Calluna vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Calluna vulgaris - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID64400edf45c7a470410653
Scientific name Calluna vulgaris
Authority (L.) Hill
First published in Brit. Fl. , ed. 2, 1: 114 (1808)

Description Top

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Calluna vulgaris, also known as common heather, ling, or simply heather, is a low-growing evergreen shrub found in Europe and Asia Minor. It is the only species in the genus Calluna and is part of the flowering plant family Ericaceae. This plant is typically found in open sunny areas or in moderate shade on acidic soils. It is the dominant plant in heathland and moorland in Europe, and can also be found in bog vegetation and acidic pine and oak woodland. Calluna is able to withstand grazing and can regenerate after occasional burning. It is often managed in nature reserves and grouse moors through grazing and light burning. The genus Calluna was named by Richard Anthony Salisbury and is believed to have originated from the Ancient Greek word Kallyno, meaning "beautify, sweep clean". The specific epithet vulgaris means 'common' in Latin. Calluna can be distinguished from the closely related genus Erica by its four-part corolla and calyx, as opposed to five parts in Erica.

Synonyms Top

Scientific name Authority First published in
Calluna atlantica Seem. J. Bot. 4: 306 (1866)
Calluna beleziana Rouy Bull. Soc. Bot. France 42: 500 (1895)
Calluna ciliaris Schur Enum. Pl. Transsilv. : 447 (1866)
Calluna elegantissima Sennen Bol. Soc. Ibér. Ci. Nat. 28: 177 (1929 publ. 1930)
Calluna erica DC. Fl. Franç. , ed. 3, 3: 680 (1805)
Calluna genuina Ducommun Taschenb. Schweiz. Bot. : 491 (1869)
Calluna sagittifolia Gray Nat. Arr. Brit. Pl. 2: 399 (1821 publ. 1822)
Calluna vulgaris var. alba (Weston) G.Don Gen. Hist. 3: 828 1834
Calluna vulgaris f. alba (Weston) Braun-Blanq. Ill. Fl. Mitt.-Eur. 5(3): 1691 1926
Calluna vulgaris subsp. elegantissima (Sennen) Mateo Fl. Montiberica 29: 92 (2005)
Calluna vulgaris var. purpurea G.Don Gen. Hist. 3: 828 1834
Calluna vulgaris f. purpurea (G.Don) Braun-Blanq. Ill. Fl. Mitt.-Eur. 5(3): 1691 1926
Erica confusa Gand. Fl. Lyon. : 149 (1875)
Erica glabra Gilib. Fl. Lit. Inch. i. 3. 1782
Erica herbacea Georgi Beschr. Nation. Russ. Reich 3(4): 935 (1800)
Erica lutescens K.Koch Dendrologie 2(2): 138 (1873)
Erica nana K.Koch Dendrologie 2(2): 138 (1873)
Erica prostrata K.Koch Dendrologie 2(1): 138 (1872)
Erica reginae K.Koch Dendrologie 2(1): 138 (1872)
Erica sagittifolia Stokes Bot. Mat. Med. 2: 370 (1812)
Erica vulgaris L. Sp. Pl. : 352 (1753)
Erica vulgaris var. alba Weston Bot. Univ. 1: 98 (1770)
Ericoides vulgaris (L.) Merino Fl. Galicia 2: 260 (1906)
Erica vulgaris var. hirsuta K.F.Waitz Beschr. Gatt. Art. Heid. 91. 1805
Erica vulgaris var. squarrosa K.F.Waitz Beschr. Gatt. Art. Heid. 91. 1805
Erica vulgaris var. plena K.F.Waitz Beschr. Gatt. Art. Heid. 92. 1805

Common names Top

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Language Common/alternative name
English heather
English scotch heather
English ling
English scottish heather
Spanish quirola
Spanish urz
Spanish bermeja
Spanish argana
Spanish argaña
Spanish azuleja
Spanish bercol
Spanish bércol
Spanish berecilla
Spanish bereza
Spanish berezo
Spanish berezo negro
Spanish bierco
Spanish biercol
Spanish biercol merino
Spanish biércol merino
Spanish brecina
Spanish brecinilla
Spanish brezo comun
Spanish brezo común
Spanish brezo de lastra
Spanish bruga
Spanish bruza
Spanish charliza
Spanish cherliz
Spanish corroucha
Spanish erica sagittifolia var villosa
Spanish erica sagittifolia var. villosa
Spanish escobas de brecina
Spanish escobas mogarizas
Spanish garbena
Spanish garbeña
Spanish gorbiza
Spanish mogariza
Spanish orbezo
Spanish pica la miel
Spanish queirino
Spanish queiriño
Spanish querihuela
Spanish quirihuela
Spanish quírola
Spanish reguarno
Spanish reguazno
Spanish sardino
Spanish urce
Spanish urcias
Spanish urcina
Arabic حشيشة المكنسة
ba Ябай арса
Belarusian Верас
Bulgarian обикновена калуна
Catalan bruguerola
Czech vřes obecný
Czech vřes
Welsh grug cyffredin
Welsh grug ysgub
Welsh grug mêl
Danish hedelyng
German heidekraut
German besenheide
Esperanto kaluno
Estonian harilik kanarbik
Estonian kanarbik
Basque txilar arrunt
Basque ainar arrunt
Persian علف جاروب
Finnish kangaskanerva
Finnish kanerva
Faroese vanligur heiðalyngur
French callune
French bruyere callune
French bruyère callune
French callune vulgaire
frr hiaskrüüs
Irish fraoch coiteann
Irish fraoch mór
Irish fraoch
Galician queiroga
Galician queiroa
Hebrew אברש מצוי
Croatian vrijesak
Croatian vrijes
Hungarian csarabfű
Hungarian közönséges csarab
Hungarian csarab
Armenian հավամրգի
Icelandic beitilyng
Italian brugo
Japanese ギョリュウモドキ
Japanese カルーナ属
Kazakh Көкбұта
Korean 칼루나
lmo brugh
Lithuanian viržiai
Lithuanian viržis
Lithuanian Šilinis viržis
Latvian parastais virsis
Latvian sila virsis
Malayalam കാലൂണ
mrj Йӓнгӓршуды
myv Урядыця куракш
Norwegian Bokmål røsslyng
Dutch struikhei
Dutch struikheide
Norwegian Nynorsk røsslyng
olo kanabro
os Вереск
os Мыдæг
Polish wrzos pospolity
Polish wrzos zwyczajny
Romansh brutg
Romanian mărtăloagă
Russian Вереск обыкновенный
se heavušdaŋas
se livdnju
Samogitian Šėlā
Serbo-Croatian vrijes
sjd Нуҏҏт
Slovak šedivník
Slovak vres obyčajný
Slovak vres
Serbian vres
stq fodderheede
stq riesheede
Swedish callluna
Swedish ljungsläktet
Swedish vanlig ljung
Swedish ljung
Turkish süpürge otu
tt Арчан
Ukrainian Верес звичайний
vep kanabr'
Chinese 帚石南
Chinese 帚石南屬
Chinese 红方柏
Chinese 蘇格蘭石楠
Chinese 帚石楠
Chinese 彩萼石楠

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

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-0000580837
UNII DTE28NXG2W
Canadensys 5496
USDA Plants CAVU
UConn 77
Tropicos 12300012
INPN 87501
Flora of Italy 3725
KEW urn:lsid:ipni.org:names:327305-1
The Plant List kew-2692970
Plantarium 7722
Missouri Botanical Garden 279934
PFAF Calluna vulgaris
Open Tree Of Life 519874
Observations.org 6509
NCBI Taxonomy 13385
NBN Atlas NBNSYS0000003902
Nature Serve 2.150845
IPNI 327304-1
iNaturalist 119450
GBIF 2882482
Freebase /m/02z7y5
WisFlora 8118
FEIS plants/shrub/calvul
EPPO CUNVU
EOL 583611
Elurikkus 3309
US Library of Congress sh85059819
USDA GRIN 8605
Wikipedia Calluna_vulgaris

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
GCA_964145215.1 ddCalVulg4.hap2.1 Chromosome WELLCOME SANGER INSTITUTE 2024-06-06 66.0x 496.31 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
Co-located ecological data for exploring top- and subsoil carbon dynamics across grassland-woodland contrasts Reinsch S, Lebron I, Brentegani M, Brooks M, Busi SB, Cagnarini C, Cooper D, Day J, Emmett BA, Fitos E, Goodall T, Griffiths R, Jones B, Keenan P, Keith A, Lopes-Mazzetto JM, Mason KE, Pallett D, Pereira MG, Pinder A, Robinson DA, Smart SM, Thomas A, Benham S, Vanguelova E, Cosby BJ Sci Data 09-May-2024
PMCID:PMC11081944
doi:10.1038/s41597-024-03333-w
PMID:38724554
Relationships among Hydrogen Peroxide Concentration, Catalase, Glucose Oxidase, and Antimicrobial Activities of Honeys Osés SM, Rodríguez C, Valencia O, Fernández-Muiño MA, Sancho MT Foods 26-Apr-2024
PMCID:PMC11083411
doi:10.3390/foods13091344
PMID:38731715
Insights from a 31‐year study demonstrate an inverse correlation between recreational activities and red deer fecundity, with bodyweight as a mediator Weterings MJ, Ebbinge EY, Strijker BN, Spek G, Kuipers HJ Ecol Evol 22-Apr-2024
PMCID:PMC11035974
doi:10.1002/ece3.11257
PMID:38654717
Comprehensive Elemental Profiling of Romanian Honey: Exploring Regional Variance, Honey Types, and Analyzed Metals for Sustainable Apicultural and Environmental Practices Bora FD, Andrecan AF, Călugăr A, Bunea CI, Popescu M, Petrescu-Mag IV, Bunea A Foods 19-Apr-2024
PMCID:PMC11048993
doi:10.3390/foods13081253
PMID:38672925
Impact of floral and geographical origins on honey quality parameters in Saudi Arabian regions Alaerjani WM, Mohammed ME Sci Rep 15-Apr-2024
PMCID:PMC11018611
doi:10.1038/s41598-024-59359-y
PMID:38622258
Globe-LFMC 2.0, an enhanced and updated dataset for live fuel moisture content research Yebra M, Scortechini G, Adeline K, Aktepe N, Almoustafa T, Bar-Massada A, Beget ME, Boer M, Bradstock R, Brown T, Castro FX, Chen R, Chuvieco E, Danson M, Değirmenci CÜ, Delgado-Dávila R, Dennison P, Di Bella C, Domenech O, Féret JB, Forsyth G, Gabriel E, Gagkas Z, Gharbi F, Granda E, Griebel A, He B, Jolly M, Kotzur I, Kraaij T, Kristina A, Kütküt P, Limousin JM, Martín MP, Monteiro AT, Morais M, Moreira B, Mouillot F, Msweli S, Nolan RH, Pellizzaro G, Qi Y, Quan X, Resco de Dios V, Roberts D, Tavşanoğlu Ç, Taylor AF, Taylor J, Tüfekcioğlu İ, Ventura A, Younes Cardenas N Sci Data 04-Apr-2024
PMCID:PMC10995118
doi:10.1038/s41597-024-03159-6
PMID:38575621
Transcriptome analysis of Gossypium reveals the molecular mechanisms of Ca2+ signaling pathway on arsenic tolerance induced by arbuscular mycorrhizal fungi Gong M, Bai N, Su J, Wang Y, Wei Y, Zhang Q Front Microbiol 25-Mar-2024
PMCID:PMC11000422
doi:10.3389/fmicb.2024.1362296
PMID:38591035
Standardising bee sampling: A systematic review of pan trapping and associated floral surveys Krahner A, Dietzsch AC, Jütte T, Pistorius J, Everaars J Ecol Evol 17-Mar-2024
PMCID:PMC10944983
doi:10.1002/ece3.11157
PMID:38500849
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
Commodity risk assessment of Cornus alba and Cornus sanguinea plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Manda RR, Schulz OM, Kariampa P, Akrivou A, Antonatos S, Beris D, Debode J, Kritikos C, Kormpi M, Manceau C, Papachristos D, Reppa C, Gardi C, Potting R EFSA J 12-Mar-2024
PMCID:PMC10928767
doi:10.2903/j.efsa.2024.8657
PMID:38476319
Fecal DNA metabarcoding reveals seasonal and annual variation in willow ptarmigan diet Ingvaldsen EW, Østnes JE, Kleven O, Davey M, Fossøy F, Nilsen EB R Soc Open Sci 28-Feb-2024
PMCID:PMC10898975
doi:10.1098/rsos.231518
PMID:38420626
Diurnal fuel moisture content variations of live and dead Calluna vegetation in a temperate peatland Lewis CH, Little K, Graham LJ, Kettridge N, Ivison K Sci Rep 27-Feb-2024
PMCID:PMC10899638
doi:10.1038/s41598-024-55322-z
PMID:38413683
Traditional Use of Wild Edible Plants in Slovenia: A Field Study and an Ethnobotanical Literature Review Papež Kristanc A, Kreft S, Strgulc Krajšek S, Kristanc L Plants (Basel) 24-Feb-2024
PMCID:PMC10934440
doi:10.3390/plants13050621
PMID:38475472
Soil Microbes and Plant-Associated Microbes in Response to Radioactive Pollution May Indirectly Affect Plants and Insect Herbivores: Evidence for Indirect Field Effects from Chernobyl and Fukushima Sakauchi K, Otaki JM Microorganisms 10-Feb-2024
PMCID:PMC10892324
doi:10.3390/microorganisms12020364
PMID:38399767
Land cover preferences and spatiotemporal associations of ungulates within a Scottish mammal community Lovell C, Pettorelli N, Dawson TP Ecol Evol 09-Feb-2024
PMCID:PMC10857944
doi:10.1002/ece3.11015
PMID:38343580

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol 10436 Click to see CC1=CC(=CC(=C1)O)O 124.14 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-8a-(hydroxymethyl)-4,4,6a,6b,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 293273 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1007/BF00598555
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0005-2760(92)90157-Q
Uvaol 92802 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)CO 442.70 unknown https://doi.org/10.1007/BF00598555
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00598555
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00598555
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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/10.1016/0031-9422(82)80150-7
Isochlorogensaure 12310829 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/10.1016/0031-9422(82)80150-7
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
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/10.1016/0031-9422(82)80150-7
5-hydroxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44583907 Click to see C1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
5-Hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163096285 Click to see C1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone 5281343 Click to see C1=COC2=CC(=CC(=C2C1=O)O)O 178.14 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,3R,3'R)-2,2'-Bis(3,4-dihydroxyphenyl)-3,3',4,4'-tetrahydro-2H,2'H-4,8'-bichromene-3,3',5,5',7,7'-hexol 5320711 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Cinnamtannin A2 16130899 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1155.00 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Procyanidin B2, (+)- 122738 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Procyanidin C1 169853 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> 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/10.1016/0031-9422(82)80150-7
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/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-3,5,7,8-Tetrahydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 468911 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O 304.25 unknown https://doi.org/10.1007/BF00565535
4',5,7,8-Tetra-hydroxyflavanonol 11722549 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O 304.25 unknown https://doi.org/10.1007/BF00565535
> 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/10.1016/0031-9422(82)80150-7
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/10.1007/BF00567713
https://doi.org/10.1111/J.1469-8137.1913.TB05680.X
https://doi.org/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
methyl (2S,3S,4S,5R,6S)-5-acetyloxy-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 101609672 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C(=O)OC)O)O 502.40 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
methyl (2S,3S,4S,5S,6S)-5-acetyloxy-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 162999450 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C(=O)OC)O)O 502.40 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
Methyl 5-acetyloxy-3,4-dihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylate 74977523 Click to see CC(=O)OC1C(C(C(OC1OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC=C(C=C4)O)O)C(=O)OC)O)O 502.40 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(3S,4S,5R,6R)-4,5-diacetyloxy-6-[[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxan-3-yl] acetate 162963443 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC3=CC(=CC4=C3C(=O)C(=C(O4)C5=CC(=C(C=C5)O)O)O)O)O)O)O 722.60 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
[(3S,4S,5R,6R)-4,5-diacetyloxy-6-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxan-3-yl] acetate 162963442 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC3=CC(=CC4=C3C(=O)C(=C(O4)C5=CC(=C(C=C5)O)O)O)O)O)O)O 722.60 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
[4,5-Diacetyloxy-6-[[6-[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-4-oxochromen-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxan-3-yl] acetate 162963441 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC3=CC(=CC4=C3C(=O)C(=C(O4)C5=CC(=C(C=C5)O)O)O)O)O)O)O 722.60 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4R,5R)-3,4-diacetyloxy-5-[[(2S,3S,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxolan-2-yl]methyl acetate 162873350 Click to see CC(=O)OCC1C(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)OC(=O)C)OC(=O)C 706.60 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
[(2S,3S,4R,5R)-3,4-diacetyloxy-5-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxolan-2-yl]methyl acetate 163085070 Click to see CC(=O)OCC1C(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)OC(=O)C)OC(=O)C 722.60 unknown https://doi.org/10.1016/0031-9422(93)85056-W
[(2S,3S,4R,5R)-3,4-diacetyloxy-5-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxolan-2-yl]methyl acetate 162873351 Click to see CC(=O)OCC1C(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)OC(=O)C)OC(=O)C 706.60 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
[(3S,4S,5R,6R)-4,5-diacetyloxy-6-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxan-3-yl] acetate 102080059 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O 706.60 unknown https://doi.org/10.1016/0031-9422(93)85056-W
[3,4-Diacetyloxy-5-[[6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxolan-2-yl]methyl acetate 74978178 Click to see CC(=O)OCC1C(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)OC(=O)C)OC(=O)C 722.60 unknown https://doi.org/10.1016/0031-9422(93)85056-W
[3,4-Diacetyloxy-5-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxolan-2-yl]methyl acetate 74978035 Click to see CC(=O)OCC1C(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)OC(=O)C)OC(=O)C 706.60 unknown https://doi.org/10.1016/S0031-9422(00)98261-X
[4,5-Diacetyloxy-6-[[6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]oxan-3-yl] acetate 74978036 Click to see CC(=O)OC1COC(C(C1OC(=O)C)OC(=O)C)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O 706.60 unknown https://doi.org/10.1016/0031-9422(93)85056-W
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12304330 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00567713
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
https://doi.org/10.1016/0031-9422(93)85253-N
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00567713
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Guaijaverin 5481224 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/0031-9422(93)85253-N
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
https://doi.org/10.1111/J.1469-8137.1913.TB05680.X
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Peltatoside 5484066 Click to see C1C(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 596.50 unknown https://doi.org/10.1016/0031-9422(93)85253-N
Quercetin-3-O-vicianoside 13887800 Click to see C1C(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 596.50 unknown https://doi.org/10.1016/0031-9422(93)85253-N
Reynoutrin 5878729 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1016/0031-9422(93)85253-N
Trifolin 5282149 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 101923621 Click to see C1C(OC2=C(C1=O)C(=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)C4=CC=C(C=C4)O 450.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
(2S,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163097780 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
(2S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 101265354 Click to see C1C(OC2=C(C1=O)C(=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)C4=CC=C(C=C4)O 450.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(2R,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]oxy]oxan-3-yl] acetate 101923622 Click to see CC(=O)OC1C(C(C(OC1OC2=C(C=C(C3=C2OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O)CO)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
[4,5-Dihydroxy-6-(hydroxymethyl)-2-[[3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4-oxo-2,3-dihydrochromen-8-yl]oxy]oxan-3-yl] acetate 163021955 Click to see CC(=O)OC1C(C(C(OC1OC2=C(C=C(C3=C2OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O)CO)O)O 508.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163097779 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown https://doi.org/10.1016/0031-9422(93)85253-N
https://doi.org/10.1016/0031-9422(82)80150-7
https://doi.org/10.1016/0031-9422(94)00910-L
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 73715829 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00565535
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 74819436 Click to see C1C(OC2=C(C1=O)C(=CC(=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)C4=CC=C(C=C4)O 450.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
Herbacin 5748571 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1007/BF00565535
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown https://doi.org/10.1007/978-0-387-77335-3_9

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