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Stryphnodendron adstringens

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

Description Top

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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

Suggest others/fix!
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
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
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
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
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
Diaporthe species associated with the maritime grass Festuca rubra subsp. pruinosa Toghueo RM, Vázquez de Aldana BR, Zabalgogeazcoa I Front Microbiol 16-Feb-2023
PMCID:PMC9978114
doi:10.3389/fmicb.2023.1105299
PMID:36876098
Vulvovaginal candidiasis and vaginal microflora interaction: Microflora changes and probiotic therapy Sun Z, Ge X, Qiu B, Xiang Z, Jiang C, Wu J, Li Y Front Cell Infect Microbiol 03-Feb-2023
PMCID:PMC9936092
doi:10.3389/fcimb.2023.1123026
PMID:36816582
Bio-Prospecting of Crude Leaf Extracts from Thirteen Plants of Brazilian Cerrado Biome on Human Glioma Cell Lines Silva VA, Rosa MN, Gomes IN, Vital PD, Alves AL, Evangelista AF, Longato GB, Carloni AC, Oliveira BG, Pinto FE, Romão W, Rezende AR, Araújo AA, Oliveira LS, Souza AA, Oliveira SC, Ribeiro RI, Reis RM Molecules 01-Feb-2023
PMCID:PMC9921846
doi:10.3390/molecules28031394
PMID:36771057
Dibenzylideneacetone Induces Apoptosis in Cervical Cancer Cells through Ros-Mediated Mitochondrial Damage Zani AP, Zani CP, Din ZU, Rodrigues-Filho E, Ueda-Nakamura T, Garcia FP, de Oliveira Silva S, Nakamura CV Antioxidants (Basel) 30-Jan-2023
PMCID:PMC9952489
doi:10.3390/antiox12020317
PMID:36829876
Major Phytochemicals: Recent Advances in Health Benefits and Extraction Method Kumar A, P N, Kumar M, Jose A, Tomer V, Oz E, Proestos C, Zeng M, Elobeid T, K S, Oz F Molecules 16-Jan-2023
PMCID:PMC9862941
doi:10.3390/molecules28020887
PMID:36677944
Herbal Products and Their Active Constituents for Diabetic Wound Healing—Preclinical and Clinical Studies: A Systematic Review Herman A, Herman AP Pharmaceutics 14-Jan-2023
PMCID:PMC9865817
doi:10.3390/pharmaceutics15010281
PMID:36678910

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 C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1055/S-2006-959826
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R)-2alpha,2'alpha-Bis(3,4,5-triacetoxyphenyl)-4beta,8'-bichroman-3alpha,3'alpha,5,5',7,7'-hexol hexaacetate 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,2'R)-2alpha,2'alpha-Bis(3,4,5-triacetoxyphenyl)-4beta,8'-bichroman-3alpha,3'beta,5,5',7,7'-hexol hexaacetate 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,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 C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)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,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 C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)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,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 C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)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
(4alpha->8)-bis-4'-O-methylgallocatechin 53344581 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C(=C6)O)OC)O)O)O)O 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 CC(=O)OC1CC2=C(C(=C(C=C2OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C4C(C(OC5=C4C(=CC(=C5)OC(=O)C)OC(=O)C)C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)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-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 C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)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 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 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,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 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)OC(=O)C)OC(=O)C)OC1C6=CC(=C(C(=C6)OC(=O)C)OC)OC(=O)C 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 CC(=O)OC1CC2=C(C(=C(C=C2OC1C3=CC(=C(C(=C3)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C4C(C(OC5=C4C(=CC(=C5)OC(=O)C)OC(=O)C)C6=CC(=C(C(=C6)OC(=O)C)OC(=O)C)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-(3,4,5-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 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
[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 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)OC(=O)C)OC(=O)C)OC1C6=CC(=C(C(=C6)OC(=O)C)OC)OC(=O)C 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 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
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 COC1=C(C=C(C=C1O)C2C(CC3=C(O2)C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C(=C6)O)OC)O)O)O)O 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 C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C(=C5)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
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
CID 16179206 16179206 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
CID 16179208 16179208 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
CID 16179209 16179209 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
Epigallocatechin-(4beta->8)-epigallocatechin 3-O-(4-hydroxybenzoate) 163184558 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)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 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 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
> 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 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)OC(=O)C)OC)C(=C1)OC(=O)C 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 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
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] 4-acetyloxy-3,5-dimethoxybenzoate 162899249 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)OC(=O)C)OC)C(=C1)OC(=O)C 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 COC1=CC(=CC(=C1O)OC)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 486.40 unknown https://doi.org/10.1016/0031-9422(95)00686-9
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 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 COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 320.29 unknown https://doi.org/10.1016/0031-9422(95)00686-9
(2R,3R)-2-(3,4,5-Triacetoxyphenyl)chroman-3,5,7-triol triacetate 21769542 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
[(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 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)00953-1
[5,7-diacetyloxy-2-(3,4,5-triacetyloxyphenyl)-3,4-dihydro-2H-chromen-3-yl] acetate 13768245 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)00953-1
https://doi.org/10.1016/0031-9422(95)00686-9
4'-O-Methylgallocatechin 44257120 Click to see COC1=C(C=C(C=C1O)C2C(CC3=C(C=C(C=C3O2)O)O)O)O 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 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/10.1055/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 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
Epigallocatechin 3-O-vanillate 44257119 Click to see COC1=C(C=CC(=C1)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O)O 456.40 unknown https://doi.org/10.1016/0031-9422(95)00686-9

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