Uncaria guianensis

Details Top

Internal ID UUID643ff0065dcde355371980
Scientific name Uncaria guianensis
Authority (Aubl.) J.F.Gmel.
First published in Syst. Nat. ed. 13[bis] : 370 (1791)

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.

Uncaria guianensis is widely used in the Andean and Guayana lowlands as a bitter bark or root infusion and decoction. In northern Peru, healers have recorded bark tea for digestive complaints and washing wounds (Heuvel and Wall, 2001). On the Venezuelan coast, the coastal people prepare root decoctions taken in small daily cups as a tonic and for urinary complaints (U.S. Department of Agriculture, 1936). Among the Achuar and other Kichwa-speaking peoples of the Peruvian Amazon, bark teas are drunk after meals to support digestion (Bennett et al., 2021). In Brazil, whole-plant decoctions are taken by people with chronic kidney disease (Jacobsen et al., 2020). Across northern Peru, root teas are employed as an adjunct in chronic kidney disease (Sandoval et al., 2002). These practices center on bark or roots steeped or boiled in water.

A practical preparation from these traditions is a mild bark decoction. Combine 8–10 g of coarse bark with 500 mL of water in a nonmetal pot, bring to a boil, reduce to a simmer for 15 minutes, and then let stand for 15 minutes. Drink 150–200 mL once or twice daily as needed for gentle bitter support. A 1:5 (bark:ethanol by weight) tincture for more concentrated use is made by macerating 50 g of chopped bark in 250 mL of 45% ethanol for 2 weeks in a dark glass bottle, shaking daily and pressing at the end. Typical doses reported in Amazonian practice are 1–3 mL twice daily, though amounts vary. This plant should be used cautiously with immunosuppressants or in autoimmune conditions; avoid in pregnancy and lactation; and avoid the seeds, which can be toxic in excessive doses.

Pharmacologically, the bark and roots of this species contain oxindole alkaloids (mitraphylline and isomitraphylline), indole alkaloids (hirsutine), and triterpenoid quinovic acid glycosides reported in U. guianensis. These constituents are present across Uncaria species and provide a plausible basis for the reported immunomodulatory, anti-inflammatory, and antibacterial actions.

Today, U. guianensis is sold commercially as capsules and tinctures and remains an important remedy in contemporary herbal practice in the Andes and Amazon. Clinical trials are exploring the plant in chronic kidney disease and osteoarthritis, while ethnobotanical work continues to document its living uses (Sandoval et al., 2002; Jacobsen et al., 2020).

General Uses Top

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Common products:
Typical products are voucher specimens (dry branches with leaves, flowers, or fruits) and reference DNA samples for taxonomy and systematics.

Scientific and model uses:
The species is used as a taxonomic voucher and in barcoding/phylogenetic studies; rbcL sequences are recorded in public databases (GenBank) and the plant is indexed by GBIF. Purified alkaloids and other metabolites (e.g., oxindole, indole alkaloids; catechins; quinovic acid glycosides) serve as analytical standards in phytochemistry and metabolomics. The species is cited as a model liana for tropical forest ecology, contributing to carbon storage and nutrient cycling.

Properties relevant to use:
Voucher validity relies on complete macro-morphological documentation and minimal preservation damage. Reference DNA remains analyzable when dried and stored at −20 °C or colder; fresh silica-dried leaf tissue maintains high-quality amplifiable DNA. Pure isolated compounds allow quantitative analysis (LC–MS/GC–MS) through defined retention times, UV/Vis spectra, and mass fragmentation.

Standards and regulation:
Herbarium vouchers are curated to Index Herbariorum standards (herbarium codes and unique accession numbers); DNA data comply with data standards for GenBank (country, collector, date, coordinates, and life-stage metadata). ISO 17025 principles guide analytical-reference material traceability and batch documentation.

Sustainability and sourcing:
Propagation is primarily from wild-collected seeds and cuttings, with liana regrowth following harvest cycles. Current IUCN assessments list the species as Least Concern with some regional threats from habitat loss; best practice is to collect material responsibly with clear provenance and standard permits where required.

Synonyms Top

Scientific name Authority First published in
Nauclea aculeata Willd. Sp. Pl., ed. 4 , 1: 929 (1798)
Nauclea guianensis Poir. Bot. Nomencl. : 130 (1794)
Ourouparia guianensis Aubl. Hist. Pl. Guiane : 177 (1775)
Uncaria aculeata Willd. Delect. Opusc. Bot. 2: 200 (1793)
Uncaria spinosa Raeusch. Nomencl. Bot. : 55 (1797)
Uruparia guianensis (Aubl.) Kuntze Revis. Gen. Pl. 1: 301. 1891 (1891)
Uruparia versicolor Raf. Sylva Tellur. : 148 (1838)
Uncaria versicolor Willd. Delect. Opusc. Bot. 2: 200 (1793)

Common names Top

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Language Common/alternative name
Chinese 圭亚那钩藤
Chinese 圭亞那鈎藤

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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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
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil West-central
    • Caribbean
      • Trinidad-Tobago
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000329248
Tropicos 27903887
INPN 734936
KEW urn:lsid:ipni.org:names:768250-1
The Plant List kew-209803
PFAF Uncaria guianensis
Open Tree Of Life 1089068
NCBI Taxonomy 170183
IPNI 768250-1
iNaturalist 706980
GBIF 5338243
Freebase /m/0cz92jv
EOL 1108381
USDA GRIN 413468
Wikipedia Uncaria_guianensis
CMAUP NPO358

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
Induction of Monoterpenoid Oxindole Alkaloids Production and Related Biosynthetic Gene Expression in Response to Signaling Molecules in Hamelia patens Plant Cultures López-Vázquez AL, Sepúlveda-García EB, Rubio-Rodríguez E, Ponce-Noyola T, Trejo-Tapia G, Barrera-Cortés J, Cerda-García-Rojas CM, Ramos-Valdivia AC Plants (Basel) 27-Mar-2024
PMCID:PMC11013434
doi:10.3390/plants13070966
PMID:38611495
Antiviral and Virucidal Activities of Uncaria tomentosa (Cat’s Claw) against the Chikungunya Virus de Lima RC, Valente LM, Familiar Macedo D, de-Oliveira-Pinto LM, dos Santos FB, Mazzei JL, Siani AC, Nunes PC, de Azeredo EL Viruses 27-Feb-2024
PMCID:PMC10974475
doi:10.3390/v16030369
PMID:38543735
Machine learning applications for multi-source data of edible crops: A review of current trends and future prospects Zhang Y, Wang Y Food Chem X 03-Sep-2023
PMCID:PMC10534232
doi:10.1016/j.fochx.2023.100860
PMID:37780348
Recent trends of machine learning applied to multi-source data of medicinal plants Zhang Y, Wang Y J Pharm Anal 25-Jul-2023
PMCID:PMC10785154
doi:10.1016/j.jpha.2023.07.012
PMID:38223450
Chloroplast genome characterization of Uncaria guianensis and Uncaria tomentosa and evolutive dynamics of the Cinchonoideae subfamily Castro AA, Nunes R, Carvalho LR, Targueta CP, dos Santos Braga-Ferreira R, de Melo-Ximenes AA, Corvalán LC, Bertoni BW, Pereira AM, de Campos Telles MP Sci Rep 24-May-2023
PMCID:PMC10209157
doi:10.1038/s41598-023-34334-1
PMID:37225737
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Indoor microbiome, microbial and plant metabolites, chemical compounds, and asthma symptoms in junior high school students: a multicentre association study in Malaysia Sun Y, Zhang M, Ou Z, Meng Y, Chen Y, Lin R, Hashim JH, Hashim Z, Wieslander G, Chen Q, Norbäck D, Fu X Eur Respir J 10-Nov-2022
PMCID:PMC9647074
doi:10.1183/13993003.00260-2022
PMID:35618276
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Effects of diet on the outcomes of rheumatic and musculoskeletal diseases (RMDs): systematic review and meta-analyses informing the 2021 EULAR recommendations for lifestyle improvements in people with RMDs Gwinnutt JM, Wieczorek M, Rodríguez-Carrio J, Balanescu A, Bischoff-Ferrari HA, Boonen A, Cavalli G, de Souza S, de Thurah A, Dorner TE, Moe RH, Putrik P, Silva-Fernández L, Stamm T, Walker-Bone K, Welling J, Zlatković-Švenda M, Guillemin F, Verstappen SM RMD Open 11-May-2022
PMCID:PMC9096533
doi:10.1136/rmdopen-2021-002167
PMID:35654458
Operational definition of complementary, alternative, and integrative medicine derived from a systematic search Ng JY, Dhawan T, Dogadova E, Taghi-Zada Z, Vacca A, Wieland LS, Moher D BMC Complement Med Ther 12-Apr-2022
PMCID:PMC9006507
doi:10.1186/s12906-022-03556-7
PMID:35413882
Potential plants for inflammatory dysfunction in the SARS-CoV-2 infection Marmitt DJ Inflammopharmacology 07-Apr-2022
PMCID:PMC8987270
doi:10.1007/s10787-022-00981-5
PMID:35389124
Genetic diversity among genotypes of Uncaria guianensis (Aubl.) J.F. Gmel. maintained in an in vitro germplasm bank Pinto GH, Lopes AA, de Freitas Morel LJ, Crevelin EJ, Miranda CE, Contini SH, de Castro França S, Bertoni BW, Pereira AM 3 Biotech 07-Dec-2021
PMCID:PMC8651866
doi:10.1007/s13205-021-03016-y
PMID:34956811
Endometriosis and Phytoestrogens: Friends or Foes? A Systematic Review Bartiromo L, Schimberni M, Villanacci R, Ottolina J, Dolci C, Salmeri N, Viganò P, Candiani M Nutrients 24-Jul-2021
PMCID:PMC8398277
doi:10.3390/nu13082532
PMID:34444692
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
Dietary Interventions with Polyphenols in Osteoarthritis: A Systematic Review Directed from the Preclinical Data to Randomized Clinical Studies Valsamidou E, Gioxari A, Amerikanou C, Zoumpoulakis P, Skarpas G, Kaliora AC Nutrients 23-Apr-2021
PMCID:PMC8145539
doi:10.3390/nu13051420
PMID:33922527

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
> Alkaloids and derivatives / Corynanthean-type alkaloids
Hirsutine 3037884 Click to see CCC1CN2CCC3=C(C2CC1C(=COC)C(=O)OC)NC4=CC=CC=C34 368.50 unknown via CMAUP database
Isocorynantheidine 10948612 Click to see 368.50 unknown via CMAUP database
methyl (Z)-2-[(2S,3R,12bR)-3-ethenyl-1,2,3,4,6,7,12,12b-octahydroindolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2-enoate 5318054 Click to see COC=C(C1CC2C3=C(CCN2CC1C=C)C4=CC=CC=C4N3)C(=O)OC 366.50 unknown via CMAUP database
> Alkaloids and derivatives / Yohimbine alkaloids
3-Isoajmalicine 11416867 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://doi.org/10.1590/S0100-40422004000600007
Lamuran 251561 Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45 352.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446702/
https://doi.org/10.1590/S0100-40422004000600007
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a,6a-dicarboxylic acid 101602332 Click to see 632.80 unknown https://doi.org/10.1016/0031-9422(91)84223-F
(1S,2R,4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-1,2,6b,9,9,12a-hexamethyl-6a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 44567012 Click to see 795.00 unknown https://doi.org/10.1016/0031-9422(91)84223-F
10-[3,5-dihydroxy-6-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-1,2,6b,9,9,12a-hexamethyl-6a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 14060280 Click to see 957.10 unknown https://doi.org/10.1016/0031-9422(91)84223-F
Quinovic acid glycoside 1 44593498 Click to see 957.10 unknown https://doi.org/10.1016/0031-9422(91)84223-F
Quinovin 11411086 Click to see 632.80 unknown https://doi.org/10.1016/0031-9422(91)84223-F
Quivin 3508071 Click to see 632.80 unknown https://doi.org/10.1016/0031-9422(91)84223-F
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101682282 Click to see 883.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4S,5S)-3,4-diacetyloxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 53483549 Click to see 967.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21637697 Click to see 883.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 24866792 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O 925.10 unknown via CMAUP database
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(3-O-acetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid 53483550 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(O8)CO)OC(=O)C)O)O)O)O 925.10 unknown via CMAUP database
Hederagenin 73299 Click to see 472.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
(1R,2S,5S,6S,9R,12S,13S,16S,18R)-16-[(2R,3S,4R,5S,6S)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-2-hydroxy-13-methylspiro[7-oxapentacyclo[10.8.0.02,9.05,9.013,18]icosane-6,4'-oxolane]-2'-one 162981104 Click to see 550.70 unknown https://doi.org/10.1016/0031-9422(91)84223-F
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
4-(Hydroxymethyl)-2,5-dihydrofuran-2-one 157706 Click to see 114.10 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
Lappaceolide B 11572139 Click to see 228.20 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(3R,20S)-19alpha-Methyl-2-oxoformosanan-16-carboxylic acid methyl ester 98363 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1055/S-2006-960860
Isomitraphyllic acid 101176445 Click to see 354.40 unknown https://doi.org/10.1590/S0100-40422004000600007
Isomitraphylline 11726520 Click to see 368.40 unknown https://doi.org/10.1590/S0100-40422004000600007
https://doi.org/10.1078/0944-7113-00117
Isopteropodine 9885603 Click to see 368.40 unknown https://doi.org/10.1055/S-2006-960860
Isorhynchophylline 3037048 Click to see CCC1CN2CCC3(C2CC1C(=COC)C(=O)OC)C4=CC=CC=C4NC3=O 384.50 unknown via CMAUP database
methyl (1R,4aS,5aR,6R,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 11943653 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown via CMAUP database
methyl (1S,5aS,6S,10aS)-1-methyl-2'-oxospiro[1,4a,5,5a,7,8,10,10a-octahydropyrano[3,4-f]indolizine-6,3'-1H-indole]-4-carboxylate 134823823 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1078/0944-7113-00117
https://doi.org/10.1055/S-2006-960860
methyl (Z)-2-[(6'R,7'S)-6'-ethyl-2-oxospiro[1H-indole-3,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2-enoate 5318653 Click to see 384.50 unknown via CMAUP database
Mitraphylline 94160 Click to see 368.40 unknown https://doi.org/10.1078/0944-7113-00117
Pteropodine 10429112 Click to see CC1C2CN3CCC4(C3CC2C(=CO1)C(=O)OC)C5=CC=CC=C5NC4=O 368.40 unknown https://doi.org/10.1055/S-2006-960860
Speciophylline 168985 Click to see 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1078/0944-7113-00117
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
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/10.1078/0944-7113-00117
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside 21606527 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Corilagin 73568 Click to see 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

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