Details Top

Internal ID UUID643ffb1f63429627503069
Scientific name Vaccinium angustifolium
Authority Aiton
First published in Hort. Kew. [W. Aiton] 2: 11. 1789

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.

Ethnobotanical Uses

Lowbush blueberry (Vaccinium angustifolium), widespread in boreal and subboreal northeastern and north‑central North America, has a well‑documented medicinal tradition centered on infusions and decoctions of its leaves and tender twigs. Among the Saulteaux (Ojibwe) peoples of Manitoba and Saskatchewan, leaf infusions were taken as a remedy for stomach troubles and vomiting, and the same preparation was used as a general tonic for a “sick stomach” (Johns et al., 1991). On the Atlantic coast, Mi’kmaq communities of New Brunswick prepared hot water infusions of the leaves for colds, coughs, and stomachaches, and also used them in baths or washes for sore eyes (Marett, 2005). Northwest Coast peoples including the Haida and Coast Salish used cold or hot infusions of blueberries (Vaccinium spp.) for scurvy and as a tonic; the same drink was valued as a carminative to “sooth a hearty stomach” (Turner & Hebda, 1990).

For a practical tea, steep 1–2 heaping teaspoons (roughly 1–2 g) of dried leaves in 250 ml of just‑boiled water for 5–10 minutes; some preparers add a few fresh twigs to the leaf infusion and strain before drinking. Traditional accounts recommend frequent small cups for stomach upset, and many contemporary herbalists suggest 1–3 cups daily for 1–2 weeks as a short course. Safety: the leaves contain significant tannins and should be taken in modest amounts; avoid very strong or prolonged daily use during pregnancy; discontinue if stomach irritation occurs and consult a clinician if symptoms persist.

The leaves are rich in flavonols (notably quercetin), phenolic acids such as chlorogenic and caffeic acids, and proanthocyanidins; anthocyanins, principally cyanidin glycosides, occur primarily in the berries. These compounds are well known in Vaccinium angustifolium and plausibly support the reported carminative and vitamin‑C‑supporting effects of the infusions (Turner & Hebda, 1990).

Modern relevance: lowbush blueberry leaves remain in limited commercial use for herbal teas and tonic blends, and ongoing studies continue to explore their antioxidant and anti‑inflammatory activities alongside ongoing traditional tea use in Indigenous communities.

General Uses Top

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**Common products:**
The berries of *Vaccinium angustifolium* are commercially cultivated and harvested as fresh fruit, frozen products, juice concentrates, dried berries, powders, and purees. Berries are also processed into jams, jellies, syrups, and baked goods fillings.

**Industrial and craft applications:**
The fruit skins (peels) contain high levels of anthocyanins and are used as a natural source of purple-blue colorants in food products, beverages, and dietary supplements. Extracts standardized for anthocyanin content may also function as natural antioxidants in certain food applications. No significant industrial or craft uses beyond food/colorant extraction are documented for other plant parts.

**Food and beverages (non-medicinal):**
Processed products include juice concentrate, frozen berries, dried/candied berries, and fruit purées. Berries are used as ingredients in baked goods, dairy products (e.g., yogurt), cereals, confectionery, and sauces. Juice concentrate serves as a base for beverages, syrups, and fermented products like wine or mead.
Anthocyanin-rich extracts derived from berry skins are utilized as food colorants (E163 classification) and antioxidant supplements.

**Colorants and tanning:**
Anthocyanins extracted from the fruit skins act as natural water-soluble colorants (purple-blue hues) in foods, beverages, supplements, and some cosmetics. These colorants exhibit sensitivity to pH and light stability challenges typical of anthocyanins. No documented use in leather tanning.

**Wood and fiber:**
*Vaccinium angustifolium* is a low-growing shrub (typically

Synonyms Top

Scientific name Authority First published in
Vaccinium pensylvanicum Lam. Encycl. [J. Lamarck & al.] 1(1): 74 (pensilvanicum). 1783 [2 Dec 1783]
Vaccinium angustifolium var. laevifolium House Bull. New York State Mus. Nat. Hist. 243-244: 61 (1923)
Cyanococcus angustifolius (Aiton) Rydb. Brittonia 1: 94 (1931)
Cyanococcus angustifolius var. laevifolius (House) Moldenke Observed Fl. Warren : 20 (1944)
Cyanococcus pensylvanicus (Lam.) Rydb. Fl. Rocky Mts. : 645 (1917)
Vaccinium ramulosum Willd. Enum. Pl. Hort. Berol. , Suppl.: 20 (1814)
Vaccinium humile Willd. Enum. Pl. Hort. Berol. , Suppl.: 21 (1814)
Vaccinium minutiflorum P.Watson Dendrol. Brit. 2: t. 125 C (1825)
Vaccinium multiflorum Dunal Prodr. 7: 572 (1839)
Vaccinium brittonii Porter ex E.P.Bicknell Bull. Torrey Bot. Club 41: 421 (1914)
Vaccinium lamarckii Camp Bull. Torrey Bot. Club 71: 180 (1944)
Vaccinium angustifolium f. leucocarpum (W.Deane) Rehder J. Arnold Arbor. 20: 426. 1939
Vaccinium angustifolium f. chiococcum (W.Deane) B.Boivin Naturaliste Canad. 93: 437. 1966
Vaccinium angustifolium f. nigrum (Alph.Wood) B.Boivin Naturaliste Canad. 93: 437 (1966)

Common names Top

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Language Common/alternative name
English lowbush blueberry
English early low-bush blueberry
English low sweet blueberry
English northern lowbush blueberry
English sugarberry
Arabic عنبية ضيقة الورق
Estonian ahtalehine mustikas
Finnish kanadanmustikka
French bleuet feuilles troites
French bleuet à feuilles étroites
Italian mirtillo di terra
Vietnamese việt quất bụi thấp
Chinese 矮叢藍莓
Chinese 矮丛越橘
Chinese 矮丛蓝莓
Chinese 狭叶越橘

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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No germination or propagation data was added yet.

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

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Database ID/link to page
World Flora Online wfo-0000422967
KEW urn:lsid:ipni.org:names:859106-1
IPNI 859106-1
GBIF 4168754
KEW urn:lsid:ipni.org:names:858970-1
IPNI 858970-1
GBIF 4172151
KEW urn:lsid:ipni.org:names:859037-1
IPNI 859037-1
GBIF 4170472
Tropicos 12302767
KEW urn:lsid:ipni.org:names:334287-1
The Plant List kew-2458389
PFAF Vaccinium brittonii
IPNI 334287-1
USDA GRIN 40993
UNII R3538BZ1BW
Cornell Woody Plants 359
Canadensys 5566
USDA Plants VAAN
UConn 518
Tropicos 12300044
INPN 761957
KEW urn:lsid:ipni.org:names:858831-1
The Plant List kew-2458810
PFAF Vaccinium angustifolium
Open Tree Of Life 3900375
NCBI Taxonomy 472369
Nature Serve 2.143176
IPNI 261779-2
iNaturalist 84542
GBIF 2882868
Freebase /m/0b6ttz
WisFlora 5317
FEIS plants/shrub/vacang
EPPO VACAN
EOL 583661
USDA GRIN 40981
Wikipedia Vaccinium_angustifolium
Tropicos 12300669
KEW urn:lsid:ipni.org:names:262087-2
The Plant List tro-12300669
IPNI 262087-2
GBIF 2882871
USDA GRIN 41027

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Dietary Sources, Stabilization, Health Benefits, and Industrial Application of Anthocyanins—A Review Saini RK, Khan MI, Shang X, Kumar V, Kumari V, Kesarwani A, Ko EY Foods 17-Apr-2024
PMCID:PMC11049351
doi:10.3390/foods13081227
PMID:38672900
A cryptic syngameon within Betula shrubs revealed: Implications for conservation in changing subarctic environments Touchette L, Godbout J, Lamothe M, Porth I, Isabel N Evol Appl 17-Apr-2024
PMCID:PMC11022622
doi:10.1111/eva.13689
PMID:38633131
Wild Blueberry Extract Intervention in Healthy Older Adults: A Multi-Study, Randomised, Controlled Investigation of Acute Cognitive and Cardiovascular Effects Cheng N, Barfoot KL, Le Cozannet R, Fança-Berthon P, Lamport DJ, Williams CM Nutrients 16-Apr-2024
PMCID:PMC11054866
doi:10.3390/nu16081180
PMID:38674870
Sea Cucumber and Blueberry Extracts Suppress Inflammation and Reduce Acute Lung Injury through the Regulation of NF-κB/MAPK/JNK Signaling Pathway in Lipopolysaccharide-Treated C57BL/6 Mice Fagbohun OF, Thilakarathna WP, Zhou J, Lehmann C, Jiao G, Rupasinghe HP Molecules 28-Mar-2024
PMCID:PMC11013731
doi:10.3390/molecules29071511
PMID:38611791
A deep multi-task learning approach to identifying mummy berry infection sites, the disease stage, and severity Qu H, Zheng C, Ji H, Huang R, Wei D, Annis S, Drummond F Front Plant Sci 28-Mar-2024
PMCID:PMC11007028
doi:10.3389/fpls.2024.1340884
PMID:38606063
The effects of protein supplementation, fumagillin treatment, and colony management on the productivity and long-term survival of honey bee (Apis mellifera) colonies Peirson M, Ibrahim A, Ovinge LP, Hoover SE, Guarna MM, Melathopoulos A, Pernal SF PLoS One 15-Mar-2024
PMCID:PMC10942092
doi:10.1371/journal.pone.0288953
PMID:38489327
Transcriptome-Based Identification of Candidate Flowering-Associated Genes of Blueberry in a Plant Factory with Artificial Lighting (PFAL) under Short-Day-Length Conditions An H, Zhang J, Li S, Zhang X Int J Mol Sci 11-Mar-2024
PMCID:PMC10969908
doi:10.3390/ijms25063197
PMID:38542171
Structures and Biological Activities of Secondary Metabolites from Xylaria spp. Chen W, Yu M, Chen S, Gong T, Xie L, Liu J, Bian C, Huang G, Zheng C J Fungi (Basel) 29-Feb-2024
PMCID:PMC10971283
doi:10.3390/jof10030190
PMID:38535199
Vaccinium uliginosum L. (bog bilberry) and the search for its alleged toxicity: a review Vaneková Z, Holloway P, Rollinger JM Front Toxicol 31-Jan-2024
PMCID:PMC10864615
doi:10.3389/ftox.2024.1358840
PMID:38357417
Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW J Fungi (Basel) 26-Jan-2024
PMCID:PMC10890244
doi:10.3390/jof10020105
PMID:38392777
Role of a Polyphenol-Enriched Blueberry Preparation on Inhibition of Melanoma Cancer Stem Cells and Modulation of MicroRNAs Alsadi N, Yahfoufi N, Nessim C, Matar C Biomedicines 16-Jan-2024
PMCID:PMC10813708
doi:10.3390/biomedicines12010193
PMID:38255297
In Vitro and In Vivo Evaluation of Bioactive Compounds from Berries for Wound Healing Vendrame S, Alaba T, Marchi N, Tsakiroglou P, Klimis-Zacas D Curr Dev Nutr 14-Jan-2024
PMCID:PMC10862523
doi:10.1016/j.cdnut.2024.102078
PMID:38351974
The Role of Natural Extracts in the Management of Infantile Hemangiomas and Vascular Tumors Roca IC, Cojocaru E, Rusu CD, Trandafir LM, Săveanu CI, Lupu VV, Butnariu LI, Ţarcă V, Moscalu M, Bernic J, Lupu A, Ţarcă E Pediatric Health Med Ther 06-Jan-2024
PMCID:PMC10778175
doi:10.2147/PHMT.S439537
PMID:38213420
Diversity of potential nitrogen-fixing bacteria from rhizosphere of the Coffea arabica L. and Coffea canephora L. Bullergahn VB, Menezes KM, Veloso TG, da Luz JM, Castanheira LF, Pereira LL, da Silva MD 3 Biotech 02-Jan-2024
PMCID:PMC10758376
doi:10.1007/s13205-023-03875-7
PMID:38173824
Protective Mechanisms of Polyphenol-Enriched Blueberry Preparation in Preventing Inflammation in the Skin against UVB-Induced Damage in an Animal Model Alsadi N, Yasavoli-Sharahi H, Mueller R, Cuenin C, Chung F, Herceg Z, Matar C Antioxidants (Basel) 21-Dec-2023
PMCID:PMC10812677
doi:10.3390/antiox13010025
PMID:38275645

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 / Benzoic acid esters
Methyl Benzoate 7150 Click to see 136.15 unknown https://doi.org/10.1021/JF00085A053
> 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/J.PHYMED.2006.08.005
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown https://doi.org/10.1021/JF00085A053
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see 108.14 unknown https://doi.org/10.1021/JF00085A053
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tridecane 12388 Click to see 184.36 unknown https://doi.org/10.1021/JF00085A053
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl 3,3-dimethylacrylate 12516 Click to see CCOC(=O)C=C(C)C 128.17 unknown https://doi.org/10.1021/JF00085A053
Ethyl butyrate 7762 Click to see CCCC(=O)OCC 116.16 unknown https://doi.org/10.1021/JF00085A053
Methyl 3-methyl-2-butenoate 13546 Click to see 114.14 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl butyrate 12180 Click to see 102.13 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
2-Methylbutanoic Acid 8314 Click to see 102.13 unknown https://doi.org/10.1021/JF00085A053
Isovaleric Acid 10430 Click to see 102.13 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
[(1S,5R,8R,9S,10R,11S,13R,14S,16S,17R,18S,19S)-10,13-dihydroxy-5-methyl-12-methylidene-3-oxo-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-yl] benzoate 101933335 Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7O)OC(=O)C8=CC=CC=C8 447.50 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00085A053
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,5R,6S,7R,7aS)-7-methyl-1-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5,6,7-triol 162845885 Click to see 364.34 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> 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/10.1111/J.1365-2621.1994.TB08189.X
https://doi.org/10.1111/J.1365-2621.1985.TB13789.X
> 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/10.1021/JF00085A053
Ethyl isobutyrate 7342 Click to see CCOC(=O)C(C)C 116.16 unknown https://doi.org/10.1021/JF00085A053
Ethyl propionate 7749 Click to see CCC(=O)OCC 102.13 unknown https://doi.org/10.1021/JF00085A053
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Methyl esters
Methyl isobutyrate 11039 Click to see CC(C)C(=O)OC 102.13 unknown https://doi.org/10.1021/JF00085A053
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Aralkylamines
(2R)-1-[(2S,6S)-6-[(2S)-2-hydroxy-2-phenylethyl]-1-methylpiperidin-2-yl]propan-2-ol 163194695 Click to see 277.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> 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/J.PHYMED.2006.08.005
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Nonanone 13187 Click to see 142.24 unknown https://doi.org/10.1021/JF00085A053
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown https://doi.org/10.1021/JF00085A053
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
13-Deacetoxyaustalide I 139588403 Click to see 428.50 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3,6,6a-trimethyl-3a,4-dihydro-3H-cyclopenta[b]furan-2-one 163010358 Click to see 166.22 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
2-hydroxy-2-methyl-N-[(2S)-1-[(E)-3-phenylprop-2-enoyl]pyrrolidin-2-yl]propanamide 162854059 Click to see 302.37 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/S0963-9969(00)00086-7
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
https://doi.org/10.1016/S0963-9969(00)00086-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1021/JF0307595
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,5R)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256953 Click to see 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
(2S,5S)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256977 Click to see 493.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Chrysanthemin 44256715 Click to see 449.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Cyanidin 3-(6''-acetyl-galactoside) 122396785 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C=C4)O)O)O)O)O)O)O 491.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Cyanidin 3-b-L-arabinoside 131752259 Click to see 419.40 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Cyanidin 3-O-galactoside 441699 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Delphinidin 3-(6''-acetylglucoside) 15385440 Click to see 507.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Malvidin 3-(6-acetylglucoside) 74977116 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)OC)O)OC)O)O)O)O)O 535.50 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Malvidin 3-(6''-acetyl-galactoside) 157009722 Click to see 535.50 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Malvidin 3-O-galactoside 5484292 Click to see 493.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
pelargonidin 3-O-rutinoside 443917 Click to see 579.50 unknown https://doi.org/10.1002/(SICI)1097-0010(199702)73:2<207::AID-JSFA703>3.0.CO;2-8
Peonidin-3-glucoside 443654 Click to see 463.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-galactoside 14311149 Click to see 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-Glucoside 443651 Click to see 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-O-(6''-acetyl-glucoside) 101922116 Click to see 521.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4R,5R)-2-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxyoxane-3,4,5-triol 163194737 Click to see 449.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
2-[5,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxane-3,4,5-triol 22283733 Click to see C1C(C(C(C(O1)OC2=CC3=C(C=C(C=C3[O+]=C2C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O 435.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Delphinidin 3-o-arabinoside 25087690 Click to see 435.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
> Phenylpropanoids and polyketides / Macrolides and analogues
Avermectin A1b 9940924 Click to see 873.10 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X

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