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Alchornea cordifolia

Alchornea cordifolia - 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 UUID644037b2e262a113812745
Scientific name Alchornea cordifolia
Authority (Schumach.) Müll.Arg.
First published in Linnaea 34: 170 (1865)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Schousboea cordifolia Schumach. & Thonn. Beskr. Guin. Pl. : 449 (1827)
Cacoucia cordifolia (Schumach. & Thonn.) Walp. Repert. Bot. Syst. (Walpers) ii. 68.
Alchornea cordata Benth. Niger Fl. : 507 (1849)

Common names Top

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Language Common/alternative name
Spanish alchornea cordata
Spanish cacoucia cordifolia
Spanish schousboea cordifolia
Bambara kɔgira
Sango mbonzi
Chinese 心叶山杆麻
Chinese 心叶山麻杆
Chinese 心葉山杆麻
Chinese 心葉山麻桿

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000938571
UNII 776X35H09F
Tropicos 12804083
KEW urn:lsid:ipni.org:names:338380-1
The Plant List kew-5722
Open Tree Of Life 1033167
NCBI Taxonomy 316697
IUCN Red List 144311802
IPNI 338380-1
iNaturalist 507088
GBIF 3055371
Freebase /m/047ptsp
EPPO AHQCO
EOL 1146148
USDA GRIN 2177
Wikipedia Alchornea_cordifolia
CMAUP NPO2330

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 packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Soil seed bank dynamics of two invasive alien plants in Nigeria: implications for ecosystem restoration Akomolafe GF, Rosazlina R, Omomoh B AoB Plants 20-Jan-2024
PMCID:PMC10880880
doi:10.1093/aobpla/plae003
PMID:38384340
Sickle Cell Disease Update: New Treatments and Challenging Nutritional Interventions Bell V, Varzakas T, Psaltopoulou T, Fernandes T Nutrients 15-Jan-2024
PMCID:PMC10820494
doi:10.3390/nu16020258
PMID:38257151
Effect of Alchornea cordifolia on Glycemic Indices of Varieties of Fufu Among Healthy Subjects Otoo ET, Tandoh MA, Mills-Robertson FC Curr Dev Nutr 10-Jan-2024
PMCID:PMC10847058
doi:10.1016/j.cdnut.2024.102076
PMID:38328775
Antifungal Activity of Thirty Essential Oils to Control Pathogenic Fungi of Postharvest Decay Allagui MB, Moumni M, Romanazzi G Antibiotics (Basel) 28-Dec-2023
PMCID:PMC10812670
doi:10.3390/antibiotics13010028
PMID:38247587
Nature’s Green Potential: Anticancer Properties of Plants of the Euphorbiaceae Family Jiménez-González V, Kowalczyk T, Piekarski J, Szemraj J, Rijo P, Sitarek P Cancers (Basel) 25-Dec-2023
PMCID:PMC10778523
doi:10.3390/cancers16010114
PMID:38201542
Croton macrostachyus Leaf Extract-Mediated Green Synthesis of ZnO Nanoparticles and ZnO/CuO Nanocomposites for the Enhanced Photodegradation of Methylene Blue Dye with the COMSOL Simulation Model Endeshaw SB, Tufa LT, Goddati M, Lee J, Silalahi VC, Lee D, Murthy HC, Sabir FK ACS Omega 19-Dec-2023
PMCID:PMC10785675
doi:10.1021/acsomega.3c06155
PMID:38222549
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
Herbs Used in Antimalarial Medicines: A Study in the Greater Accra Region of Ghana Nortey NN, Korsah S, Tagoe M, Apenteng JA, Owusu FA, Oppong J, Attah AE, Allotey S Evid Based Complement Alternat Med 19-Aug-2023
PMCID:PMC10460277
doi:10.1155/2023/6697078
PMID:37636997
Effect of clove buds powder supplementation on hematological profile, biochemical parameters, lymphoid organs, and cell-mediated immunity of broilers Ben Naser KM, Sherif BM, Othman SM, Asheg AA Open Vet J 31-Jul-2023
PMCID:PMC10443825
doi:10.5455/OVJ.2023.v13.i7.7
PMID:37614736
Ethnobotanical Survey and Cercaricidal Activity Screening of Medicinal Plants Used for Schistosomiasis Treatment in Atwima-Nwabiagya District, Ashanti Region, Ghana Asante-Kwatia E, Gyimah L, Forkuo AD, Anyan WK, Gbemu MA, Armah FA, Mensah AY J Parasitol Res 19-Jul-2023
PMCID:PMC10372336
doi:10.1155/2023/6707157
PMID:37520159
The Use of Natural Bioactive Nutraceuticals in the Management of Tick-Borne Illnesses Shor SM, Schweig SK Microorganisms 05-Jul-2023
PMCID:PMC10384908
doi:10.3390/microorganisms11071759
PMID:37512931
Phytopharmaceutical practices of traditional health practitioners in Burkina Faso: a cross-sectional study Ouoba K, Lehmann H, Zongo A, Semdé R, Pabst JY BMC Complement Med Ther 30-Jun-2023
PMCID:PMC10311739
doi:10.1186/s12906-023-04055-z
PMID:37391813
Medicinal Plants as a Natural Greener Biocontrol Approach to “The Grain Destructor” Maize Weevil (Sitophilus zeamais) Motschulsky Phokwe OJ, Manganyi MC Plants (Basel) 30-Jun-2023
PMCID:PMC10346355
doi:10.3390/plants12132505
PMID:37447066

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
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydrochelerythrine 485077 Click to see CN1CC2=C(C=CC(=C2OC)OC)C3=C1C4=CC5=C(C=C4C=C3)OCO5 349.40 unknown via CMAUP database
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Secobenzophenanthridine alkaloids
Formamide, N-(6-(2-hydroxy-3,4-dimethoxyphenyl)naphtho(2,3-d)-1,3-dioxol-5-yl)-N-methyl- 3085181 Click to see CN(C=O)C1=C(C=CC2=CC3=C(C=C21)OCO3)C4=C(C(=C(C=C4)OC)OC)O 381.40 unknown via CMAUP database
> Alkaloids and derivatives / Harmala alkaloids
methyl 9H-pyrido[3,4-b]indole-1-carboxylate 597266 Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 226.23 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1002/PTR.2650040508
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl 4-hydroxy-3,5-dimethoxybenzoate 70164 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC 212.20 unknown via CMAUP database
> 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/10.1002/PTR.2650040508
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see COC(=O)C1=CC=C(C=C1)O 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
3,4,5-Trimethoxybenzyl alcohol 77449 Click to see COC1=CC(=CC(=C1OC)OC)CO 198.22 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3-methoxycinnamaldehyde 5280536 Click to see COC1=C(C=CC(=C1)C=CC=O)O 178.18 unknown via CMAUP database
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
CID 12443227 12443227 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin 179651 Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C 470.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
CID 9848259 9848259 Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C 486.50 unknown via CMAUP database
Evodol 185481 Click to see CC1(C2=C(C(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C 484.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
1,1,2-Tris(3-methylbut-3-enyl)guanidine 163189609 Click to see CC(=C)CCN=C(N)N(CCC(=C)C)CCC(=C)C 263.42 unknown https://doi.org/10.1002/PTR.2650040508
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Methyl chlorogenate 6476139 Click to see COC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O 368.30 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(S)-alpha,4'-Dihydroxy-3'-methoxypropiophenone 12181418 Click to see CC(C(=O)C1=CC(=C(C=C1)O)OC)O 196.20 unknown via CMAUP database
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
1H-Pyrido(3,4-b)indol-1-one, 2,3,4,9-tetrahydro-2-methyl- 162871 Click to see CN1CCC2=C(C1=O)NC3=CC=CC=C23 200.24 unknown via CMAUP database
Hortiacine 378227 Click to see COC1=CC2=C(C=C1)NC3=C2CCN4C3=NC5=CC=CC=C5C4=O 317.30 unknown via CMAUP database
Rutaecarpine 65752 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4 287.30 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
Decarine 179640 Click to see COC1=C(C=CC2=C3C=CC4=CC5=C(C=C4C3=NC=C21)OCO5)O 319.30 unknown via CMAUP database
Norchelerythrine 443719 Click to see COC1=C(C2=CN=C3C(=C2C=C1)C=CC4=CC5=C(C=C43)OCO5)OC 333.30 unknown via CMAUP database
Oxychelerythrine 147279 Click to see CN1C2=C(C=CC3=CC4=C(C=C32)OCO4)C5=C(C1=O)C(=C(C=C5)OC)OC 363.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown via CMAUP database
gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown via CMAUP database
Robustine 164950 Click to see COC1=C2C=COC2=NC3=C1C=CC=C3O 215.20 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
4-Methoxy-1-methylquinolin-2-one 182073 Click to see CN1C2=CC=CC=C2C(=CC1=O)OC 189.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
n-cis-Feruloyltyramine 6440659 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
Paprazine 5372945 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Evofolin C 44445795 Click to see CC(=CCOC1=CC=C(C=C1)C=CCO)C 218.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Fraxin 5273568 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O 370.31 unknown via CMAUP database
Isofraxoside 11508953 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC3C(C(C(C(O3)CO)O)O)O 370.31 unknown via CMAUP database
Skimmin 99693 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1002/PTR.2650040508
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Sophoraflavone B 5491513 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 416.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see C1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 436.40 unknown https://doi.org/10.1002/PTR.2650040508
4',5,7-Trihydroxy-3-(alpha-D-arabinopyranosyloxy)flavone 11625890 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 unknown via CMAUP database
Hyperoside 5281643 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 https://doi.org/10.1002/PTR.2650040508
kaempferol 3-O-beta-D-xyloside 21310440 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 418.30 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
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 / Stilbenes
(-)-Evofolin B 46229015 Click to see COC1=C(C=CC(=C1)C(CO)C(=O)C2=CC(=C(C=C2)O)OC)O 318.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
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 via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1016/S0378-8741(02)00121-6

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