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Zanthoxylum americanum

Zanthoxylum americanum - 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 UUID64404d8463962221698982
Scientific name Zanthoxylum americanum
Authority Mill.
First published in Gard. Dict. ed. 8 : n.º 2 (1768)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Zanthoxylum parvum Shinners Field & Lab. 24: 19 (1956)
Zanthoxylum ramiflorum Michx. Fl. Bor.-Amer. 2: 235 (1803)
Zanthoxylum fraxinifolium Marshall Arbust. Amer. : 167 (1785)
Zanthoxylum fraxineum Willd. Sp. Pl., ed. 4 , 4: 757 (1806)
Thylax fraxineum (Willd.) Raf. Med. Fl. 2: 114 (1830)
Zanthoxylum mite Willd. Enum. Pl. : 1013 (1809)
Mioptrila odorata Raf. Amer. Manual Mulberry Trees 37. 1839
Zanthoxylum americanum f. armatius F.C.Gates Trans. Kansas Acad. Sci. 42: 136 (1939 publ. 1940)
Zanthoxylum clava-herculis var. americanum Du Roi Diss. Inaug. Obs. Bot. : 57 (1771)

Common names Top

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Language Common/alternative name
English american prickly-ash
English toothachetree
English toothache tree
English prickly ash
English northern prickly-ash
English common pricklyash
English common prickly-ash
English prickly-ash
Arabic ديش شوكي
Arabic فاغرة أمريكية
Danish tandpinetræ
Persian زانتکسیلوم امریکنوم
French clavalier d'amérique
French frêne épineux
Croatian zuboboljno drvo
Chinese 美洲花椒

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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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
  • Northern America
    • Eastern Canada
      • Nova Scotia
      • Ontario
      • Québec
    • Mexico
      • Mexico Northeast
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Indiana
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Alabama
      • Arkansas
      • Delaware
      • District Of Columbia
      • Florida
      • Georgia
      • Kentucky
      • Louisiana
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001132898
UNII NCL1TT8GSN
Florida Plant Atlas 1063
Flora of Alabama 3309
Canadensys 9041
USDA Plants ZAAM
UConn 553
Tropicos 28100527
INPN 717710
KEW urn:lsid:ipni.org:names:775568-1
The Plant List tro-28100527
Missouri Botanical Garden 286754
PFAF Zanthoxylum americanum
Open Tree Of Life 760765
NCBI Taxonomy 354526
Nature Serve 2.133451
IUCN Red List 135956405
IPNI 775568-1
iNaturalist 54836
GBIF 3190089
Freebase /m/06w6d7x
WisFlora 5451
EPPO ZANAM
EOL 484217
USDA GRIN 42186
Wikipedia Zanthoxylum_americanum
CMAUP NPO29030
CMAUP NPO6480

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
Evaluation of Factors Affecting Tree and Shrub Bark’s Antioxidant Status Golubkina N, Plotnikova U, Lapchenko V, Lapchenko H, Sheshnitsan S, Amagova Z, Matsadze V, Naumenko T, Bagrikova N, Logvinenko L, Sakhno T, Shevchuk O, Pirogov N, Caruso G Plants (Basel) 04-Oct-2022
PMCID:PMC9571727
doi:10.3390/plants11192609
PMID:36235475
Insect Floral Visitors of Ptelea trifoliata (Rutaceae) in Iowa, United States Talcott Stewart AJ, O’Neal ME, Graves WR Ann Entomol Soc Am 08-Jul-2022
PMCID:PMC9467031
doi:10.1093/aesa/saac012
PMID:36105848
Reinventory of the vascular plants of Mormon Island Crane Meadows after forty years of restoration, invasion, and climate change Caven AJ, Wiese JD Heliyon 03-Jun-2022
PMCID:PMC9192816
doi:10.1016/j.heliyon.2022.e09640
PMID:35711997
Purification and Identification of Natural Inhibitors of Protein Arginine Methyltransferases from Plants Wang Z, Xiong L, Xiong Q Mol Cell Biol 21-Mar-2022
PMCID:PMC9022574
doi:10.1128/mcb.00523-21
PMID:35311588
Pharmacological Properties to Pharmacological Insight of Sesamin in Breast Cancer Treatment: A Literature-Based Review Study Sohel M, Islam MN, Hossain MA, Sultana T, Dutta A, Rahman MS, Aktar S, Islam K, Al Mamun A Int J Breast Cancer 17-Feb-2022
PMCID:PMC8872699
doi:10.1155/2022/2599689
PMID:35223101
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Beneficial Role of Antioxidant Secondary Metabolites from Medicinal Plants in Maintaining Oral Health Kumar M, Prakash S, Radha, Kumari N, Pundir A, Punia S, Saurabh V, Choudhary P, Changan S, Dhumal S, Pradhan PC, Alajil O, Singh S, Sharma N, Ilakiya T, Singh S, Mekhemar M Antioxidants (Basel) 30-Jun-2021
PMCID:PMC8300643
doi:10.3390/antiox10071061
PMID:34209152
Autumn larval cold tolerance does not predict the northern range limit of a widespread butterfly species Tremblay P, MacMillan HA, Kharouba HM Ecol Evol 22-May-2021
PMCID:PMC8216912
doi:10.1002/ece3.7663
PMID:34188890
The potential of ODFs as carriers for drugs/vaccines against COVID-19 Gupta MS, Kumar TP Drug Dev Ind Pharm 18-Dec-2020
PMCID:PMC7784830
doi:10.1080/03639045.2020.1862180
PMID:33300820
Antimicrobial potential of toothpaste formulated from extracts of Syzygium aromaticum, Dennettia tripetala and Jatropha curcas latex against some oral pathogenic microorganisms Oluwasina OO, Ezenwosu IV, Ogidi CO, Oyetayo VO AMB Express 04-Feb-2019
PMCID:PMC6362185
doi:10.1186/s13568-019-0744-2
PMID:30715633
The Phytochemistry of Cherokee Aromatic Medicinal Plants Setzer WN Medicines (Basel) 12-Nov-2018
PMCID:PMC6313439
doi:10.3390/medicines5040121
PMID:30424560
A Randomized, Active Comparator-controlled Clinical Trial of a Topical Botanical Cream for Skin Hydration, Elasticity, Firmness, and Cellulite Yimam M, Lee YC, Jiao P, Hong M, Brownell L, Jia Q J Clin Aesthet Dermatol 01-Aug-2018
PMCID:PMC6122510
PMID:30214668
The Influence of Prescribed Fire, Habitat, and Weather on Amblyomma americanum (Ixodida: Ixodidae) in West-Central Illinois, USA Gilliam ME, Rechkemmer WT, McCravy KW, Jenkins SE Insects 22-Mar-2018
PMCID:PMC6023455
doi:10.3390/insects9020036
PMID:29565805
Mast cell degranulation and calcium influx are inhibited by an Echinacea purpurea extract and the alkylamide dodeca-2E,4E-dienoic acid isobutylamide Gulledge TV, Collette NM, Mackey E, Johnstone SE, Moazami Y, Todd DA, Moeser AJ, Pierce JG, Cech NB, Laster SM J Ethnopharmacol 14-Oct-2017
PMCID:PMC5818717
doi:10.1016/j.jep.2017.10.012
PMID:29042288
A Standardized Composition Comprised of Extracts from Rosmarinus officinalis, Annona squamosa and Zanthoxylum clava-herculis for Cellulite Yimam M, Lee YC, Jiao P, Hong M, Brownell L, Jia Q Pharmacognosy Res 01-Oct-2017
PMCID:PMC5717783
doi:10.4103/pr.pr_70_17
PMID:29263624

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
> Lignans, neolignans and related compounds / Furanoid lignans
5-[(3aR,6R,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-1,3-benzodioxole 102004873 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/PTR.686
CID 233333 233333 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/PTR.686
Episesamin 5204 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/PTR.686
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown https://doi.org/10.1002/PTR.686
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Methyl 3-phenylpropionate 7643 Click to see COC(=O)CCC1=CC=CC=C1 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,2R,4As,8aS)-1-[(3S)-5-hydroxy-3-methylpentyl]-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-2-ol 11130717 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CCO 310.50 unknown via CMAUP database
(3S)-5-[(1S,4aS,8aR)-2,5,5,8a-tetramethyl-4-oxo-4a,6,7,8-tetrahydro-1H-naphthalen-1-yl]-3-methylpentanoic acid 93233226 Click to see CC1=CC(=O)C2C(CCCC2(C1CCC(C)CC(=O)O)C)(C)C 320.50 unknown via CMAUP database
(4aalpha)-2-Hydroxy-2beta,5,5,8abeta-tetramethyldecalin-1beta-((R)-3-methylvaleric acid) 11868539 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
Labdanic Acid Methyl Ester 7057547 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)OC 338.50 unknown via CMAUP database
Labdanolic acid 11186394 Click to see CC(CCC1C2(CCCC(C2CCC1(C)O)(C)C)C)CC(=O)O 324.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Ledol 92812 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
Viridiflorol 11996452 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Trichothecenes
(1S,2R,7R,9R,10R,11S,12R)-3,10,11-trihydroxy-2-(hydroxymethyl)-1,5-dimethylspiro[8-oxatricyclo[7.2.1.02,7]dodec-5-ene-12,2'-oxirane]-4-one 6325746 Click to see CC1=CC2C(C(C1=O)O)(C3(C(C(C(C34CO4)O2)O)O)C)CO 312.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Glutinol Acetate 1781002 Click to see CC(=O)OC1CCC2C(=CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C1(C)C 468.80 unknown via CMAUP database
Urs-9(11),12-diene-3beta-ol 13996053 Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 424.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
(3aS,5aR,9aS,9bR)-3a,6,6,9a-tetramethyl-2,4,5,5a,7,8,9,9b-octahydro-1H-benzo[e][1]benzofuran 12838593 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
8,12-Epoxy-13,14,15,16-tetranorlabdane 11861328 Click to see CC1(CCCC2(C1CCC3(C2CCO3)C)C)C 236.39 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Nitidine 4501 Click to see C[N+]1=CC2=CC(=C(C=C2C3=C1C4=CC5=C(C=C4C=C3)OCO5)OC)OC 348.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown https://doi.org/10.1002/PTR.2650040604
Pentosalen 10212 Click to see CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 270.28 unknown https://doi.org/10.1002/PTR.2650040604
https://doi.org/10.1016/J.PHYMED.2003.12.005
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1016/J.PHYMED.2003.12.005
https://doi.org/10.1002/PTR.2650040604
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-methoxypsoralens
Cnidilin 821449 Click to see CC(=CCOC1=C2C=COC2=C(C3=C1C=CC(=O)O3)OC)C 300.30 unknown https://doi.org/10.1002/PTR.2650040604
Methoxsalen 4114 Click to see COC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2 216.19 unknown https://doi.org/10.1016/J.PHYMED.2003.12.005
https://doi.org/10.1002/PTR.2650040604
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Alloxanthoxyletin 5317485 Click to see CC1(C=CC2=C(C=C3C(=C2O1)C=CC(=O)O3)OC)C 258.27 unknown https://doi.org/10.1002/PTR.686
https://doi.org/10.1039/JR9370001545
Dipetalin 5316928 Click to see CC(=CCC1=C(C2=C(C3=C1OC(=O)C=C3)OC(C=C2)(C)C)OC)C 326.40 unknown https://doi.org/10.1002/PTR.686
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1002/PTR.686
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1039/JR9360001828
https://doi.org/10.1002/PTR.686
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
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 via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2S,3R,4S,5S,6R)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-chromen-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)tetrahydropyran-3-yl] 3,4,5-trihydroxybenzoate 5480249 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)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5315208 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 596.50 unknown via CMAUP database
3-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 42613954 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(6-O-I(2)-D-xylopyranosyl-I(2)-D-glucopyranosyl)oxy]-4H-1-benzopyran-4-one 102148697 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Isoquercetin 5280804 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
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin-3-O-rutinoside 21577860 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O 626.50 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Acacetin 5280442 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 284.26 unknown via CMAUP database
Ermanin 5352001 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Genkwanin 5281617 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O 284.26 unknown via CMAUP database
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
Xenognosin A 5281296 Click to see COC1=C(C=CC(=C1)O)CC=CC2=CC=C(C=C2)O 256.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Phenylpropanoic acids
3-Phenylpropionic acid 107 Click to see C1=CC=C(C=C1)CCC(=O)O 150.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
1-O,2-O,6-O-Trigalloyl-alpha-D-glucopyranose 11969002 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)O)O 636.50 unknown via CMAUP database
1,3,6-tri-O-galloyl-beta-D-glucose 452707 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)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 636.50 unknown via CMAUP database
3,4,6-tri-O-galloyl-beta-d-glucose 14188641 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 636.50 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
CID 442674 442674 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C(C(C(=O)O3)CC(=O)O)C(C(=O)O6)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O 954.70 unknown via CMAUP database

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