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Ajuga genevensis

Ajuga genevensis - 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 UUID6440372100e3d280276683
Scientific name Ajuga genevensis
Authority L.
First published in Sp. Pl. : 561 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Teucrium genevense Crantz Stirp. Austr. Fasc. , ed. 2, 2: 253 (1769)
Bugula alpina All. Fl. Pedem. 1: 45 (1785)
Bugula genevensis Crantz Inst. Rei Herb. 1: 518 (1766)
Bugula tomentosa Gilib. Fl. Lit. Inch. 1: 94 (1782)
Ajuga genevensis var. alpina (L.) Nyman Consp. Fl. Eur. 567. 1881
Ajuga genevensis var. foliosa (Tratt.) Beck Fl. Nieder-Osterreich 2: 1025. 1893
Ajuga genevensis var. longistyla St.-Lag. Étude Fl. éd. 8, 2: 685. 1889
Ajuga genevensis var. arida Fr. Novit. Fl. Suec. Alt. 175. 1828
Ajuga genevensis var. integrifolia Sanio Term. Füz. 1889: iii, t. XII.
Ajuga genevensis var. grossidens Briq. Lab. Alp. Mar. 105. 1891
Ajuga genevensis var. elatior Fr. Novit. Fl. Suec. Alt. 175. 1828
Ajuga alpestris Dumort. Fl. Belg. : 42 (1827)
Ajuga alpicola Dalla Torre Alpenfl. : 188 (1899)
Ajuga alpina L. Mant. Pl. 1: 80 (1767)
Ajuga foliosa Tratt. Arch. Gewächsk. 1: 25 (1811)
Ajuga genevensis var. alpicola Beck Fl. Nieder-Osterreich 2: 1025. 1893
Ajuga genevensis var. glabrifolia St.-Lag. Étude Fl. ed. 8, 2: 685 1889
Ajuga glabrifolia (St.-Lag.) Bonnier Fl. Ill. France 9: 31 (1927)
Ajuga interrupta Dulac Fl. Hautes-Pyrénées : 407 (1867)
Ajuga lanata F.Mart. ex Steud. Nomencl. Bot. , ed. 2, 1: 46 (1840)
Ajuga latifolia Host Fl. Austriac. 2: 119 (1831)
Ajuga montana Rchb. Fl. Germ. Excurs. : 314 (1831)
Ajuga pyramidalis M.Bieb. Fl. Taur.-Caucas. 2: 32 (1808)
Ajuga rugosa Host Fl. Austriac. 2: 120 (1831)

Common names Top

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Language Common/alternative name
English blue bugleweed
English upright bugle
English geneva bugleweed
English geneva bugle
English blue bugle
Spanish búgula de ginebra
Spanish bugula de ginebra
Arabic عجوقة جنيفية
Azerbaijani cenevrə dirçəyi
Belarusian гарлянка жэнеўская
Bulgarian женевско срещниче
Czech zběhovec lesní
Welsh glesyn cernyw
German heide-günsel
German genfer günsel
Estonian karvane akakapsas
Finnish hammasakankaali
French bugle de geneve
French bugle de genève
Croatian ledinska ivica
Upper Sorbian kosmaty zběhowc
Georgian პირწმინდა
Lithuanian gauruotoji vaisgina
Dutch harig zenegroen
Dutch heidezenegroen
Polish dąbrówka genewska
Polish dąbrówka kosmata
Romanian gubănaş
Romanian suliman
Russian Живучка женевская
Russian Живучка мохнатая
Slovak zbehovec ženevský
Swedish kritsuga
Ukrainian Горлянка женевська
xmf ცეიშელა
Chinese 歐洲筋骨草
Chinese 欧洲筋骨草
Chinese 直立筋骨草
Chinese 喇叭草
Chinese 日内瓦筋骨草
Chinese 下草

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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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
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Turkey-in-Europe
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Southeastern U.S.A.
      • Maryland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000933858
Canadensys 6355
USDA Plants AJGE
Tropicos 17600013
INPN 80980
Flora of Italy 4412
KEW urn:lsid:ipni.org:names:444576-1
The Plant List kew-5266
Open Tree Of Life 6086026
Observations.org 6339
NCBI Taxonomy 1532251
NBN Atlas NBNSYS0000004270
Nature Serve 2.160359
IPNI 444576-1
iNaturalist 61326
GBIF 2927079
Freebase /m/04gj3d4
WisFlora 2469
EPPO AIUGE
EOL 579638
Elurikkus 2602
Wikipedia Ajuga_genevensis
CMAUP NPO12101

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
Phytochemical, In Vitro, In Vivo, and In Silico Research on the Extract of Ajuga chamaepitys (L.) Schreb. Ionus E, Schröder V, Chiţescu CL, Bucur LA, Lupu CE, Dumitrescu DE, Popescu L, Mihai DP, Olaru OT, Nițulescu GM, Boscencu R, Gîrd CE Plants (Basel) 25-Apr-2024
PMCID:PMC11085171
doi:10.3390/plants13091192
PMID:38732407
Characterization and comparative evaluation of wound healing potential of Ajugarin I and Ajuga bracteosa Wall. ex Benth Wasti Y, Muntaqua D, Majid M, Naz I, Zafar A, Khan SU, Kazmi ST, Rehman TU, Irshad N, Fatima H Front Chem 31-Jan-2024
PMCID:PMC10867974
doi:10.3389/fchem.2023.1325578
PMID:38362004
A Possible Perspective of Recultivation with Arbuscular Mycorrhiza-Inoculated Drought-Tolerant Herbaceous Plants Papp L, Habtemariam AA, Brandt S, Cseh P, Heller Á, Péter B, Szakály ÁP, Kiszel P, Codogno B, Bratek Z, Tóth Z Plants (Basel) 06-Dec-2023
PMCID:PMC10747347
doi:10.3390/plants12244088
PMID:38140415
Skin cancer, including related pathways and therapy and the role of luteolin derivatives as potential therapeutics Juszczak AM, Wöelfle U, Končić MZ, Tomczyk M Med Res Rev 21-Feb-2022
PMCID:PMC9303584
doi:10.1002/med.21880
PMID:35187675
Phytochemical Characterization of Phenolic Compounds by LC-MS/MS and Biological Activities of Ajuga reptans L., Ajuga salicifolia (L.) Schreber and Ajuga genevensis L. from Turkey GÖGER G, KÖSE YB, DEMİRCİ F, GÖGER F Turk J Pharm Sci 28-Oct-2021
PMCID:PMC8562120
doi:10.4274/tjps.galenos.2021.33958
PMID:34719190
Phagocytosis, Degranulation and Extracellular Traps Release by Neutrophils—The Current Knowledge, Pharmacological Modulation and Future Prospects Gierlikowska B, Stachura A, Gierlikowski W, Demkow U Front Pharmacol 04-May-2021
PMCID:PMC8129565
doi:10.3389/fphar.2021.666732
PMID:34017259
Lipoxygenase Inhibition by Plant Extracts Lončarić M, Strelec I, Moslavac T, Šubarić D, Pavić V, Molnar M Biomolecules 25-Jan-2021
PMCID:PMC7911790
doi:10.3390/biom11020152
PMID:33503885
Abstracts of the 12th Edition of the Biopharmacy - Pharmacokinetics & Industrial Pharmacy Symposium: 8 November 2019, Cluj-Napoca N/A Med Pharm Rep 10-Nov-2019
PMCID:PMC7010337
Comparative Phytochemical Profile, Antioxidant, Antimicrobial and In Vivo Anti-Inflammatory Activity of Different Extracts of Traditionally Used Romanian Ajuga genevensis L. and A. reptans L. (Lamiaceae) Toiu A, Mocan A, Vlase L, Pârvu AE, Vodnar DC, Gheldiu AM, Moldovan C, Oniga I Molecules 23-Apr-2019
PMCID:PMC6515068
doi:10.3390/molecules24081597
PMID:31018502
Biologically Active Ajuga Species Extracts Modulate Supportive Processes for Cancer Cell Development Rauca VF, Vlase L, Casian T, Sesarman A, Gheldiu AM, Mocan A, Banciu M, Toiu A Front Pharmacol 05-Apr-2019
PMCID:PMC6460044
doi:10.3389/fphar.2019.00334
PMID:31024305
Development of a NIR Method for the In-Line Quantification of the Total Polyphenolic Content: A Study Applied on Ajuga genevensis L. Dry Extract Obtained in a Fluid Bed Process Gavan A, Colobatiu L, Mocan A, Toiu A, Tomuta I Molecules 27-Aug-2018
PMCID:PMC6225481
doi:10.3390/molecules23092152
PMID:30150579
Ethnopharmacological in vitro studies on Austria's folk medicine—An unexplored lore in vitro anti-inflammatory activities of 71 Austrian traditional herbal drugs Vogl S, Picker P, Mihaly-Bison J, Fakhrudin N, Atanasov AG, Heiss EH, Wawrosch C, Reznicek G, Dirsch VM, Saukel J, Kopp B J Ethnopharmacol 07-Oct-2013
PMCID:PMC3791396
doi:10.1016/j.jep.2013.06.007
PMID:23770053
Are Autumn Foliage Colors Red Signals to Aphids? Chittka L, Döring TF PLoS Biol 14-Aug-2007
PMCID:PMC1945073
doi:10.1371/journal.pbio.0050187
PMID:17696643
Species groups can be transferred across different scales Petřík P, Bruelheide H J Biogeogr 12-Jun-2006
PMCID:PMC7159123
doi:10.1111/j.1365-2699.2006.01514.x
PMID:32313357
Iridoids ofStachys inflata andS. iberica N. F. Komissarenko, A. I. Derkach, I. P. Sheremet, D. A. Pakaln Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00570872

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Roseoside 9930064 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[(1S,4aR,7S,7aS)-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7-yl] acetate 23640094 Click to see CC(=O)OC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)C 390.40 unknown https://doi.org/10.1007/BF00570872
[5-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-7-yl] acetate 14355412 Click to see CC(=O)OC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)C 390.40 unknown https://doi.org/10.1007/BF00570872
Ajugol 6325127 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 348.34 unknown https://doi.org/10.1007/BF00570872
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1R,4R,4aR,5S,7R,8S,8aR)-8-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (E)-2-methylbut-2-enoate 101619546 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 534.60 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[(1S,4R,4aR,5S,7R,8S,8aR)-8-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (2R)-2-methylbutanoate 162988326 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 536.70 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[(1S,4R,4aR,5S,7R,8S,8aR)-8-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] (E)-2-methylbut-2-enoate 162918334 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 534.60 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[(1S,4R,4aR,5S,7R,8S,8aR)-8-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 101619545 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 536.70 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[8-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbut-2-enoate 162918333 Click to see CC=C(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 534.60 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[8-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-4a-(acetyloxymethyl)-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-1-yl] 2-methylbutanoate 53463834 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 536.70 unknown https://doi.org/10.1016/0031-9422(91)83472-W
Ajugavensin A 197434 Click to see CCC(C)C(=O)OC1CCC2(CO2)C3(C1C(C(CC3OC(=O)C)C)(C)C4CC5CCOC5O4)COC(=O)C 536.70 unknown https://doi.org/10.1016/0031-9422(91)83472-W
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(3-hydroxy-5-methoxy-4-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 11723266 Click to see CC1=C(C=C(C=C1OC)OC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown via CMAUP database
[2,6-dihydroxy-3-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone 10393178 Click to see CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C3C(C(C(C(O3)CO)O)O)O)O)C(=O)C4=CC=CC=C4)O 568.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azepines
4-hydroxy-7-(2-hydroxy-2-methylpropyl)-1H-azepine-2,5-dione 54749584 Click to see CC(C)(CC1=CC(=O)C(=CC(=O)N1)O)O 211.21 unknown via CMAUP database
Pestalactam A 54749583 Click to see CC(C)(CC1=CC(=O)C(=C(C(=O)N1)Cl)O)O 245.66 unknown via CMAUP database
Pestalactam C 54749585 Click to see CC(=CC1=CC(=O)C(=C(C(=O)N1)Cl)O)C 227.64 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
[(1R,4R,4aR,5S,7R,8S,8aR)-8-[(3aR,5S,6aS)-2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl]-5-acetyloxy-1-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl (E)-2-methylbut-2-enoate 101619547 Click to see CC=C(C)C(=O)OCC12C(CC(C(C1C(CCC23CO3)O)(C)C4CC5CCOC5O4)C)OC(=O)C 492.60 unknown https://doi.org/10.1016/0031-9422(91)83472-W
[8-(2,3,3a,4,5,6a-hexahydrofuro[2,3-b]furan-5-yl)-5-acetyloxy-1-hydroxy-7,8-dimethylspiro[2,3,5,6,7,8a-hexahydro-1H-naphthalene-4,2'-oxirane]-4a-yl]methyl 2-methylbut-2-enoate 162844614 Click to see CC=C(C)C(=O)OCC12C(CC(C(C1C(CCC23CO3)O)(C)C4CC5CCOC5O4)C)OC(=O)C 492.60 unknown https://doi.org/10.1016/0031-9422(91)83472-W
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
(2S,3S,4S,5R,6S)-6-[6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 11798847 Click to see C1=CC(=C(C(=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Myricetin 3-O-glucuronide 5487413 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 3,4,5-trihydroxybenzoate 5316590 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 10961589 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=C(C(=C3C2=O)O)O)O)O)C4=CC=C(C=C4)O)O)O)O 464.40 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 via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricitrin 5281673 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)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 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)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
6''-O-(3,4,5-Trihydroxybenzoyl)quercimeritrin 100968215 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O 616.50 unknown via CMAUP database

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