaves are boiled into a decoction and applied as a poultice to treat skin infections and eczema, according to Shukla et al., 2018. In southwestern Nigeria, the Yoruba gather the roots, dry them, and grind them into a powder that is mixed with water to make a decoction used to reduce fever and relieve headaches; Olatunde et al., 2015 report that this preparation is also taken orally for stomach upset. In Jamaica, the leaves are steeped in hot water to produce a mild tea that is drunk to alleviate coughs and sore throats, as documented by Smith et al., 2019. In all three cultures, the plant parts used are leaves, roots, and sometimes the pods, and the preparations are typically infusions or decoctions rather than tinctures or macerations.

A simple, safe recipe for a mild leaf tea is as follows: take 5 g of dried pigeon‑pea leaves, place them in a cup, pour 250 ml of boiling water over them, cover, and let steep for 10 minutes. Strain the liquid and drink one cup in the morning and one in the evening. This dosage is considered safe for most adults; however, high intake may cause mild gastrointestinal upset, and pregnant women are advised to avoid the tea because the plant contains compounds that may stimulate uterine contractions.

The therapeutic effects of pigeon pea are linked to several well‑established phytochemicals. The leaves contain flavonoids such as quercetin and kaempferol, which have anti‑inflammatory and antioxidant activities. They also contain saponins and tannins that contribute to antimicrobial action, and lectins that may help modulate immune responses. The roots and pods are rich in phenolic acids and alkaloids that have been shown in laboratory studies to reduce fever and inhibit bacterial growth.

Modern research continues to explore the antidiabetic, anti‑inflammatory, and antimicrobial potential of Cajanus cajan extracts, and the plant is now available in some markets as a herbal tea blend. Its long history of use in diverse cultures underscores its relevance as a natural remedy that bridges traditional knowledge and contemporary science.

General Uses Top

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Common products:
- Green pods and mature seeds are a vegetable and pulse legume; mature seeds are dehulled to split peas.
- Seed flour produced after dehulling and grinding.
- Fodder from leaves and young shoots; hay or silage.
- Fuelwood from mature stems.
- Green manure, cover crop, and mulch.

Industrial and craft applications:
- Stems provide fuelwood for household energy and small-scale industry; coppiced stems yield charcoal.
- Leaf and stem residues used as compost or green manure.
- Seed flour used as an adhesive and binder in paper and plywood; used as a paste and sizing agent in papermaking; also as a carrier and binder in feed pellets.
- Lignocellulose residues from threshing and processing used as fuel or composted.

Food and beverages (non-medicinal):
- Green pods consumed as a vegetable; mature seeds sold as dried peas or split peas.
- Dehulling and milling yields split peas and pea flour.
- Processing includes soaking, cooking, pressure cooking, sprouting, and fermentation.

Colorants and tanning:
- Leaves and stems contain tannins but are not reported as commercial tanning agents.

Wood and fiber:
- Mature stems used as fuelwood and for charcoal; also employed as stakes and light construction poles.

Fragrance and cosmetics:
- No documented fragrance or cosmetic uses.

Properties relevant to use:
- High protein content (about 20–25% in mature seeds) makes seed flour valuable as a binder in adhesives and sizing.
- Starch and protein content support binding action in paper and plywood; water solubility enables paste and sizing preparation.
- Leaf and stem biomass provides moderate organic matter and nutrients as green manure or compost.
- Fodder value derives from relatively high protein and digestibility of leaves and young shoots; palatability varies with stage of growth.

Standards and regulation:
- Food uses comply with national food standards for dried pulses and flour; conformity with general food labeling and hygiene regulations.
- Industrial uses such as animal feed and adhesives follow general product safety and compositional standards where applicable.

Sustainability and sourcing:
- Nitrogen-fixing ability improves soil fertility, reducing fertilizer requirements.
- Short rotation and adaptability enable multiple harvests per year in suitable climates, supporting resource efficiency and smallholder livelihoods.

Synonyms Top

Scientific name Authority First published in
Cajanus inodorum Medik.
Cajanus obcordifolius V.Singh
Phaseolus balicus L.
Cajan indorum Medik.
Cajan cajan (L.) Millsp. Publ. Field Columb. Mus., Bot. Ser. ii. 53. 1900 (as Cajan(us) cajan)
Cajan inodorum Medik. Vorles. Churpfälz. Phys.-Öcon. Ges. ii. (1787) 363.
Cytisus guineensis Schum. & Thonn.

Common names Top

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Language Common/alternative name
English pigeonpea
English tur
English pigeon pea
English gungo peas
English red gram
Spanish guandu
Spanish cytisus pseudo cajan
Spanish cytisus pseudo-cajan
Spanish guandul
Spanish cajan indorum
Spanish cajanus inodorum
Spanish cajanus obcordifolius
Spanish phaseolus balicus
ami fata'an
Arabic البازلاء الهندية (البسلة)
Azerbaijani göyərçin noxudu
azb گؤیرچین نوخودو
ban undis
Bulgarian гълъбов грах
bjn akar gudai
Bengali অড়হর ডাল
Bengali অড়হর
Catalan pèsol d'angola
Czech mestelice
Czech kajan indický
dag adua
German erbsenbohne
German taubenerbse
German straucherbse
dv މުގު ތޮޅި
Esperanto kajano
Estonian ambrevade
Estonian tuvihernes
Estonian harilik tuvihernes
Persian نخود کفتری
Finnish kyyhkyherne
Finnish kyyhkynherne
French ambrevade
French embrevade
French pois cajan
French pois d’angole
French pois-congo
French pois d'angole
French pois d'angole ( cajanus cajan)
gn kumanda yvyra'i
Gujarati તુવર
Gujarati તુવેર
Hausa wáákén sàntànbûl
Hausa waaken santanbul
Hebrew אפונת יונה
Hindi अरहर
Hindi अरहर की दाल
Hindi तुअर दाल
Hindi तुवर दाल
Hindi तूअर दाल
Hindi तूवर
Hindi अरहर दाल
ht pwa kongo
Hungarian kajánbab
Hungarian galambborsó
Indonesian gude
Indonesian kacang gude
ilo kardis
Icelandic dúfnabaun
Italian caiano
Japanese キマメ
jv kacang dara
Georgian მტრედიცერცვა
Kannada ತೊಗರಿ ಕಾಳು
Korean 비둘기콩
Latvian baložu zirņi
Latvian cūku zirņi
Latvian kajāns
mad guḍi
mai अरहर दाल
Malagasy amberivatry
Malagasy ambarivatry
Malagasy antsotry
Malagasy ambatry
Macedonian гулабов грашок
Malayalam pigeon pea
Malayalam തുവര
Marathi तुरी
Marathi तूर
Malay kacang dal
Norwegian Bokmål ertebønne
Nepali रहर(दाल)
Dutch duivenerwt
Norwegian Nynorsk ertebønne
ny nandalo
Oriya ହରଡ଼
Punjabi ਅਰਹਰ
pap wandu
Punjab ارہر
Portuguese guando
Portuguese guandu
pwn puk
Russian Голубиный горох
Russian Каянус
Russian Каянус индийский
Kinyarwanda itenderwa
Kinyarwanda umukunde
sa तुवरी
Slovenian golobji grah
su hiris
Swedish duvärt
Swahili mbaazi
szy taung
Tamil துவரம் பருப்பு
Tamil துவரை
Telugu ఎర్ర కంది పప్పు
Telugu క౦ది పప్పు
Telugu కజానస్ కజాన్
Telugu కందులు
Telugu కంది పప్పు
Thai ถั่วมะแฮะ
Tonga pī kula
trv sunguc
Urdu ارہر
Vietnamese Đậu triều
xmf ტორონხაჯი
Chinese 山豆根
Chinese 木豆
Chinese 木豆叶
Chinese 木豆根
Chinese 三叶豆
Chinese 扭豆
Chinese 官渡豆

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
      • Mauritius
      • Réunion
      • Seychelles
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • Caucasus
      • Transcaucasus
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
    • Middle Asia
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
  • Northern America
    • Mexico
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida
      • Maryland
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Marquesas
      • Society Islands
    • Southwestern Pacific
      • Nauru
      • New Caledonia
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
    • Caribbean
      • Bahamas
      • Bermuda
      • Cayman Islands
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Honduras
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000179103
UNII S1KB8A6Y1B
Florida Plant Atlas 1834
USDA Plants CACA27
Tropicos 13046795
INPN 448617
KEW urn:lsid:ipni.org:names:1152177-2
The Plant List ild-2524
PFAF Cajanus cajan
Open Tree Of Life 612448
Observations.org 115693
NCBI Taxonomy 3821
Nature Serve 2.141441
IPNI 1152177-2
iNaturalist 139444
GBIF 2960383
Freebase /m/0b2r0
EPPO CAJCA
EOL 643268
USDA GRIN 8319
Wikipedia Pigeon_pea
Plantarium 7275

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
GCF_000230855.1 NIPB_CcT2T_4 Chromosome AKI-PGI 2025-08-12 97 715.69 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
The association of protein-bound methionine sulfoxide with proteomic basis for aging in beech seeds Kalemba EM, Gevaert K, Impens F, Dufour S, Czerwoniec A BMC Plant Biol 08-May-2024
PMCID:PMC11077735
doi:10.1186/s12870-024-05085-6
PMID:38714916
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Synergistic Inhibition of Synbiotic Cultures among Lactobacilli and Plant Extracts against Vaginal Discharge Causing Candida albicans Sookkhee S, Khamnoi P, Sastraruji T, Boonkum S, Wikan N, Nimlamool W Nutrients 30-Apr-2024
PMCID:PMC11085874
doi:10.3390/nu16091372
PMID:38732618
Understanding the interactions of genotype with environment and management (G×E×M) to maize productivity in Conservation Agriculture systems of Malawi Mhlanga B, Gama M, Museka R, Thierfelder C PLoS One 29-Apr-2024
PMCID:PMC11057976
doi:10.1371/journal.pone.0298009
PMID:38683809
Exploring Gluten Assessment in Marketed Products through a Sandwich ELISA Methodology Based on Novel Recombinant Antibodies Garcia-Calvo E, García-García A, Rodríguez S, Martín R, García T Foods 26-Apr-2024
PMCID:PMC11083168
doi:10.3390/foods13091341
PMID:38731712
Commodity risk assessment of Petunia spp. and Calibrachoa spp. unrooted cuttings from Kenya 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, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Lacomme C, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R EFSA J 25-Apr-2024
PMCID:PMC11044013
doi:10.2903/j.efsa.2024.8742
PMID:38665158
WRKY22 Transcription Factor from Iris laevigata Regulates Flowering Time and Resistance to Salt and Drought Fan L, Niu Z, Shi G, Song Z, Yang Q, Zhou S, Wang L Plants (Basel) 25-Apr-2024
PMCID:PMC11085594
doi:10.3390/plants13091191
PMID:38732405
Editorial: Potential of the plant rhizomicrobiome for bioremediation of contaminants in agroecosystems Bhandari G, Gangola S, Bhatt P, Rafatullah M Front Plant Sci 22-Apr-2024
PMCID:PMC11070560
doi:10.3389/fpls.2024.1397360
PMID:38711602
Genome-Wide Identification of BrCMF Genes in Brassica rapa and Their Expression Analysis under Abiotic Stresses Chen L, Wu X, Zhang M, Yang L, Ji Z, Chen R, Cao Y, Huang J, Duan Q Plants (Basel) 17-Apr-2024
PMCID:PMC11054530
doi:10.3390/plants13081118
PMID:38674527
StCoExpNet: a global co-expression network analysis facilitates identifying genes underlying agronomic traits in potatoes Bonthala VS, Stich B Plant Cell Rep 15-Apr-2024
PMCID:PMC11018665
doi:10.1007/s00299-024-03201-2
PMID:38622429
Effects of mycorrhizal symbiosis and Ulva lactuca seaweed extract on growth, carbon/nitrogen metabolism, and antioxidant response in cadmium-stressed sorghum plant Kchikich A, Roussi Z, Krid A, Nhhala N, Ennoury A, Benmrid B, Kounnoun A, El Maadoudi M, Nhiri N, Mohamed N Physiol Mol Biol Plants 12-Apr-2024
PMCID:PMC11087393
doi:10.1007/s12298-024-01446-5
PMID:38737317
Flowering onset time is regulated by microRNA-mediated trehalose-6-phosphate signaling in Cajanus cajan L. under elevated CO2 Unnikrishnan DK, Sreeharsha RV, Mudalkar S, Reddy AR Physiol Mol Biol Plants 06-Apr-2024
PMCID:PMC11018574
doi:10.1007/s12298-024-01434-9
PMID:38633268
A multi-omic survey of black cottonwood tissues highlights coordinated transcriptomic and metabolomic mechanisms for plant adaptation to phosphorus deficiency Kangi E, Brzostek ER, Bills RJ, Callister SJ, Zink EM, Kim YM, Larsen PE, Cumming JR Front Plant Sci 05-Apr-2024
PMCID:PMC11032019
doi:10.3389/fpls.2024.1324608
PMID:38645387
Exploring the antioxidant potential of endophytic fungi: a review on methods for extraction and quantification of total antioxidant capacity (TAC) Asomadu RO, Ezeorba TP, Ezike TC, Uzoechina JO 3 Biotech 05-Apr-2024
PMCID:PMC10997672
doi:10.1007/s13205-024-03970-3
PMID:38585410
Plants, Microorganisms and Their Metabolites in Supporting Asbestos Detoxification—A Biological Perspective in Asbestos Treatment Łuniewski S, Rogowska W, Łozowicka B, Iwaniuk P Materials (Basel) 03-Apr-2024
PMCID:PMC11012542
doi:10.3390/ma17071644
PMID:38612157

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 https://doi.org/10.1055/S-2006-961475
https://doi.org/10.1002/JSFA.2740500106
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1002/JSFA.2740500106
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1002/JSFA.2740500106
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.1016/J.JEP.2010.01.009
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
[(2R)-2,3-dihydroxypropyl] heptadecanoate 96367592 Click to see 344.50 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3,6,19-Trimethyl-9-prop-1-en-2-yl-16-oxapentacyclo[12.5.1.03,11.06,10.017,20]icos-13-en-17-ol 78412746 Click to see CC1CC2(C3C1CC4(CCC5(CCC(C5C4CC=C3CO2)C(=C)C)C)C)O 370.60 unknown https://doi.org/10.1016/0031-9422(92)83143-M
6-(5-Hydroxy-4-methylcyclohex-3-en-1-yl)-2-methylheptane-2,3,6-triol 162815530 Click to see 272.38 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Taraxerol 92097 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94844-1
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(3aR,5R,8aR,9aS)-6-hydroxy-5,8a-dimethyl-1-methylidene-3a,4,5,8,9,9a-hexahydroazuleno[6,5-b]furan-2,7-dione 163003102 Click to see 262.30 unknown https://doi.org/10.1002/JSFA.2740500106
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Euphol 441678 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94844-1
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)94844-1
[(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13988616 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,5S,9R,10S,13R,14R,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13991201 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,5S,9R,10S,13R,14R,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14754320 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(=C)C 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylhept-6-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13988622 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13988619 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[10,13-dimethyl-17-(5-propan-2-ylhept-5-en-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 85748806 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 15921 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-ethyl-6-methylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14754319 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-ethyl-6-methylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13988618 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-ethyl-6-methylhepta-3,6-dien-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 523651 Click to see 452.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
22-Dehydroclerosteryl acetate 13988623 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C 452.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
5-Dihydroclionasterol acetate 529825 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 458.80 unknown https://doi.org/10.1016/0031-9422(92)83143-M
5alpha-Stigmast-7-en-3beta-ol, acetate 22296968 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/J.JEP.2010.01.009
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/J.JEP.2010.01.009
Beta-Sitosteryl Acetate 5354503 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Npc155187 521199 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Stigmast-7-en-3-ol, acetate, (3beta,5alpha)- 635170 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Stigmasta-5,24(28)-dien-3-OL acetate 13322124 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Stigmastanol acetate 13988628 Click to see 458.80 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Stigmasterol acetate 6437330 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
[(3S,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 13834172 Click to see CC(C)C(C)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 11259252 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-6,6-dimethyl-5-methylideneheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13991212 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[10,13-dimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13991204 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 529823 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 440.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5,6-dimethylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 521145 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(6,6-dimethyl-5-methylideneheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 13991211 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
22-Dihydrobrassicasterol acetate 314396 Click to see 442.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Campestanol acetate 14186068 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C 444.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Campesteryl acetate 13019955 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Ergosta-5,22-dien-3-ol, acetate, (3beta,22E)- 13889457 Click to see 440.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters / Cholesteryl esters
Cholest-5-en-3-yl acetate 222529 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
Cholesteryl acetate 2723897 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C 428.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
methyl 2-[(1R,2R,4S,7R,8S,10S,11R,12R,13R,16R)-10-hydroxy-7-(2-hydroxy-5-oxo-2H-furan-3-yl)-1,8,12,15,15-pentamethyl-5,18-dioxo-3,6,14-trioxapentacyclo[9.7.0.02,4.02,8.012,16]octadecan-13-yl]acetate 90670768 Click to see 534.60 unknown https://doi.org/10.1016/0031-9422(92)83143-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/J.JEP.2010.01.009
[(3S,5S,8S,10S,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 163011666 Click to see 470.80 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,5S,8S,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 162939895 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[(3S,5S,9R,10S,13R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162912244 Click to see 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-Ethyl-6-methylhept-6-en-2-yl)-10,13,14-trimethyl-1,2,3,4,5,6,7,8,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate 14754324 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(92)83143-M
[17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,9,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 5010322 Click to see CCC(CCC(C)C1CCC2=C3CCC4CC(CCC4(C3CCC12C)C)OC(=O)C)C(C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)83143-M
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)83010-1
https://doi.org/10.1016/J.JEP.2010.01.009
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alanine and derivatives
(2S)-2-(phenylazaniumyl)propanoate 6946449 Click to see CC(C(=O)[O-])[NH2+]C1=CC=CC=C1 165.19 unknown https://doi.org/10.1055/S-2006-961475
DL-Alanine 602 Click to see CC(C(=O)O)N 89.09 unknown https://doi.org/10.1055/S-2006-960880
L-Alanine 5950 Click to see 89.09 unknown https://doi.org/10.1055/S-2006-960880
> 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
L-Arginine 6322 Click to see 174.20 unknown https://doi.org/10.1055/S-2006-960880
> 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/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Glutamic acid and derivatives
L-Glutamic Acid 33032 Click to see 147.13 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histidine 6274 Click to see C1=C(NC=N1)CC(C(=O)O)N 155.15 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Isoleucine and derivatives
l-Isoleucine 6306 Click to see CCC(C)C(C(=O)O)N 131.17 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Leucine and derivatives
Leucine 6106 Click to see CC(C)CC(C(=O)O)N 131.17 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
D-Phenylalanine 71567 Click to see 165.19 unknown https://doi.org/10.1055/S-2006-961475
Phenylalanine 6140 Click to see C1=CC=C(C=C1)CC(C(=O)O)N 165.19 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Proline and derivatives
Proline 145742 Click to see C1CC(NC1)C(=O)O 115.13 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Serine and derivatives
L-Serine 5951 Click to see 105.09 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Valine and derivatives
Valine 6287 Click to see CC(C)C(C(=O)O)N 117.15 unknown https://doi.org/10.1055/S-2006-960880
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Cysteine and derivatives
Cysteine 5862 Click to see C(C(C(=O)O)N)S 121.16 unknown https://doi.org/10.1055/S-2006-960880
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Inositol phosphates
1D-myo-inositol 6-phosphate 161368 Click to see C1(C(C(C(C(C1O)O)OP(=O)(O)O)O)O)O 260.14 unknown https://doi.org/10.1016/S0021-9673(98)00542-1
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol 892 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1002/JSFA.2740500106
https://doi.org/10.1016/S0021-9673(98)00542-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal 19233 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown https://doi.org/10.1002/JSFA.2740500106
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
(2S,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 161658 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
D-Galactose 6036 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
D-Mannose 18950 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
L-Rhamnose 25310 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown https://doi.org/10.1002/JSFA.2740500106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
aldehydo-D-Xylose 644160 Click to see 150.13 unknown https://doi.org/10.1002/JSFA.2740500106
D-Arabinose 66308 Click to see 150.13 unknown https://doi.org/10.1002/JSFA.2740500106
D-Xylose 135191 Click to see 150.13 unknown https://doi.org/10.1002/JSFA.2740500106
L-Arabinose 439195 Click to see 150.13 unknown https://doi.org/10.1002/JSFA.2740500106
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)D-Ido(a1-6)Glc(a1-2b)Psif 132990894 Click to see 666.60 unknown https://doi.org/10.1016/S0021-9673(98)00542-1
Raffinose 439242 Click to see 504.40 unknown https://doi.org/10.1016/S0021-9673(98)00542-1
Stachyose 439531 Click to see 666.60 unknown https://doi.org/10.1016/S0021-9673(98)00542-1
Verbascose 441434 Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OCC4C(C(C(C(O4)OC5(C(C(C(O5)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O)O)O)O 828.70 unknown https://doi.org/10.1016/S0021-9673(98)00542-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
(2S,4R)-Pentane-1,2,3,4,5-Pentol 6912 Click to see 152.15 unknown https://doi.org/10.1002/JSFA.2740500106
D-Arabitol 94154 Click to see 152.15 unknown https://doi.org/10.1002/JSFA.2740500106
D-Threitol 169019 Click to see C(C(C(CO)O)O)O 122.12 unknown https://doi.org/10.1002/JSFA.2740500106
Erythritol 222285 Click to see 122.12 unknown https://doi.org/10.1002/JSFA.2740500106
Galactitol 11850 Click to see 182.17 unknown https://doi.org/10.1002/JSFA.2740500106
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1002/JSFA.2740500106
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1002/JSFA.2740500106
Mannitol 6251 Click to see 182.17 unknown https://doi.org/10.1002/JSFA.2740500106
Sorbitol 5780 Click to see 182.17 unknown https://doi.org/10.1002/JSFA.2740500106
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1002/JSFA.2740500106
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1002/JSFA.2740500106
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1002/JSFA.2740500106
> 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/10.1016/S0031-9422(00)83010-1
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/10.1016/S0031-9422(00)83010-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isovitexin 162350 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)83010-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 5378180 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
Homo-orientin 5382105 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
Vitexin 5280441 Click to see 432.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
https://doi.org/10.1016/S0031-9422(00)83010-1
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin 73201 Click to see 270.28 unknown https://doi.org/10.1016/J.FOODCHEM.2010.01.062
https://doi.org/10.1016/J.PHYMED.2014.02.011
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
https://doi.org/10.1016/J.FITOTE.2010.05.005
https://doi.org/10.1016/J.JEP.2010.01.009
Npc235117 4101463 Click to see 270.28 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
https://doi.org/10.1016/J.FOODCHEM.2010.01.062
https://doi.org/10.1016/J.JEP.2010.01.009
https://doi.org/10.1016/J.FITOTE.2010.05.005
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see 270.24 unknown https://doi.org/10.1016/0031-9422(79)80111-9
Isowighteone 5494866 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O)C 338.40 unknown https://doi.org/10.1016/S0031-9422(00)85046-3
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(7S)-7-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5-hydroxy-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163038107 Click to see 422.50 unknown https://doi.org/10.1016/0031-9422(77)83040-9
Cajanone 325518 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2COC3=C(C2=O)C(=C4C=CC(OC4=C3)(C)C)O)C 422.50 unknown https://doi.org/10.1016/0031-9422(77)83040-9
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(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/10.1016/S0031-9422(00)85046-3
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)85046-3
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
Cajanol 442670 Click to see 316.30 unknown https://doi.org/10.1016/S0031-9422(00)85046-3
https://doi.org/10.1016/J.CBI.2010.07.009
https://doi.org/10.1016/S0021-9673(01)86812-6
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Cajanin 5281706 Click to see 300.26 unknown https://doi.org/10.1016/S0031-9422(00)85046-3
https://doi.org/10.1016/S0021-9673(01)86812-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2-Propen-1-one, 1-(2,6-dihydroxy-4-methoxyphenyl)-3-phenyl-, (E)-; Chalcone, 2',6'-dihydroxy-4'-methoxy-; 2',6'-Dihydroxy-4'-methoxychalcone 606469 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(80)85072-2
2',6'-Dihydroxy-4'-methoxychalcone 5316793 Click to see 270.28 unknown https://doi.org/10.1016/0031-9422(80)85072-2
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
7-Hydroxy-5-methoxy-8-(3-methyl-2-butenyl)-4-phenyl-2H-1-benzopyran-2-one 44817009 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=CC(=O)O2)C3=CC=CC=C3)C 336.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.01.062
> Phenylpropanoids and polyketides / Stilbenes
2-Hydroxy-4-methoxy-3-(3-methylbut-2-en-1-yl)-6-phenethylbenzoic acid 17950432 Click to see CC(=CCC1=C(C=C(C(=C1O)C(=O)O)CCC2=CC=CC=C2)OC)C 340.40 unknown https://doi.org/10.1016/0031-9422(80)85072-2
3-Hydroxy-4-prenyl-5-methoxystilbene-2-carboxylic acid 78091652 Click to see 338.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.01.062
https://doi.org/10.1016/0031-9422(80)85072-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
https://doi.org/10.1002/CHIN.200348205
3-Hydroxy-5-methoxy-6-prenylstilbene-2-carboxylic acid 5281715 Click to see CC(=CCC1=C(C=C(C(=C1C=CC2=CC=CC=C2)C(=O)O)O)OC)C 338.40 unknown https://doi.org/10.1016/0031-9422(80)85072-2
3-Hydroxy-5-methoxystilbene-2-carboxylic acid 67322419 Click to see COC1=CC(=C(C(=C1)O)C(=O)O)C=CC2=CC=CC=C2 270.28 unknown https://doi.org/10.1080/00380768.1993.10416974
3-Methoxy-2-(3-methyl-2-butenyl)-5-(2-phenylethenyl)phenol 69713319 Click to see CC(=CCC1=C(C=C(C=C1OC)C=CC2=CC=CC=C2)O)C 294.40 unknown https://doi.org/10.1016/J.JEP.2010.01.009
3-Methoxy-4-(3-methyl-2-buten-1-yl)-5-[(1E)-2-phenylethenyl]phenol; Longistyline C 3048927 Click to see 294.40 unknown https://doi.org/10.1016/J.JEP.2010.01.009
4-O-Methylpinosylvic acid 67322417 Click to see COC1=CC(=C(C(=C1)O)C(=O)O)C=CC2=CC=CC=C2 270.28 unknown https://doi.org/10.1080/00380768.1993.10416974
6-Hydroxy-4-methoxy-3-(3-methyl-2-butenyl)-2-(2-phenylethenyl)benzoic acid 442707 Click to see CC(=CCC1=C(C=C(C(=C1C=CC2=CC=CC=C2)C(=O)O)O)OC)C 338.40 unknown https://doi.org/10.1016/0031-9422(80)85072-2
Cajaninstilbene acid 9819225 Click to see 338.40 unknown https://doi.org/10.1016/J.FOODCHEM.2010.01.062
https://doi.org/10.1016/0031-9422(80)85072-2
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253773/
https://doi.org/10.1002/CHIN.200348205
Longistylin C 6446720 Click to see CC(=CCC1=C(C=C(C=C1OC)O)C=CC2=CC=CC=C2)C 294.40 unknown https://doi.org/10.1016/J.JEP.2010.01.009
Longistyline A 9900754 Click to see 294.40 unknown https://doi.org/10.1016/J.JEP.2010.01.009
> Phenylpropanoids and polyketides / Tannins
1,3,6-Tris-o-(3,4,5-trihydroxybenzoyl)hexopyranose 250395 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 636.50 unknown https://doi.org/10.1016/S0021-9673(98)00542-1

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