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Onobrychis viciifolia

Onobrychis viciifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Onobrychis viciifolia - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

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

Details Top

Internal ID UUID643fdd3ac5187793559188
Scientific name Onobrychis viciifolia
Authority Scop.
First published in Fl. Carniol., ed. 2, 2: 76 (1771)

Description Top

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Synonyms Top

Scientific name Authority First published in
Onobrychis viciifolia subsp. sativa Thell. Mém. Soc. Sci. Nat. Cherbourg38: 341 (1912)
Hedysarum onobrychis L. Sp. Pl. 2: 751. 1753 [1 May 1753]
Onobrychis viciifolia subsp. sativum (Lam.) Thell.
Onobrychis viciifolia var. viciifolia Scop.
Onobrychis glabra Desv. J. Bot. Agric.3: 82 (1814)
Onobrychis incana Gueldenst. Reis. Russland2: 19 (1791)
Onobrychis spicata Moench Methodus: 122 (1794)
Onobrychis pallescens Schur Verh. Naturf. Vereins Brünn15(2): 183 (1877)
Onobrychis pallens Láng ex Neilr. Aufz. Ungarn Slavon. Gefässpfl.: 349 (1865)
Onobrychis procumbens Fisch. ex Schrank Denkschr. Königl.-Baier. Bot. Ges. Regensburg2: 64 (1822)
Onobrychis collina Jord. Index Seminum (GR, Gratianopolis)1851: 8 (1851)
Onobrychis esponellae Sennen Diagn. Nouv.: 15 (1936)
Onobrychis vicioides Medik. Vorles. Churpfälz. Phys.-Ökon. Ges.2: 372 (1787)
Hedysarum onobrychioides Winkl. Arch. Naturk. Liv- Ehst- Kurlands, Ser. 2, Biol. Naturk.7: 490 (1877)
Hedysarum onobrychis L. Sp. Pl.: 751 (1753)
Onobrychis viciifolia subsp. collina (Jord.) P.D.Sell Fl. Great Britain Ireland3: 517 (2009)
Onobrychis sativa var. bifera Alef. Landw. Fl.: 70 (1866)
Onobrychis sativa var. calvescens Schur Verh. Naturf. Vereins Brünn15(2): 183 (1877)
Onobrychis sativa var. communis Alef. Landw. Fl.: 70 (1866)
Onobrychis sativa var. hirsuta Schur Verh. Naturf. Vereins Brünn15(2): 183 (1877)
Onobrychis sativa var. pseudosupina Ball J. Linn. Soc., Bot.16: 435 (1878)
Onobrychis sativa var. silvestris Alef. Landw. Fl.: 70 (1866)
Onobrychis viciifolia f. albiflora Rouy G.Rouy & J.Foucaud, Fl. France5: 285 (1899)
Onobrychis viciifolia f. glabrescens Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 146 (1902)
Onobrychis viciifolia f. inermis Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 146 (1902)
Onobrychis viciifolia f. nivea Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 146 (1902)
Onobrychis viciifolia f. pallens (Láng ex Neilr.) Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 146 (1902)
Onobrychis viciifolia f. pallidiflora Stelzhamer ex Gams G.Hegi, Ill. Fl. Mitt.-Eur.4: 1493 (1924)
Onobrychis viciifolia f. roseola Beck H.G.L.Reichenbach, Icon. Fl. Germ. Helv.22: 146 (1902)
Onobrychis viciifolia f. subvillosa (DC.) Širj. Spisy Prír. Fak. Masarykovy Univ.56: 181 (1925)
Onobrychis viciifolia var. collina (Jord.) St.-Lag. A.Cariot, Étude Fl., éd. 8, 2: 276 (1889)
Onobrychis viciifolia var. comosa Pluskal Abh. Zool.-Bot. Ges. Österreich3: 8 (1853)
Onobrychis viciifolia var. culta Gren. & Godr. Fl. France Corse1: 505 (1848)
Onobrychis viciifolia var. subvillosa DC. Prodr.2: 344 (1825)
Onobrychis vulgaris var. sativa Gaudin Fl. Helv.4: 571 (1829)
Onobrychis viciifolia var. braunii Širj. Spisy Prír. Fak. Masarykovy Univ.56: 182 (1925)
Onobrychis viciifolia var. comosa (Pluskal) Širj. Spisy Prír. Fak. Masarykovy Univ.56: 182 (1925)
Onobrychis viciifolia var. ramosa Širj. Spisy Prír. Fak. Masarykovy Univ.76: 156 (1926)
Hedysarum onobrychis var. canone S.L.Welsh Great Basin Naturalist38: 314 (1978)
Onobrychis vulgaris Gueldenst. Reis. Russland2: 19 (1791)
Hedysarum montanum Pers. Syn. Pl.2: 324 (1807)

Common names Top

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Language Common/alternative name
English common sainfoin
English esparcet
English holy-clover
English sainfoin
Spanish hedysarum echinatum
Spanish pirigallo silvestre
Spanish pirigallo
Spanish esparcilla
Spanish pipirigallo común
Spanish pipirigallo
Spanish pimpirigallo
Spanish perigallo
Spanish esparcetilla
Spanish esparceta loca
Spanish esparceta común
Spanish esparceta
Spanish cresta de abubilla
Spanish arveja de asno
Spanish arbeja de asno
Arabic عرن
Arabic انوبروخيس
Arabic عنبريس بيقي الأوراق
Belarusian Эспарцэт пасяўны
Catalan esparcet
Catalan sainfoin
Catalan pipirigall
Czech vičenec ligrus
Welsh gwyran fendigaid
Welsh y godog
Danish foder-esparsette
German sainfoin
German saat-esparsette
German futteresparsette
German futter-esparsette
Estonian harilik esparsett
Basque astorki
Persian اسپرس ویکیفولیا
Finnish esparsetti
French esparcette à feuilles de vesce
French esparcette cultivée
French sainfoin
French sainfoin cultive
French sainfoin cultivé
Upper Sorbian sywny turkowski dźećel
Hungarian takarmánybaltacim
Cornish gweg benigys
Lithuanian sėjamasis esparcetas
Lithuanian sainfoin
Latvian vīķlapu esparsete
Macedonian еспарзета
Norwegian Bokmål esparsett
Dutch esparcette
Polish sparceta siewna
Romanian sparcetă
Russian Эспарцет виколистный
Russian Эспарцет горошколистный
Russian Эспарцет обыкновенный
Russian Эспарцет посевной
Slovak vičenec vikolistý
Slovenian navadna turška detelja
Swedish sainfoin
Swedish esparsett
Turkish fiğ yapraklı korunga
Chinese 紅豆草
Chinese 驴食豆
Chinese 红羊草
Chinese 驴食草
Chinese 红豆草

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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Maintain seeds at a constant 10°C.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000205013
Flora of Alabama 5602
Canadensys 5844
USDA Plants ONVI
Tropicos 13067213
INPN 110139
Flora of Italy 2791
KEW urn:lsid:ipni.org:names:510168-1
The Plant List ild-5130
Plantarium 25478
PFAF Onobrychis viciifolia
Open Tree Of Life 359899
Observations.org 7111
NCBI Taxonomy 3882
NBN Atlas NBNSYS0000003279
Nature Serve 2.151085
IUCN Red List 176379
IPNI 60457687-2
iNaturalist 55441
GBIF 2972595
Freebase /m/0gs01
WisFlora 8371
EPPO ONBVI
EOL 689248
Elurikkus 5962
Calflora (Californian flora) 5915
USDA GRIN 25737
Wikipedia Onobrychis_viciifolia
CMAUP NPO14379

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
Improving Human Diets and Welfare through Using Herbivore-Based Foods: 2. Environmental Consequences and Mitigations Caradus JR, Chapman DF, Rowarth JS Animals (Basel) 30-Apr-2024
PMCID:PMC11083977
doi:10.3390/ani14091353
PMID:38731357
Chemical Characterization and Biological Properties of Leguminous Honey Fratianni F, Amato G, Ombra MN, De Feo V, Nazzaro F, De Giulio B Antioxidants (Basel) 18-Apr-2024
PMCID:PMC11047671
doi:10.3390/antiox13040482
PMID:38671929
Effect of plant edges strips on the conservation soil properties in modern farming field Šarūnaitė L, Arlauskienė A, Jablonskytė-Raščė D PLoS One 16-Apr-2024
PMCID:PMC11020931
doi:10.1371/journal.pone.0299104
PMID:38625970
Evaluation of the Growth, Sporulation, Fungicide Efficacy, and Host Range of Ramularia sphaeroidea Shi M, Li YZ Microorganisms 10-Apr-2024
PMCID:PMC11051774
doi:10.3390/microorganisms12040766
PMID:38674710
Diet modulates strongyle infection and microbiota in the large intestine of horses Laroche N, Grimm P, Julliand S, Sorci G PLoS One 09-Apr-2024
PMCID:PMC11003623
doi:10.1371/journal.pone.0301920
PMID:38593129
Evolutionary history of an Irano-Turanian cushion-forming legume (Onobrychis cornuta) Tayebi Z, Moghaddam M, Mahmoodi M, Kazempour-Osaloo S BMC Plant Biol 20-Mar-2024
PMCID:PMC10953250
doi:10.1186/s12870-024-04895-y
PMID:38509474
Alternative Approaches to Feeding Small Ruminants and Their Potential Benefits Boudalia S, Smeti S, Dawit M, Senbeta EK, Gueroui Y, Dotas V, Bousbia A, Symeon GK Animals (Basel) 14-Mar-2024
PMCID:PMC10967440
doi:10.3390/ani14060904
PMID:38540002
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
Land‐use affects pollinator‐specific resource availability and pollinator foraging behaviour Birkenbach M, Straub F, Kiesel A, Ayasse M, Wilfert L, Kuppler J Ecol Evol 07-Mar-2024
PMCID:PMC10918743
doi:10.1002/ece3.11061
PMID:38455145
Phytochemical analysis and anthelmintic activity of Combretum mucronatum leaf extract against infective larvae of soil-transmitted helminths including ruminant gastrointestinal nematodes Belga FN, Waindok P, Raulf MK, Jato J, Orman E, Rehbein S, Spiegler V, Liebau E, Hensel A, Ndjonka D, Strube C Parasit Vectors 01-Mar-2024
PMCID:PMC10905826
doi:10.1186/s13071-024-06194-9
PMID:38429804
Microgreens on the rise: Expanding our horizons from farm to fork Lone JK, Pandey R, Gayacharan Heliyon 11-Feb-2024
PMCID:PMC10881865
doi:10.1016/j.heliyon.2024.e25870
PMID:38390124
Chicory (Cichorium intybus) reduces cyathostomin egg excretion and larval development in grazing horses Malsa J, Boudesocque-Delaye L, Wimel L, Auclair-Ronzaud J, Dumont B, Mach N, Reigner F, Guégnard F, Chereau A, Serreau D, Théry-Koné I, Sallé G, Fleurance G Int J Parasitol Drugs Drug Resist 09-Feb-2024
PMCID:PMC10884488
doi:10.1016/j.ijpddr.2024.100523
PMID:38368671
Improved muscle fatty acid composition and oxidative stability in lambs grazing on sainfoin pasture Li Z, Peng C, Wang H, Liu X Vet Anim Sci 28-Jan-2024
PMCID:PMC10847756
doi:10.1016/j.vas.2024.100337
PMID:38328742
Amino acid and fatty acid profiles of perennial Baki™ bean Craine EB, Barriball S, Şakiroğlu M, Peters T, Schlautman B Front Nutr 12-Jan-2024
PMCID:PMC10811165
doi:10.3389/fnut.2023.1292628
PMID:38283912
A chromosome-level genome assembly for Onobrychis viciifolia reveals gene copy number gain underlying enhanced proanthocyanidin biosynthesis He J, Tian D, Li X, Wang X, Wang T, Wang Z, Zang H, He X, Zhang T, Yun Q, Zhang R, Jiang J, Jia S, Zhang Y Commun Biol 05-Jan-2024
PMCID:PMC10770414
doi:10.1038/s42003-023-05754-6
PMID:38182881

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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Lariciresinol dimethyl ether 14237703 Click to see COC1=C(C=C(C=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC)OC)OC 388.50 unknown https://doi.org/10.1021/JF000388H
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
3-Phenyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyprop-2-enoic acid 76031018 Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
alpha-(beta-D-Glucopyranosyloxy)-trans-cinnamic acid 53385591 Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphates / Diacylglycerophosphates / 1,2-diacylglycerol-3-phosphates
(2-Formyloxy-3-phosphonooxypropyl) formate 5460104 Click to see C(C(COP(=O)(O)O)OC=O)OC=O 228.09 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoinositols / Phosphatidylinositols
1-Phosphatidyl-D-myo-inositol 53477912 Click to see C(C(COP(=O)(O)OC1C(C(C(C(C1O)O)O)O)O)OC=O)OC=O 390.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoserines / Phosphatidylserines
1,2-Distearoyl phosphatidyl serine 44147587 Click to see CCCC(=O)OC(COC(=O)CC)COP(=O)(O)OCC(C(=O)O)N 385.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
alpha-Vetivone 442405 Click to see CC1CC(=O)C=C2C1(CC(=C(C)C)CC2)C 218.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[[(3S,8R,9S,10R,13R,14S,15R,17R)-15-hydroxy-10,13-dimethyl-17-[1-(1-methylazepan-2-yl)ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101427855 Click to see CC(C1CCCCCN1C)C2CC(C3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C)O 591.80 unknown https://doi.org/10.1021/JF900625R
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
N(5)-Acetyl-L-ornithine 193343 Click to see CC(=O)NCCCC(C(=O)O)N 174.20 unknown https://doi.org/10.1016/S0031-9422(00)82784-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
Ndelta-acetyl-L-ornithine 90658764 Click to see CC(=O)NCCCC(C(=O)[O-])[NH3+] 174.20 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4-Trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 53420248 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF900625R
1,3,5-Trihydroxy-4-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 179719 Click to see C1C(C(C(CC1(C(=O)O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O 338.31 unknown https://doi.org/10.1021/JF900625R
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
3-p-Coumaroylquinic acid 9945785 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1021/JF900625R
3-p-Coumaroylquinic acid, (Z)- 92135690 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1021/JF900625R
4-O-Feruloylquinic acid 4635494 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(CC(CC2O)(C(=O)O)O)O)O 368.30 unknown https://doi.org/10.1021/JF900625R
5-p-Coumaroylquinic acid, (Z)- 90478782 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF900625R
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
6-Methoxycyclohexane-1,2,3,4,5-pentol 230881 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/JF000388H
D-Pinitol 164619 Click to see COC1C(C(C(C(C1O)O)O)O)O 194.18 unknown https://doi.org/10.1021/JF000388H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/JF000388H
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1021/JF000388H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Ferulic acid 4-O-beta-D-glucoside 9820054 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1021/JF900625R
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1021/JF000388H
3-(3-Methoxy-4-{[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}phenyl)prop-2-enoic acid 73021256 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1021/JF900625R
3-[3-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 271602 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 342.30 unknown https://doi.org/10.1021/JF900625R
3-[4-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 73208527 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF900625R
4-O-beta-D-glucosyl-4-coumaric acid 9840292 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF900625R
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1021/JF900625R
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1021/JF000388H
Caffeic acid 4-O-glucoside 11382279 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)OC2C(C(C(C(O2)CO)O)O)O 342.30 unknown https://doi.org/10.1021/JF900625R
Lavandoside 13916049 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1021/JF900625R
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
5,9,10-Trihydroxy-7-(3-hydroxy-3-methylbutyl)-8-(3-methylbut-2-enyl)furo[2,3-c]xanthen-6-one 162937039 Click to see CC(=CCC1=C(C2=C(C(=C1O)O)OC3=C(C2=O)C(=CC4=C3C=CO4)O)CCC(C)(C)O)C 438.50 unknown https://doi.org/10.1021/JF900625R
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
DL-Tryptophan 1148 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1021/JF000388H
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1021/JF000388H
> Organoheterocyclic compounds / Pteridines and derivatives / Alloxazines and isoalloxazines / Flavins
Riboflavin 493570 Click to see CC1=CC2=C(C=C1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(CO)O)O)O 376.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(2R)-5-hydroxy-2,8-bis(4-hydroxyphenyl)-3,4-dihydro-2H-furo[2,3-h]chromen-9-yl]-(2,4,6-trihydroxyphenyl)methanone 162886106 Click to see C1CC2=C(C3=C(C=C2O)OC(=C3C(=O)C4=C(C=C(C=C4O)O)O)C5=CC=C(C=C5)O)OC1C6=CC=C(C=C6)O 526.50 unknown https://doi.org/10.1016/S0031-9422(00)82784-3
Methylsainfuran 44260111 Click to see COC1=CC(=C(C=C1)C2=CC3=CC(=C(C=C3O2)OC)O)OC 300.30 unknown https://doi.org/10.1016/S0031-9422(00)80477-X
Sainfuran 185034 Click to see COC1=CC(=C(C=C1)C2=CC3=CC(=C(C=C3O2)OC)O)O 286.28 unknown https://doi.org/10.1016/S0031-9422(00)80477-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(2R)-2-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxybutanedioic acid 26176222 Click to see C1=CC(=CC=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O 280.23 unknown https://doi.org/10.1021/JF900625R
(3,4,5-Trihydroxy-6-methoxyoxan-2-yl)methyl 3-(4-hydroxyphenyl)prop-2-enoate 162892461 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-methoxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 15048037 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
2-[(1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexyl]acetic acid 10569992 Click to see C1C(C(C(CC1(CC(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 352.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
2-[(1S,3R,4R,5R)-1,3,4-trihydroxy-5-[(Z)-3-(4-hydroxyphenyl)prop-2-enoyl]oxycyclohexyl]acetic acid 162987586 Click to see C1C(C(C(CC1(CC(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 352.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
2-[1,3,4-Trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoyloxy]cyclohexyl]acetic acid 85189119 Click to see C1C(C(C(CC1(CC(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 352.30 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
2-{[3-(4-Hydroxyphenyl)acryloyl]oxy}butanedioic acid 68721301 Click to see C1=CC(=CC=C1C=CC(=O)OC(CC(=O)O)C(=O)O)O 280.23 unknown https://doi.org/10.1021/JF900625R
Methyl 6-O-[(Z)-3-(4-hydroxyphenyl)propenoyl]-beta-D-glucopyranoside 102371158 Click to see COC1C(C(C(C(O1)COC(=O)C=CC2=CC=C(C=C2)O)O)O)O 340.32 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,7-Bis(4-hydroxy-3-methoxyphenyl)hepta-4,6-dien-3-one 46881044 Click to see COC1=C(C=CC(=C1)CCC(=O)C=CC=CC2=CC(=C(C=C2)O)OC)O 354.40 unknown https://doi.org/10.1021/JF900625R
> 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 https://doi.org/10.1021/JF00031A010
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/JF00031A010
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Dihydromyricetin 161557 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1016/S0031-9422(96)00415-3
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1021/JF00031A010
Gallocatechin 65084 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown https://doi.org/10.1016/S0031-9422(96)00415-3
https://doi.org/10.1021/JF00031A010
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1515/ZNC-1978-1-227
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 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 https://doi.org/10.1021/JF000388H
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 https://doi.org/10.1021/JF000388H
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[4-(5,7-dihydroxy-4-oxochromen-2-yl)-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 102371159 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)O)O 504.40 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
[6-[4-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-methoxyphenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162964126 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)OC)O)O)O 504.40 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5,7-dihydroxy-2-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 14406834 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5,7-Dihydroxy-2-[3-methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 14406833 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Isoliquiritin 5318591 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4R,5R,6S)-2-[[(2R,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781229 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 916.80 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781232 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)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 786.70 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101781231 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)OC(=O)C=CC6=CC(=C(C=C6)O)OC)O)O)O)O)O 770.70 unknown via CMAUP database
[2-[[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-methyloxan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 73109610 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 932.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.01.001
2-(3,4-dihydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-4,5-dihydroxy-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxychromen-4-one 162947896 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
2-(3,4-dihydroxyphenyl)-3-[(2S,5S)-4,5-dihydroxy-3-[(2S,3S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxychromen-4-one 44259164 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-3-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-5,7-dihydroxychromen-4-one 14299117 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF000388H
3-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 124928687 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
3-[[6-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-galactopyranosyl]oxy]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one 73803273 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)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-[(2S,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 154497062 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)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162873126 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)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-4H-chromen-3-yl 6-O-(6-deoxy-alpha-D-mannopyranosyl)-beta-D-glucopyranoside 17751019 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)OC)O)O)O)O)O)O 624.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 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 594.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF000388H
5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranosyl-(1->2)-[6-deoxyhexopyranosyl-(1->6)]hexopyranoside 24978604 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-(3,5-dimethoxy-4-hydroxy-trans-cinnamoyl)-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781230 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)OC(=O)C=CC6=CC(=C(C(=C6)OC)O)OC)O)O)O)O)O 816.70 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-[4-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781226 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)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O)O 932.80 unknown via CMAUP database
5,7,3',4'-Tetrahydroxyflavone-3-yl 2-O-[4-O-(3,5-dimethoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781227 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)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C(=C7)OC)O)OC)O)O)O)O)O)O)O 962.90 unknown via CMAUP database
5,7,4'-Trihydroxyflavone-3-yl 2-O-(3,5-dimethoxy-4-hydroxy-trans-cinnamoyl)-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781233 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)OC(=O)C=CC6=CC(=C(C(=C6)OC)O)OC)O)O)O)O)O 800.70 unknown via CMAUP database
5,7,4'-Trihydroxyflavone-3-yl 2-O-[4-O-(3-methoxy-4-hydroxy-trans-cinnamoyl)-alpha-L-rhamnopyranosyl]-6-O-(alpha-L-rhamnopyranosyl)-beta-D-glucopyranoside 101781228 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)OC6C(C(C(C(O6)C)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O)O 916.80 unknown via CMAUP database
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF000388H
Amurenoside A 10653411 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC6C(C(C(C(O6)C)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O)O 932.80 unknown via CMAUP database
Amurenoside B 11803929 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC6C(C(C(C(O6)C)O)O)OC(=O)C=CC7=CC(=C(C=C7)O)OC)O)O)O)O)O 932.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2011.01.001
Clitorin 11592917 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Isorhamnetin 3-robinobioside 6223069 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)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown https://doi.org/10.1021/JF000388H
https://doi.org/10.1016/S0031-9422(00)00143-6
Manghaslin 11498684 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1021/JF000388H
https://doi.org/10.1016/S0031-9422(00)00143-6
Mauritianin 5459192 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Myricetin 3-rutinoside 44259428 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)O 626.50 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 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)O 626.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
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 https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF000388H
Vitamin P 5293655 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 https://doi.org/10.1016/S0031-9422(00)00143-6
https://doi.org/10.1021/JF000388H
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 162905976 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
5-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162913296 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/JF900625R
Kaempferol-3-O-glucoside-7-O-rhamnoside 14035324 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/JF900625R
Quercetin 3-rutinoside 7-galactoside 13942388 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
Quercetin 3-rutinoside-7-glucoside 10190763 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)OC5C(C(C(C(O5)CO)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O)O)O 772.70 unknown https://doi.org/10.1016/S0031-9422(00)00143-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one 821416 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3S)-vestitone 44446897 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
Vestitone 439310 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1016/S0031-9422(00)91022-7
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Lopac-I-3766 6603886 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1515/ZNC-1978-1-227
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzoic acid 14132336 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown https://doi.org/10.1021/JF900625R
4-(beta-D-Glucopyranosyloxy)-3-methoxybenzoic acid 14132337 Click to see COC1=C(C=CC(=C1)C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 330.29 unknown https://doi.org/10.1021/JF900625R

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