Stryphnodendron adstringens

Details Top

Internal ID UUID643fd58daed3d754906888
Scientific name Stryphnodendron adstringens
Authority (Mart.) Coville
First published in Century Dict.10: 111 (1910)

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.

In traditional practice across Brazil’s cerrado, barbatimão is used as a tannin-rich wash, infusion, or poultice to ease gums, soothe sore throats, and support external wounds. In the caatinga of Bahia, the infusion of the bark is also taken for diarrhea and other intestinal complaints, while in the pantanal communities a bark decoction is applied topically for skin infections. According to Medical Plants of Brazil, the bark is employed as an astringent gargle and wound rinse (Gertsch, 2008), and studies of Brazilian cerrado populations document the same parts and preparations for mouth and intestinal ailments (Bennett et al., 2021). In the Tramil network’s ethnomedicinal survey of northeastern Brazil, infusions of the bark are reported for treating mouth and throat irritation, and topical decoctions for cuts and ulcerations (Tramil, 2019).

A simple practical preparation is a mild barbatimão infusion for mouth and throat use. Place 5 g of dried bark in 500 mL of cold water, bring to a simmer and maintain a gentle boil for 5 minutes, then remove from heat and steep, covered, for an additional 15–20 minutes. Cool, strain, and use the liquid as a gargle or swish for 1–2 minutes up to three times a day, avoiding swallowing. Do not exceed this dose, and stop use if irritation occurs. Because of the high tannin content, barbatimão should not be taken during pregnancy; people with gastric ulcers or sensitivities to astringents should also avoid internal use. The bark’s strong astringency may also bind with iron or medications, so allow at least two hours between barbatimão use and any oral drugs or iron supplements.

Barbatimão’s activity is linked to its condensed tannins, notably procyanidins and robinetinidins, which are well documented for this species, together with simpler phenolics such as gallic acid. These constituents are responsible for the marked astringency and known protein-binding effects, and they underpin reported anti-inflammatory, wound‑healing, and antiulcer activities (Barros et al., 2008; Gertsch, 2008). In animal studies, extracts reduce gastric lesions and skin inflammation, supporting traditional uses as astringents and topical protectors (Gertsch, 2008; Bennett et al., 2021).

Today, research continues into the tannin profile and mucosal-protective potential of barbatimão, and the dried bark remains widely available in Brazilian herbal markets. It is still used in home care for gums, throats, and minor wounds, while commercial preparations such as mouthwashes and gels feature the plant’s tannins for astringent action.

General Uses Top

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Common products:
Bark is the primary commercial product. An aqueous extract (often called “barbatimão extract”) is traded as a natural vegetable tanning material.

Industrial and craft applications:
Leather tanning. Bark or extract is used to tan hides and skins, providing firm, dark brown leather. The material contains condensed (proanthocyanidin) tannins with high protein-binding capacity, enabling efficient crosslinking of collagen fibers.

Natural brown dye. The bark extract is used as a non-medicinal dye for protein fibers such as wool, producing stable brown shades.

Packaging and film additives. Proanthocyanidins extracted from barbatimão bark have been used as antioxidant additives in edible/composite films and coatings to limit oxidative reactions in packaged products.

Food and beverages (non-medicinal):
Extracts are used as natural colorants and antioxidants in packaged foods and beverages to stabilize color and flavor; they are not consumed as beverages themselves.

Colorants and tanning:
Color class: brown. The brown hue derives from condensed tannins and their complexes. The bark’s high tannin content and fast dye uptake on protein fibers provide consistent coloration for leather and textile dyeing.

Wood and fiber:
Wood is dense and used locally for poles and posts where durability is required. Bark fibers are also collected for tanning and dyeing.

Fragrance and cosmetics:
No documented non-medicinal uses in perfumery or cosmetics were found.

Properties relevant to use:
The bark contains condensed proanthocyanidin tannins that precipitate proteins and readily complex with metal ions, a chemical basis for tanning and dyeing. Proanthocyanidins also provide antioxidant activity exploited in food packaging contexts.

Standards and regulation:
Tannin extracts for leather tanning may be traded under national or regional timber/tannin material standards; such frameworks vary by country. For food-contact uses of bark extracts in packaging, regulatory requirements for colorants and additives apply at the national level.

Sustainability and sourcing:
Bark is harvested from wild or cultivated trees; regeneration through reseeding and sustainable harvesting cycles is commonly practiced to maintain supplies. This is a source of non-timber forest product revenue in parts of Brazil.

Synonyms Top

Scientific name Authority First published in
Mimosa barbadetimam Vell. Fl. Flumin.11: t. 7 (1831)
Mimosa virginalis Arruda H.Koster, Trav. Brazil: 500 (1816)
Acacia adstringens Mart. Reise Bras.1: 548 (1823)
Stryphnodendron barbatimam Mart. Flora 20(2, Beibl.): 117. 1837
Stryphnodendron barbadetimam (Vell.) Mart. Flora20(2 Beibl.): 117 (1837)

Common names Top

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Language Common/alternative name
Portuguese baba timão
Portuguese barbatimão-verdadeiro

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000164061
UNII 1SQL02JNZB
USDA Plants STAD
Tropicos 13001565
KEW urn:lsid:ipni.org:names:519615-1
The Plant List ild-10478
Open Tree Of Life 386248
NCBI Taxonomy 397648
IPNI 247368-2
iNaturalist 601680
GBIF 2951737
Freebase /m/0b77k1p
EPPO SRYAD
EOL 418220
USDA GRIN 70761
Wikipedia Stryphnodendron_adstringens

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
Updating the Knowledge on the Secretory Machinery of Hops (Humulus lupulus L., Cannabaceae) Ramos FP, Iwamoto L, Piva VH, Teixeira SP Plants (Basel) 17-Mar-2024
PMCID:PMC10974171
doi:10.3390/plants13060864
PMID:38592855
Emerging Trends in Ant–Pollinator Conflict in Extrafloral Nectary-Bearing Plants Calixto ES, de Oliveira Pimenta IC, Lange D, Marquis RJ, Torezan-Silingardi HM, Del-Claro K Plants (Basel) 27-Feb-2024
PMCID:PMC10935445
doi:10.3390/plants13050651
PMID:38475497
Assembly, annotation and analysis of the chloroplast genome of the Algarrobo tree Neltuma pallida (subfamily: Caesalpinioideae) Caycho E, La Torre R, Orjeda G BMC Plant Biol 16-Nov-2023
PMCID:PMC10652460
doi:10.1186/s12870-023-04581-5
PMID:37974117
Campomanesia adamantium O Berg. fruit, native to Brazil, can protect against oxidative stress and promote longevity de Araújo LC, Leite NR, da Rocha PD, Baldivia DD, Agarrayua DA, Ávila DS, da Silva DB, Carollo CA, Campos JF, Souza KD, dos Santos EL PLoS One 16-Nov-2023
PMCID:PMC10653513
doi:10.1371/journal.pone.0294316
PMID:37972127
Characterization of Sodium Alginate-Based Films Blended with Olive Leaf and Laurel Leaf Extracts Obtained by Ultrasound-Assisted Technology Moura-Alves M, Souza VG, Silva JA, Esteves A, Pastrana LM, Saraiva C, Cerqueira MA Foods 09-Nov-2023
PMCID:PMC10670003
doi:10.3390/foods12224076
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Navigating the Multidimensional Impact of Living with Hidradenitis Suppurativa: An In-Depth Netnographic Study on Social Media Platforms Bellei EA, de Carvalho AV, Eng BM, Tozato C, de Barros DH, Tamashiro EY, Duarte GV, de Fátima RT, Magalhães RF, da Silva RS, Cesar WG, Thies FG Dermatol Ther (Heidelb) 04-Oct-2023
PMCID:PMC10613171
doi:10.1007/s13555-023-01032-9
PMID:37794274
Meta-analysis of the responses of tree and herb to elevated CO2 in Brazil da Silva Fortirer J, Grandis A, Pagliuso D, de Toledo Castanho C, Buckeridge MS Sci Rep 22-Sep-2023
PMCID:PMC10517018
doi:10.1038/s41598-023-40783-5
PMID:37739974
Back to Nature: Medicinal Plants as Promising Sources for Antibacterial Drugs in the Post-Antibiotic Era Abdallah EM, Alhatlani BY, de Paula Menezes R, Martins CH Plants (Basel) 28-Aug-2023
PMCID:PMC10490416
doi:10.3390/plants12173077
PMID:37687324
Anemochorous and zoochorous seeds of trees from the Brazilian savannas differ in fatty acid content and composition Franco AC, de Melo RB, Ferreira CS, Williams TC AoB Plants 17-Aug-2023
PMCID:PMC10433789
doi:10.1093/aobpla/plad042
PMID:37600502
Development status of novel spectral imaging techniques and application to traditional Chinese medicine Wang Q, Zhang Y, Yang B J Pharm Anal 29-Jul-2023
PMCID:PMC10759257
doi:10.1016/j.jpha.2023.07.007
PMID:38174122
Screening antibiofilm activity of invasive plants growing at the Slope Merapi Mountain, Central Java, against Candida albicans Desrini S, Girardot M, Imbert C, Mustofa M, Nuryastuti T BMC Complement Med Ther 12-Jul-2023
PMCID:PMC10339508
doi:10.1186/s12906-023-04044-2
PMID:37438777
Diversity analysis of endophytes with antimicrobial and antioxidant potential from Viola odorata: an endemic plant species of the Himalayas Salwan R, Rana A, Saini R, Sharma A, Sharma M, Sharma V Braz J Microbiol 25-May-2023
PMCID:PMC10484869
doi:10.1007/s42770-023-01010-5
PMID:37227628
Paecilins Q and R: Antifungal Chromanones Produced by the Endophytic Fungus Pseudofusicoccum stromaticum CMRP4328 Iantas J, Savi DC, Ponomareva LV, Thorson JS, Rohr J, Glienke C, Shaaban KA Planta Med 28-Mar-2023
PMCID:PMC10698238
doi:10.1055/a-2063-5481
PMID:36977488
Plant-Derived Bioactive Compounds in the Management of Neurodegenerative Disorders: Challenges, Future Directions and Molecular Mechanisms Involved in Neuroprotection Shoaib S, Ansari MA, Fatease AA, Safhi AY, Hani U, Jahan R, Alomary MN, Ansari MN, Ahmed N, Wahab S, Ahmad W, Yusuf N, Islam N Pharmaceutics 23-Feb-2023
PMCID:PMC10057544
doi:10.3390/pharmaceutics15030749
PMID:36986610
Prospecting Plant Extracts and Bioactive Molecules with Antimicrobial Activity in Brazilian Biomes: A Review de Queiroz JC, Leite JR, Vasconcelos AG Antibiotics (Basel) 21-Feb-2023
PMCID:PMC10044579
doi:10.3390/antibiotics12030427
PMID:36978294

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/10.1055/S-2006-959826
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-6-[(2R,3S,4S)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101995292 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
(2R,3R)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101995287 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
(2R,3R)-8-[(2R,3S,4S)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101995288 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
(2R,3S)-6-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101995289 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
(2R,3S)-6-[(2R,3S,4S)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101995291 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
(4alpha->8)-bis-4'-O-methylgallocatechin 53344581 Click to see 638.60 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-6-[(2R,3R,4R)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 16175829 Click to see 1115.00 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4R)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 16179206 Click to see 1351.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4R)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxybenzoate 16179208 Click to see 1235.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4R)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 16175826 Click to see CC(=O)OC1CC2=C(C(=C(C=C2OC(=O)C)OC(=O)C)C3C(C(OC4=C3C(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=C(C(=C5)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC1C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)OC(=O)C 1115.00 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4S)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 163024853 Click to see CC(=O)OC1C(C2=C(C=C(C=C2OC(=O)C)OC(=O)C)OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(C(C5)OC(=O)C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)OC(=O)C)C7=CC(=C(C(=C7)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1351.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4S)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxybenzoate 162974965 Click to see CC(=O)OC1C(C2=C(C=C(C=C2OC(=O)C)OC(=O)C)OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(C(C5)OC(=O)C6=CC=C(C=C6)OC(=O)C)C7=CC(=C(C(=C7)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1235.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-8-[(2R,3R,4R)-5,7-diacetyloxy-3-(3,4,5-triacetyloxybenzoyl)oxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 16179209 Click to see 1587.30 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 4-hydroxybenzoate 101935949 Click to see 730.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-8-[(2R,3S,4R)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 101995290 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 746.60 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[(2R,3R)-8-[(2R,3S,4S)-3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 101995293 Click to see 746.60 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[(2R,3S)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[(2R,3R,4R)-3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 16175825 Click to see CC(=O)OC1CC2=C(C(=C(C=C2OC(=O)C)OC(=O)C)C3C(C(OC4=C3C(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=C(C(=C5)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC1C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)OC(=O)C 1115.00 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3S)-5,7-diacetyloxy-2-(3,5-diacetyloxy-4-methoxyphenyl)-8-[(2R,3S,4S)-3,5,7-triacetyloxy-2-(3,5-diacetyloxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 162902693 Click to see 1058.90 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-6-[3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 16175830 Click to see 1115.00 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 163024852 Click to see 1351.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxybenzoate 162974964 Click to see CC(=O)OC1C(C2=C(C=C(C=C2OC(=O)C)OC(=O)C)OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)C4=C(C=C(C5=C4OC(C(C5)OC(=O)C6=CC=C(C=C6)OC(=O)C)C7=CC(=C(C(=C7)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 1235.10 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-8-[3,5,7-triacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 16175827 Click to see CC(=O)OC1CC2=C(C(=C(C=C2OC(=O)C)OC(=O)C)C3C(C(OC4=C3C(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=C(C(=C5)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC1C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)OC(=O)C 1115.00 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,5-diacetyloxy-4-methoxyphenyl)-8-[3,5,7-triacetyloxy-2-(3,5-diacetyloxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromen-3-yl] acetate 162902692 Click to see 1058.90 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[5,7-diacetyloxy-8-[5,7-diacetyloxy-3-(3,4,5-triacetyloxybenzoyl)oxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 162999613 Click to see CC(=O)OC1=CC2=C(C(C(C(O2)C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C4=CC(=C(C(=C4)OC(=O)C)OC(=O)C)OC(=O)C)C5=C(C=C(C6=C5OC(C(C6)OC(=O)C7=CC(=C(C(=C7)OC(=O)C)OC(=O)C)OC(=O)C)C8=CC(=C(C(=C8)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C(=C1)OC(=O)C 1587.30 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[8-[3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate 162996075 Click to see 746.60 unknown https://doi.org/10.1016/0031-9422(95)00953-1
2-(3,5-dihydroxy-4-methoxyphenyl)-8-[2-(3,5-dihydroxy-4-methoxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 75290667 Click to see 638.60 unknown https://doi.org/10.1016/0031-9422(95)00953-1
6-[3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 101429502 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
8-[3,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 77916041 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
Epigallocatechin-(4beta->8)-epigallocatechin 3-O-(4-hydroxybenzoate) 163184558 Click to see 730.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Prodelphinidin B5 163184605 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C(=C5)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O 610.50 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Robinetinidol-(4alpha,8)-gallocatechin 70697956 Click to see 594.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxy-3,5-dimethoxybenzoate 15281606 Click to see 738.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 3,4,5-triacetyloxybenzoate 14890499 Click to see 794.70 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxy-3,5-dimethoxybenzoate 162899249 Click to see 738.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
EGCG Octaacetate 11787645 Click to see CC(=O)OC1=CC2=C(CC(C(O2)C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C4=CC(=C(C(=C4)OC(=O)C)OC(=O)C)OC(=O)C)C(=C1)OC(=O)C 794.70 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Epigallocatechin 3-O-(3,5-di-O-methylgallate) 9913276 Click to see 486.40 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Epigallocatechin Gallate 65064 Click to see 458.40 unknown https://doi.org/10.1055/S-2006-959826
https://doi.org/10.1016/0031-9422(95)00686-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Egc-4'-O-ME 53463000 Click to see 320.29 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] acetate 21769542 Click to see 558.50 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2R,3S)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] acetate 5317460 Click to see CC(=O)OC1CC2=C(C=C(C=C2OC(=O)C)OC(=O)C)OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C 558.50 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[(2S,3S)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] acetate 13768246 Click to see 558.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] acetate 13768245 Click to see 558.50 unknown https://doi.org/10.1016/0031-9422(95)00953-1
https://doi.org/10.1016/0031-9422(95)00686-9
4'-O-Methyl-Gallocatechin 44257120 Click to see 320.29 unknown https://doi.org/10.1055/S-2006-959826
https://doi.org/10.1016/0031-9422(95)00686-9
Epigallocatechin 72277 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/10.1016/0031-9422(95)00686-9
https://doi.org/10.1016/S0031-9422(98)00715-8
Gallocatechin 65084 Click to see 306.27 unknown https://doi.org/10.1016/0031-9422(95)00686-9
https://doi.org/10.1055/S-2006-959826
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(2R,3R)-5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxy-3-methoxybenzoate 15281607 Click to see CC(=O)OC1=C(C=C(C=C1)C(=O)OC2CC3=C(C=C(C=C3OC(=O)C)OC(=O)C)OC2C4=CC(=C(C(=C4)OC(=O)C)OC(=O)C)OC(=O)C)OC 708.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxy-3-methoxybenzoate 162937159 Click to see 708.60 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Epigallocatechin 3-O-vanillate 44257119 Click to see 456.40 unknown https://doi.org/10.1016/0031-9422(95)00686-9

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