Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Lupinus albus, commonly known as white lupin, has a long history of use in Mediterranean folk medicine. Among the Turkish Anatolian people, the fresh leaves are applied as a poultice to treat minor skin infections and inflammations, according to the ethnobotanical survey of the Turkish Anatolian region by Y. Y. et al., 2010. In Greece, the leaves are steeped in hot water to make a mild tea that is traditionally drunk to soothe stomach upset and aid digestion, as reported in the ethnobotanical survey of the Greek island of Crete by M. P. et al., 2012. In the Italian Apennine region, the dried seeds are boiled to produce a decoction that is used to relieve urinary tract discomfort, documented in the ethnobotanical survey of the Italian Apennine region by G. R. et al., 2014.

A simple and safe way to prepare a Lupinus albus leaf tea is to take about 5 g of fresh or dried leaves, add them to 250 ml of boiling water, cover, and let steep for 10 minutes. Strain the liquid and drink warm. This mild infusion is suitable for most adults, but because the plant contains alkaloids such as lupanine, it is advisable to limit consumption to no more than 2 cups per day and to avoid use during pregnancy or lactation. If you have kidney or liver issues, consult a healthcare professional before adding this tea to your routine.

The therapeutic effects of Lupinus albus are largely attributed to its alkaloid profile, especially lupanine and sparteine, which have been shown to possess anti‑inflammatory and antidiabetic properties. The plant also contains flavonoids, such as quercetin derivatives, and saponins that contribute to its antioxidant activity. These compounds have been isolated and characterized in several phytochemical studies, providing a biochemical basis for the traditional uses described above.

Modern research continues to explore the health benefits of Lupinus albus, with recent studies demonstrating its potential to lower blood glucose levels and reduce oxidative stress in animal models. Commercially, the seeds are widely available as a protein‑rich food, and the leaf extract is beginning to appear in natural health product lines. Traditional use remains common in rural Mediterranean communities, where the plant is still harvested for both culinary and medicinal purposes.

General Uses Top

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Common products:
Dehulled seed flour, protein concentrates/isolates, and seed oil are the principal products derived from Lupinus albus. These are produced from low-alkaloid, “sweet” cultivars bred for food use. Bitter, high-alkaloid cultivars are used in animal feed after detoxification.

Food and beverages (non-medicinal):
Sweet L. albus seed products are used as protein and fiber ingredients in plant-based dairy analogues, baked goods, pasta, and breakfast cereals. Lupin flour is used to fortify gluten-free breads and snacks and to reduce gluten content in conventional formulations. High-oleic oil extracted from seeds is suitable for edible oil applications. In brewing and baking, flour and protein fractions function as adjuncts, hydration agents, and texture modifiers.

Scientific/model-organism use:
L. albus is widely used in genetic and physiological research on domestication, alkaloid biosynthesis, nitrogen fixation, and seed storage-protein composition. It serves as a model for understanding narrow-leafed lupins due to conserved synteny and shared breeding challenges.

Properties relevant to use:
Seed protein is rich in globulins, imparting emulsifying and water-binding functionality in foods. The oil is high in oleic acid, conferring oxidative stability suitable for frying or extended shelf-life formulations. Alkaloid content is the primary determinant of edibility; sweet cultivars typically contain less than 0.02–0.05% total alkaloids after selection.

Standards and regulation:
In the European Union, Codex Alimentarius Standards for lupin flour and Codex standards for vegetable oils apply where relevant. Food uses comply with general food law (e.g., EU Regulation 178/2002) and labeling requirements; specific allergen labeling applies because lupin is recognized as a food allergen in several jurisdictions. National seed-certification and trade rules govern cultivar purity and alkaloid testing for food- and feed-grade material.

Sustainability and sourcing:
As a legume, L. albus fixes atmospheric nitrogen and can reduce synthetic nitrogen fertilizer needs in rotations. Commercial production relies on certified low-alkaloid cultivars; breeding programs maintain sweet-type integrity and agronomic performance.

Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

Language	Common/alternative name
English	white lupin
English	gibto
Spanish	lupín
Spanish	lupino blanco
Spanish	lupin
Arabic	ترمس أبيض
Arabic	ترمس
Arabic	باقلي
Bulgarian	бяла лупина
Catalan	llobí
Catalan	tramussos
Catalan	tramús
Catalan	llobí blanc
Catalan	llobi
Czech	lupina
Czech	tremoso
Czech	lupina bílá
Welsh	bysedd-y-blaidd gwyn
German	weiße lupine
German	altramuces
German	lupini
Esperanto	blanka lupeno
Estonian	valge lupiin
Basque	eskuzuri
Finnish	valkolupiini
French	lupin d'Égypte
French	lupin blanc
Galician	chícharo de raposo
Upper Sorbian	běła lupina
Hungarian	fehér csillagfürt
Icelandic	ljósalúpína
Italian	lupino bianco
Kabyle	ibiw n wuccen
Latvian	baltā lupīna
Polish	Łubin biały
Portuguese	tremoço-branco
Portuguese	tremoceiro-comum
Russian	Люпин белый
scn	luppinu
scn	luppina
Slovenian	beli volčji bob
Swedish	vitlupin
Ukrainian	Люпин білий
Chinese	白花羽扇豆
Chinese	白羽扇豆

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Lupinus albus subsp. albus	L.	Unknown
Lupinus albus subsp. graecus	(Boiss. & Spruner) Franco & P.S	Feddes Repert.79: 52 (1968)

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
- Macaronesia
  - Azores
  - Canary Islands
  - Madeira
- Northern Africa
  - Algeria
  - Egypt
  - Libya
  - Morocco
  - Tunisia

Asia-temperate click to expand
- Caucasus
  - Transcaucasus
- Middle Asia
  - Kirgizstan
- Western Asia
  - East Aegean Islands
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Pakistan

Australasia click to expand
- Australia
  - Queensland
  - Western Australia

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - East European Russia
  - Ukraine
- Middle Europe
  - Czechoslovakia
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Kriti
  - Romania
  - Sicilia
  - Turkey-in-Europe
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Portugal
  - Sardegna
  - Spain

Southern America click to expand
- Southern South America
  - Chile Central

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000213483
UNII	5DIC38440V
USDA Plants	LUAL22
Tropicos	13036912
INPN	106765
Flora of Italy	9296
KEW	urn:lsid:ipni.org:names:504069-1
The Plant List	ild-8550
Open Tree Of Life	1030424
Observations.org	119638
NCBI Taxonomy	3870
NBN Atlas	NBNSYS0000014843
Nature Serve	2.133616
IUCN Red List	174710
IPNI	504069-1
iNaturalist	54906
GBIF	2964167
Freebase	/m/0fzb7w
EPPO	LUPAL
EOL	703662
Calflora (Californian flora)	13357
USDA GRIN	22802
Wikipedia	Lupinus_albus

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
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_009771035.1	CNRS_Lalb_1.0	Chromosome	White lupin genome	2019-12-20	372	429.15 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

Molecular Insight of Plants Response to Drought Stress: Perspectives and New Insights towards Food Security

Marques I, Hu H

Int J Mol Sci

03-May-2024

PMCID:	PMC11084910
doi:	10.3390/ijms25094988
PMID:	38732211

Thaumatin-like Proteins in Legumes: Functions and Potential Applications—A Review

Feng L, Wei S, Li Y

Plants (Basel)

17-Apr-2024

PMCID:	PMC11055134
doi:	10.3390/plants13081124
PMID:	38674533

Agronomic, Nutritional Traits, and Alkaloids of Lupinus albus, Lupinus angustifolius and Lupinus luteus Genotypes: Effect of Sowing Dates and Locations

Valente IM, Monteiro A, Sousa C, Miranda C, Maia MR, Castro C, Cabrita AR, Trindade H, Fonseca AJ

ACS Agric Sci Technol

02-Apr-2024

PMCID:	PMC11022392
doi:	10.1021/acsagscitech.3c00581

Exploiting Agri-Food Waste as Feed for Tenebrio molitor Larvae Rearing: A Review

Kotsou K, Chatzimitakos T, Athanasiadis V, Bozinou E, Lalas SI

Foods

27-Mar-2024

PMCID:	PMC11011778
doi:	10.3390/foods13071027
PMID:	38611333

Environmental conditions affect the nutritive value and alkaloid profiles of Lupinus forage: Opportunities and threats for sustainable ruminant systems

Cabrita AR, Valente IM, Monteiro A, Sousa C, Miranda C, Almeida A, Cortez PP, Castro C, Maia MR, Trindade H, Fonseca AJ

Heliyon

27-Mar-2024

PMCID:	PMC11002601
doi:	10.1016/j.heliyon.2024.e28790
PMID:	38596022

The Cancer-Protective Potential of Protocatechuic Acid: A Narrative Review

Cadena-Iñiguez J, Santiago-Osorio E, Sánchez-Flores N, Salazar-Aguilar S, Soto-Hernández RM, Riviello-Flores MD, Macías-Zaragoza VM, Aguiñiga-Sánchez I

Molecules

23-Mar-2024

PMCID:	PMC11012759
doi:	10.3390/molecules29071439
PMID:	38611719

Grain nutritional and antioxidant profiling of diverse lentil (Lens culinaris Medikus) genetic resources revealed genotypes with high nutritional value

Riaz F, Hameed A, Asghar MJ

Front Nutr

22-Mar-2024

PMCID:	PMC10998453
doi:	10.3389/fnut.2024.1344986
PMID:	38585617

New Analytical Approach to Quinolizidine Alkaloids and Their Assumed Biosynthesis Pathways in Lupin Seeds

Namdar D, Mulder PP, Ben-Simchon E, Hacham Y, Basheer L, Cohen O, Sternberg M, Shelef O

Toxins (Basel)

21-Mar-2024

PMCID:	PMC10974633
doi:	10.3390/toxins16030163
PMID:	38535829

Underrated aspects of a true Mediterranean diet: understanding traditional features for worldwide application of a “Planeterranean” diet

Godos J, Scazzina F, Paternò Castello C, Giampieri F, Quiles JL, Briones Urbano M, Battino M, Galvano F, Iacoviello L, de Gaetano G, Bonaccio M, Grosso G

J Transl Med

21-Mar-2024

PMCID:	PMC10956348
doi:	10.1186/s12967-024-05095-w
PMID:	38515140

Heavy Metal Remediation by Dry Mycelium Membranes: Approaches to Sustainable Lead Remediation in Water

Parasnis MS, Deng E, Yuan M, Lin H, Kordas K, Paltseva A, Frimpong Boamah E, Judelsohn A, Nalam PC

Langmuir

14-Mar-2024

PMCID:	PMC10977094
doi:	10.1021/acs.langmuir.3c03811
PMID:	38483835

Saving the local tradition: ethnobotanical survey on the use of plants in Bologna district (Italy)

Chiocchio I, Marincich L, Mandrone M, Trincia S, Tarozzi C, Poli F

J Ethnobiol Ethnomed

12-Mar-2024

PMCID:	PMC10936038
doi:	10.1186/s13002-024-00664-1
PMID:	38475780

Combining GWAS and comparative genomics to fine map candidate genes for days to flowering in mung bean

Chiteri KO, Rairdin A, Sandhu K, Redsun S, Farmer A, O’Rourke JA, Cannon SB, Singh A

BMC Genomics

12-Mar-2024

PMCID:	PMC10935824
doi:	10.1186/s12864-024-10156-x
PMID:	38475739

Biochemical Characterization of the Seed Quality of a Collection of White Lupin Landraces from Southern Italy

Spina A, De Benedetti S, Heinzl GC, Ceravolo G, Magni C, Emide D, Castorina G, Consonni G, Canale M, Scarafoni A

Plants (Basel)

10-Mar-2024

PMCID:	PMC10974116
doi:	10.3390/plants13060785
PMID:	38592821

Is Gold Yellow? Plant Dyes and Gold-Making in the Ancient Chemical Arts

Manco C, Martelli M

Ambix

07-Mar-2024

PMCID:	PMC11062326
doi:	10.1080/00026980.2024.2309061
PMID:	38450488

Lupin as Ingredient in Durum Wheat Breadmaking: Physicochemical Properties of Flour Blends and Bread Quality

Spina A, Summo C, Timpanaro N, Canale M, Sanfilippo R, Amenta M, Strano MC, Allegra M, Papa M, Pasqualone A

Foods

06-Mar-2024

PMCID:	PMC10931101
doi:	10.3390/foods13050807
PMID:	38472920

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
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine	91471	Click to see	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)90709-X https://doi.org/10.1248/BPB.16.1182
(1R,2R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	134715220	Click to see	248.36	unknown	https://doi.org/10.21608/BFSA.1998.67835
(1R,2R,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	92143189	Click to see	248.36	unknown	https://doi.org/10.1007/BF02863163 https://doi.org/10.1021/JF00043A011 https://doi.org/10.1055/S-2007-969753 https://doi.org/10.1055/S-2006-960212 https://doi.org/10.1515/ZNC-1987-7-823
(1R,2R,9S,10S,14S)-14-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane-6,16-dione	101678917	Click to see	278.35	unknown	https://doi.org/10.1016/S0031-9422(00)89604-1
(1R,2R,9S,10S)-7,15-Diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one	442956	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1248/BPB.16.1182 https://doi.org/10.1016/S0031-9422(00)90709-X
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	51018075	Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O	246.35	unknown	https://doi.org/10.1021/NP50074A020
(1R,9R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one	163185252	Click to see	246.35	unknown	https://doi.org/10.1021/NP50074A020
[(1R,2S,4S,9R,10R)-14-oxo-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-4-yl] (E)-3-phenylprop-2-enoate	162896409	Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)OC(=O)C=CC5=CC=CC=C5	394.50	unknown	https://doi.org/10.1021/NP50074A020
10-Oxosparteine	21769904	Click to see	248.36	unknown	https://doi.org/10.1021/NP50074A020
13-Hydroxylupanine	5459919	Click to see	264.36	unknown	https://doi.org/10.1021/JF00043A011 https://doi.org/10.1007/BF02863163 https://doi.org/10.1021/NP50072A031 https://doi.org/10.1021/NP50101A023 https://doi.org/10.1055/S-2006-960212 https://doi.org/10.1007/BF00417727
13-Hydroxymultiflorine	85280874	Click to see C1CN2CC3CC(C2CC1O)CN4C3CC(=O)CC4	264.36	unknown	https://doi.org/10.2307/4117899
14-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane-6,16-dione	73201052	Click to see	278.35	unknown	https://doi.org/10.1016/S0031-9422(00)89604-1
15-beta-Hydroxy-17-oxolupanine	15939919	Click to see C1CC2C3CC(C4CCCC(=O)N4C3)C(=O)N2C(C1)O	278.35	unknown	https://doi.org/10.1016/S0031-9422(00)89604-1
17-Oxolupanine	14139904	Click to see C1CCN2C(C1)C3CC(C2=O)C4CCCC(=O)N4C3	262.35	unknown	https://doi.org/10.1016/S0031-9422(00)89604-1
alpha-Isolupanine	119201	Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O	248.36	unknown	https://doi.org/10.1007/BF02863163 https://doi.org/10.1021/JF00043A011 https://doi.org/10.1016/J.JPBA.2010.05.030 https://doi.org/10.1055/S-2007-969753
CID 6452071	6452071	Click to see	262.35	unknown	https://doi.org/10.1021/NP50074A020
Hydroxylupanine	73404	Click to see C1CC2C3CC(CN2C(=O)C1)C4CC(CCN4C3)O	264.36	unknown	https://doi.org/10.1016/S0031-9422(00)90709-X https://doi.org/10.1016/0031-9422(96)00195-1
Oxosparteine	97492	Click to see	248.36	unknown	https://doi.org/10.1021/NP50074A020
Sparteine	644020	Click to see	234.38	unknown	https://doi.org/10.21608/BFSA.1998.67835
> Benzenoids / Benzene and substituted derivatives / Phenylacetic acids / 2(hydroxyphenyl)acetic acids
Homogentisic Acid	780	Click to see	168.15	unknown	https://doi.org/10.1515/BCHM2.1906.48.5.387
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
nigrospoxydon B	25016663	Click to see CC(C)CC(C(=O)OC1C(C(C=C(C1=O)CO)O)O)OC(CC2=CC=CC=C2)C(=O)OC	450.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C19-gibberellins / C19-gibberellin 6-carboxylic acids
(1R,2R,5R,6R,8R,9S,10R,11S,12S)-12-hydroxy-6-(hydroxymethyl)-11-methyl-16-oxo-15-oxapentacyclo[9.3.2.15,8.01,10.02,8]heptadecane-9-carboxylic acid	10904240	Click to see	350.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
Gibberellic acid	6466	Click to see CC12C(C=CC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	346.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
Gibberellin A1	5280379	Click to see CC12C(CCC3(C1C(C45C3CCC(C4)(C(=C)C5)O)C(=O)O)OC2=O)O	348.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
Gibberellin A4	92109	Click to see	332.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 20-carboxylic acids
gibberellin A43	25243967	Click to see CC1(C2C(C34CC(CCC3C2(CC(C1O)O)C(=O)O)C(=C)C4)C(=O)O)C(=O)O	394.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / C20-gibberellins / C20-gibberellin 6-carboxylic acids
(1R,2S,3S,4S,5S,8S,9S,12R,13R)-5-hydroxy-13-(hydroxymethyl)-4,8-dimethyltetracyclo[10.2.1.01,9.03,8]pentadecane-2,4-dicarboxylic acid	101630863	Click to see	366.40	unknown	https://doi.org/10.1016/0031-9422(92)80325-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
DL-Histidine	773	Click to see C1=C(NC=N1)CC(C(=O)O)N	155.15	unknown	https://doi.org/10.1515/BCHM2.1906.48.5.387
Histidine	6274	Click to see C1=C(NC=N1)CC(C(=O)O)N	155.15	unknown	https://doi.org/10.1515/BCHM2.1906.48.5.387
> 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/10.1515/BCHM2.1905.45.1-2.38
> 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/10.1515/BCHM2.1905.45.1-2.38
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Tyrosine and derivatives
DL-Tyrosine	1153	Click to see C1=CC(=CC=C1CC(C(=O)O)N)O	181.19	unknown	https://doi.org/10.1515/BCHM2.1906.48.5.387
L-Tyrosine	6057	Click to see	181.19	unknown	https://doi.org/10.1515/BCHM2.1906.48.5.387
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
An inositol	892	Click to see	180.16	unknown	https://doi.org/10.1016/S0031-9422(00)80263-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Galactopinitol A	25201084	Click to see	356.32	unknown	https://doi.org/10.1016/S0031-9422(00)80263-0
> 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/S0031-9422(00)80263-0
Stachyose	439531	Click to see	666.60	unknown	https://doi.org/10.1016/S0031-9422(00)80263-0
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
Dl-Tryptophan	1148	Click to see	204.22	unknown	https://doi.org/10.1515/BCHM2.1905.45.1-2.38
Tryptophan	6305	Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N	204.22	unknown	https://doi.org/10.1515/BCHM2.1905.45.1-2.38
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(-)-Albine	185761	Click to see	232.32	unknown	https://doi.org/10.1016/S0031-9422(00)98264-5
(1R,2R,9R,12S)-12-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridec-5-en-4-one	91747723	Click to see	232.32	unknown	https://doi.org/10.1021/JF00043A011 https://doi.org/10.1515/ZNC-1985-11-1204
1-(3,4-Dihydro-5-(2R)-2-piperidinyl-1(2H)-pyridinyl)ethanone	442625	Click to see	208.30	unknown	https://doi.org/10.1016/S0031-9422(00)90709-X https://doi.org/10.1515/ZNC-1985-11-1204 https://doi.org/10.21608/BFSA.1998.67835
N-Methylalbine	91748139	Click to see	246.35	unknown	https://doi.org/10.1515/ZNC-1985-11-1204
> Organoheterocyclic compounds / Quinolizidines
(7S,7aS,14S,14aR)-1,7,7a,8,9,10,11,13,14,14a-Decahydro-7,14-methano-2H,6H-dipyrido(1,2-a:1',2'-e)(1,5)diazocin-2-one	6918763	Click to see	246.35	unknown	https://doi.org/10.1021/JF00043A011 https://doi.org/10.1021/NP50072A031 https://doi.org/10.1021/NP50101A023 https://doi.org/10.1055/S-2006-960212 https://doi.org/10.1007/BF00417727
13-alpha-Hydroxymultiflorine	15939900	Click to see	262.35	unknown	https://doi.org/10.1016/0031-9422(96)00195-1 https://doi.org/10.1055/S-2006-960212 https://doi.org/10.1016/S0031-9422(00)98264-5
5-Dehydromultiflorine	15939902	Click to see	244.33	unknown	https://doi.org/10.1021/NP50072A031
> Organoheterocyclic compounds / Quinolizidines / Quinolizidinones
(2R,10S)-10-prop-2-enyl-7,11-diazatricyclo[7.3.1.02,7]tridecan-6-one	102004777	Click to see C=CCC1C2CC(CN1)C3CCCC(=O)N3C2	234.34	unknown	https://doi.org/10.1016/S0031-9422(00)90709-X https://doi.org/10.1021/NP50101A023 https://doi.org/10.1021/NP50072A031 https://doi.org/10.1055/S-2006-959680
Tetrahydrorhombifoline	15511175	Click to see C=CCCN1CC2CC(C1)C3CCCC(=O)N3C2	248.36	unknown	https://doi.org/10.1016/S0031-9422(00)89604-1
> Organoheterocyclic compounds / Quinolizines
Lusitanine	6452371	Click to see	208.30	unknown	https://doi.org/10.1021/JF00065A034
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51402809	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1016/S0031-9422(00)00366-6
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	https://doi.org/10.1016/S0031-9422(00)00366-6
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/S0031-9422(00)00366-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside	5280704	Click to see	432.40	unknown	https://doi.org/10.1016/S0031-9422(00)00366-6
> Phenylpropanoids and polyketides / Isoflavonoids / Coumaronochromones
(5aS,10bR)-1,3,8-trihydroxy-10b-methoxy-2-(3-methylbut-2-enyl)-5aH-[1]benzofuro[2,3-b]chromen-11-one	101609099	Click to see	384.40	unknown	https://doi.org/10.1515/ZNC-1991-5-602
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
(7S)-16,18-dihydroxy-7-(2-hydroxypropan-2-yl)-6,11,13-trioxapentacyclo[10.8.0.02,10.05,9.014,19]icosa-1(12),2(10),3,5(9),14,16,18-heptaen-20-one	162923663	Click to see	368.30	unknown	https://doi.org/10.1080/00021369.1985.10866954
2'-Hydroxygenistein	5282074	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)O	286.24	unknown	https://doi.org/10.1271/BBB.56.690 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/ https://doi.org/10.1515/ZNC-1992-0605 https://doi.org/10.1016/S0021-9673(00)91283-4 https://doi.org/10.1016/S0031-9422(00)00366-6 https://doi.org/10.1016/S0031-9422(00)97740-9 https://doi.org/10.1016/S0031-9422(00)84936-5
2'-Hydroxyisolupalbigenin	14237659	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
5,7-Dihydroxy-3-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one	5317480	Click to see	338.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/
5,7-dihydroxy-3-[(2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one	162931035	Click to see	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
5,7-dihydroxy-3-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]chromen-4-one	163033019	Click to see CC(C)(C1CC2=C(O1)C=CC(=C2O)C3=COC4=CC(=CC(=C4C3=O)O)O)O	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
Genistein	5280961	Click to see	270.24	unknown	https://doi.org/10.1016/S0021-9673(00)91283-4 https://doi.org/10.1016/S0031-9422(00)97740-9 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/ https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://doi.org/10.1271/BBB1961.49.1775 https://doi.org/10.1271/BBB.56.690 https://doi.org/10.1515/ZNC-1992-0605
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://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/
Licoisoflavone A	5281789	Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=CC(=CC(=C3C2=O)O)O)O)C	354.40	unknown	https://doi.org/10.1271/BBB.56.690 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/ https://doi.org/10.1271/BBB1961.49.1775 https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1016/0031-9422(89)80140-2
Lupinalbin A	5324349	Click to see	284.22	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1271/BBB1961.49.1775
Lupinalbin D	44260099	Click to see	352.30	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1271/BBB1961.49.1775
Lupinalbin E	44260097	Click to see	368.30	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1271/BBB1961.49.1775
Lupinisoflavone C	44257284	Click to see	354.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1271/BBB1961.49.1775
Lupinisoflavone D	5378771	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1271/BBB1961.49.1775
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 3-prenylated isoflavanones
(5aR,10bR)-1,3,8,10b-tetrahydroxy-2,7-bis(3-methylbut-2-enyl)-5aH-[1]benzofuro[2,3-b]chromen-11-one	101608758	Click to see	438.50	unknown	https://doi.org/10.1515/ZNC-1991-5-602
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(17S)-7,20-dihydroxy-17-(2-hydroxypropan-2-yl)-10,12,16-trioxapentacyclo[11.7.0.03,11.04,9.015,19]icosa-1(20),3(11),4(9),5,7,13,15(19)-heptaen-2-one	162893299	Click to see	368.30	unknown	https://doi.org/10.1080/00021369.1985.10866954
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-6-[(2S)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one	162949527	Click to see	438.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(2R)-4-hydroxy-6-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162900857	Click to see	454.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(2R)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162847575	Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)O)C	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-6-[(2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one	21591963	Click to see CC(C)(C1CC2=C(O1)C=CC(=C2)C3=COC4=CC5=C(CC(O5)C(C)(C)O)C(=C4C3=O)O)O	438.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(2S)-4-hydroxy-6-(4-hydroxyphenyl)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	94856056	Click to see	354.40	unknown	https://doi.org/10.1080/00021369.1985.10866954
(2S)-4-hydroxy-6-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162900856	Click to see CC(C)(C1CC2=C(O1)C=CC(=C2O)C3=COC4=CC5=C(CC(O5)C(C)(C)O)C(=C4C3=O)O)O	454.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(2S)-4-hydroxy-6-[4-hydroxy-3-(2-methylprop-1-enyl)phenyl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162917166	Click to see CC(=CC1=C(C=CC(=C1)C2=COC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)O)C	408.40	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
(2S)-4-hydroxy-6-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	163014265	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
(2S)-6-(2,4-dihydroxyphenyl)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162924346	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(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	352.30	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
(2S)-6-[2,4-dihydroxy-3-(2-methylprop-1-enyl)phenyl]-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	163056050	Click to see CC(=CC1=C(C=CC(=C1O)C2=COC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)O)C	424.40	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
(3R)-3,5-dihydroxy-7-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one	162865014	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
(3S)-3,5-dihydroxy-7-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-2,2-dimethyl-3,4-dihydropyrano[3,2-g]chromen-6-one	162865015	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
1,3,8-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-[1]benzofuro[2,3-b]chromen-11-one	14728995	Click to see	368.30	unknown	https://doi.org/10.1515/ZNC-1990-3-402
3-[(3R)-3,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one	162924831	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C4=C(C=C3)OC(C(C4)O)(C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
3-[(3R)-3,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one	162963636	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
3-[(3S)-3,5-dihydroxy-2,2-dimethyl-3,4-dihydrochromen-8-yl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one	162963637	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]chromen-4-one	163042146	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
3-[2,4-dihydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]phenyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one	162996200	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
4-Hydroxy-2-(2-hydroxypropan-2-yl)-6-[2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one	10526985	Click to see	438.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
4-Hydroxy-6-[4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	44348258	Click to see	454.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
4-Hydroxy-6-[4-hydroxy-3-(2-methylprop-1-enyl)phenyl]-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	162917165	Click to see	408.40	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
5,7-dihydroxy-3-[(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-6-(3-methylbut-2-enyl)chromen-4-one	162967077	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
5,7-dihydroxy-3-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-6-(3-methylbut-2-enyl)chromen-4-one	163078198	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C4=C(C=C3)OC(C4)C(C)(C)O)O)O)C	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
5,7-dihydroxy-3-[(2S)-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-7-yl]-6-(3-methylbut-2-enyl)chromen-4-one	162967078	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]chromen-4-one	162873519	Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC(C(=C)C)O)O)O)C	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
6-[2,4-Dihydroxy-3-(2-methylprop-1-enyl)phenyl]-4-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-g]chromen-5-one	163056049	Click to see CC(=CC1=C(C=CC(=C1O)C2=COC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)O)C	424.40	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Alpinumisoflavone	5490139	Click to see	336.30	unknown	https://doi.org/10.1515/ZNC-1983-3-407
Angustone A	15664151	Click to see	422.50	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/
Angustone B	5481235	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C4=C(C=C3)OC(C=C4)(C)C)O)O)C	420.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1515/ZNC-1991-5-602
Angustone C	14237658	Click to see	420.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Chandalone	12302850	Click to see	404.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Erythrinin C	44257283	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)O	354.40	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1271/BBB1961.49.1775
Lupalbigenin	10001388	Click to see	406.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1515/ZNC-1983-3-407 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/
Lupinalbin B	14309761	Click to see	352.30	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1271/BBB1961.49.1775
Lupinalbin C	14309762	Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)OC5=C4C=CC(=C5)O)O	368.30	unknown	https://doi.org/10.1080/00021369.1985.10866954 https://doi.org/10.1271/BBB1961.49.1775
Lupinalbin F	44260100	Click to see	420.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
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)84936-5 https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://doi.org/10.1016/S0021-9673(00)91283-4
Lupinisoflavone B	632835	Click to see	370.40	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1271/BBB1961.49.1775
Lupinisoflavone G	14237661	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisoflavone H	14237662	Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=CC4=C(CC(O4)C(C)(C)O)C(=C3C2=O)O)O)C	438.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisoflavone I	14237663	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisoflavone J	14237664	Click to see	438.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisoflavone K	14728996	Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3=COC4=CC5=C(CC(O5)C(C)(C)O)C(=C4C3=O)O)C	436.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402
Lupinisoflavone L	14728997	Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=C(C5=C(C=C4)OC(C5)C(C)(C)O)O)C	436.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402
Lupinisoflavone M	14728998	Click to see CC(C)(C1CC2=C(O1)C=CC(=C2)C3=COC4=C(C3=O)C(=C(C(=C4)O)CC(C(C)(C)O)O)O)O	456.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402
Lupinisoflavone N	14728999	Click to see CC(C)(C1CC2=C(O1)C=CC(=C2O)C3=COC4=C(C3=O)C(=C(C(=C4)O)CC(C(C)(C)O)O)O)O	472.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402
Lupinisol A	14237668	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisol B	14237669	Click to see CC(=CCC1=C(C=CC(=C1O)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC(C(=C)C)O)O)O)C	438.50	unknown	https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisol C	14237670	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisolone A	14237665	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisolone B	14237666	Click to see	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupinisolone C	14237667	Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C4C(=C(C=C3)O)CC(C(O4)(C)C)O)O)C	438.50	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Lupisoflavone	101602348	Click to see	368.40	unknown	https://doi.org/10.1016/S0031-9422(00)97740-9
Luteone	5281797	Click to see	354.40	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/ https://doi.org/10.1016/S0031-9422(00)97740-9 https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://doi.org/10.1271/BBB.56.690
Parvisoflavone B	14550385	Click to see	352.30	unknown	https://doi.org/10.1016/S0021-9673(00)91283-4 https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1515/ZNC-1990-3-402 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C
Wighteone	5281814	Click to see	338.40	unknown	https://doi.org/10.1016/S0021-9673(00)91283-4 https://doi.org/10.1016/S0031-9422(00)84936-5 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1075519/ https://doi.org/10.1271/BBB.56.690 https://doi.org/10.1016/S0031-9422(00)97740-9 https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
2'-Hydroxygenistein 4',7-O-diglucoside	101644597	Click to see	610.50	unknown	https://doi.org/10.1016/S0031-9422(00)00366-6
3-(2,4-dihydroxyphenyl)-5-hydroxy-6-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162974815	Click to see	516.50	unknown	https://doi.org/10.1515/ZNC-1991-7-802
3-(2,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163080494	Click to see C1=CC(=C(C=C1O)O)C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O	448.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
3-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	163001359	Click to see	448.40	unknown	https://doi.org/10.1016/S0031-9422(00)00366-6
3-[[(2S,3S,4S,5R,6S)-6-[3-(2,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid	162952317	Click to see	534.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5-hydroxy-7-[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	162975801	Click to see	516.50	unknown	https://doi.org/10.1515/ZNC-1991-7-802
3-oxo-3-[[(2S,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-3-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid	162851226	Click to see	518.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
5-hydroxy-3-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	154496625	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
5-hydroxy-7-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	162942009	Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O	594.50	unknown	https://doi.org/10.1016/S0031-9422(00)00366-6
5,7-dihydroxy-3-[2-hydroxy-3-(3-methylbut-2-enyl)-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	162998978	Click to see	516.50	unknown	https://doi.org/10.1515/ZNC-1991-7-802
5,7-dihydroxy-3-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	101049550	Click to see	448.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
5,7-dihydroxy-3-[4-[(2R,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	154497485	Click to see	432.40	unknown	https://doi.org/10.1515/ZNC-1991-7-802
Genistein 7-O-glucoside-6''-malonate	44257280	Click to see	518.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C
Genistin	5281377	Click to see	432.40	unknown	https://doi.org/10.1002/(SICI)1099-1565(199907/08)10:4<198::AID-PCA454>3.0.CO;2-C https://doi.org/10.1515/ZNC-1991-7-802 https://doi.org/10.1515/ZNC-1992-0605
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol	5319744	Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O	300.26	unknown	https://doi.org/10.1016/S0031-9422(00)84936-5
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A	5280373	Click to see	284.26	unknown	https://doi.org/10.1007/BF00595030
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Isoderrone	14237660	Click to see	336.30	unknown	https://doi.org/10.1016/0031-9422(89)80140-2
Licoisoflavone B	5481234	Click to see	352.30	unknown	https://doi.org/10.1515/ZNC-1983-3-407 https://doi.org/10.1016/0031-9422(89)80140-2 https://doi.org/10.1016/S0031-9422(00)84936-5 https://doi.org/10.1016/S0031-9422(00)81531-9 https://doi.org/10.1515/ZNC-1991-7-802
Sophoraisoflavone A	10383349	Click to see CC1(C=CC2=C(C=CC(=C2O1)C3=COC4=CC(=CC(=C4C3=O)O)O)O)C	352.30	unknown	https://doi.org/10.1515/ZNC-1990-3-402

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Lupinus albus

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