Details Top

Internal ID UUID643fdb3ac8629783227887
Scientific name Lotus japonicus
Authority (Regel) K.Larsen
First published in Bot. Tidsskr.52: 13 (1955)

Ethnobotanical Use Top

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General Uses Top

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Scientific and model-organism uses:
Lotus japonicus is a widely used model legume for genetics and molecular biology, especially for symbiotic nitrogen fixation, nodulation, arbuscular mycorrhizal symbiosis, root development, and comparative legume genomics. It is diploid, has a compact, low-repeat genome (~472–480 Mb) and is short-lived and readily cultivable under controlled conditions. These properties enable forward and reverse genetics, transcriptomics, mutant screens (including TILLING), and community mapping populations. Standard protocols are established for Agrobacterium tumefaciens–mediated transformation and regeneration, alongside growth in axenic and controlled-environment systems, supporting reproducible experimentation across laboratories.

Databases and community resources:
Genome assemblies and annotations are publicly available through major databases, including the Kyoto Encyclopedia of Genes and Genomes (KEGG), the National Center for Biotechnology Information (NCBI), Ensembl Plants, and the Legume Information System (LIS). The Lotus genome is curated by the Lotus Base portal, which provides datasets and tools for functional genomics and community data sharing. These resources support standard genome browsers, BLAST queries, and comparative analyses with other legumes.

Properties relevant to use:
Genome attributes include modest size and diploidy, facilitating mapping and positional cloning. The species exhibits self-compatibility, a short life cycle (~8–12 weeks from seed to seed under controlled conditions), and a small stature suitable for controlled-environment growth. These traits allow genetic screens, time-resolved studies of symbiosis, and high-throughput phenotyping, with standard growth media and inoculation protocols documented for rhizobia and mycorrhizal fungi.

Note on commercial and industrial uses:
No documented commercial, industrial, craft, culinary, timber, fiber, resin/gum, colorant/tanning, fragrance/cosmetic, or food/beverage uses have been established for Lotus japonicus as a species.

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
Japanese ミヤコグサ
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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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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
Name Level Submitter Released Coverage Size
GCF_012489685.1 LjGifu_v1.2 Chromosome Aarhus University 2022-11-15 100 528.06 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
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
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
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!
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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 328.27 unknown via CMAUP database
Demethylbergenin 90476206 Click to see 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 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 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 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 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 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 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 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 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-dihydroxy-6-(4-hydroxy-3-methoxyphenoxy)-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 102147465 Click to see 606.50 unknown via CMAUP database
[(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 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 454.40 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 196.20 unknown via CMAUP database
1-(2,6-Dihydroxy-4-methoxy-3,5-dimethylphenyl)ethanone 14602301 Click to see 210.23 unknown via CMAUP database
Butyrylmallotochromene 189457 Click to see 470.50 unknown via CMAUP database
Isomallotochromene 10433453 Click to see 442.50 unknown via CMAUP database
Mallotochromene 126969 Click to see 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
Catechin 9064 Click to see 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 3-Gallate 5276454 Click to see 442.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Hibiscetin 15559735 Click to see 334.23 unknown via CMAUP database
Isorhamnetin 5281654 Click to see 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 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 240.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown via CMAUP database
1,2,4,6-Tetra-O-galloyl-beta-D-glucose 11297287 Click to see 788.60 unknown via CMAUP database
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 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
Penta-O-galloyl-beta-D-glucose 65238 Click to see 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 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 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 786.60 unknown via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11,14-bis[(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 10557787 Click to see 938.70 unknown via CMAUP database
1,2-DI-O-GALLOYL-3,6-(R)-HEXAHYDROXYDIPHENOYL-| cent-D-GLUCOSE 14284664 Click to see 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 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 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 330.24 unknown via CMAUP database
Casuarictin 73644 Click to see 936.60 unknown via CMAUP database
Corilagin 73568 Click to see 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Mallonin 21668995 Click to see 808.60 unknown via CMAUP database
Mallotinic Acid 10056140 Click to see 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 1278.90 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown via CMAUP database

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