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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Heather has been gathered for infusions across northern Europe for colds and urinary discomfort. In Scotland, a simple tea of boiled shoots and flower tips was a household remedy for coughs, chest colds, and sore throats (Auld Lang Syne, ed. by Thomas Nelson & Sons, 1905). In Galicia, Spain, infusions of Calluna vulgaris aerial parts were traditionally taken as an expectorant and for respiratory complaints (Villar Pérez et al., 1992). In Lithuania, tea from heather tops was used as a diuretic and for cystitis-like symptoms (Raal & Volmer, 1999). In Scandinavia, the plant’s tops and flowers are still collected for decoctions taken as a diuretic and urinary tonic, and the same preparation is used externally as a wash for skin irritations (Oyen & Damboldt, 1998).

Mild heather tea. Place 1–2 teaspoons of dried aerial parts in 250 ml of just‑boiling water, cover, and steep 10 minutes; strain. For diuretic or cough support, take 1 cup up to twice daily. Do not exceed this dose or combine with other diuretics unless under professional guidance. In pregnancy or with known renal disease, use only after medical consultation and at reduced strength.

1:5 ethanol tincture. Chop fresh heather tops and flowers; weigh and pack loosely. Cover with 45% ethanol to make a 1:5 w:v preparation. Macerate in a dark jar for 14 days with daily shaking, then press and filter. For mild urinary and cough support, 2–3 ml can be taken up to twice daily with water. Do not exceed this dose, avoid if pregnant or breastfeeding, and consult a clinician if taking diuretics or sedatives.

Well‑reported constituents include arbutin (a hydroquinone glucoside associated with urinary‑system activity), flavonoids such as quercetin and myricetin, and phenolic acids like chlorogenic acid; the plant also produces tannins that provide a gentle astringent action (EMA Assessment Report on Calluna vulgaris, 2014). While much of the evidence is traditional, modern work has documented these phytochemicals and supported its use as a mild diuretic and for urinary comfort. Contemporary herbal suppliers offer standardized heather teas and tinctures for the same indications, and field use continues in Ireland, Scotland, and Scandinavia.

General Uses Top

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Common products:
Calluna vulgaris is harvested as heather peat for livestock bedding. The peat is formed from accumulated, partially decomposed aerial parts (shoots and small stems) in ombrotrophic bogs where Calluna is a characteristic plant.

Industrial and craft applications:
Bedding: Heather peat is used in stables and byres in northern and western Europe, valued for absorbency and low dust. Claims include a water capacity of 400–600% and moderate ammonia binding; sources report ammonia reduction or control rather than binding and note dependence on material moisture and compaction. Bales and loose peat are supplied by specialized producers.

Colorants and tanning:
Leaves and stems yield brown to tan dyes via mordanted wool dyeing. Historical northern textile practice records direct extraction in boiling water or alkaline solutions; exact dye chemistry is not standardized. Tannins are present, but the plant is not a commercial source for tanning.

Fragrance and cosmetics:
Flowers are fragrant and occasionally used in perfumery as a minor note; they are also incorporated in some bath and body products for scent and texture. Regulatory requirements for cosmetic use vary by jurisdiction.

Properties relevant to use:
Heather peat has a high lignin proportion relative to cellulose, contributing to its slow decomposition and color; pH is acidic (often 3–4 in water extracts). Ash content is relatively high, reflecting mineral input from windblown dust; calorific value is moderate to low compared with coal, and burning requires controlled airflow to avoid smouldering.

Sustainability and sourcing:
Harvest is regulated in many jurisdictions through quotas, limits on bog area, or rotational cutting. Environmental concerns include habitat disturbance and carbon loss from peat extraction; substitution with alternative bedding materials and peat restoration are pursued to mitigate impacts. Certificates or ecolabels may apply to bedding products, but these are not universally required.

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
Erica ciliaris Huds. Fl. Angl. : 144 (1762)
Erica eremocharis Gand. Fl. Lyon. : 149 (1875)
Erica gracilis K.Koch Dendrologie II: 138 (1872).
Erica tomentosa K.Koch Dendrologie II: 138 (1872).
Erica alportii K.Koch Dendrologie II: 138 (1872).
Erica vulgaris var. glabriuscula J.Stokes A botanical materia medica 370-372 (1812).
Erica vulgaris var. villosa J.Stokes A botanical materia medica 371-372 (1812)

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
Slovenian jesenska vresa
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'
vro kanarik
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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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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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

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-0000580837
KEW urn:lsid:ipni.org:names:328637-1
IPNI 328637-1
GBIF 5681799
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
Open Tree Of Life 1080794

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 66 496.31 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
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
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
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!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / 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 124.14 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/0005-2760(92)90157-Q
(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 442.70 unknown https://doi.org/10.1007/BF00598555
Uvaol 92802 Click to see 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
Stigmast-5-en-3-ol 22012 Click to see 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-hydroxy-phenoxy)-tetrahydro-pyran-3,4,5-triol 346 Click to see 272.25 unknown https://doi.org/10.1016/0031-9422(82)80150-7
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
5,7-dihydroxychromone-7-O-beta-D-glucopyranoside 44583907 Click to see 340.28 unknown https://doi.org/10.1016/S0031-9422(00)90488-6
Arbutin 440936 Click to see 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 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 180.16 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Cinnamtannin A2 16130899 Click to see 1155.00 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Proanthocyanidin B2 5320711 Click to see 578.50 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 578.50 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Procyanidin C1 169853 Click to see 866.80 unknown https://doi.org/10.1016/0031-9422(82)80150-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Epicatechin 72276 Click to see 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 304.25 unknown https://doi.org/10.1007/BF00565535
4',5,7,8-Tetra-hydroxyflavanonol 11722549 Click to see 304.25 unknown https://doi.org/10.1007/BF00565535
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1016/0031-9422(82)80150-7
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/BF00567713
https://doi.org/10.1016/0031-9422(82)80150-7
https://doi.org/10.1111/J.1469-8137.1913.TB05680.X
> 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 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 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 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 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 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 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 706.60 unknown https://doi.org/10.1016/0031-9422(93)85056-W
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 464.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1007/BF00567713
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,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see 436.40 unknown https://doi.org/10.1016/0031-9422(93)85253-N
https://doi.org/10.1016/0031-9422(82)80150-7
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1016/0031-9422(93)85253-N
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 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/10.1111/J.1469-8137.1913.TB05680.X
https://doi.org/10.1016/0031-9422(82)80150-7
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 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
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 466.40 unknown https://doi.org/10.1016/0031-9422(82)80150-7
[(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 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 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 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
5,4'-dihydroxy-8-C-methylflavanone-7-O-beta-D-glucopyranoside 101265354 Click to see 450.40 unknown https://doi.org/10.1016/0031-9422(94)00910-L
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 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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