Lathyrus nissolia, also known as grass vetchling or grass pea, is a flowering plant in the pea and bean family found in Europe, Maghreb, Levant, and the Caucasus. Despite its name, it is not a grass but belongs to the legume family. It is an annual plant with an erect stem and no true leaves, leaflets, or tendrils. Its flowers, which appear in June and July, are small and solitary with the ability to self-pollinate. The plant produces long, slender pods that contain peas and can be found in grasslands, banks, and field margins on neutral to acid soil. While rare in Scotland and localized in England and Wales, there are indications that it is spreading in the United Kingdom. It has not been recorded in Ireland.

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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Filter by language:

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
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

Africa click to expand
- Northern Africa
  - Algeria
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - North Caucasus
  - Transcaucasus
- Western Asia
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine

Australasia click to expand
- Australia
  - Tasmania
  - Victoria
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- 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

Northern America click to expand
- Northwestern U.S.A.
  - Oregon
  - Washington

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

Add a new one!

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
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 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-[(2S,3R,5S)-5-(4-hydroxy-3-methoxyphenyl)-3-methyl-4-methylideneoxolan-2-yl]-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
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 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
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 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
(E,E)-1,4,4-Trimethyl-8-methylene-1,5-cycloundecadiene	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
(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
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-O-beta-D-glucoside	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-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-(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 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
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
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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Lathyrus nissolia

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