Piper acutifolium

Details Top

Internal ID UUID64404a76d6403843602237
Scientific name Piper acutifolium
Authority Ruiz & Pav.
First published in Fl. Peruv. 1: 38 (1798)

Ethnobotanical Use Top

Suggest a correction!
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 Andean and Amazonian medicine, Piper acutifolium (matico) is prepared as a leaf or aerial-part infusion or decoction for both internal and external care. Among the Mapuche of southern Chile, a leaf decoction is used as a wash for bleeding wounds and to help close and protect cuts, according to Bennett et al. (2021). In coastal Peru, dried leaf is infused as a tea for dysentery, colic, and the afterbirth period, while the same infusion or decoction is used to wash wounds and mouth sores, per De Feo (2003). In Andean Bolivia, a strong leaf infusion is taken for stomachache and as a digestive tea, and the boiled leaf is applied as a poultice to bruises and inflamed areas (Cruz et al., 2015). In Amazonian Peru, a leaf infusion is also consumed to ease colds and coughs (Ostolaza, 2011). These preparations consistently involve the leaves and tender stems.

A practical mild leaf tea for digestive or general support can be made by placing 1–2 grams of dried, chopped leaves in 250 mL of just‑boiling water, covering, and letting it steep for 5–10 minutes before straining. Adults typically drink 1 cup up to twice daily as needed; do not use during pregnancy or breastfeeding, and discontinue if allergic symptoms develop. For wound care, a decoction suitable for washing can be prepared by simmering 6–10 grams of fresh or dried leaf in 500 mL of water for 10–15 minutes, cooling, and applying as a wash or compress two to three times daily; avoid contact with eyes. A 1:5 ethanol tincture is made by macerating 20 grams of chopped dried leaf in 100 mL of 45% ethanol for 2–4 weeks in a dark place, shaking daily and filtering; the finished tincture can be used for topical care or in a very small dilution as directed by a trained practitioner; the adult dose of 10–20 drops diluted in water can be taken 1–2 times daily for short periods; do not use in pregnancy.

Piper acutifolium contains an essential oil rich in safrole, elemicin, myristicin, asaricin, and related phenylpropanoids, as well as the alkaloid piperine, compounds that have been identified in this species and are consistent with its reported antimicrobial and antispasmodic actions (Bennett et al., 2021; De Feo, 2003). These constituents help explain the traditional use for wound washing and as a digestive tea.

Today, matico remains a widely used remedy in Andean and Amazonian communities, and clinical interest in its antimicrobial and anti-inflammatory potential continues to grow.

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Artanthe acutifolia Miq. Syst. Piperac. : 428 (1844)
Piper mandonii C.DC. Prodr. 16(1): 275 (1869)
Steffensia acutifolia Kunth Linnaea 13: 650 (1840)
Piper acutifolium var. stuebelii Trel. in J.F.Macbr. Publ. Field Columb. Mus., Bot. Ser. 13(2): 131 (1936)
Artanthe acutifolia f. minor Miq. London J. Bot. 4: 455. 1845
Piper velutinum Opiz Reliq. Haenk. 1: 157 (1828)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
    • Western South America
      • Bolivia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001092473
Tropicos 25001226
KEW urn:lsid:ipni.org:names:680277-1
The Plant List tro-25001226
Open Tree Of Life 5699593
Observations.org 350327
IPNI 680277-1
iNaturalist 564657
GBIF 7305400
Elurikkus 625092
CMAUP NPO20637

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)!
Title Authors Publication Released IDs
Benzoic acid derivatives from Piper species and their antiparasitic activity. Flores N, Jiménez IA, Giménez A, Ruiz G, Gutiérrez D, Bourdy G, Bazzocchi IL J Nat Prod 01-Sep-2008
doi:10.1021/NP800104P
PMID:18712933

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxy-3-(2-hydroxy-3-methylbut-3-enyl)-5-(3-methylbut-2-enyl)benzoic acid 25111594 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)CC(C(=C)C)O)O)C 290.40 unknown https://doi.org/10.1021/NP800104P
4-hydroxy-3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-5-(3-methylbut-2-enyl)benzoic acid 162937536 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)CC(C(=C)C)O)O)C 290.40 unknown https://doi.org/10.1021/NP800104P
4-Hydroxy-3,5-bis(2-hydroxy-3-methylbut-3-enyl)benzoic acid 102411352 Click to see CC(=C)C(CC1=CC(=CC(=C1O)CC(C(=C)C)O)C(=O)O)O 306.40 unknown https://doi.org/10.1021/NP800104P
4-hydroxy-3,5-bis[(2R)-2-hydroxy-3-methylbut-3-enyl]benzoic acid 162908643 Click to see CC(=C)C(CC1=CC(=CC(=C1O)CC(C(=C)C)O)C(=O)O)O 306.40 unknown https://doi.org/10.1021/NP800104P
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-(2-Hydroxy-3-methylbut-3-enyl)-4-methoxy-5-(3-methylbut-2-enyl)benzoic acid 101447973 Click to see 304.40 unknown https://doi.org/10.1021/NP800104P
3-(3-Hydroxy-3-methylbut-1-enyl)-4-methoxy-5-(3-methylbut-2-enyl)benzoic acid 162940626 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)O)C=CC(C)(C)O)OC)C 304.40 unknown https://doi.org/10.1021/NP800104P
3-[(2R)-2-hydroxy-3-methylbut-3-enyl]-4-methoxy-5-(3-methylbut-2-enyl)benzoic acid 162955325 Click to see 304.40 unknown https://doi.org/10.1021/NP800104P
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methyl 3,4-dihydroxy-5-(3'-methyl-2'-butenyl)benzoate 25058114 Click to see CC(=CCC1=C(C(=CC(=C1)C(=O)OC)O)O)C 236.26 unknown https://doi.org/10.1021/NP800104P
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
Yangambin 443028 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(-)-Citronellol 7793 Click to see CC(CCC=C(C)C)CCO 156.26 unknown via CMAUP database
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 unknown via CMAUP database
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-Isopulegol 170833 Click to see CC1CCC(C(C1)O)C(=C)C 154.25 unknown via CMAUP database
1Alpha,3beta,4beta-p-menthane-3,8-diol 22214620 Click to see 172.26 unknown via CMAUP database
Menthoglycol 19100 Click to see 172.26 unknown via CMAUP database
Neomenthoglycol 9920491 Click to see CC1CCC(C(C1)O)C(C)(C)O 172.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
Alpha-Tocopherol 14985 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
Calamenene, trans-(+)- 6429022 Click to see 202.33 unknown via CMAUP database
epi-alpha-Muurolol 3084331 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Erythrodiol 101761 Click to see 442.70 unknown via CMAUP database
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 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
Morolic Acid 489944 Click to see 456.70 unknown via CMAUP database
Squalene 638072 Click to see 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloeucalenol 101690 Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C 426.70 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
Daucosterin acetate 12895763 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C(C)C 745.00 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
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Glutaric acid 743 Click to see C(CC(=O)O)CC(=O)O 132.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
Fustin 5317435 Click to see 288.25 unknown via CMAUP database
Garbanzol 442410 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(O2)C=C(C=C3)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnocitrin 5320946 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R,3R)-3,4'-Dihydroxy-5,7-dimethoxyflavone 10403456 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(C(O2)C3=CC=C(C=C3)O)O 316.30 unknown via CMAUP database
Aromadendrin 7-methyl ether 181132 Click to see 302.28 unknown via CMAUP database
Eucalyptin 76573 Click to see CC1=C(C2=C(C(=C1OC)C)OC(=CC2=O)C3=CC=C(C=C3)OC)O 326.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.