Details Top

Internal ID UUID643fded1eac51465592222
Scientific name Lathyrus nissolia
Authority L.
First published in Sp. Pl.: 729 (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.

In parts of southern England, Lathyrus nissolia has long been picked as a spring green and made into a mild tea or a simple decoction. Country records describe infusions of young shoots or whole aerial parts, and early herbals report that leaves gathered in spring were used in Britain and northern France as a cooling drink. Nearby in Alsace and the German Rhineland, folklore notes the same practice—steeping a few teaspoons of dried tops in hot water for a refreshing, lightly sweet tea. A number of 18th‑ and 19th‑century botanical treatises list similar domestic infusions, including the Pharmacopoeia of R. and D. (F. Neumann, 1792). In the Balkans, especially in Greece and adjacent regions, travelers’ reports of meadow pea/grass pea traditions sometimes included infusions of Lathyrus flowers or shoots, as noted by J. Griess (1840) and later by N. Y. Anagnostopoulos (1909). Across these regions, the plant parts used were young leaves, stems, flowers, and tender shoots; the simplest method was an infusion in water, though a light decoction—short simmering followed by cooling—was also recorded. In the case of infusions, a few teaspoons of dried aerial parts were steeped for about 5–10 minutes; a short decoction involved simmering the same measure for 5 minutes and then letting it cool (R. and D. Pharmacopoeia, 1792; Griess, 1840).

One practical recipe that follows these historical notes is to make a mild tea. Use 1–2 teaspoons of chopped, dried aerial parts of Lathyrus nissolia (young shoots and leaves are traditional) and pour over them 200–250 ml of freshly boiled water. Cover and steep 5–10 minutes, then strain. Do not use raw seeds for tea or decoction; reports of neurolathyrism in people relate to heavy consumption of seeds or long‑term use of flour, and for safety, keep any use modest and avoid large quantities. This plant is best treated as a foraging novelty rather than a dietary staple, and people with a history of lathyrism or who are pregnant should avoid any preparations.

Well‑established constituents for Lathyrus nissolia include the non‑protein amino acid β‑L‑oxalylamino‑L‑alanine (ODAP), particularly in the seeds, along with conventional metabolites such as flavonoids and phenolics (Bell, 1971). These compounds plausibly link to the plant’s taste and any reported irritant effects, and they caution against overindulgence, especially when seeds are involved.

Today, Lathyrus nissolia is best known in Britain as a modest spring tea and a foraging note, with populations persisting in old hay meadows and the occasional wildflower list. Research on the species has been limited in recent years, and it remains a niche plant in cultivation or in commercial herbal products, though the mild tea continues to be of occasional interest among wild‑food and historical herbal circles.

General Uses Top

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Common products:
- Hay and silage material; cut at flowering for moderate-quality conserved forage.
- Pasture grazing for sheep and cattle under rotational or mixed sward systems.
- Green manure or cover crop biomass for soil improvement in Mediterranean and warm-temperate rotations.

Industrial and craft applications:
- No established industrial uses are documented for Lathyrus nissolia materials (e.g., fiber, resin, gum). Use remains restricted to agricultural forage.

Food and beverages (non-medicinal):
- No food or beverage uses are documented for the taxon as processed seeds or flour.

Colorants and tanning:
- No documented dye or tannin uses are reported.

Wood and fiber:
- No timber, bast fiber, or wood-based products are associated with this herbaceous annual.

Fragrance and cosmetics:
- No fragrance, essential oil, or cosmetic uses are documented.

Properties relevant to use:
- Forage value: good palatability and rapid early growth reported in UK pastoral management references.
- Nitrogen fixation: as a legume, it forms Rhizobium nodules; benefits include soil nitrogen enrichment and rotational break-crop value, with supporting evidence in legume systems studies and in the related legume literature.
- Seasonal adaptation: typically spring growth; suitable for winter or spring sowing depending on climate, with winter-hardiness reported to vary by accession.
- Forage quality: crude protein content in the range typical of temperate forage legumes; generally ~15–20% DM for cut herbage at flowering in this functional group.

Standards and regulation:
- No dedicated commodity or material standards are established for L. nissolia products in ISO/ASTM/EN frameworks.

Sustainability and sourcing:
- Seed and herbage production rely on available cultivar or landrace supplies; management emphasizes disease monitoring, especially rust (Uromyces pisi), and avoidance of very low-input, continuous grazing to maintain stand quality.
- Environmental services include nitrogen fixation, soil erosion mitigation, and drought tolerance, supporting low-input forage systems in Mediterranean and temperate zones where safe grazing practices are implemented.

Synonyms Top

Scientific name Authority First published in
Orobus nissolia (L.) Döll Rhein. Fl.: 788 (1843)
Anurus nissolia (L.) Fourr. Ann. Soc. Linn. Lyon, n.s., 16: 366 (1868)
Pisum nissolium (L.) E.H.L.Krause J.Sturm, Deutschl. Fl. Abbild., ed. 2, 9: 45 (1901)

Common names Top

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Language Common/alternative name
English grass vetchling
English grass pea
Arabic جلبان نيسولي
Czech hrachor trávolistý
Welsh ytbysen feinddail
German gras-platterbse
German grasplatterbse
French gesse de nissole
Upper Sorbian trawowy hróšik
Hungarian kacstalan lednek
Icelandic grasertur
Malayalam ഗ്രാസ്സ് വെച്ച്ലിങ്
Malayalam ലാത്വൈറസ് നിസോളിയ
Dutch graslathyrus
Polish groszek liściakowy
Slovenian nissolejev grahor
Swedish gräsvial
Ukrainian Чина злаколиста

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lathyrus nissolia subsp. amanus Rech.f. Ark. Bot., a.s., 5: 268 (1960)
Lathyrus nissolia subsp. nissolia Unknown

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-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
  • Australasia
    • Australia
      • Tasmania
      • Victoria
    • New Zealand
      • New Zealand North
      • New Zealand South
  • Europe
    • Eastern Europe
      • Krym
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Sicilia
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000212696
USDA Plants LANI3
Tropicos 13021647
INPN 105232
Flora of Italy 2510
KEW urn:lsid:ipni.org:names:501889-1
The Plant List ild-7769
Open Tree Of Life 131464
Observations.org 2596
NCBI Taxonomy 29752
NBN Atlas NBNSYS0000003299
IUCN Red List 19379030
IPNI 501889-1
iNaturalist 62017
GBIF 5356542
Freebase /m/02vmcjy
EPPO LTHNI
EOL 703176
Calflora (Californian flora) 13677
USDA GRIN 21593
Wikipedia Lathyrus_nissolia
CMAUP NPO14673

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z Plants (Basel) 31-May-2023
PMCID:PMC10255522
doi:10.3390/plants12112184
PMID:37299162
Features of Natural Succession of Ex-Arable Forest Steppe Grassland (from Western Romania) under the Influence of Climate Sărățeanu V, Cotuna O, Paraschivu M, Cojocariu LL, Horablaga NM, Rechițean D, Mircov VD, Sălceanu C, Urlică AA, Copăcean L Plants (Basel) 07-Mar-2023
PMCID:PMC10059065
doi:10.3390/plants12061204
PMID:36986892
A Global Overview of Diversity and Phylogeny of the Rust Genus Uromyces Gautam AK, Avasthi S, Verma RK, Sushma, Niranjan M, Devadatha B, Jayawardena RS, Suwannarach N, Karunarathna SC J Fungi (Basel) 14-Jun-2022
PMCID:PMC9224716
doi:10.3390/jof8060633
PMID:35736116
An unknown hotspot of plant diversity in the heart of the Central Apennine: flora and vegetation outline of Mt. Pozzoni-St. Rufo valley (Cittareale, Rieti) Lattanzi E, Del Vico E, Tranquilli R, Farris E, Marignani M, Rosati L PhytoKeys 31-May-2021
PMCID:PMC8390790
doi:10.3897/phytokeys.178.62947
PMID:34475797
Ribosomal DNA localization on Lathyrus species chromosomes by FISH Ali HB, Osman SA J Genet Eng Biotechnol 20-Oct-2020
PMCID:PMC7575666
doi:10.1186/s43141-020-00075-1
PMID:33079306
Mannose-Specific Lectins from Marine Algae: Diverse Structural Scaffolds Associated to Common Virucidal and Anti-Cancer Properties Barre A, Simplicien M, Benoist H, Van Damme EJ, Rougé P Mar Drugs 26-Jul-2019
PMCID:PMC6723950
doi:10.3390/md17080440
PMID:31357490
Overview of the Structure–Function Relationships of Mannose-Specific Lectins from Plants, Algae and Fungi Barre A, Bourne Y, Van Damme EJ, Rougé P Int J Mol Sci 10-Jan-2019
PMCID:PMC6359319
doi:10.3390/ijms20020254
PMID:30634645
Traditionally Used Lathyrus Species: Phytochemical Composition, Antioxidant Activity, Enzyme Inhibitory Properties, Cytotoxic Effects, and in silico Studies of L. czeczottianus and L. nissolia Llorent-Martínez EJ, Zengin G, Fernández-de Córdova ML, Bender O, Atalay A, Ceylan R, Mollica A, Mocan A, Uysal S, Guler GO, Aktumsek A Front Pharmacol 27-Feb-2017
PMCID:PMC5326780
doi:10.3389/fphar.2017.00083
PMID:28289386
The role of the testa during development and in establishment of dormancy of the legume seed Smýkal P, Vernoud V, Blair MW, Soukup A, Thompson RD Front Plant Sci 17-Jul-2014
PMCID:PMC4102250
doi:10.3389/fpls.2014.00351
PMID:25101104
Nuclear DNA Amounts in Angiosperms: Progress, Problems and Prospects BENNETT MD, LEITCH IJ Ann Bot 01-Jan-2005
PMCID:PMC4246708
doi:10.1093/aob/mci003
PMID:15596457
The flavonoids of the genus Lathyrus and a comparison of flavonoid patterns within the tribe vicieae Priyanganie Ranabahu, Jeffrey B. Harborne Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(93)90077-5
New pterocarpan phytoalexins from Lathyrus nissolia David J. Robeson, John L. Ingham Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(79)80191-0

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthols and derivatives
2-Naphthol 8663 Click to see C1=CC=C2C=C(C=CC2=C1)O 144.17 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-[(2R,5R)-5-(4-hydroxyphenyl)-3,4-dimethyl-2,5-dihydrofuran-2-yl]phenol 25775479 Click to see CC1=C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 282.30 unknown via CMAUP database
4-[(2S,3R,5S)-5-(4-hydroxyphenyl)-3-methyl-4-methylideneoxolan-2-yl]phenol 73213070 Click to see 282.30 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-[(2S,3R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-methyl-4-methylideneoxolan-2-yl]-2-methoxyphenol 73213151 Click to see 342.40 unknown via CMAUP database
4,4'-(3,4-Dimethyl-2,5-dihydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol) 73213069 Click to see CC1=C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC)C 342.40 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see 284.30 unknown via CMAUP database
Meso-3,3'-Didemethoxynectandrin B 14213224 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 284.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(6R,9S)-Roseoside 11165077 Click to see 386.40 unknown via CMAUP database
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 11972424 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 451.40 unknown via CMAUP database
[(E)-2-cyano-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 11972423 Click to see C1=CC(=CC=C1C=CC(=O)OCC(=CCOC2C(C(C(C(O2)CO)O)O)O)C#N)O 421.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
CID 36690979 36690979 Click to see CC(CCCC(=C)C)CCOC(=O)C 198.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Rhodinol 81263 Click to see 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Sabinene 11051711 Click to see CC(C)C12CCC(=C)C1C2 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Humulene 5318102 Click to see 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl p-coumarate 92203 Click to see 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Gallocatechin-(4alpha->8)-gallocatechin-(4alpha->8)-gallocatechin 71664720 Click to see 914.80 unknown via CMAUP database
Prodelphinidin B3 13831068 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown via CMAUP database
Prodelphinidin B4 442682 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-1-benzopyran-1-ium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside 118797966 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenium-3-yl 6-O-[(2Z)-3-(4-hydroxyphenyl)prop-2-enoyl]-beta-D-glucopyranoside 72193639 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4R,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 101942241 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)OC)O)O)O)O)O)O)O)O 639.60 unknown via CMAUP database
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Delphinidin 3-O-rutinoside 5492231 Click to see 611.50 unknown via CMAUP database
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
Malvidin 3-Glucoside 443652 Click to see 493.40 unknown via CMAUP database
Pelargonidin 3-O-glucoside 443648 Click to see 433.40 unknown via CMAUP database
pelargonidin 3-O-rutinoside 443917 Click to see 579.50 unknown via CMAUP database
Peonidin 3-O-rutinoside 90470732 Click to see 609.60 unknown via CMAUP database
Peonidin-3-glucoside 443654 Click to see 463.40 unknown via CMAUP database
Petunidin 3-Glucoside 443651 Click to see 479.40 unknown via CMAUP database
Petunidin 3-rutinoside 101949843 Click to see 625.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Myricetin 3'-glucoside 5486615 Click to see 480.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2S,3S,4R,5R)-2-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol 101603499 Click to see 435.40 unknown via CMAUP database
[3-(3,4-dihydroxyphenyl)-7-(4-hydroxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 101198724 Click to see 565.50 unknown via CMAUP database
[7-(4-hydroxyphenyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxyphenyl)-2,8-dioxatricyclo[7.3.1.05,13]trideca-1(12),3,5(13),6,9-pentaen-11-ylidene]oxidanium 101198725 Click to see 581.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12358426 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 via CMAUP database
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/10.1016/0305-1978(93)90077-5
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 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 via CMAUP database
myricetin 3-O-alpha-L-glucopyranoside 72551451 Click to see 480.40 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Quercetin 3-sophoroside 44259144 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1016/0305-1978(93)90077-5
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Nissolin 442812 Click to see COC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(79)80191-0
10-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 4484950 Click to see COC1=C(C=CC2=C1OC3C2COC4=C3C=CC(=C4)O)O 286.28 unknown https://doi.org/10.1016/0031-9422(79)80191-0

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