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Quercus acutissima

Quercus acutissima - Unknown
Part: Unknown
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 UUID643fea44e3aca032735373
Scientific name Quercus acutissima
Authority Carruth.
First published in J. Proc. Linn. Soc., Bot. 6: 33 (1861)

Description Top

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Synonyms Top

Scientific name Authority First published in
Quercus acutissima var. lioui Kozlov Mat. Etud. Chen. Monog. Mandsh. Chine 79. 1933
Quercus acutissima var. septentrionalis Liou Contr. Inst. Bot. Natl. Acad. Peiping 4: 12. 1936
Quercus serrata var. attenuata Blume Mus. Bot. 1: 297. 1851
Quercus serrata var. nana Blume Mus. Bot. 1: 297. 1851
Quercus serrata var. obtusata Blume Mus. Bot. 1: 297. 1851
Quercus serrata var. tanbakuri Blume Mus. Bot. 1: 297. 1851

Common names Top

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Language Common/alternative name
English saw-tooth oak
English sawtooth oak
English bristle oak
English chinese oak
Afrikaans saagtandeik
Afrikaans stekeleik
Arabic سنديان حاد
Czech dub špičatolistý
Czech dub nejšpičatější
German seidenraupen-eiche
German japanische kastanien-eiche
Esperanto japana marona kverko
Esperanto segildenta kverko
Persian بلوط برگارهای
French chêne du japon
Hungarian hegyeslevelű tölgy
Japanese ボクソク
Japanese 椚
Japanese 椚木
Japanese つるばみ
Japanese くぬぎ
Japanese クヌギ
Japanese 樸樕
Japanese ツルバミ
Japanese 椢
Korean 상수리 나무
Korean 상수리나무
Dutch gezaagdbladige eik
Portuguese carvalho do japão
Portuguese carvalho japonês
Portuguese kunugi
Russian Дуб острейший
Turkish japon kestane meşesi
Ukrainian Дуб найгостріший
Chinese 栎
Chinese 橡碗树
Chinese 麻櫟
Chinese 麻栎
Chinese 橡木皮
Chinese 橡实壳
Chinese 橡实

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Quercus acutissima subsp. acutissima Unknown
Quercus acutissima subsp. kingii Menitsky Novosti Sist. Vyssh. Rast. 10: 120 (1973)

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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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 North-central
      • China South-central
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
  • Northern America
    • North-central U.S.A.
      • Missouri
    • Northeastern U.S.A.
      • Pennsylvania
    • Southeastern U.S.A.
      • Alabama
      • District Of Columbia
      • Kentucky
      • Louisiana
      • Maryland
      • Mississippi
      • North Carolina
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000289386
UNII 0TVP714IPW
Flora of Alabama 2149
Cornell Woody Plants 201
USDA Plants QUAC80
UConn 380
Tropicos 13100182
KEW urn:lsid:ipni.org:names:295743-1
The Plant List kew-171430
Missouri Botanical Garden 280732
PFAF Quercus acutissima
PaleoBotany 83438
Open Tree Of Life 272706
NCBI Taxonomy 58330
Nature Serve 2.144243
IUCN Red List 194048
IPNI 295743-1
iNaturalist 167634
GBIF 2877959
Freebase /m/07xx52
EPPO QUEAS
EOL 1151810
US Library of Congress sh99000696
USDA GRIN 70535
Wikipedia Quercus_acutissima

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
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
The Potential of Acorn Extract Treatment on PUFAs Oxidative Stability: A Case Study on Fish Cooking Wastewater Araújo-Rodrigues H, Ribeiro TB, Machado M, Pereira CD, Pintado ME Foods 19-Mar-2024
PMCID:PMC10969428
doi:10.3390/foods13060935
PMID:38540925
Applicability analysis of flame height estimation based on Byram’s fireline intensity model under flat and windless conditions Zhang Y, Luo A Sci Rep 23-Feb-2024
PMCID:PMC10891076
doi:10.1038/s41598-024-55132-3
PMID:38396250
The Potential of Wood Vinegar to Replace Antimicrobials Used in Animal Husbandry—A Review Gama GS, Pimenta AS, Feijó FM, de Azevedo TK, de Melo RR, de Andrade GS Animals (Basel) 25-Jan-2024
PMCID:PMC10854697
doi:10.3390/ani14030381
PMID:38338024
Fine-Root Distribution and Soil Physicochemical Property Variations in Four Contrasting Urban Land-Use Types in South Korea Tran LT, An JY, Carayugan MB, Hernandez JO, Rahman SA, Youn WB, Carvalho JI, Jo MS, Han SH, Nguyen HH, Park BB Plants (Basel) 07-Jan-2024
PMCID:PMC10821101
doi:10.3390/plants13020164
PMID:38256718
Anti-Inflammatory Herbal Extracts and Their Drug Discovery Perspective in Atopic Dermatitis Lee JW, Kim EN, Jeong GS Biomol Ther (Seoul) 01-Jan-2024
PMCID:PMC10762282
doi:10.4062/biomolther.2023.102
PMID:38148551
A new species and new records of Hymenopellis and Xerula (Agaricales, Physalacriaceae) from China Liu YJ, Qi ZX, Li Y, Yue L, Zhao GP, Gui XY, Dong P, Wang Y, Zhang B, Li X PeerJ 20-Dec-2023
PMCID:PMC10748483
doi:10.7717/peerj.16681
PMID:38144183
Editorial: Highly contiguous plant genome assembly and transcriptional regulation Tian XC, Jia KH Front Plant Sci 13-Dec-2023
PMCID:PMC10751298
doi:10.3389/fpls.2023.1331498
PMID:38152147
Natural Substances vs. Approved Drugs in the Treatment of Main Cardiovascular Disorders—Is There a Breakthrough? Grujić-Milanović J, Rajković J, Milanović S, Jaćević V, Miloradović Z, Nežić L, Novaković R Antioxidants (Basel) 07-Dec-2023
PMCID:PMC10740850
doi:10.3390/antiox12122088
PMID:38136208
Chromosome-scale genome assembly of sweet tea (Lithocarpus polystachyus Rehder) Liu H, Zhang R, Zhou BF, Shen Z, Chen XY, Gao J, Wang B Sci Data 06-Dec-2023
PMCID:PMC10700502
doi:10.1038/s41597-023-02791-y
PMID:38057329
Factors influencing the difference in dissolved ion inputs to the forest floor between deciduous and coniferous stands: comparison under high and low atmospheric deposition conditions Imamura N, Ohte N, Tanaka N Environ Monit Assess 02-Dec-2023
PMCID:PMC10693530
doi:10.1007/s10661-023-12132-6
PMID:38041704
The Prospect of Hydrolytic Enzymes from Bacillus Species in the Biological Control of Pests and Diseases in Forest and Fruit Tree Production Ajuna HB, Lim HI, Moon JH, Won SJ, Choub V, Choi SI, Yun JY, Ahn YS Int J Mol Sci 29-Nov-2023
PMCID:PMC10707167
doi:10.3390/ijms242316889
PMID:38069212
Assembly and analysis of the complete mitochondrial genome of Forsythia suspensa (Thunb.) Vahl Song Y, Du X, Li A, Fan A, He L, Sun Z, Niu Y, Qiao Y BMC Genomics 23-Nov-2023
PMCID:PMC10666317
doi:10.1186/s12864-023-09821-4
PMID:37996801
Favorite Parts of a Single Leaf for Giant Flying Squirrels to Eat in Three Species of Food Trees Ito M, Tamura N, Hayashi F Biology (Basel) 22-Oct-2023
PMCID:PMC10604700
doi:10.3390/biology12101352
PMID:37887062

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/0031-9422(95)00378-K
https://doi.org/10.1007/S12272-011-0205-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[3,4,5-Trihydroxy-6-(4-hydroxy-3-methoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 385552 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 454.40 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
[3,4,5-Trihydroxy-6-(4-hydroxy-3,5-dimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 162872516 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
2-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]oxybenzoic acid 15698963 Click to see C1=CC(=C(C=C1OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)C(=O)O)O 468.40 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
3-Methoxy-4-hydroxyphenyl 6-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranoside 102442448 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O 454.40 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
4-Hydroxy-3,5-dimethoxyphenyl 6-O-galloyl-beta-D-glucopyranoside 100916644 Click to see COC1=CC(=CC(=C1O)OC)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O 484.40 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
Phomoxydiene A 139585368 Click to see CC1C(C2C=CC=CC1(O2)O)C3C(C=CC(=O)O3)OC(=O)C 306.31 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 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/10.1016/0031-9422(95)00378-K
https://doi.org/10.1007/S12272-011-0205-1
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/10.1007/S12272-011-0205-1
https://doi.org/10.1016/0031-9422(95)00378-K
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
Flavan-3,3',4',5,5',7-hexol 1249 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/10.1007/S12272-011-0205-1
Gallocatechin 65084 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/10.1007/S12272-011-0205-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 163188139 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown https://doi.org/10.1007/S12272-011-0205-1
Glucodistylin 14187088 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 466.40 unknown https://doi.org/10.1007/S12272-011-0205-1
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose 374874 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1016/0031-9422(95)00378-K
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4,5-trihydroxybenzoate 4628122 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown https://doi.org/10.1016/0031-9422(95)00378-K
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown https://doi.org/10.1016/0031-9422(95)00378-K
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1016/0031-9422(95)00378-K
> Phenylpropanoids and polyketides / Tannins / Complex tannins
(1R,2R,20R,42S,46S)-46-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 16167199 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown https://doi.org/10.1248/CPB.35.602
(1S,2S,20S,42S,46R)-46-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-6-yl]-7,8,9,12,13,14,25,26,27,30,31,32,35,36,37-pentadecahydroxy-3,18,21,41,43-pentaoxanonacyclo[27.13.3.138,42.02,20.05,10.011,16.023,28.033,45.034,39]hexatetraconta-5,7,9,11,13,15,23,25,27,29(45),30,32,34(39),35,37-pentadecaene-4,17,22,40,44-pentone 101676953 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown https://doi.org/10.1248/CPB.35.602
CID 16167195 16167195 Click to see C1C(C(OC2=C1C(=CC(=C2C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown https://doi.org/10.1248/CPB.35.602
CID 16167198 16167198 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C4C5C6C(COC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O6)O)O)O)O)O)O)OC(=O)C9=CC(=C(C(=C9C1=C(C(=C(C(=C1O)O)O)C1=C(C3=C(C(=C1O)O)O)C(=O)O4)C(=O)O5)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1206.90 unknown https://doi.org/10.1248/CPB.35.602
Mongolicain A 44576149 Click to see C1C(C(OC2=C1C(=CC3=C2C4C5C6C7C(COC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O7)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C(=C1O)O)O)C1=C(C(=O)C4(C1C(=O)O5)O3)O)C(=O)O6)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1176.90 unknown https://doi.org/10.1248/CPB.36.857
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11R)-10-[(15S,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601179 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(95)00378-K
[(10R,11R)-10-[(15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 101601178 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(95)00378-K
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trimethoxybenzoate 162997516 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)OC)OC)OC)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
[3,4,5-Trihydroxy-6-(3,4,5-trimethoxyphenoxy)oxan-2-yl]methyl 3,4,5-trimethoxybenzoate 162997515 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)OCC2C(C(C(C(O2)OC3=CC(=C(C(=C3)OC)OC)OC)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)82367-5
1-O-Galloylpedunculagin 452242 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 936.60 unknown https://doi.org/10.1016/0031-9422(95)00378-K
3-(beta-D-Glucopyranosyloxy)-4,5-dihydroxybenzoic acid 101683334 Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C(=O)O 332.26 unknown https://doi.org/10.1016/0031-9422(95)00378-K
3-Glucogallic acid 14345564 Click to see C1=C(C=C(C(=C1O)O)OC2C(C(C(C(O2)CO)O)O)O)C(=O)O 332.26 unknown https://doi.org/10.1016/0031-9422(95)00378-K
CID 12302513 12302513 Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 934.60 unknown https://doi.org/10.1016/0031-9422(95)00378-K
Eugeniin 442679 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 938.70 unknown https://doi.org/10.1016/0031-9422(95)00378-K
Pedunculagin 442688 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/0031-9422(95)00378-K

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