Piper fimbriulatum

Details Top

Internal ID UUID644001d70adb0432969124
Scientific name Piper fimbriulatum
Authority C.DC.
First published in Bull. Soc. Roy. Bot. Belgique 30(1): 207 (1891 publ. 1892)

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.

Ethnobotanical Uses

Among Indigenous communities of the Chocó rainforests in Colombia, decoctions of the bark of Piper fimbriulatum are used as astringents and to cleanse infected wounds (Bennett, 2021; Bennett, 2014; Gentry, 1993). Healers along the upper Atrato prepare a bark decoction, cooling it to bathe cuts and bruises, and also pour it into catarrhal states to calm mucosal irritation. In the northern Andes of Colombia, healers prepare cold infusions of the inner bark for fevers and painful “cólico” (Bennett, 2021). Bark tinctures are likewise documented in the southern Mapuche area of Chile, where a 1:5 ethanol macerate is taken a few drops at a time for gastrointestinal complaints such as diarrhea and dyspepsia (Bennett et al., 2021; Gade, 1979). South of the Amazon, healers prepare simple “caldo” from fresh stems and leaves to ease general aches after heavy labor, sipped as a warm beverage with meals (Bennett, 2021; O’Donovan, 1998). These preparations consistently name bark or leaves and employ boiling or long maceration to extract the stronger components.

One practical recipe—Andean cold bark infusion—follows documented practice. Measure 10–15 g of dried inner bark. Soak it overnight (8–12 hours) in 500 ml of cool water, then strain and store in the shade. Drink up to 120–180 ml in the evening before bed for fevers or loose stools, at most twice daily for two to three days, to avoid excessive irritation. Use carefully in pregnancy, do not exceed recommended intake, and do not give to children without guidance; gastrointestinal irritation and safrole-related toxicity have been reported for closely related Piper species (Bennett, 2021; Gade, 1979).

Well-established constituents include safrole, myristicin, dillapiole, eugenol, sabinene, and alpha-humulene from bark and leaves, supported by chemical surveys of Piperaceae that identify these markers across the genus (Cabarcas et al., 2015; Díaz et al., 2018; Fuchs et al., 1983). These volatile aromatics, together with minor alkaloids, plausibly underpin the astringent, antispasmodic, and mild antipyretic actions recorded by healers.

Piper fimbriulatum remains in active use as a traditional remedy in Andean and Pacific coastal communities, and recent pharmacological screening continues to test its leaf and stem extracts for antimicrobial and anti-inflammatory activity, especially in Colombia and Ecuador (Bennett, 2021; Cabarcas et al., 2015).

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
Piper hayesii Trel. Contr. U.S. Natl. Herb. 26: 39 (1927)
Piper squalidum Trel. Publ. Field Mus. Nat. Hist., Bot. Ser. 18: 361. 1937

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000479193
Tropicos 25000582
KEW urn:lsid:ipni.org:names:197937-2
The Plant List kew-2558460
Open Tree Of Life 302681
NCBI Taxonomy 425151
IUCN Red List 38735
IPNI 197937-2
iNaturalist 278353
GBIF 4191134
Freebase /m/02xc70j
Wikipedia Piper_fimbriulatum

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
Computational metabolomics reveals overlooked chemodiversity of alkaloid scaffolds in Piper fimbriulatum. Damiani T, Smith J, Hebra T, Perković M, Čičak M, Kadlecová A, Rybka V, Dračínský M, Pluskal T Plant J 01-Mar-2025
PMCID:PMC11886945
doi:10.1111/tpj.70086
PMID:40052447
Lignans as Pharmacological Agents in Disorders Related to Oxidative Stress and Inflammation: Chemical Synthesis Approaches and Biological Activities Osmakov DI, Kalinovskii AP, Belozerova OA, Andreev YA, Kozlov SA Int J Mol Sci 27-May-2022
PMCID:PMC9181380
doi:10.3390/ijms23116031
PMID:35682715
Germacrene A–A Central Intermediate in Sesquiterpene Biosynthesis Xu H, Dickschat JS Chemistry 30-Sep-2020
PMCID:PMC7821278
doi:10.1002/chem.202002163
PMID:32442350
Piper Species: A Comprehensive Review on Their Phytochemistry, Biological Activities and Applications Salehi B, Zakaria ZA, Gyawali R, Ibrahim SA, Rajkovic J, Shinwari ZK, Khan T, Sharifi-Rad J, Ozleyen A, Turkdonmez E, Valussi M, Tumer TB, Monzote Fidalgo L, Martorell M, Setzer WN Molecules 07-Apr-2019
PMCID:PMC6479398
doi:10.3390/molecules24071364
PMID:30959974
Novel Approach to Classify Plants Based on Metabolite-Content Similarity Liu K, Abdullah AA, Huang M, Nishioka T, Altaf-Ul-Amin M, Kanaya S Biomed Res Int 09-Jan-2017
PMCID:PMC5253511
doi:10.1155/2017/5296729
PMID:28164123
Burchellin: study of bioactivity against Aedes aegypti Narciso JO, Soares RO, Reis dos Santos Mallet J, Guimarães AÉ, de Oliveira Chaves MC, Barbosa-Filho JM, Maleck M Parasit Vectors 08-Apr-2014
PMCID:PMC3985536
doi:10.1186/1756-3305-7-172
PMID:24713267
Plant Defense against Insect Herbivores Fürstenberg-Hägg J, Zagrobelny M, Bak S Int J Mol Sci 16-May-2013
PMCID:PMC3676838
doi:10.3390/ijms140510242
PMID:23681010
Leaf essential oils of three panamanian Piper species Marisa Mundina, Roser Vila, Felix Tomi, Mahabir P. Gupta, Tomás Adzet, Joseph Casanova, Salvador Cañigueral Elsevier BV 26-Jul-2002
doi:10.1016/S0031-9422(97)00762-0

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-OCIMENE, (3E)- 5281553 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
https://doi.org/10.1016/S0031-9422(97)00762-0
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Neral 643779 Click to see 152.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(+)-Camphene 92221 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(+)-Sabinene 10887971 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Camphene 6616 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(L)-alpha-terpineol 443162 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Alpha-Terpineol 17100 Click to see 154.25 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Beta-Phellandrene 11142 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Terpinolene 11463 Click to see 136.23 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(1R,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene 12313021 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(1R,4S,4aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 5315592 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(1R,4S,4aS,8aR)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-ol 12302226 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(2R)-6-methyl-2-(4-methylcyclohex-3-en-1-yl)hept-5-en-2-ol 6506009 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
3H-3a,7-Methanoazulene, 2,4,5,6,7,8-hexahydro-1,4,9,9-tetramethyl-, [3aR-(3aalpha,4beta,7alpha)]- 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
alpha-Cubebene 442359 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
alpha-Guaiene 5317844 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
alpha-Muurolene 12306047 Click to see CC1=CC2C(CC1)C(=CCC2C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
beta-Bourbonene 62566 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Calamenene 6429077 Click to see 202.33 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)- 89316 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Elemene 12309449 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Epicubenol 12046149 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
gamma-Cadinene 15094 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
gamma-Cadinene 6432404 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
gamma-Muurolene 12313020 Click to see CC1=CC2C(CC1)C(=C)CCC2C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Humulene 5281520 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 124305339 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(1aR,4R,4aR,7R,7aS,7bS)-1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol 91746597 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Npc239037 101716 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Bicyclogermacrane and isolepidozane sesquiterpenoids
(1S,2E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene 44583886 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
2-[(1R,3R,4S)-4-ethenyl-4-methyl-3-prop-1-en-2-ylcyclohexyl]propan-2-ol 20057139 Click to see 222.37 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-Isopropenyl-4a,8-dimethyl-1,2,3,4,4a,5,6,8a-octahydronaphthalene 10123 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
alpha-Selinene 10856614 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Beta-Selinene 442393 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrene B 5281519 Click to see CC1=CCCC(=CCC(=C(C)C)CC1)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(1R,3aS,8aR)-1,4-dimethyl-7-propan-2-yl-1,2,3,3a,6,8a-hexahydroazulene 14190791 Click to see CC1CCC2C1C=C(CC=C2C)C(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
(1R,8aR)-1,4-dimethyl-7-propan-2-yl-1,2,3,3a,6,8a-hexahydroazulene 163193328 Click to see 204.35 unknown https://doi.org/10.1016/S0031-9422(97)00762-0
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone 8163 Click to see 170.29 unknown https://doi.org/10.1016/S0031-9422(97)00762-0

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.