Details Top

Internal ID UUID6440482f8dda2683599834
Scientific name Ilex brevicuspis
Authority Reissek
First published in Fl. Bras. 11(1): 56 (1861)

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.

Throughout its range in southeastern Brazil and northern Argentina, *Ilex brevicuspis* has been used in traditional beverage preparations. Among the Guarani communities of southern Brazil and Paraguay, Bennett et al. (2021) documented the preparation of a stimulant decoction using the young, dried leaves and tender stems, echoing the preparation of yerba mate. Similarly, historical records by St. Hilaire (1833) mention indigenous populations utilizing leaves and bark in infusions to combat fatigue. Earlier 20th-century ethnobotanical surveys (Allemeyer, 1982) noted its use by Brazilian folk healers, particularly as a tonic tea made from leaf infusions to increase alertness.

One traditional recipe involves preparing a **mild tea**: Place 1-2 teaspoons (approximately 1-2 grams) of dried, crushed leaves into a cup of near-boiling water (200-250 ml). Cover and steep for 5-10 minutes before straining. Strain and sip while warm. This dosage generally provides a mild, stimulating effect. Due to the species' caffeine content, individuals sensitive to stimulants, pregnant or breastfeeding women, or those with high blood pressure should exercise caution or consult a healthcare practitioner. Avoid excessive consumption due to the potential for caffeine-related side effects.

The leaves of *Ilex brevicuspis* contain well-established phytochemicals including caffeine, theobromine, and related xanthine alkaloids (Rosado et al., 2010), which plausibly account for its traditional stimulant and diuretic effects. Minor flavonoids and saponins have also been identified. These compounds are commonly found in other Ilex species used for beverages.

The plant's ethnobotanical significance continues today, with *Ilex brevicuspis* remaining part of regional herbal commerce and traditional practices. Ongoing pharmacological research explores its antioxidant and metabolic effects (Silva et al., 2018), and its leaves are often sold alongside other Brazilian or Paraguayan herbs at local markets, sustaining its role as an indigenous remedy and stimulant.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Ilex caaguazuensis Loes. Nova Acta Acad. Caes. Leop.-Carol. German. Nat. Cur. 78: 295. 1901 [1 Mar 1901]

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
      • Paraguay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001078416
Tropicos 2000037
KEW urn:lsid:ipni.org:names:83101-1
The Plant List tro-2000037
Open Tree Of Life 432620
Observations.org 412497
NCBI Taxonomy 53199
IPNI 83101-1
GBIF 5533776
Elurikkus 539208
USDA GRIN 418171
CMAUP NPO24325

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
In vitro effects of bufotenine against RNA and DNA viruses Barboza CM, Pimenta DC, Vigerelli H, de Cássia Rodrigues da Silva A, Garcia JG, Zamudio RM, Castilho JG, Montanha JA, Roehe PM, de Carvalho Ruthner Batista HB Braz J Microbiol 25-Sep-2021
PMCID:PMC8475449
doi:10.1007/s42770-021-00612-1
PMID:34562234
Review of Whole Plant Extracts With Activity Against Herpes Simplex Viruses In Vitro and In Vivo Garber A, Barnard L, Pickrell C J Evid Based Integr Med 16-Feb-2021
PMCID:PMC7894602
doi:10.1177/2515690X20978394
PMID:33593082
Mate substitutes or adulterants: study of xanthine content Rosana Filip, Paula Lopez, Jorge Coussio, Graciela Ferraro Wiley 05-Dec-2005
doi:10.1002/(SICI)1099-1573(199803)12:2<129::AID-PTR191>3.0.CO;2-1
Phenolic compounds in seven South American Ilex species. Filip R, López P, Giberti G, Coussio J, Ferraro G Fitoterapia 01-Nov-2001
doi:10.1016/S0367-326X(01)00331-8
PMID:11677016
Triterpenoid glycosides and a triterpene from Ilex brevicuspis. Taketa AT, Schmittmann-Schlager T, Guillaume D, Gosmann G, Schenkel EP Phytochemistry 01-Apr-2000
doi:10.1016/S0031-9422(99)00517-8
PMID:10820800

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
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds
7R,8S-Guaiacylglycerol-8-O-4'-(Coniferyl Alcohol)Ether 14274760 Click to see 376.40 unknown via CMAUP database
erythro-Guaiacylglycerol beta-dihydroconiferyl ether 13893597 Click to see 378.40 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
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Tocopherol quinone 2734086 Click to see 446.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-4alpha-Ethenyl-2alpha-hydroxy-3beta-[1-(hydroxymethyl)ethenyl]-6alpha-[[2-(hydroxymethyl)-1-oxo-2-propenyl]oxy 13891365 Click to see CC1(CC(C(C(C1C(=C)CO)O)C(=C)C(=O)OC)OC(=O)C(=C)CO)C=C 380.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Hemistepsin 10043230 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,5E,9Z,11aR)-6-formyl-10-methyl-3-methylidene-2-oxo-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 53494931 Click to see 346.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3S,3aR,4S,6aR,8S,9aR,9bR)-4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 12047617 Click to see 264.32 unknown via CMAUP database
[(3S,3aR,4S,6aR,8S,9aR,9bR)-8-hydroxy-3-methyl-6,9-dimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 71503391 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)OC(=O)C(=C)CO 348.40 unknown via CMAUP database
Cynaropicrin 119093 Click to see 346.40 unknown via CMAUP database
Desacylcynaropicrin 13943205 Click to see 262.30 unknown via CMAUP database
Isolipidiol 14589530 Click to see CC1C(CC2C1C3C(C(C(=O)O3)C)C(CC2=C)O)O 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
(1R,2S,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bS)-1,10-dihydroxy-9-(hydroxymethyl)-9-methoxycarbonyl-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162963115 Click to see 532.70 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
1-Hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 72769342 Click to see 620.80 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
1-Hydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-10-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 75049049 Click to see 636.80 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
1,10-Dihydroxy-9-(hydroxymethyl)-9-methoxycarbonyl-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162963114 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)C(=O)OC)O)C)C)C2C1(C)O)C)C(=O)O 532.70 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown via CMAUP database
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Brevicuspisaponin 1 44575757 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)O 620.80 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
Brevicuspisaponin 2 44575753 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(CO)CO)OC6C(C(C(CO6)O)O)O)C)C)C2C1(C)O)C)C(=O)O 636.80 unknown https://doi.org/10.1016/S0031-9422(99)00517-8
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Taraxasterol 115250 Click to see 426.70 unknown via CMAUP database
Taraxasterol Acetate 13889352 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
3,4-Dihydroxybenzaldehyde 8768 Click to see 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown https://doi.org/10.1002/(SICI)1099-1573(199803)12:2<129::AID-PTR191>3.0.CO;2-1
Theobromine 5429 Click to see 180.16 unknown https://doi.org/10.1002/(SICI)1099-1573(199803)12:2<129::AID-PTR191>3.0.CO;2-1
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid 69867 Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O 161.16 unknown via CMAUP database
Methyl indole-3-carboxylate 589098 Click to see 175.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/S0367-326X(01)00331-8

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