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Vaccinium angustifolium

Vaccinium angustifolium - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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Vaccinium angustifolium, also known as the wild lowbush blueberry, is a species of blueberry native to eastern and central Canada and the northeastern United States. It is the most common species of commercially used wild blueberries and is known for its "low sweet" berries. The plant has glossy blue-green leaves and produces white or pink bell-shaped flowers, followed by small dark blue to black berries. It grows best in wooded areas with well-drained acidic soils and is fire-tolerant, often increasing in numbers after a forest fire. The lowbush blueberry is an important food source for many animals and is also used in traditional burning and mowing techniques by farmers to stimulate production. During the fruit-bearing year, blueberry growers rent honey bee hives for pollination, and also rely on wild bees. The lowbush blueberry is the state fruit of Maine and the provincial berry of Nova Scotia, and is celebrated in the town of Oxford, Nova Scotia as the "Wild Blueberry Capital of Canada."

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)

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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No subspecies added yet.

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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Name Authority First published in
Vaccinium angustifolium f. chiococcum (W.Deane) B.Boivin Naturaliste Canad. 93: 437. 1966
Vaccinium angustifolium f. leucocarpum (W.Deane) Rehder J. Arnold Arbor. 20: 426. 1939
Vaccinium angustifolium f. nigrum (Alph.Wood) B.Boivin Naturaliste Canad. 93: 437 (1966)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000422967
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

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
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
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
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
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
Shade Effect on Phenology, Fruit Yield, and Phenolic Content of Two Wild Blueberry Species in Northwestern Ontario, Canada Dyukaryeva V, Mallik AU Plants (Basel) 07-Dec-2023
PMCID:PMC10747682
doi:10.3390/plants12244099
PMID:38140426
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
A mixture of Nordic berries improves cognitive function, metabolic function and alters the gut microbiota in C57Bl/6J male mice Huang F, Marungruang N, Martinsson I, Camprubí Ferrer L, Nguyen TD, Gondo TF, Karlsson EN, Deierborg T, Öste R, Heyman-Lindén L Front Nutr 03-Oct-2023
PMCID:PMC10580983
doi:10.3389/fnut.2023.1257472
PMID:37854349
Rust Fungi on Medicinal Plants in Guizhou Province with Descriptions of Three New Species Wu Q, He M, Liu T, Hu H, Liu L, Zhao P, Li Q J Fungi (Basel) 21-Sep-2023
PMCID:PMC10532644
doi:10.3390/jof9090953
PMID:37755061
In vitro and ex vitro propagation of Turkish myrtles through conventional and plantform bioreactor systems Şimşek Ö, Dönmez D, Sarıdaş MA, Acar E, Aka Kaçar Y, Paydaş Kargı S, İzgü T PeerJ 18-Sep-2023
PMCID:PMC10512933
doi:10.7717/peerj.16061
PMID:37744226
Modification of the existing maximum residue levels for mefentrifluconazole in various commodities Bellisai G, Bernasconi G, Carrasco Cabrera L, Castellan I, del Aguila M, Ferreira L, Santonja GG, Greco L, Jarrah S, Leuschner R, Perez JM, Miron I, Nave S, Pedersen R, Reich H, Ruocco S, Santos M, Scarlato AP, Theobald A, Tiramani M, Verani A EFSA J 15-Sep-2023
PMCID:PMC10502649
doi:10.2903/j.efsa.2023.8237
PMID:37719918
The complete chloroplast genome of Vaccinium oxycoccos (Ericaceae) Qiao X, Gu Q, Ye R, Cai J, Zhu N Mitochondrial DNA B Resour 04-Sep-2023
PMCID:PMC10478597
doi:10.1080/23802359.2023.2252943
PMID:37674913

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 / Benzoic acid esters
Methyl benzoate 7150 Click to see COC(=O)C1=CC=CC=C1 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 C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1021/JF00085A053
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1021/JF00085A053
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tridecane 12388 Click to see CCCCCCCCCCCCC 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 CC(=CC(=O)OC)C 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 CCCC(=O)OC 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 CCC(C)C(=O)O 102.13 unknown https://doi.org/10.1021/JF00085A053
Isovaleric acid 10430 Click to see CC(C)CC(=O)O 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 CC1=CC=C(C=C1)C(C)C 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 CC1(C2C(C=COC2OC3C(C(C(C(O3)CO)O)O)O)C(C1O)O)O 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 CCOC(=O)C 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 CC(CC1CCCC(N1C)CC(C2=CC=CC=C2)O)O 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 CCCCCCCC(=O)C 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 CC1=C2COC(=O)C2=C(C3=C1OC4(CCC5C(OC(=O)CCC5(C4C3)C)(C)C)C)OC 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 CC1C2CC=C(C2(OC1=O)C)C 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 CC(C)(C(=O)NC1CCCN1C(=O)C=CC2=CC=CC=C2)O 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-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0963-9969(00)00086-7
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0963-9969(00)00086-7
https://doi.org/10.1016/J.PHYMED.2006.08.005
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/JF0307595
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/J.PHYMED.2006.08.005
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2S,3R,4S,5R,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 5484292 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 493.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
(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 COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 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
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 C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(O4)CO)O)O)O)O)O)O 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-(acetylglucoside) 15385440 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)O 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 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-O-beta-D-glucopyranoside 44256977 Click to see COC1=CC(=CC(=C1O)OC)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 493.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Pelargonidin 3-O-rutinoside 443917 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 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 COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 463.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-galactoside 14311149 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-glucoside 443651 Click to see COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 479.40 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X
Petunidin 3-O-(6''-acetyl-glucoside) 101922116 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)O)O)O)O)O)O 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 COC1=CC(=CC(=C1O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(CO4)O)O)O)O)O 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 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
> Phenylpropanoids and polyketides / Macrolides and analogues
Avermectin A1b 9940924 Click to see CC1C=CC=C2COC3C2(C(C=C(C3OC)C)C(=O)OC4CC(CC=C(C1OC5CC(C(C(O5)C)OC6CC(C(C(O6)C)O)OC)OC)C)OC7(C4)C=CC(C(O7)C(C)C)C)O 873.10 unknown https://doi.org/10.1111/J.1365-2621.1994.TB08189.X

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