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Vaccinium dunalianum

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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 UUID644044222927d645527584
Scientific name Vaccinium dunalianum
Authority Wight
First published in Calcutta J. Nat. Hist. 8: 175 (1847)

Description Top

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Synonyms Top

Scientific name Authority First published in
Epigynium dunalianum (Wight) Klotzsch Linnaea 24: 51 (1852)

Common names Top

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Language Common/alternative name
Chinese 大透骨草
Chinese 尾叶越橘
Chinese 樟叶越桔
Chinese 樟叶越橘
Chinese 长尾越桔
Chinese 饭米果

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Vaccinium dunalianum var. caudatifolium (Hayata) H.L.Li Woody Fl. Taiwan 700. 1963 (1963)
Vaccinium dunalianum var. megaphyllum Sleumer Bot. Jahrb. Syst. 71: 448. 1941 (1941)
Vaccinium dunalianum var. urophyllum Rehder & E.H.Wilson Pl. Wilson. 1: 560. 1913 (1913)

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001048413
Tropicos 12304471
KEW urn:lsid:ipni.org:names:858913-1
The Plant List tro-12304471
Open Tree Of Life 348403
NCBI Taxonomy 174251
IUCN Red List 146526711
IPNI 858913-1
iNaturalist 736594
GBIF 4173549
EOL 2891456
USDA GRIN 41010

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
Hypolipidemic and Antithrombotic Effect of 6′-O-Caffeoylarbutin from Vaccinium dunalianum Based on Zebrafish Model, Network Pharmacology, and Molecular Docking Wu B, Li C, Kan H, Zhang Y, Rao X, Liu Y, Zhao P Molecules 08-Feb-2024
PMCID:PMC10893483
doi:10.3390/molecules29040780
PMID:38398534
Re-identification of Colletotrichum gloeosporioides Species Complex Isolates in Korea and Their Host Plants Thao LD, Choi H, Choi Y, Mageswari A, Lee D, Kim DH, Shin HD, Choi H, Ju HJ, Hong SB Plant Pathol J 01-Feb-2024
PMCID:PMC10850535
doi:10.5423/PPJ.OA.09.2023.0133
PMID:38326955
Characterization of the Chemical Composition and Biological Activities of Bog Bilberry (Vaccinium uliginosum L.) Leaf Extracts Obtained via Various Extraction Techniques Ștefănescu BE, Socaci SA, Fărcaș AC, Nemeș SA, Teleky BE, Martău GA, Călinoiu LF, Mitrea L, Ranga F, Grigoroaea D, Vodnar DC, Socaciu C Foods 13-Jan-2024
PMCID:PMC10814626
doi:10.3390/foods13020258
PMID:38254559
6′-O-Caffeoylarbutin from Quezui Tea: A Highly Effective and Safe Tyrosinase Inhibitor Xie D, Fu W, Yuan T, Han K, Lv Y, Wang Q, Jiang Q, Zhang Y, Zhu G, Xu J, Zhao P, Yang X Int J Mol Sci 12-Jan-2024
PMCID:PMC10816276
doi:10.3390/ijms25020972
PMID:38256044
The profiles of free, esterified and insoluble-bound phenolics in peach juice after high pressure homogenization and evaluation of their antioxidant capacities, cytoprotective effect, and inhibitory effects on α-glucosidase and dipeptidyl peptidase-Ⅳ Bie S, Zhao S, Cai S, Yi J, Zhou L Food Chem X 25-Dec-2023
PMCID:PMC10784678
doi:10.1016/j.fochx.2023.101092
PMID:38223527
First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand Norphanphoun C, Hyde KD Pathogens 10-Dec-2023
PMCID:PMC10747506
doi:10.3390/pathogens12121436
PMID:38133319
Antioxidant Capacity of Free and Bound Phenolics from Olive Leaves: In Vitro and In Vivo Responses Li T, Wu W, Zhang J, Wu Q, Zhu S, Niu E, Wang S, Jiang C, Liu D, Zhang C Antioxidants (Basel) 23-Nov-2023
PMCID:PMC10740763
doi:10.3390/antiox12122033
PMID:38136153
Multi-Locus Phylogenetic Analysis Revealed the Association of Six Colletotrichum Species with Anthracnose Disease of Coffee (Coffea arabica L.) in Saudi Arabia Alhudaib K, Ismail AM, Magistà D J Fungi (Basel) 27-Jun-2023
PMCID:PMC10381574
doi:10.3390/jof9070705
PMID:37504694
Neuroprotective Effects of Agri-Food By-Products Rich in Phenolic Compounds Rojas-García A, Fernández-Ochoa Á, Cádiz-Gurrea MD, Arráez-Román D, Segura-Carretero A Nutrients 14-Jan-2023
PMCID:PMC9865516
doi:10.3390/nu15020449
PMID:36678322
Pestalotioid Species Associated with Medicinal Plants in Southwest China and Thailand Sun YR, Jayawardena RS, Sun JE, Wang Y Microbiol Spectr 10-Jan-2023
PMCID:PMC9927317
doi:10.1128/spectrum.03987-22
PMID:36625649
Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent Nahar L, Al-Groshi A, Kumar A, Sarker SD Molecules 11-Dec-2022
PMCID:PMC9787540
doi:10.3390/molecules27248786
PMID:36557918
Phenolic Constituents, Antioxidant and Cytoprotective Activities, Enzyme Inhibition Abilities of Five Fractions from Vaccinium dunalianum Wight Cheng CS, Gu QH, Zhang JK, Tao JH, Zhao TR, Cao JX, Cheng GG, Lai GF, Liu YP Molecules 26-May-2022
PMCID:PMC9181978
doi:10.3390/molecules27113432
PMID:35684371
Bioactivity-Guided Isolation of Phytochemicals from Vaccinium dunalianum Wight and Their Antioxidant and Enzyme Inhibitory Activities Zhao T, Sun M, Kong L, Xue Q, Wang Y, Wang Y, Khan A, Cao J, Cheng G Molecules 04-Apr-2021
PMCID:PMC8038501
doi:10.3390/molecules26072075
PMID:33916551
Caffeoyl arbutin and related compounds from the buds of Vaccinium dunalianum. Zhao P, Tanaka T, Hirabayashi K, Zhang YJ, Yang CR, Kouno I Phytochemistry 01-Dec-2008
doi:10.1016/J.PHYTOCHEM.2008.06.001
PMID:18639307

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(2S)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-2,8-dimethyl-3,4-dihydrochromen-6-ol 163194297 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCC=C(C)CCC=C(C)C)O 328.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid 3488508 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (1S,4aR,7R,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 162879139 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OCC4C(C(C(C(O4)OC5=CC=C(C=C5)O)O)O)O)(CO)O 644.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 7-hydroxy-7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylate 162879138 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OCC4C(C(C(C(O4)OC5=CC=C(C=C5)O)O)O)O)(CO)O 644.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Desacetyl asperulosidic acid 12315348 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Monotropein 73466 Click to see C1=CC(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)(CO)O 390.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3,4-trihydroxy-5-[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]cyclohexane-1-carboxylic acid 163194013 Click to see C1C(C(C(CC1(C(=O)O)O)OCC=CC2=CC=C(C=C2)O)O)O 324.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
(1R,3R,4S,5R)-1,3,4-trihydroxy-5-[3-(4-hydroxyphenyl)prop-2-enoxy]cyclohexane-1-carboxylic acid 162926018 Click to see C1C(C(C(CC1(C(=O)O)O)OCC=CC2=CC=C(C=C2)O)O)O 324.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 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.PHYTOCHEM.2008.06.001
3-Feruloylquinic acid 10133609 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)O)O)O 368.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
5-O-Feruloylquinic acid 73210496 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)O)O)O 368.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
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.PHYTOCHEM.2008.06.001
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
3,4,5-Trihydroxy-1-cyclohexene-1-carboxylic acid 1094 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
methyl (3S,5S)-5-hydroxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]hexanoate 162954139 Click to see CC(CC(CC(=O)OC)C1C(C(C(C(O1)CO)O)O)O)O 308.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Methyl 5-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]hexanoate 162954138 Click to see CC(CC(CC(=O)OC)C1C(C(C(C(O1)CO)O)O)O)O 308.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-[[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol 162896316 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
2-(Hydroxymethyl)-6-phenylmethoxyoxane-3,4,5-triol 4984739 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-phenylmethoxyoxane-3,4,5-triol 14079044 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
6-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-one 14774596 Click to see CC1CC(CC(=O)O1)OC2C(C(C(C(O2)CO)O)O)O 292.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Parasorboside 3050414 Click to see CC1CC(CC(=O)O1)OC2C(C(C(C(O2)CO)O)O)O 292.28 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(4-hydroxyphenoxy)-6-[[(E)-3-(4-hydroxyphenyl)prop-2-enoxy]methyl]oxane-3,4,5-triol 163189247 Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 404.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 72737666 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (E)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 101023291 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate 72737673 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-6-(2,4-dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 72737672 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)O)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-6-(3,4-dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 72737665 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C=C3)O)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[3-Acetyloxy-4,5-dihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74424257 Click to see CC(=O)OC1C(OC(C(C1O)O)OC2=CC=C(C=C2)O)COC(=O)C=CC3=CC(=C(C=C3)O)O 476.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[3,4,5-Trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74424182 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[3,4,5-Trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 3-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 162972664 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 596.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[6-(2,4-Dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74424180 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(C=C(C=C3)O)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[6-(3,4-Dihydroxyphenoxy)-3,4,5-trihydroxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74424181 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C=C3)O)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
2-(4-Hydroxyphenoxy)-6-[3-(4-hydroxyphenyl)prop-2-enoxymethyl]oxane-3,4,5-triol 162890773 Click to see C1=CC(=CC=C1C=CCOCC2C(C(C(C(O2)OC3=CC=C(C=C3)O)O)O)O)O 404.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
2-(Hydroxymethyl)-6-(4-hydroxyphenoxy)oxane-3,4,5-triol 346 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
3-[3-Methoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 73021256 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
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/10.1016/J.PHYTOCHEM.2008.06.001
6-O-Caffeoylarbutin 15689808 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 434.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
coumaroyl(3-OH)(-6)Glc4Ac(b)-O-Ph(4-OH) 72737667 Click to see CC(=O)OC1C(OC(C(C1O)O)OC2=CC=C(C=C2)O)COC(=O)C=CC3=CC(=C(C=C3)O)O 476.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Lavandoside 13916049 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 356.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Pyroside 5315513 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/10.1016/J.PHYTOCHEM.2008.06.001
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
DL-Tryptophan 1148 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (2R,3R)-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(E)-3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methoxy]prop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 72737671 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC4=C(C(=C3)O)OC(C4C(=O)OCC5C(C(C(C(O5)OC6=CC=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O)O)O 866.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl (2S,3S)-2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[(E)-3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methoxy]prop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 72737670 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC4=C(C(=C3)O)OC(C4C(=O)OCC5C(C(C(C(O5)OC6=CC=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O)O)O 866.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
[3,4,5-Trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl 2-(3,4-dihydroxyphenyl)-7-hydroxy-5-[3-oxo-3-[[3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methoxy]prop-1-enyl]-2,3-dihydro-1-benzofuran-3-carboxylate 74424258 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC4=C(C(=C3)O)OC(C4C(=O)OCC5C(C(C(C(O5)OC6=CC=C(C=C6)O)O)O)O)C7=CC(=C(C=C7)O)O)O)O)O 866.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(3,4,5,6-Tetrahydroxyoxan-2-yl)methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 85140196 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
6-O-caffeoyl-beta-glucose 101419460 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)O)O)O)O)O)O 342.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
13-(3,4-dihydroxyphenyl)-7-[2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-5-(4-hydroxyphenyl)-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 14586201 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)C1=CC(=C(C=C1)O)O)O 848.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3,7-Dihydroxy-2-(4-hydroxyphenyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978064 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
kaempferol 5-O-beta-D-glucopyranoside 72551448 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
bis[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl] (1R,2R,3R,4R)-3,4-bis(3,4-dihydroxyphenyl)cyclobutane-1,2-dicarboxylate 72737664 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3C(C(C3C(=O)OCC4C(C(C(C(O4)OC5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)C7=CC(=C(C=C7)O)O)O)O)O 868.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001
Bis[[3,4,5-trihydroxy-6-(4-hydroxyphenoxy)oxan-2-yl]methyl] 3,4-bis(3,4-dihydroxyphenyl)cyclobutane-1,2-dicarboxylate 163057631 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)COC(=O)C3C(C(C3C(=O)OCC4C(C(C(C(O4)OC5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)C7=CC(=C(C=C7)O)O)O)O)O 868.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.06.001

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