Lotus japonicus is a wild legume from the Fabaceae family, which is known for its diversity with about 20,000 species. This plant is significant in agriculture and biology due to its high protein and oil content and its ability to fix atmospheric nitrogen. It has become a popular model plant for studying legume genomes, particularly in relation to symbiotic relationships with rhizobia and mycorrhizal fungi. With a small genome size, diploid genome, short life cycle, and perennial nature, it is a convenient plant for research. While it shares some characteristics with the legume Medicago truncatula, they are phylogenetically different and have different nodulation development systems. L. japonicus has determinate nodules.

Synonyms Top

Scientific name	Authority	First published in
Lotus corniculatus subsp. japonicus	(Regel) H.Ohashi	Fl. Japan2b: 240 (2001)
Lotus corniculatus var. japonicus	Regel	Index Seminum (LE, Petropolitanus)1864(Suppl.): 23 (1865)
Lotus corniculatus f. semibarbatus	Nakai	Bot. Mag. (Tokyo)45: 120 (1931)
Lotus corniculatus f. hirtellus	Nakai	Bot. Mag. (Tokyo)45: 120 (1931)

Common names Top

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Language	Common/alternative name
Arabic	لوطس ياباني
Persian	آهوماش ژاپنی
Chinese	百脉根

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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 click to expand
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000194760
Tropicos	13044155
KEW	urn:lsid:ipni.org:names:503703-1
Open Tree Of Life	1081728
NCBI Taxonomy	34305
IPNI	503703-1
iNaturalist	1429824
GBIF	5357027
USDA GRIN	22722
CMAUP	NPO13504
Wikipedia	Lotus_japonicus

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
GCF_012489685.1	LjGifu_v1.2	Chromosome	Aarhus University	2022-11-15	100.0x	528.06 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

TML1 AND TML2 SYNERGISTICALLY REGULATE NODULATION AND AFFECT ARBUSCULAR MYCORRHIZA IN MEDICAGO TRUNCATULA

Chaulagain D, Schnabel E, Kappes M, Lin EX, Müller LM, Frugoli JA

bioRxiv

09-Oct-2024

PMCID:	PMC10723381
doi:	10.1101/2023.12.07.570674
PMID:	38106087

Strigolactones promote flowering by inducing the miR319-LA-SFT module in tomato

Visentin I, Ferigolo LF, Russo G, Korwin Krukowski P, Capezzali C, Tarkowská D, Gresta F, Deva E, Nogueira FT, Schubert A, Cardinale F

Proc Natl Acad Sci U S A

03-May-2024

PMCID:	PMC11087791
doi:	10.1073/pnas.2316371121
PMID:	38701118

Arbuscular Mycorrhizal Fungi Improve Lycium barbarum Potassium Uptake by Activating the Expression of LbHAK

Zhang Y, Han X, Ren W, Zhang H, Tang M

Plants (Basel)

30-Apr-2024

PMCID:	PMC11085931
doi:	10.3390/plants13091244
PMID:	38732459

A minimal Fanconi Anemia complex in early diverging fungi

Barua D, Płecha M, Muszewska A

Sci Rep

30-Apr-2024

PMCID:	PMC11061109
doi:	10.1038/s41598-024-60318-w
PMID:	38688950

Plant Cyanogenic-Derived Metabolites and Herbivore Counter-Defences

Martinez M, Diaz I

Plants (Basel)

29-Apr-2024

PMCID:	PMC11085660
doi:	10.3390/plants13091239
PMID:	38732453

Synergistic effects of plant genotype and soil microbiome on growth in Lotus japonicus

Bamba M, Akyol TY, Azuma Y, Quilbe J, Andersen SU, Sato S

FEMS Microbiol Ecol

27-Apr-2024

PMCID:	PMC11068475
doi:	10.1093/femsec/fiae056
PMID:	38678008

Recent advances in research on phosphate starvation signaling in plants

Puga MI, Poza-Carrión C, Martinez-Hevia I, Perez-Liens L, Paz-Ares J

J Plant Res

26-Apr-2024

PMCID:	PMC11081996
doi:	10.1007/s10265-024-01545-0
PMID:	38668956

RinRK1 enhances NF receptors accumulation in nanodomain-like structures at root-hair tip

Zhou N, Li X, Zheng Z, Liu J, Downie JA, Xie F

Nat Commun

26-Apr-2024

PMCID:	PMC11053012
doi:	10.1038/s41467-024-47794-4
PMID:	38670968

Nitrogen and Nod factor signaling determine Lotus japonicus root exudate composition and bacterial assembly

Tao K, Jensen IT, Zhang S, Villa-Rodríguez E, Blahovska Z, Salomonsen CL, Martyn A, Björgvinsdóttir ÞN, Kelly S, Janss L, Glasius M, Waagepetersen R, Radutoiu S

Nat Commun

23-Apr-2024

PMCID:	PMC11039659
doi:	10.1038/s41467-024-47752-0
PMID:	38653767

A receptor required for chitin perception facilitates arbuscular mycorrhizal associations and distinguishes root symbiosis from immunity

Zhang J, Sun J, Chiu CH, Landry D, Li K, Wen J, Mysore KS, Fort S, Lefebvre B, Oldroyd GE, Feng F

Curr Biol

22-Apr-2024

PMCID:	PMC11037463
doi:	10.1016/j.cub.2024.03.015
PMID:	38574729

Comparative Genomics of Lotus japonicus Reveals Insights into Proanthocyanidin Accumulation and Abiotic Stress Response

Sun Z, Liu Z, Zhi M, Ran Q, Xue W, Tang Y, Wu Y

Plants (Basel)

20-Apr-2024

PMCID:	PMC11054356
doi:	10.3390/plants13081151
PMID:	38674560

Biological Activity of Artificial Plant Peptides Corresponding to the Translational Products of Small ORFs in Primary miRNAs and Other Long “Non-Coding” RNAs

Erokhina TN, Ryazantsev DY, Zavriev SK, Morozov SY

Plants (Basel)

18-Apr-2024

PMCID:	PMC11055055
doi:	10.3390/plants13081137
PMID:	38674546

2-oxoglutarate-dependent dioxygenases and BAHD acyltransferases drive the structural diversification of orobanchol in Fabaceae plants

Homma M, Uchida K, Wakabayashi T, Mizutani M, Takikawa H, Sugimoto Y

Front Plant Sci

18-Apr-2024

PMCID:	PMC11063326
doi:	10.3389/fpls.2024.1392212
PMID:	38699535

Setting up Agrobacterium tumefaciens-mediated transformation of the tropical legume Aeschynomene evenia, a powerful tool for studying gene function in Nod Factor-independent symbiosis

Tisseyre P, Cartieaux F, Chabrillange N, Gully D, Hocher V, Svistoonoff S, Gherbi H

PLoS One

16-Apr-2024

PMCID:	PMC11020691
doi:	10.1371/journal.pone.0297547
PMID:	38625963

Antifungal Activity of Ribosome-Inactivating Proteins

Iglesias R, Citores L, Gay CC, Ferreras JM

Toxins (Basel)

15-Apr-2024

PMCID:	PMC11054410
doi:	10.3390/toxins16040192
PMID:	38668617

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
Bergenin	66065	Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)O)O)OC2=O)O	328.27	unknown	via CMAUP database
Norbergenin	90476206	Click to see C1=C2C(=C(C(=C1O)O)O)C3C(C(C(C(O3)CO)O)O)OC2=O	314.24	unknown	via CMAUP database
> 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
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	11968480	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O	332.26	unknown	via CMAUP database
[(2S)-2,3-dihydroxypropyl] 3,4,5-trihydroxybenzoate	51543740	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC(CO)O	244.20	unknown	via CMAUP database
11-O-Galloylbergenin	56680102	Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)OC2=O)O	480.40	unknown	via CMAUP database
5-Galloylshikimic acid	460897	Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O	326.25	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Diphenylmethanes
1-[3-[(3-Acetyl-2,4-dihydroxy-6-methoxy-5-methylphenyl)methyl]-2,4,6-trihydroxy-5-(3-methyl-2-butenyl)phenyl]-1-butanone	5315573	Click to see CCCC(=O)C1=C(C(=C(C(=C1O)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)CC=C(C)C)O	472.50	unknown	via CMAUP database
Mallotojaponin	122659	Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)CC=C(C)C)O)C(=O)C)O)O)C(=O)C)O	444.50	unknown	via CMAUP database
Mallotophenone	179090	Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C(C(=C2O)C(=O)C)O)C)OC)O)C(=O)C)O	404.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rhodiocyanoside A	6442274	Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)C#N	259.26	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
(2Z,6Z,10Z,14Z,18Z,22E,26E,30E)-3,7,11,15,19,23,27,31,35-nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol	12442866	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C	631.10	unknown	via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26E,30E,34E)-3,7,11,15,19,23,27,31,35,39-decamethyltetraconta-2,6,10,14,18,22,26,30,34,38-decaen-1-ol	12866490	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C	699.20	unknown	via CMAUP database
(2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E,42E)-3,7,11,15,19,23,27,31,35,39,43,47-dodecamethyloctatetraconta-2,6,10,14,18,22,26,30,34,38,42,46-dodecaen-1-ol	14380582	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C)C	835.40	unknown	via CMAUP database
3,7,11,15,19,23,27,31,35-Nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaen-1-ol	83218	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C	631.10	unknown	via CMAUP database
Ficaprenol 11	11411688	Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C	767.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
[(2R,3R,4R,4aS,10bS)-8,10-dihydroxy-2-(hydroxymethyl)-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-3-yl] 3,4,5-trihydroxybenzoate	71571588	Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)CO)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O	632.50	unknown	via CMAUP database
[(2R,3R,4S,4aS,10bS)-3,8,10-trihydroxy-9-methoxy-6-oxo-4-(3,4,5-trihydroxybenzoyl)oxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-2-yl]methyl 3,4,5-trihydroxybenzoate	102314951	Click to see COC1=C(C=C2C(=C1O)C3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC2=O)O	632.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Epilotaustralin	185818	Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O	261.27	unknown	via CMAUP database
Rhodiocyanoside D	6442230	Click to see CC=C(COC1C(C(C(C(O1)CO)O)O)O)C#N	259.26	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	102442447	Click to see COC1=C(C=CC(=C1)O)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	454.40	unknown	via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-2,6-dimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	25262417	Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)OC)O	484.40	unknown	via CMAUP database
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	102442448	Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O	454.40	unknown	via CMAUP database
4-Hydroxy-3-methoxyphenyl 2-O,6-O-bis(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside	102147465	Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O	606.50	unknown	via CMAUP database
I(2)-D-Glucopyranoside, 3,4,5-trimethoxyphenyl, 2,6-bis(3,4,5-trihydroxybenzoate)	102469980	Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	650.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxy-3-methylphenyl)ethanone	14602300	Click to see CC1=C(C=C(C(=C1O)C(=O)C)O)OC	196.20	unknown	via CMAUP database
Butyrylmallotochromene	189457	Click to see CCCC(=O)C1=C2C(=C(C(=C1O)CC3=C(C(=C(C(=C3O)C(=O)C)O)C)OC)O)C=CC(O2)(C)C	470.50	unknown	via CMAUP database
Isomallotochromene	10433453	Click to see CC1=C(C(=C(C(=C1OC)CC2=C3C(=C(C(=C2O)C(=O)C)O)C=CC(O3)(C)C)O)C(=O)C)O	442.50	unknown	via CMAUP database
Mallophenone	14602301	Click to see CC1=C(C(=C(C(=C1OC)C)O)C(=O)C)O	210.23	unknown	via CMAUP database
Mallotochromene	126969	Click to see CC1=C(C(=C(C(=C1OC)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C)O)O)C(=O)C)O	442.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxamides / Nicotinamides
Nicotinamide	936	Click to see C1=CC(=CN=C1)C(=O)N	122.12	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate	107905	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
(+)-Catechin gallate	5276454	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
Epigallocatechin Gallate	65064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin	15559735	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O	334.23	unknown	via CMAUP database
Isorhamnetin	5281654	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	316.26	unknown	via CMAUP database
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 / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin	128861	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O	287.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Peonidin	441773	Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O	301.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Vestitol, (-)-	182259	Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Eucomic acid, (-)-	23757219	Click to see C1=CC(=CC=C1CC(CC(=O)O)(C(=O)O)O)O	240.21	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,4,6-Tetragalloylglucose	11297287	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	via CMAUP database
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	via CMAUP database
NP-003686	73178	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O	788.60	unknown	via CMAUP database
Pentagalloylglucose	65238	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione	11754973	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O	482.30	unknown	via CMAUP database
[(10R,11R,13R,14R,15S)-3,4,5,11,20,21,22-heptahydroxy-8,17-dioxo-14-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate	14284542	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	786.60	unknown	via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,14,20,21,22-heptahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-13-yl]methyl 3,4,5-trihydroxybenzoate	14429414	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)O	786.60	unknown	via CMAUP database
[(1S,19R,21S,22R,23R)-6,7,8,11,12,13,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-22-yl] 3,4,5-trihydroxybenzoate	14284664	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)O	786.60	unknown	via CMAUP database
2-[[(1R,7R,8S,26R,28S,29R,38R)-1,14,15,18,19,20,34,35,39,39-decahydroxy-2,5,10,23,31-pentaoxo-28-(3,4,5-trihydroxybenzoyl)oxy-6,9,24,27,30,40-hexaoxaoctacyclo[34.3.1.04,38.07,26.08,29.011,16.017,22.032,37]tetraconta-3,11,13,15,17,19,21,32,34,36-decaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid	16201525	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)OC1=C(C(=C(C=C1C(=O)O)O)O)O	1120.70	unknown	via CMAUP database
2-[[(1S,19R,21S,22R,23R)-6,7,8,11,12,22,23-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-13-yl]oxy]-3,4,5-trihydroxybenzoic acid	46905124	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O)O)O)O)O)O	802.60	unknown	via CMAUP database
3,3a(2),4a(2)-Tri-O-methylellagic acid	11674590	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O	344.30	unknown	via CMAUP database
4,4'-Di-O-methylellagic acid	11580745	Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4O)OC)C(=O)O2)O	330.24	unknown	via CMAUP database
Casuarictin	73644	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	via CMAUP database
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database
Geraniin	3001497	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	via CMAUP database
Giadmmrdajabjm-oaqcrpkasa-	21668995	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C(C(C(OC8OC(=O)C9=CC(=C(C(=C9)O)O)O)CO)OC5=O)O)O)O)O)O)O)O	808.60	unknown	via CMAUP database
Mahtabin A	10557787	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	938.70	unknown	via CMAUP database
Mallotinic Acid	10056140	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)OC6=C(C(=C(C=C6C(=O)O)O)O)O)O	802.60	unknown	via CMAUP database
Mallotusinin	514180	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7=C(O6)C(=C(C=C7C(=O)O3)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	918.60	unknown	via CMAUP database
Pmgvhtaltibnie-gloqphdasa-	21668994	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)OC1=C(C(=C(C=C1C(=O)O)O)O)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1278.90	unknown	via CMAUP database
Punicafolin	5320800	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O	938.70	unknown	via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa-	21636130	Click to see C1C(C2C(O1)(C3(C(=O)O2)C45CC(=O)C(O3)(C6(C4C7=C(O6)C(=C(C=C7C(=O)OC8C9C(C(COC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O9)O)O)O)O)O)O)OC8OC(=O)C1=CC(=C(C(=C1)O)O)O)OC5=O)O)O)O)O)O)O	1110.80	unknown	via CMAUP database

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Lotus japonicus

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