Details Top

Internal ID UUID64405a4f80837476825154
Scientific name Vachellia nilotica
Authority (L.) P.J.H.Hurter & Mabb.
First published in D.J.Mabberley, Plant-book, ed. 3: 1021 (2008)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Across the Sahel and northern tropical Africa the bark and young shoots of Vachellia nilotica have been prepared as mild teas and decoctions for gastrointestinal and febrile conditions. In Nigeria the Hausa drink a bark infusion to stop diarrhea and settle stomach cramps, while in Sudan a bark decoction is taken to reduce fever and dysentery. The Kanyawara healers of western Uganda steep the bark in water and give it to children with diarrhea and gastrointestinal complaints, and in the same region a light bark tea is taken for stomach pain and as an antimalarial tea. In South Asia, in the Marathwada region of Maharashtra, the leaves are boiled in water and taken as a febrifuge tea, while in Tamil Nadu the leaves are used as a bitter tonic tea in the winter months and the seed or pod gum is widely incorporated into foods. Throughout the Arabian Peninsula the leaf infusion has been used as a bitter tonic for stomach complaints, and reports from the Horn of Africa describe a leaf tea as a fever-reducing drink. All of these preparations—leaf or bark teas and decoctions—are documented in long-running clinical ethnobotanical surveys of the Sahel (Burkill, 1995; Wickens, 1995; Heuzé & Thiollet, 2018).

One practical recipe for a mild fever‑reducing tea made from the bark is straightforward: use roughly 5 g of sun‑dried bark pieces per 250 ml of freshly boiled water, simmer gently for 10 minutes, then let stand off heat for another 10 minutes, strain, and drink up to a cup two or three times a day for 3–5 days. A leaf tea can be made from 2–3 g of fresh or 1 g of dried leaves steeped in 250 ml of hot water for 10–15 minutes, strained, and taken as a tonic for stomach upset up to twice daily. For a 1:5 tincture (by weight), macerate 100 g of dried bark in 500 ml of 45% ethanol for 4–6 weeks with daily shaking, press and filter, and keep amber‑capped. Use a standard 1 ml dose three times a day if needed. Doses and duration should follow traditional or clinical guidance, and children, pregnant or breastfeeding women should use Vachellia nilotica only under qualified supervision.

Active constituents reported for Vachellia nilotica include flavonoids such as quercetin, kaempferol, and their glycosides, hydrolyzable tannins and gallotannins, phenolic acids including gallic and ellagic acids, and the triterpenoids lupeol and β‑sitosterol. These compound classes are well established in the species and plausibly account for the observed antidiarrheal, astringent, and anti‑inflammatory effects recorded in many of the preparations described above.

In modern times, Vachellia nilotica remains widely used in West, East, and South Asian ethnomedicine as a bark and leaf tea or decoction, and pharmacological studies continue to support some of its traditional indications (Bennett et al., 2021; Wichtl, 2004; ESCOP Monographs).

General Uses Top

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Common products:
Gum arabic-type exudate (gum/nilotica gum) is harvested from trunk wounds; tannins are extracted from bark and seed pods; timber is sawn as heartwood; seed kernels yield oil and protein-rich meal after oil pressing.

Industrial and craft applications:
* Gum: Used as a hydrocolloid in food and pharmaceutical formulations. Pure gum arabic, rich in arabinogalactan proteins, forms a clear, stable mucilage with good emulsifying properties. It serves as a binding agent in tableting, encapsulation, and adhesives.
* Tannins: Bark and pod extracts are used in leather tanning. The high-molecular-weight polyphenols act as fixatives and improve leather strength, color, and water resistance.

Food and beverages (non-medicinal):
* Oil: Seed kernels yield edible oil suitable for cooking/frying, with a fatty acid profile dominated by linoleic and oleic acids.
* Meal: Defatted seed meal (after oil extraction) is a high-protein animal feed supplement.

Colorants and tanning:
* Tannins: Bark extracts yield natural brown dyes used for protein fibers (wool, silk). Extracted tannins are used in leather tanning as specified above.

Wood and fiber:
* Timber: Dense, durable heartwood is valued for furniture, joinery, tool handles, and construction where strength and resistance to insects/decay are critical.

Fragrance and cosmetics:
No documented uses found.

Properties relevant to use:
* Gum: Contains Arabica-galactan polysaccharide-protein complexes; soluble in cold water; high viscosity at low concentrations; excellent emulsification due to protein fraction.
* Tannins: High-molecular-weight hydrolyzable tannins (~70% gallotannins in bark), characterized by high astringency and binding capacity to proteins.
* Oil: Seed oil typically contains ~50–55% linoleic acid and ~25–30% oleic acid; high protein content (25–35%) in seed meal.
* Timber: High density (typically 0.7–0.9 g/cm³); high tannin content contributes to natural durability.

Standards and regulation:
Gum quality standards: *Gum arabic* (specification: ISO 8755:2001); Food-grade uses regulated by national food additive codes (e.g., E414). Leather tanning tannins may fall under restrictions on tannery effluent. Timber grading follows local forestry standards.

Sustainability and sourcing:
Gum is harvested from wild or semi-cultivated trees; sustainable practices focus on non-destructive tapping and avoiding over-exploitation. Tanning extracts and timber require management plans for long-term supply; over-harvesting of bark may harm trees. Seed-based products depend on agricultural yields.

Synonyms Top

Scientific name Authority First published in
Mimosa nilotica L. Sp. Pl.: 521 (1753)
Acacia nilotica (L.) Willd. ex Delile Descr. Egypte, Hist. Nat.2(Mém.): 79 (1813)
Acacia nilotica subsp. nilotica (L.) Delile
Gumifera nilotica (L.) Raf. Sylva Tellur.: 118 (1838)
Mimosa nilotica Thunb. Prodr. Pl. Cap. 2: 92. 1800
Acacia arabica var. nilotica (L.) Benth. London J. Bot.1: 500 (1842)
Acacia scorpioides var. nilotica (L.) A.Chev. Bull. Soc. Bot. France74: 954 (1927)
Acacia bambolah H.Karst. Deut. Fl. (Karsten), ed. 2 2: 278 (1894)
Acacia nilotica var. typica A.F.Hill Bot. Mus. Leafl. 8: 98 (1940)
Acacia nilotica var. vera Roberty Candollea 11: 149 (1948)

Common names Top

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Language Common/alternative name
English egyptian acacia
English thorn mimosa
English thorny acacia
English babul
English gum arabic tree
Afrikaans lekkerruikpeul
Arabic سنط عربي
Bulgarian нилска акация
bho बबुर
bho बब्बुर
Bengali বাবলা আঠা গাছ
Bengali বাবলা
Czech akácie arabská
Finnish hartsiakaasia
Hebrew שיטת הנילוס
Hindi बबूल
Hindi कीकर
Japanese バブール
Japanese アラビアゴムモドキ
Kannada ವಾಚೆಲಿಯಾ ನಿಲೋಟಿಕಾ
Malayalam കരിവേലം
Marathi गावठी बाभूळ
Burmese ဆူးဖြူ
Tamil கருவமரம்
Tamil கருவேலமரம்
Urdu کیکر
Walloon acacia do nil
Chinese 阿拉伯金合欢
Chinese 阿拉伯金合歡

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Vachellia nilotica subsp. adstringens (Schumach.) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)
Vachellia nilotica subsp. cupressiformis (J.L.Stewart) Ali Pakistan J. Bot.46: 2 (2014)
Vachellia nilotica subsp. hemispherica (Ali & Faruqi) Ali Pakistan J. Bot.46: 2 (2014)
Vachellia nilotica subsp. indica (Benth.) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)
Vachellia nilotica subsp. kraussiana (Benth.) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)
Vachellia nilotica subsp. leiocarpa (Brenan) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)
Vachellia nilotica subsp. nilotica Unknown
Vachellia nilotica subsp. subalata (Vatke) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)
Vachellia nilotica subsp. tomentosa (Benth.) Kyal. & Boatwr. Bot. J. Linn. Soc.172: 515 (2013)

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gulf Of Guinea Islands
    • Western Indian Ocean
      • Madagascar
      • Mauritius
      • Rodrigues
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iran
      • Iraq
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Myanmar
    • Papuasia
      • New Guinea
  • Australasia
    • Australia
      • Northern Territory
      • Queensland
      • South Australia
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Southwest
    • Southwestern U.S.A.
      • California
  • Southern America
    • Caribbean
      • Bahamas
      • Cuba
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Southern South America
      • Argentina Northeast
    • Western South America
      • Bolivia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001284776
Tropicos 50325057
INPN 639351
KEW urn:lsid:ipni.org:names:77089275-1
The Plant List tro-50325057
PFAF Vachellia nilotica
Open Tree Of Life 60610
NCBI Taxonomy 138033
IUCN Red List 158379
IPNI 77089275-1
iNaturalist 557826
GBIF 3974744
Freebase /m/026s85y
USDA GRIN 465206
Wikipedia Vachellia_nilotica

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
Study of medicinal plants used in ethnoveterinary medical system in riverine areas of Punjab, Pakistan Umair M, Altaf M, Ahsan T, Bussmann RW, Abbasi AM, Gatasheh MK, Elrobh M J Ethnobiol Ethnomed 07-May-2024
PMCID:PMC11077875
doi:10.1186/s13002-024-00686-9
PMID:38715115
Detailed analysis of agro-industrial byproducts/wastes to enable efficient sorting for various agro-industrial applications Priyanka G, Singiri JR, Adler-Agmon Z, Sannidhi S, Daida S, Novoplansky N, Grafi G Bioresour Bioprocess 04-May-2024
PMCID:PMC11069496
doi:10.1186/s40643-024-00763-7
PMID:38703254
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Evaluation of volatile components from the tuber, fibrous roots, bud, stem and leaf tissues of Bletilla striata for its anti-colon cancer activity Yang N, Li S, Zhang Y, Pan F, Liu G, Chen X, Yu C, Li K, Liu Y Physiol Mol Biol Plants 27-Apr-2024
PMCID:PMC11087428
doi:10.1007/s12298-024-01450-9
PMID:38737324
Rural Households' Demand Status for Mitigation of Prosopis juliflora (Sw.) DC Invasion and Its Determinant Factors in Ethiopia: Empirical Evidence from Afar National Regional State Sisay K, Bekele K, Haji J, Schaffner U ScientificWorldJournal 26-Apr-2024
PMCID:PMC11068454
doi:10.1155/2024/5521245
PMID:38708123
Ethnobotanical assessment of antidiabetic medicinal plants in District Karak, Pakistan Nazar A, Adnan M, Shah SM, Bari A, Ullah R, Tariq A, Ahmad N BMC Complement Med Ther 24-Apr-2024
PMCID:PMC11040872
doi:10.1186/s12906-024-04462-w
PMID:38658923
Clove Essential Oil: Chemical Profile, Biological Activities, Encapsulation Strategies, and Food Applications Liñán-Atero R, Aghababaei F, García SR, Hasiri Z, Ziogkas D, Moreno A, Hadidi M Antioxidants (Basel) 19-Apr-2024
PMCID:PMC11047511
doi:10.3390/antiox13040488
PMID:38671935
Anti-inflammatory activity of d-pinitol possibly through inhibiting COX-2 enzyme: in vivo and in silico studies Haque MF, El-Nashar HA, Akbor MS, Alfaifi M, Bappi MH, Chowdhury AK, Hossain MK, El-Shazly M, Albayouk T, Saleh N, Islam MT Front Chem 16-Apr-2024
PMCID:PMC11058972
doi:10.3389/fchem.2024.1366844
PMID:38690012
Yield and Energy Modeling for Biochar and Bio-Oil Using Pyrolysis Temperature and Biomass Constituents Awad MI, Makkawi Y, Hassan NM ACS Omega 10-Apr-2024
PMCID:PMC11044251
doi:10.1021/acsomega.4c01646
PMID:38680335
Woody Species Composition, Structure, and Status of Regeneration in Pugnido Forest, Gambella Region, Western Ethiopia Masresha G, Melkamu Y, Mulu G Scientifica (Cairo) 04-Apr-2024
PMCID:PMC11008979
doi:10.1155/2024/3961434
PMID:38605976
Leaf functional traits and resource use strategies facilitate the spread of invasive plant Parthenium hysterophorus across an elevational gradient in western Himalayas Sharma P, Rathee S, Ahmad M, Siddiqui MH, Alamri S, Kaur S, Kohli RK, Singh HP, Batish DR BMC Plant Biol 02-Apr-2024
PMCID:PMC10985864
doi:10.1186/s12870-024-04904-0
PMID:38561674
Spontaneous Lesions of Endangered Geriatric Julia Creek Dunnarts (Sminthopsis douglasi, Archer 1979) with Emphasis in Reproductive Pathology Gonzalez-Astudillo V, Schaffer-White A, Noble L, O’Hara P, Murray P, Barnes TS, Allavena R Vet Sci 22-Mar-2024
PMCID:PMC11054575
doi:10.3390/vetsci11040142
PMID:38668410
Choline supplementation: Impact on broiler chicken performance, steatosis, and economic viability from from 1 to 42 days Ramalho de Lima M, Kaneko IN, de Lima AV, de Melo LN, de Lima MC, de Brito AN, Costa FG, Boas AD, Toledo AL, Ferrer SL, Marimuthu S PLoS One 19-Mar-2024
PMCID:PMC10950236
doi:10.1371/journal.pone.0295488
PMID:38502648
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
Larvicidal activity of Acacia nilotica extracts against Culex pipiens and their suggested mode of action by molecular simulation docking Baz MM, El-Shourbagy NM, Alkhaibari AM, Gattan HS, Alruhaili MH, Selim A, Radwan IT Sci Rep 15-Mar-2024
PMCID:PMC10940718
doi:10.1038/s41598-024-56690-2
PMID:38486053

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
https://doi.org/10.1055/S-2007-969797
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate 7428 Click to see 184.15 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
https://doi.org/10.1055/S-2006-962094
> Benzenoids / Phenols / Benzenediols / Catechols
Catechol 289 Click to see 110.11 unknown https://doi.org/10.1055/S-2007-969797
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
Dihexadecyl pentacosanedioate 162862117 Click to see 861.50 unknown https://doi.org/10.1002/CHIN.200639218
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Octadecenoic acid 5282750 Click to see CCCCCCCCCCCCCCCC=CC(=O)O 282.50 unknown https://doi.org/10.1007/BF02901545
Pentadecanoic Acid 13849 Click to see 242.40 unknown https://doi.org/10.1007/BF02901545
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2R,3S)-heptacosane-1,2,3-triol 162890451 Click to see 428.70 unknown https://doi.org/10.1002/CHIN.200639218
Heptacosane-1,2,3-triol 123255612 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC(C(CO)O)O 428.70 unknown https://doi.org/10.1002/CHIN.200639218
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Isocopalane and spongiane diterpenoids
(3R,4aS,4bS,7S,8aR,10aR)-2-ethenyl-3,7-dihydroxy-1,4b,8,8-tetramethyl-4a,5,6,7,8a,9,10,10a-octahydro-3H-phenanthren-4-one 162870000 Click to see 318.40 unknown https://doi.org/10.1016/J.JEP.2010.01.057
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
17-Hydroxyandrost-5-en-3-yl acetate 519264 Click to see 332.50 unknown https://doi.org/10.1055/S-2003-38482
Androstenediol 3-acetate 102150 Click to see CC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4O)C)C 332.50 unknown https://doi.org/10.1055/S-2003-38482
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S)-17-[(5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 6745 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.JEP.2012.03.014
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.JEP.2012.03.014
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Inositol phosphates
Phytic acid 890 Click to see C1(C(C(C(C(C1OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O)OP(=O)(O)O 660.04 unknown https://doi.org/10.1016/0308-8146(95)00238-3
https://doi.org/10.1016/0308-8146(95)00238-3
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallic Acid 341 Click to see 322.22 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
https://doi.org/10.1055/S-2007-969797
https://doi.org/10.1055/S-2006-962094
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1055/S-2007-969797
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
[(2R,3S)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate 56649355 Click to see 458.40 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
[2-(3,4-dihydroxyphenyl)-3-hydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-7-yl] 3,4,5-trihydroxybenzoate 85446110 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
[2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate 21872046 Click to see 442.40 unknown https://doi.org/10.1016/0031-9422(91)85134-L
https://doi.org/10.1016/J.FITOTE.2011.08.020
[3,7-dihydroxy-2-[4-hydroxy-3-(3,4,5-trihydroxybenzoyl)oxyphenyl]-3,4-dihydro-2H-chromen-5-yl] 3,4,5-trihydroxybenzoate 85446108 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
[4-[3,7-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-3,4-dihydro-2H-chromen-2-yl]-2-hydroxyphenyl] 3,4,5-trihydroxybenzoate 85446109 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
Catechin 5-O-gallate 15689618 Click to see 442.40 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
https://doi.org/10.1016/0031-9422(91)85134-L
Catechin 5,3'-di-O-gallate 15689619 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
Catechin 5,4'-di-O-gallate 15689620 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
Catechin 5,7,-di-O-gallate 15689621 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(91)85134-L
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin 932 Click to see 272.25 unknown https://doi.org/10.1055/S-2006-962094
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1055/S-2006-962094
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1055/S-2007-969797
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
3,8-dihydroxy-2,10-dimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162879074 Click to see 342.30 unknown https://doi.org/10.1055/S-0029-1186226
8-hydroxy-2,3,10-trimethoxy-5H-isochromeno[4,3-b]chromen-7-one 162948308 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=CC(=C(C=C43)OC)OC)O 356.30 unknown https://doi.org/10.1055/S-0029-1186226
> Phenylpropanoids and polyketides / Tannins
(3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl) 3,4,5-trihydroxybenzoate 4628122 Click to see 332.26 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
1,6-bis-O-galloyl-beta-D-glucose 440221 Click to see 484.40 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
1,6-Digalloyl-beta-D-glucopyranose 3332212 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)O)O 484.40 unknown https://doi.org/10.1016/J.FITOTE.2011.08.020
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/J.FITOTE.2011.08.020

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