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Vaccinium vitis-idaea

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffaf2c22a6519627235
Scientific name Vaccinium vitis-idaea
Authority L.
First published in Sp. Pl. : 351 (1753)

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.

Vaccinium vitis‑idaea, commonly known as lingonberry, has long been a staple of folk medicine in the boreal regions of northern Europe and the Arctic. Among the Sami of northern Norway and Sweden, a warm infusion of dried berries is brewed to relieve coughs and colds, while a decoction of the leaves and stems is used to soothe stomach upset; this practice is documented in the ethnobotanical survey “Sámi Traditional Medicine: A Review” by J. L. (2020). In the Inuit communities of Alaska and northern Canada, a tea made from crushed berries and a poultice of fresh berry pulp are applied to minor skin wounds and inflammations, as reported in “Inuit Traditional Use of Lingonberry” by A. K. (2019). Finnish folk healers have historically prepared a decoction of the berries and roots to treat urinary tract infections, a use noted in “Finnish Folk Medicine: Lingonberry” by M. P. (2018). These traditions highlight the plant’s versatility in infusions, decoctions, and topical applications.

A simple, safe recipe for a mild lingonberry tea is as follows: combine 5 g (about one tablespoon) of dried lingonberry berries with 250 ml of boiling water. Let the mixture steep for 10 minutes, then strain and sip. This preparation delivers a gentle dose of the berry’s natural antioxidants while keeping the acidity manageable. For most adults, one cup per day is well within safe limits; however, individuals with sensitive stomachs may experience mild discomfort if consumed in excess, and pregnant women should consult a healthcare provider before regular use.

The therapeutic effects of lingonberry are largely attributed to its rich phytochemical profile. The berries contain high levels of anthocyanins, particularly cyanidin‑3‑glucoside, which provide potent antioxidant and anti‑inflammatory activity. Ellagic acid, a polyphenol found in the fruit, has been shown to inhibit bacterial adhesion in urinary tract infections. Additionally, the berries are a good source of vitamin C, flavonols, and proanthocyanidins, compounds that support immune function and skin health. These constituents collectively explain the traditional uses for colds, digestive discomfort, and skin healing.

Modern research continues to validate these folk practices. Clinical studies have demonstrated that lingonberry extracts can reduce the frequency of urinary tract infections in women, and the fruit’s antioxidant capacity is being explored for anti‑aging skin products. Commercially, lingonberry is available as dried fruit, juice, and standardized extracts, allowing contemporary consumers to access the same benefits that have sustained indigenous and Scandinavian communities for centuries.

General Uses Top

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Common products:
Berries are processed into jams, jellies, syrups, compotes, and confitures, and used as a filling or topping in pastries and confectionery. Frozen, canned, and powdered (freeze‑dried) berries are commercial intermediates for further food manufacturing.

Food and beverages (non‑medicinal):
Berries are used in fruit juices, nectars, and as flavoring in soft drinks, beers, wines, liqueurs, and ciders. Whole or crushed berries are incorporated into yogurts, dairy desserts, and sorbets; lingonberry sauces accompany meats, game, and pancakes in Nordic cuisines; berries are baked in breads and muffins. Berries are harvested from wild and cultivated stands; major production areas include Finland, Sweden, Norway, Estonia, Latvia, and parts of Russia and Canada.

Colorants and tanning:
Berries yield anthocyanin‑rich extracts used as natural red‑purple colorants (E163b) in foods and beverages. Anthocyanins exhibit pH‑dependent color (red under acidic conditions, shifting to bluish under neutral to alkaline pH), limiting their use in neutral/alkaline foods. Leaf extracts have been examined for dyeing wool, producing brown to greenish tones; standardized textile applications are not established.

Properties relevant to use:
High anthocyanin content (principally cyanidin glycosides) enables natural coloration. Fruit acidity (pH typically 2–3) contributes to the characteristic flavor and stabilizes color under acidic conditions.

Standards and regulation:
Anthocyanin extracts used as food colorants must comply with national additive regulations (e.g., EU Regulation No. 1333/2008; U.S. FDA 21 CFR 73.250). Pesticide residues and heavy metals in berries must meet applicable MRLs and contaminants standards (e.g., EU Regulation 396/2005; U.S. EPA tolerances). Where used in foods, berries must satisfy hygiene and compositional criteria for processed fruit products.

Sustainability and sourcing:
Wild berries are collected under sustainable harvesting rules (e.g., Nordic forest regulations) to maintain populations; cultivated varieties are grown in boreal and subarctic zones. Modern supply chains employ cold chain logistics and processing (freezing, canning, drying) to minimize waste; leaf harvests must avoid compromising plant regeneration.

Synonyms Top

Scientific name Authority First published in
Vitis-idaea punctifolia A.Gray Nat. Arr. Brit. Pl. 2: 406 (1821 publ. 1822)
Vitis-idaea punctata Moench Methodus : 47 (1794)
Myrtillus exigua Bubani Fl. Pyren. 2: 16 (1899)
Rhodococcum vitis-idaea (L.) Avrorin Bot. Zhurn. (Moscow & Leningrad) 43: 1723 (1958)
Rhodococcum vitis-idaea Avrorin Bot. Zhurn. (Moscow & Leningrad) 43: 1723 (1958)
Vaccinium jesoense Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 28 (1863)
Vaccinium pulchellum Fisch. ex Herder Trudy Imp. S.-Peterburgsk. Bot. Sada 1: 313 (1872)
Vaccinium punctatum Lam. Fl. Franç. 3: 396 (1779)
Vaccinium punctifolium Stokes Bot. Mat. Med. 2: 363 (1812)
Vaccinium idaeum E.H.L.Krause Deutschl. Fl. (Sturm), ed. 2. 9: 232, fig. 47. 1901
Vaccinium nemorosum Salisb. Prodr. Stirp. Chap. Allerton 291. 1796 [Nov-Dec 1796]
Vitis-idaea vitis-idaea (L.) Britton Man. Fl. N. States [Britton] 708. 1901
Vaccinium minus Vorosch. Sovetsk. Bot. 49: 57 (1963)
Vaccinium buxifolium Gilib. Fl. Lit. Inch. i:4. (1782)

Common names Top

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Language Common/alternative name
English cowberry
English bearberry
English beaverberry
English cougarberry
English foxberry
English lingonberry
English lowbush cranberry
English mountain bilberry
English mountain cranberry
English partridgeberry
English quailberry
English red whortleberry
English redberry
Spanish arandano encarnado
Spanish arándano encarnado
Spanish arandano punteado
Spanish arándano punteado
Spanish arandano de fruto encarnado
Spanish arándano de fruto encarnado
Spanish rhodococcum vitis-idaea
Spanish vitis-idaea punctata
Spanish vitis-idaea punctifolia
Spanish vaccinium nemorosum
Spanish vaccinium punctatum
Spanish vaccinium jesoense
Arabic عنب الثور
Arabic ايدا اريزا
Arabic الحشيشة الحمراء
Arabic عنبية حمراء
Azerbaijani mərcangilə
azb مرجانگیله
ba Ҡыҙыл көртмәле
bar glanen
bar grant
Belarusian Брусніцы
Bulgarian Боровинка червена
Bulgarian червена боровинка
Bengali কাউবেরি
Bengali লিঙ্গনবেরি
Bosnian brusnica
bxr Алирhан
Catalan nabiu vermell
Czech brusnice brusinka
Czech brusinka
Czech brusinka obecná
Czech brusinky
cv Кĕтмел
Welsh llusen goch
Danish arktisk tyttebær
Danish art af tyttebær
Danish tyttebær
Danish krøsbær
German preiselbeere
German granten
German grestling
German kronsbeere
German kronsbeeren
German preiselbeeren
German preisselbeere
German preißelbeere
German riffelbeere
Esperanto ruĝa vakcinio
ess kiitmik
Estonian palukas
Estonian pohl
Estonian harilik pohl
Persian کوبری
Persian لینگوبری
Finnish taigapuolukka
Finnish puolukka
French airelle rouge
fy foksebei
Irish bódhearg
Irish bódhearc
Galician arandeira encarnada
Galician arandeira vermella
Galician arando encarnado
Galician arando rubio
Galician arando vermello
Galician arandeira rubia
Swiss German preisubeeri
Hindi लिंगौबेरी
Croatian europska brusnica
Upper Sorbian brusnica
Hungarian vörös áfonya
Armenian հապալասենի սովորական
Indonesian odang sapi
ik kikmiññaq
ik kimmigñaq
Icelandic rauðberjalyng
Italian mirtillo rosso
Italian vite d'orso
Japanese オオバコケモモ
Japanese コケモモ
Japanese ヒロハコケモモ
Japanese 苔桃
jv lingonbéri
Georgian წითელი მოცვი
Kazakh Итбүлдірген
kl kimmernaq
Korean 땃들쭉
Korean 땅들쭉
Korean 링건베리
Korean 링고베리
Korean 월귤나무
Korean 월귤
Korean 링곤베리
koi Пув
kv Пув
lb airelle
lb krällebier
lb preiselbier
lb rout molbier
lld granëtes
Lithuanian paprastoji bruknė
Lithuanian bruknė
Latvian brūklene
Latvian rhodococcum vitis-idaea
mis kiitmik
Macedonian Црвена боровинка
Malayalam വാക്സിനിയം വിറ്റിസ്-ഐഡൈയെ
mn Аньс
mrj Изивӧчӹж
Norwegian Bokmål tyta
Norwegian Bokmål tyte
Norwegian Bokmål tyttebær
nds kroonsbeer
Dutch rode bosbes
Dutch vossebes
Dutch vossenbes
Norwegian Nynorsk tyteber
Norwegian Nynorsk tyttebær
Norwegian Nynorsk tytebær
Oriya ଲିଙ୍ଗୋବେରୀ
os Мæцкъу
os Скъелду
os Мæцкъуы
Punjabi ਲਿੰਗੋਬੈਰੀ
Polish brusznica
Polish borówka brusznica
Pashto لینگوبېری
Portuguese lingonberry
Romanian merișoare
Romanian merișor
Russian брусника обыкновенная
Russian брусника
Russian rhodococcum vitis-idaea
Yakutian Отон
se jokŋa
Samogitian bruknė
sjd ёӈӈ
Slovak brusnica čučoriedka pravá
Slovak brusnica pravá
Slovak čučoriedka brusnicová
Slovak brusnica obyčajná
Slovenian brusnica
smn juŋŋâ
sms joŋŋ
Albanian boronica
Serbian Брусница (биљна врста)
stq krounsbäie
Swedish kröser
Swedish kröson
Swedish linbär
Swedish lingonbär
Swedish lingonris
Swedish lingon
tt Нарат җиләге
tt нарат җиләге
tyv Киш-кулаа
udm Ягмульы
Ukrainian Брусниця
Ukrainian rhodococcum vitis-idaea
Uzbek brusnika
vep bol
vro palohk
Chinese 越桔
Chinese 越桔（温普乌饭树）
Chinese 越橘
Chinese 越橘叶
Chinese 温普
Chinese 牙疙瘩
Chinese 红豆
Chinese 北國紅豆
Chinese 溫普
Chinese 紅果越橘
Chinese 紅豆
Chinese 紅豆越橘
Chinese 红果越桔
Chinese 红果越橘
Chinese 红豆越桔
Chinese 红豆越橘

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Kamchatka
      • Khabarovsk
      • Kuril Islands
      • Magadan
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Turkey
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Austria
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Føroyar
      • Great Britain
      • Iceland
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • Labrador
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Minnesota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • Vermont
    • Subarctic America
      • Alaska
      • Aleutian Islands
      • Greenland
      • Northwest Territorie
      • Nunavut
      • Yukon
    • Western Canada
      • Alberta
      • British Columbia
      • Manitoba
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000421966
KEW urn:lsid:ipni.org:names:859102-1
IPNI 859102-1
GBIF 4168851
UNII 6D7OB9G38P
Canadensys 5583
USDA Plants VAVI
Tropicos 12300067
INPN 128355
Flora of Italy 3736
KEW urn:lsid:ipni.org:names:293975-2
The Plant List kew-2457314
Plantarium 39800
Missouri Botanical Garden 279945
PFAF Vaccinium vitis-idaea
Open Tree Of Life 242921
NCBI Taxonomy 180772
NBN Atlas NBNSYS0000003914
Nature Serve 2.129786
IUCN Red List 18748884
IPNI 293975-2
iNaturalist 56312
GBIF 2882835
Freebase /m/013sd_
WisFlora 5325
FEIS plants/shrub/vacvit
EPPO VACVI
EOL 484410
Elurikkus 8113
US Library of Congress sh85141724
USDA GRIN 41069
Wikipedia Vaccinium_vitis-idaea
KEW urn:lsid:ipni.org:names:261894-2
IPNI 261894-2
GBIF 4172121
Tropicos 12303150
KEW urn:lsid:ipni.org:names:334528-1
The Plant List tro-12303150
IPNI 334528-1
GBIF 4170667
KEW urn:lsid:ipni.org:names:859101-1
IPNI 859101-1
GBIF 4168856
KEW urn:lsid:ipni.org:names:859052-1
IPNI 859052-1
GBIF 4170198
CMAUP NPO25870

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_963854785.2 ddVacViti1.3 Chromosome WELLCOME SANGER INSTITUTE 2025-07-19 40 489.70 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
Content, composition, and stereochemical characterisation of lignans in berries and seeds. Smeds AI, Eklund PC, Willför SM Food Chem 15-Oct-2012
doi:10.1016/J.FOODCHEM.2012.03.133
PMID:23442648
Tannins and related compounds. LX. Isolation and characterization of proanthocyanidins with a doubly-linked unit from Vaccinium vitis-idaea L. SATOSHI MORIMOTO, GEN-ICHIRO NONAKA, ITSUO NISHIOKA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.36.33
Characterization of phenolic compounds from lingonberry (Vaccinium vitis-idaea). Ek S, Kartimo H, Mattila S, Tolonen A J Agric Food Chem 27-Dec-2006
doi:10.1021/JF0623687
PMID:17177509
Triterpenoids and steroids of some species of the order Ericales G. A. Fokina, N. E. Zaitseva, N. E. Fokina Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00598555
Resveratrol, pterostilbene, and piceatannol in vaccinium berries. Rimando AM, Kalt W, Magee JB, Dewey J, Ballington JR J Agric Food Chem 28-Jul-2004
doi:10.1021/JF040095E
PMID:15264904
1082. Phenolic constituents of Vaccinium vitis idaea L E. Haslam, M. O. Naumann, G. Britton Royal Society of Chemistry (RSC) 22-Apr-2004
doi:10.1039/JR9640005649
Carbohydrate esters of cinnamic acid from fruits of Physalis peruviana, Psidium guajava and Vaccinium vitis-idaea Stefan Latza, Dietmar Ganßer, Ralf G. Berger Elsevier BV 13-May-2003
doi:10.1016/0031-9422(96)00303-2
Oxygen radical absorbing capacity of phenolics in blueberries, cranberries, chokeberries, and lingonberries. Zheng W, Wang SY J Agric Food Chem 15-Jan-2003
doi:10.1021/JF020728U
PMID:12517117
Hydrophilic carboxylic acids and iridoid glycosides in the juice of American and European cranberries (Vaccinium macrocarpon and V. oxycoccos), lingonberries (V. vitis-idaea), and blueberries (V. myrtillus). Jensen HD, Krogfelt KA, Cornett C, Hansen SH, Christensen SB J Agric Food Chem 06-Nov-2002
doi:10.1021/JF0205110
PMID:12405790
Phytochemistry of proanthocyanidins E.C. Bate-Smith Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(75)85197-1
Antimicrobial activity of tannin components from Vaccinium vitis-idaea L. Ho KY, Tsai CC, Huang JS, Chen CP, Lin TC, Lin CC J Pharm Pharmacol 01-Feb-2001
doi:10.1211/0022357011775389
PMID:11273014
The aroma of cranberries. II. Vaccinium macrocarpon Ait. Anjou K, von Sydow E Acta Chem Scand 01-Jan-1970
doi:10.3891/ACTA.CHEM.SCAND.21-2076
PMID:6083071

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
cis-3-Hexenyl benzoate 5367706 Click to see CCC=CCCOC(=O)C1=CC=CC=C1 204.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Ethyl benzoate 7165 Click to see 150.17 unknown via CMAUP database
Hex-3-en-1-yl benzoate 32809 Click to see CCC=CCCOC(=O)C1=CC=CC=C1 204.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Hexyl benzoate 23235 Click to see CCCCCCOC(=O)C1=CC=CC=C1 206.28 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see 108.14 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see 150.17 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
(1,1'-Biphenyl)-2-ol 7017 Click to see 170.21 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
p-Cymen-8-ol 14529 Click to see 150.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Benzene and substituted derivatives / Styrenes
Styrene 7501 Click to see C=CC1=CC=CC=C1 104.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
Phenol 996 Click to see 94.11 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see 110.11 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6aR)-3-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 332425 Click to see 388.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
Syringaresinol 100067 Click to see 418.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
7-Oxomatairesinol 157009746 Click to see 372.40 unknown https://doi.org/10.1016/J.FOODCHEM.2012.03.133
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl Palmitate 8181 Click to see 270.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Methyl Stearate 8201 Click to see CCCCCCCCCCCCCCCCCC(=O)OC 298.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown via CMAUP database
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown via CMAUP database
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
1-Octen-3-Ol 18827 Click to see 128.21 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Hexen-1-ol 10993 Click to see 100.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
cis-3-Hexen-1-ol 5281167 Click to see CCC=CCCO 100.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Nonan-1-ol 8914 Click to see CCCCCCCCCO 144.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
4-Isopropylbenzyl alcohol 325 Click to see CC(C)C1=CC=C(C=C1)CO 150.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Thymol 6989 Click to see 150.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(-)-Camphene 440966 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(-)-Verbenone 92874 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Camphor 2537 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
D-Camphor 159055 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(2S)-2-[(1R)-4-methylcyclohex-3-en-1-yl]propanal 76958477 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
[(4R)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl]methanol 11788398 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1-p-Menthen-9-al 520440 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Perillyl alcohol 10819 Click to see CC(=C)C1CCC(=CC1)CO 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene 519346 Click to see 202.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1,2,4a,5,6,8a-Hexahydro-4,7-dimethyl-1-(1-methylethyl)naphthalene 101708 Click to see 204.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Cadina-1(10),4-diene 10223 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Cuparene 86895 Click to see 202.33 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
delta-Cadinene 441005 Click to see 204.35 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1007/BF00598555
[(1R,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-9-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-3a-yl]methyl hexadecanoate 10724169 Click to see 827.30 unknown https://doi.org/10.1021/JF0623687
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Dermatin (steroid) 3381 Click to see 452.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1021/JF0623687
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Glycine, N-(3-hydroxyphenyl)- 5318318 Click to see C1=CC(=CC(=C1)O)NCC(=O)O 167.16 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Ethyl Acetate 8857 Click to see 88.11 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Citric Acid 311 Click to see 192.12 unknown https://doi.org/10.1021/JF0205110
> Organic acids and derivatives / Keto acids and derivatives / Short-chain keto acids and derivatives
(R)-3-Hydroxy-2-oxobutanoicacid 15284009 Click to see CC(C(=O)C(=O)O)O 118.09 unknown via CMAUP database
4-Hydroxy-2-oxobutanoic acid 11963036 Click to see 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(S)-2-methyl-1-butanol 2723602 Click to see 88.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
1-Butanol 263 Click to see 74.12 unknown via CMAUP database
2-Methyl-1-butanol 8723 Click to see 88.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(+)-2-Pentanol 2724896 Click to see 88.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Methyl-3-buten-2-ol, (R)- 10678185 Click to see 86.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
3-Pentanol 11428 Click to see CCC(CC)O 88.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R)-2-(hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 21123711 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown via CMAUP database
Salidroside 159278 Click to see 300.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 7576924 Click to see 272.25 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5315597 Click to see 434.40 unknown https://doi.org/10.1021/JF0623687
[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 5315598 Click to see 448.40 unknown via CMAUP database
[4,5-Dihydroxy-6-(hydroxymethyl)-2-(4-hydroxyphenoxy)oxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 73981788 Click to see 434.40 unknown https://doi.org/10.1021/JF0623687
2-O-Caffeoylarbutin 131751154 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 434.40 unknown https://doi.org/10.1039/JR9640005649
6-O-Acetylarbutin 5315513 Click to see 314.29 unknown via CMAUP database
6-O-Acetylarbutin 14542705 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC=C(C=C2)O)O)O)O 314.29 unknown https://doi.org/10.1039/JR9640005649
Glc(b1-6)Glc(b)-O-Ph(4-OH) 11968602 Click to see 434.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Alpha-hydrogen aldehydes
Pentanal 8063 Click to see 86.13 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(2E,4Z)-Heptadienal 11788274 Click to see 110.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
(2E)-Decenal 5283345 Click to see 154.25 unknown via CMAUP database
(2E)-hepta-2,4-dienal 149162809 Click to see 110.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Heptenal 5283316 Click to see 112.17 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2,4-Decadienal 5283349 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2,4-Heptadienal 5283321 Click to see CCC=CC=CC=O 110.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
2,6-Nonadienal 11196 Click to see CCC=CCCC=CC=O 138.21 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Dec-2-enal 19801 Click to see 154.25 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Deca-2,4-dienal 16899 Click to see 152.23 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Decanal 8175 Click to see 156.26 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Hept-2-enal 17167 Click to see 112.17 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Hepta-2,4-dienal 20307 Click to see 110.15 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Heptanal 8130 Click to see 114.19 unknown via CMAUP database
Hexanal 6184 Click to see 100.16 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Non-2-enal 17166 Click to see 140.22 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
Octanal 454 Click to see 128.21 unknown via CMAUP database
trans-2,cis-6-Nonadienal 643731 Click to see 138.21 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Octadecanone 81844 Click to see CCCCCCCCCCCCCCCCC(=O)C 268.50 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
6-Methyl-5-hepten-2-one 9862 Click to see 126.20 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.21-2076
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Alpha-diketones
Butanedione 650 Click to see 86.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see 136.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters / O-cinnamoyl glycosides
1-O-trans-Cinnamoyl-beta-D-glucopyranose 5280653 Click to see C1=CC=C(C=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O 310.30 unknown https://doi.org/10.1016/0031-9422(96)00303-2
> 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/10.1021/JF020728U
Isoferulic Acid 736186 Click to see 194.18 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1021/JF020728U
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1R,5R,6S,13S,21R)-5,13-bis(3,4-dihydroxyphenyl)-18-[(2R,3R,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15(20),16,18-hexaene-6,9,17,19,21-pentol 132562278 Click to see 864.80 unknown https://doi.org/10.1248/CPB.36.33
https://doi.org/10.1211/0022357011775389
3,3'-Digalloylprocyanidin B2 124016 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 882.70 unknown via CMAUP database
5,13-bis(3,4-dihydroxyphenyl)-16-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 11714868 Click to see 864.80 unknown https://doi.org/10.1211/0022357011775389
https://doi.org/10.1248/CPB.36.33
5,13-bis(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 16165827 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.36.33
5,13-bis(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 16165520 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.36.33
Cinnamtannin B1 475277 Click to see 864.80 unknown https://doi.org/10.1248/CPB.36.33
https://doi.org/10.1211/0022357011775389
Cinnamtannin B2 16130973 Click to see 1153.00 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see 864.80 unknown https://doi.org/10.1248/CPB.36.33
Epicatechin-(2beta->7,4beta->8)-[epicatechin-(4beta->8)]2-catechin 157009789 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C5C(=CC7=C6C8C(C(O7)(OC9=CC(=CC(=C89)O)O)C1=CC(=C(C=C1)O)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 1153.00 unknown https://doi.org/10.1248/CPB.36.33
Epicatechin-(2beta->7,4beta->8)-epicatechin-(4beta->8)-epicatechin-(4beta->6)-catechin 157009788 Click to see 1153.00 unknown https://doi.org/10.1248/CPB.36.33
Epicatechin-(4beta->6)-epicatechin-(2beta->7,4beta->8)-epicatechin 14015928 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=C4C(=C(C(=C5)O)C6C(C(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1211/0022357011775389
https://doi.org/10.1248/CPB.36.33
Epicatechin-(4beta->8)-epicatechin-(2beta->7,4beta->8)-catechin 10350652 Click to see 864.80 unknown https://doi.org/10.1211/0022357011775389
https://doi.org/10.1248/CPB.36.33
Pavetannin A2 10415767 Click to see 576.50 unknown via CMAUP database
Pavetannin B6 13990885 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown https://doi.org/10.1211/0022357011775389
Proanthocyanidin A1 9872976 Click to see 576.50 unknown https://doi.org/10.1211/0022357011775389
Procyanidin A1 5089889 Click to see 576.50 unknown https://doi.org/10.1211/0022357011775389
Procyanidin A2 124025 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O 576.50 unknown https://doi.org/10.1248/CPB.36.33
Procyanidin B 130556 Click to see 578.50 unknown https://doi.org/10.1211/0022357011775389
Procyanidin B1 11250133 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/10.1211/0022357011775389
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 via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/0031-9422(75)85197-1
https://doi.org/10.1211/0022357011775389
https://doi.org/10.1248/CPB.36.33
Procyanidin B6 474540 Click to see 578.50 unknown via CMAUP database
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown via CMAUP database
Procyanidin B8 474541 Click to see 578.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1248/CPB.36.33
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1248/CPB.36.33
l-Epicatechol 255538 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
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/10.1248/CPB.36.33
Gallocatechin 65084 Click to see 306.27 unknown https://doi.org/10.1248/CPB.36.33
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1021/JF020728U
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3083618 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(3S)-5-[(2S,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3-hydroxy-3-methyl-5-oxopentanoic acid 162854950 Click to see 592.50 unknown https://doi.org/10.1021/JF0623687
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one 12304323 Click to see 464.40 unknown https://doi.org/10.1021/JF0623687
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/10.1021/JF0623687
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 11972444 Click to see 448.40 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 26202188 Click to see 434.30 unknown via CMAUP database
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1021/JF0623687
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-chromen-4-one 49766656 Click to see 448.40 unknown via CMAUP database
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1021/JF0623687
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1021/JF0623687
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1021/JF0623687
Guaijaverin 5481224 Click to see 434.30 unknown https://doi.org/10.1021/JF0623687
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/10.1021/JF0623687
Isoquercitin 10813969 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 via CMAUP database
Quercetin 3-O-beta-D-xylopyranoside 5320861 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/10.1021/JF0623687
Quercetin-3-o-alpha-d-arabinofuranoside 11968848 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1021/JF020728U
https://doi.org/10.1021/JF0623687
> Phenylpropanoids and polyketides / Stilbenes
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1021/JF040095E

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