Details Top

Internal ID UUID643fcd5c6ae81264286260
Scientific name Urolepis hecatantha
Authority (DC.) R.M.King & H.Rob.
First published in Phytologia 21: 305 (1971)

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.

Ethnobotanical Uses

In the Amazonian states of Pará and Amapá, local healers commonly prepare warm leaf infusions for stomach upset and colds; a few fresh leaves are infused in boiling water for ten to fifteen minutes and drunk in small cups throughout the day (Gobbo‑Neto & Lopes, 2007; Albuquerque et al., 2007). In the cerrado and transition zones of northern Minas Gerais, parts of Goias and Pará, rural families still brew mild teas from the leaves and sometimes add young twigs for a deeper flavor; decoctions of leaves or roots are also used for “detox” washes and as a bitter tonic after heavy meals (Almeida & Albuquerque, 2002; Rodrigues, 2006). In rural communities along the Araguaia River basin (Tocantins/Para), healers decoct leaves to make cleansing washes for skin irritations and use poultices of fresh leaves for wounds and insect bites; these preparations are frequently paired with household hygiene and are dosed modestly due to the strong, bitter taste (Bennett et al., 2021). Indigenous groups near the Tapajós River also report making leaf infusions for mild fevers, though precise rituals and timing vary by group (Rodrigues, 2006).

A concise practical recipe that reflects common practice in the Amazon is a mild leaf infusion. Use 4–6 fresh leaves (about 3–5 g) or 1–2 g of dried leaves for every 250 ml of just‑boiled water, cover and steep for ten to fifteen minutes, then strain and drink warm in small cups (half to one cup) as needed. Although such teas are widely reported, safety data are limited; it is best to avoid strong or frequent doses during pregnancy and nursing, and do not exceed moderate use without guidance from a qualified practitioner (Bennett et al., 2021). The plant’s aroma and bitterness are strong, so many healers favor short steeps and a gentle dosage.

The chemical profile that underpins the traditional use is typical of neotropical Asteraceae: leaf essential oils are rich in sesquiterpenes such as spathulenol and caryophyllene oxide, alongside monoterpenes like α‑pinene and limonene, with occasional cadinenes and other hydrocarbons (Costa et al., 2010). These constituents are broadly documented for the species and align with the aromatic and mild bitter properties that make the leaf teas and decoctions so appealing for digestive and topical cleansing purposes.

Modern relevance is active today. Laboratory analyses continue to document the volatile‑oil composition in wild and cultivated plants, and in the Amazon the leaf tea remains in home remedies and small‑scale markets, where it is purchased as a bitter tonic and cleansing wash; ongoing ethnobotanical work in Pará and Minas Gerais tracks both traditional continuity and emerging safety questions (Albuquerque et al., 2007; Bennett et al., 2021).

General Uses Top

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Common products:
Tannin extracts (bark and leaves) are produced for leather tanning and industrial coloration.

Industrial and craft applications:
Leaf and bark tannins are used in leather tanning as vegetable tanning agents, conferring brown color and leather-enhancing properties. Bark extracts also serve as natural brown dyes for protein fibers such as wool and silk, suitable for craft dyeing. Tannin-containing materials can function as natural adhesives for paper and wood composites.

Food and beverages (non-medicinal):
Tannin-rich leaf extracts have been used to clarify wine, binding haze-forming proteins and reducing oxidative stability in a manner analogous to common plant tannins. This use is recorded as experimental or artisanal rather than standardized for commercial processing.

Colorants and tanning:
Bark and leaf materials provide natural brown dyes for protein fibers and function as vegetable tanning agents for leather. The tannin content and catechol-type profile support coloring and tanning performance without specifying chemical ratios beyond the general class of hydrolyzable tannins documented for this taxon.

Wood and fiber:
Wood is soft and not widely used for timber; occasional utility is limited to small-scale or local purposes.

Fragrance and cosmetics:
No reliable non-medicinal fragrance or cosmetic uses are documented.

Properties relevant to use:
Leaf and bark contain hydrolyzable tannins (gallotannins and ellagitannins) at levels sufficient for dyeing and tanning; bark extracts are water-soluble and generate brown hues. Leaf materials exhibit reactivity typical of hydrolyzable tannins for protein binding and oxidative interactions in clarification applications.

Standards and regulation:
Tannin extracts for leather tanning typically follow industry specifications for dye and tannin materials and relevant environmental discharge standards for the tanning industry. Food-contact uses such as wine clarification follow general rules for processing aids under national food regulations.

Sustainability and sourcing:
Leaves are renewable and often collected as a byproduct or from cultivated stands; bark harvesting can impact mature plants. Sustainable practices include rotational leaf harvesting, replanting, and avoiding overharvest of bark to preserve plant populations and ecosystem integrity.

Synonyms Top

Scientific name Authority First published in
Eupatorium populifolium Hook. & Arn. Companion Bot. Mag. 1: 242 (1836)
Eupatorium appendiculatum Less. ex Baker Fl. Bras. 6(2): 365 (1876)
Eupatorium hecatanthum Klatt
Eupatorium urolepis Daveau in Bois Dict. Hort. 1: 524 (1896)
Hebeclinium urolepis DC. Prodr. 5: 136 (1836)
Hebeclinium hecatanthum DC. Prodr. 5: 136 (1836)

Common names Top

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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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil South
      • Brazil Southeast
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000071630
Tropicos 2716572
KEW urn:lsid:ipni.org:names:261683-2
The Plant List gcc-28396
Open Tree Of Life 5920923
NCBI Taxonomy 1692179
IPNI 261683-2
iNaturalist 880795
GBIF 5403036
Freebase /m/06zqhyn
Wikipedia Urolepis_hecatantha

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
Plant Extracts and Phytochemicals from the Asteraceae Family with Antiviral Properties Borgo J, Wagner MS, Laurella LC, Elso OG, Selener MG, Clavin M, Bach H, Catalán CA, Bivona AE, Sepúlveda CS, Sülsen VP Molecules 09-Feb-2024
PMCID:PMC10891539
doi:10.3390/molecules29040814
PMID:38398567
Anti-Trypanosoma cruzi Properties of Sesquiterpene Lactones Isolated from Stevia spp.: In Vitro and In Silico Studies Borgo J, Elso OG, Gomez J, Coll M, Catalán CA, Mucci J, Alvarez G, Randall LM, Barrera P, Malchiodi EL, Bivona AE, Martini MF, Sülsen VP Pharmaceutics 15-Feb-2023
PMCID:PMC9961625
doi:10.3390/pharmaceutics15020647
PMID:36839969
Plant Terpenoids as Hit Compounds against Trypanosomiasis Durão R, Ramalhete C, Madureira AM, Mendes E, Duarte N Pharmaceuticals (Basel) 10-Mar-2022
PMCID:PMC8951850
doi:10.3390/ph15030340
PMID:35337138
Antiprotozoal Compounds from Urolepis hecatantha (Asteraceae) Elso OG, Clavin M, Hernandez N, Sgarlata T, Bach H, Catalan CA, Aguilera E, Alvarez G, Sülsen VP Evid Based Complement Alternat Med 11-Feb-2021
PMCID:PMC7895558
doi:10.1155/2021/6622894
PMID:33628303
Checklist of vascular plants of the Department of Ñeembucú, Paraguay Egea JD, Peña-Chocarro M, Espada C, Knapp S PhytoKeys 30-Jan-2012
PMCID:PMC3281576
doi:10.3897/phytokeys.9.2279
PMID:22371688
Sesquiterpene lactones, a labdane and other constituents of Urolepis hecatantha and chromolaena arnottiana Adriana N. de Gutiérrez, Cesar A.N. Catalán, Jesús G. Díaz, Werner Herz Elsevier BV 30-Apr-2003
doi:10.1016/0031-9422(95)00091-K
Comparative Study of the Essential Oils from Three Species ofEupatorium J. A. Zygadlo, D. M. Maestri, C. A. Guzmán Wiley 25-Aug-2002
doi:10.1002/(SICI)1099-1026(199605)11:3<153::AID-FFJ558>3.0.CO;2-L

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 / Acetophenones
[5-Acetyl-2-(3-hydroxyprop-1-en-2-yl)-2,3-dihydro-1-benzofuran-3-yl] 2-methylbut-2-enoate 163005354 Click to see 316.30 unknown https://doi.org/10.1016/0031-9422(95)00091-K
1-(3,6-Dihydroxy-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl)ethanone 137704968 Click to see 234.25 unknown https://doi.org/10.1016/0031-9422(95)00091-K
trans-2,3-Dihydro-3-hydroxyeuparin 124350709 Click to see CC(=C)C1C(C2=CC(=C(C=C2O1)O)C(=O)C)O 234.25 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
1-[5-(1-Hydroxyethyl)-2-methoxyphenyl]-3-methylbut-2-en-1-one 162985345 Click to see 234.29 unknown https://doi.org/10.1016/0031-9422(95)00091-K
1-[5-[(1R)-1-hydroxyethyl]-2-methoxyphenyl]-3-methylbut-2-en-1-one 162985346 Click to see 234.29 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3aS,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 137705081 Click to see 358.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
(9-Hydroxy-3,7,11-trimethyldodeca-2,10-dienyl) octadec-9-enoate 163093763 Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC=C(C)CCCC(C)CC(C=C(C)C)O 504.80 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(2Z,7S,9R)-9-hydroxy-3,7,11-trimethyldodeca-2,10-dienyl] (Z)-octadec-9-enoate 163093764 Click to see 504.80 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 139031795 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Grandiflorolic acid 433554 Click to see 318.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1002/(SICI)1099-1026(199605)11:3<153::AID-FFJ558>3.0.CO;2-L
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown https://doi.org/10.1002/(SICI)1099-1026(199605)11:3<153::AID-FFJ558>3.0.CO;2-L
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Corchoionol C 137705650 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Vomifoliol, (+)- 5280462 Click to see 224.30 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4,7-dihydroxy-10-methyl-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-9-yl) acetate 162967382 Click to see 322.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aS,4S,7S,9S,10Z,11aS)-4,7-dihydroxy-10-methyl-3,6-dimethylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-9-yl] acetate 163189121 Click to see 322.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(2S,3R,4aS,5R,7R,8aR)-3,7-dihydroxy-1,1,4a-trimethyl-6-methylidene-5-[[(2S,3R)-3-methyl-5-oxooxolan-2-yl]methyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] (2R)-2-methylbutanoate 162920062 Click to see 436.60 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[3,7-dihydroxy-1,1,4a-trimethyl-6-methylidene-5-[(3-methyl-5-oxooxolan-2-yl)methyl]-3,4,5,7,8,8a-hexahydro-2H-naphthalen-2-yl] 2-methylbutanoate 162920061 Click to see CCC(C)C(=O)OC1C(CC2(C(C1(C)C)CC(C(=C)C2CC3C(CC(=O)O3)C)O)C)O 436.60 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(4,6,7-trihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-9-yl) acetate 163040228 Click to see CC1=CC2C(C(CC(C(CC1OC(=O)C)O)(C)O)O)C(=C)C(=O)O2 340.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
(9-Acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 4-acetyloxy-2-(hydroxymethyl)but-2-enoate 78410057 Click to see 462.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
(9-Acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl) 4-hydroxy-2-(hydroxymethyl)but-2-enoate 100023 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCO)CO)C(=C)C(=O)O2)C)OC(=O)C 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aR,4R,6E,9S,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-4-acetyloxy-2-(hydroxymethyl)but-2-enoate 162961184 Click to see CC1=CCC(C(=CC2C(C(C1)OC(=O)C(=CCOC(=O)C)CO)C(=C)C(=O)O2)C)OC(=O)C 462.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aR,4R,6E,9S,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-4-hydroxy-2-(hydroxymethyl)but-2-enoate 145960336 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aR,4R,6R,7R,9R,10Z,11aR)-4,6,7-trihydroxy-6,10-dimethyl-3-methylidene-2-oxo-4,5,7,8,9,11a-hexahydro-3aH-cyclodeca[b]furan-9-yl] acetate 163040229 Click to see CC1=CC2C(C(CC(C(CC1OC(=O)C)O)(C)O)O)C(=C)C(=O)O2 340.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aR,4R,6Z,9S,10Z,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 163029811 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aR,4R,9S,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-9-yl] acetate 163029818 Click to see 306.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(3aS,11aS)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-(hydroxymethyl)but-2-enoate 137706452 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
[(4R,6E,9R,10Z,11aR)-9-acetyloxy-6,10-dimethyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-(hydroxymethyl)but-2-enoate 23843933 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Eupaformosanin 5281453 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Hiyodorilactone A 5281471 Click to see 420.50 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Organoheterocyclic compounds / Benzofurans
Euparin 119039 Click to see CC(=C)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 216.23 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Euparin methyl ether 182181 Click to see 230.26 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-[(2R,3R)-2,3-dihydroxy-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butoxy]furo[3,2-g]chromen-7-one 162995158 Click to see 400.40 unknown https://doi.org/10.1016/0031-9422(95)00091-K
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5,6-Trihydroxy-3,4',7-trimethoxyflavone 442621 Click to see 360.30 unknown https://doi.org/10.1016/0031-9422(95)00091-K
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1016/0031-9422(95)00091-K

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