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Lathyrus nissolia

Lathyrus nissolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

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

Details Top

Internal ID UUID643fded1eac51465592222
Scientific name Lathyrus nissolia
Authority L.
First published in Sp. Pl.: 729 (1753)

Description Top

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No description added yet. Help us by writing one.

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 pea
English grass vetchling
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
Malayalam ലാത്വൈറസ് നിസോളിയ
Malayalam ഗ്രാസ്സ് വെച്ച്ലിങ്
Dutch graslathyrus
Polish groszek liściakowy
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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Subvarieties (abbr. subvar.) Top

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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

Suggest others/fix!
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 C1=C(C=C(C(=C1O)O)O)C(=O)O 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 COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
2-(4-Methylphenyl)propan-2-ol 14529 Click to see CC1=CC=C(C=C1)C(C)(C)O 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
3,4-Dehydrolarreatricin 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 CC1C(OC(C1=C)C2=CC=C(C=C2)O)C3=CC=C(C=C3)O 282.30 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
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
4,4'-(3alpha-Methyl-4-methylenetetrahydrofuran-2alpha,5beta-diyl)bis(2-methoxyphenol) 73213151 Click to see CC1C(OC(C1=C)C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)O)OC 342.40 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Larreatricin 26389403 Click to see CC1C(C(OC1C2=CC=C(C=C2)O)C3=CC=C(C=C3)O)C 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 CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 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
[R,(+)]-3,7-Dimethyl-7-octen-1-ol acetate 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
7-Octen-1-ol, 3,7-dimethyl-, (S)- 81263 Click to see CC(CCCC(=C)C)CCO 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 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 CC1=CCC2C(C1)C2(C)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 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
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Humulene 5318102 Click to see CC1=CCC(C=CCC(=C)CCC1)(C)C 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
2-Propenoic acid, 3-(4-hydroxyphenyl)-, methyl ester 92203 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Gallocatechin-(4alpha->8)-epigallocatechin 442682 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
Gallocatechin-(4alpha->8)-gallocatechin-(4alpha->8)-gallocatechin 71664720 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C(=C7)O)O)O)O)C8=CC(=C(C(=C8)O)O)O)O)O)O)C9=CC(=C(C(=C9)O)O)O)O 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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / 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
3-[(6-O-alpha-L-Rhamnopyranosyl-beta-D-glucopyranosyl)oxy]-4',5,7-trihydroxy-3',5'-dimethoxyflavylium 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
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
Oenin 443652 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 493.40 unknown via CMAUP database
Pelargonidin 3-glucoside ion 443648 Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 433.40 unknown via CMAUP database
Pelargonidin 3-O-rutinoside 443917 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 579.50 unknown via CMAUP database
Peonidin 3-O-rutinoside 90470732 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)OC)O)O)O)O)O)O)O)O 609.60 unknown via CMAUP database
Peonidin-3-glucoside 443654 Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 463.40 unknown via CMAUP database
Petunidin 3-glucoside 443651 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown via CMAUP database
Petunidin 3-rutinoside 101949843 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)O)O)O)O)O)O)O)O)O 625.60 unknown via CMAUP database
Tulipanin 5492231 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)O 611.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Cannabiscitrin 5486615 Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C3=C(C(=O)C4=C(C=C(C=C4O3)O)O)O 480.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-beta-D-Arabinopyranosyloxy-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyrylium 101603499 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O 435.40 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 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
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 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
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
Pyranocyanin D 101198724 Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O2)O 565.50 unknown via CMAUP database
Pyranodelphinin D 101198725 Click to see C1=CC(=CC=C1C2=CC3=C4C(=CC(=[OH+])C=C4OC(=C3OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C(=C6)O)O)O)O2)O 581.50 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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