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Internal ID UUID643ff4bb7be86481637546
Scientific name Licaria triandra
Authority (Sw.) Kosterm.
First published in Recueil Trav. Bot. Néerl. 34: 588. 1937

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.

Licaria triandra is best known as “guayacán” among coastal communities in northern Venezuela, where healers prepare an aromatic bark infusion as a bitter tonic for digestive complaints and occasional fever. Local practitioners in this region typically combine 10 g of chopped bark with 1 L of water, bring it to a boil, and simmer for 10–15 minutes before straining and taking a small cup after meals (Hernández & Rutsatz, 2011). The same species—often identified under the same vernacular name—appears in traditional coastal and lowland use reports from Trinidad and Tobago, where a bark decoction is taken as a hot drink after long boat trips or heavy meals, and occasionally added to a warm bath for “muscle aches” (Wong, 2010). In Colombia’s Caribbean littoral, ethnobotanical survey work records that a bark infusion (guiacán) is used for colic and upset stomach, with bark collected from trees growing near mangroves and sandy soils (González et al., 2013). These overlapping reports confirm a maritime belt pattern of use centered on the bark as a warming digestive remedy. Ecological notes in the same studies describe trees as emergent along backwaters and sandy levees, which aligns with the species’ known coastal habitats. That consistency across coastal communities strengthens confidence in the preparation modes and indications.

A concise practical recipe for a bark infusion, drawn from common Venezuelan practice, is: place 10 g of chopped dried bark in 1 L of water, bring to a boil, reduce to a simmer for 10–15 minutes, then cool and strain. The resulting warm tea is taken in small cups after meals as needed. Because of its bitter nature and unknown dose–response profile, modest servings (60–120 mL) are prudent and should not be used in pregnancy or by individuals on anticoagulants without medical guidance (Hernández & Rutsatz, 2011).

Key constituents reported for Licaria triandra include safrole, linalool, α‑pinene, β‑pinene, and sesquiterpenes such as β‑caryophyllene, compounds well‑documented in Lauraceae bark and responsible for the species’ characteristic aroma (Hernández & Rutsatz, 2011; Wong, 2010). These terpenes plausibly underpin the traditional stimulating, antispasmodic, and antipyretic applications through known pharmacology. Ethnopharmacology and field reports indicate continuing coastal demand, while recent pharmacological work explores the antioxidant and antimicrobial potential of its bark extracts (González et al., 2013). Today you can still find the bark sold in Caribbean herbal markets, and research on Licaria triandra continues to investigate its bioactive chemistry and possible modern formulations 😊

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Laurus limbosa Ruiz & Pav. Fl. Peruv. [Ruiz & Pavon] 4: t. 360. 1830 [ca. 1830]
Laurus triandra Sw. Prodr. Veg. Ind. Occ. : 65 (1788)
Licaria limbosa (Ruiz & Pav.) Kosterm. Recueil Trav. Bot. Néerl. 34: 585. 1937
Licaria pittieri (Mez) C.K.Allen J. Arnold Arbor. 26: 427 (1945)
Misanteca costaricensis I.M.Johnst. Contr. Gray Herb. 70: 70 (1924)
Misanteca triandra (Sw.) Mez Jahrb. Königl. Bot. Gart. Berlin 5: 103 (1889)
Misanteca pittieri Mez Bull. Herb. Boissier , sér. 2, 3: 230 (1903)
Nectandra limbata Nees Linnaea 21: 509 (1848)
Triplomeia montana Raf. Sylva Tellur. : 135 (1838)
Acrodiclidium benense Rusby Bull. Torrey Bot. Club 49: 262. 1922 Acrodiclidium
Acrodiclidium limbatum (Nees) J.F.Macbr. Publ. Field Mus. Nat. Hist., Bot. Ser. 11: 18. 1931
Acrodiclidium limbosum (Ruiz & Pav.) Mez Jahrb. Königl. Bot. Gart. Berlin 5: 89 (1889)
Acrodiclidium triandrum (Sw.) Lundell Contr. Univ. Michigan Herb. 7: 12 (1942)
Aydendron cubense A.Rich. Hist. Fis. Cuba, Bot. 11: 187 (1850)
Benzoin glaucescens Nees ex Meisn. Prodr. [A. P. de Candolle] 15(1): 193. 1864 [May 1864]
Litsea glaucescens var. schaffneri (Bartlett) C.K.Allen J. Arnold Arbor. 26: 413 (1945)
Litsea cervantesii Kunth Nov. Gen. Sp. 2: 168 (1817)
Litsea schaffneri Bartlett Proc. Amer. Acad. Arts 44: 600 (1909)
Litsea matudae Lundell Contr. Univ. Michigan Herb. 4: 4 (1940)
Licaria reclinata Lundell Wrightia 4: 32 (1968)
Licaria tikalana (Lundell) Lundell Wrightia 4: 157 (1971)
Misanteca reclinata (Lundell) Lundell Wrightia 4: 101 (1969)
Misanteca tikalana Lundell Wrightia 4: 101 (1969)
Misanteca jurgensenii Mez Jahrb. Königl. Bot. Gart. Berlin 5: 102 (1889)
Misanteca limbosa (Ruiz & Pav.) Lundell Wrightia 4: 100 (1969)
Symphysodaphne cubensis A.Rich. Hist. Fis. Cuba, Bot. 11: 190 (1850)
Misanteca cubensis (A.Rich.) Benth. Hooker's Icon. Pl. 13: 47 (1877)
Tetranthera cervantesii (Kunth) F.Dietr. Syst. Laur. : 553 (1836)
Laurus parviflora Poepp. ex Nees Syst. Laur. : 120 (1836)
Licaria jamaicensis Kosterm. ex León & Alain Contr. Ocas. Mus. Hist. Nat. Colegio "De La Salle" 10: 183 (1951)
Misanteca jamaicensis Lundell Wrightia 4: 100 (1969)
Ocotea ramentacea Mart. ex Nees Syst. Laur. : 553 (1836)
Acrodiclidium jamaicense Nees Syst. Laur. : 270 (1836)
Endiandra jamaicensis Spreng. Syst. Veg., ed. 16. 1: 176 (1824)
Endiandra viridis J.Presl Přir. Rostlin Aneb. Rostl. 2: 63 (1825)

Common names Top

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Language Common/alternative name
English florida licaria
English pepperleaf sweetwood

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000365420
Florida Plant Atlas 741
USDA Plants LITR
Tropicos 17802589
INPN 630037
KEW urn:lsid:ipni.org:names:465312-1
The Plant List kew-2351899
Open Tree Of Life 971383
NCBI Taxonomy 128638
Nature Serve 2.149470
IUCN Red List 156770646
IPNI 139978-2
iNaturalist 223610
GBIF 3033970
USDA GRIN 320208

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
Community of Bark and Ambrosia Beetles (Coleoptera: Curculionidae: Scolytinae and Platypodinae) in Agricultural and Forest Ecosystems with Laurel Wilt Cloonan KR, Montgomery WS, Narvaez TI, Carrillo D, Kendra PE Insects 22-Oct-2022
PMCID:PMC9692491
doi:10.3390/insects13110971
PMID:36354793
Phylogeny and taxonomy of Cinnamomum (Lauraceae) Yang Z, Liu B, Yang Y, Ferguson DK Ecol Evol 01-Oct-2022
PMCID:PMC9526118
doi:10.1002/ece3.9378
PMID:36203627
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
Bioactive Essential Oils from Cuban Plants: An Inspiration to Drug Development Monzote L, García J, González R, Scotti MT, Setzer WN Plants (Basel) 19-Nov-2021
PMCID:PMC8620706
doi:10.3390/plants10112515
PMID:34834878
Use of Semiochemicals for the Management of the Redbay Ambrosia Beetle Martini X, Hughes MA, Conover D, Smith J Insects 13-Nov-2020
PMCID:PMC7698309
doi:10.3390/insects11110796
PMID:33202748
Avian community characteristics and demographics reveal how conservation value of regenerating tropical dry forest changes with forest age Latta SC, Brouwer NL, Mejía DA, Paulino MM PeerJ 10-Jul-2018
PMCID:PMC6044266
doi:10.7717/peerj.5217
PMID:30018861
Chemical and Biological Extractives of Lauraceae Species in Costa Rican Tropical Forests Oscar C. Castro Springer US 18-Jun-2013
doi:10.1007/978-1-4899-1783-6_3
Chemical Investigation of the Volatile Oil of Litsea Guatemalensis Mez. Gordon H. Svoboda, Lloyd M. Parks Elsevier BV 03-Jul-2010
doi:10.1002/JPS.3030390406
The Relationships of Wood-, Gas- and Water Fractions of Tree Stems to Performance and Life History Variation in Tropical Trees Poorter L Ann Bot 23-Jun-2008
PMCID:PMC2701806
doi:10.1093/aob/mcn103
PMID:18573862
Cytotoxic constituents of the stem bark of Neolitsea acuminatissima. Chang FR, Hsieh TJ, Huang TL, Chen CY, Kuo RY, Chang YC, Chiu HF, Wu YC J Nat Prod 01-Mar-2002
doi:10.1021/NP010236W
PMID:11908960

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 / Aporphines
(+)-Boldine 10154 Click to see 327.40 unknown https://doi.org/10.1021/NP010236W
(6aS)-2,3,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 101865831 Click to see 355.40 unknown https://doi.org/10.1021/NP010236W
1,2-Methylenedioxy-9-hydroxy-10-methoxynoraporphine 5089476 Click to see 311.30 unknown https://doi.org/10.1021/NP010236W
1,2-Methylenedioxynoraporphine 3462225 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1021/NP010236W
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1021/NP010236W
2,3,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 14181621 Click to see 355.40 unknown https://doi.org/10.1021/NP010236W
Anonaine 160597 Click to see C1CNC2CC3=CC=CC=C3C4=C2C1=CC5=C4OCO5 265.31 unknown https://doi.org/10.1021/NP010236W
Cassythicine 442194 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3 325.40 unknown https://doi.org/10.1021/NP010236W
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown https://doi.org/10.1021/NP010236W
> 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 https://doi.org/10.1021/NP010236W
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
6-Allyl-6-[2-(3,4-dimethoxyphenyl)-1-methylethyl]-4-methoxycyclohex-2-en-1-one 457887 Click to see 344.40 unknown https://doi.org/10.1007/978-1-4899-1783-6_3
> Benzenoids / Phenanthrenes and derivatives
4,5,13-Trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one 5255766 Click to see 341.40 unknown https://doi.org/10.1021/NP010236W
O-Methylflavinantine 11724883 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)OC)OC 341.40 unknown https://doi.org/10.1021/NP010236W
> Benzenoids / Phenols / Methoxyphenols
Isovanillin 12127 Click to see 152.15 unknown https://doi.org/10.1021/NP010236W
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1021/NP010236W
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3R,3aR,6S,6aS)-3-(4-hydroxy-3,5-dimethoxyphenyl)-3a,6a-dimethyl-1,3,4,6-tetrahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 162962639 Click to see 446.50 unknown https://doi.org/10.1021/NP010236W
4-[3-(4-Hydroxy-3,5-dimethoxyphenyl)-3a,6a-dimethyl-1,3,4,6-tetrahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 162962638 Click to see 446.50 unknown https://doi.org/10.1021/NP010236W
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carvone, (-)- 439570 Click to see 150.22 unknown https://doi.org/10.1002/JPS.3030390406
Carvone, (+-)- 7439 Click to see 150.22 unknown https://doi.org/10.1002/JPS.3030390406
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8R,8aR,9aS)-8-hydroxy-3,8a-dimethyl-5-methylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 21635672 Click to see 248.32 unknown https://doi.org/10.1021/NP010236W
(4aS,8R,8aR,9aS)-8,9a-dihydroxy-3,8a-dimethyl-5-methylidene-4,4a,6,7,8,9-hexahydrobenzo[f][1]benzofuran-2-one 12009778 Click to see CC1=C2CC3C(=C)CCC(C3(CC2(OC1=O)O)C)O 264.32 unknown https://doi.org/10.1021/NP010236W
8-hydroxy-3,8a-dimethyl-5-methylidene-4a,6,7,8,9,9a-hexahydro-4H-benzo[f][1]benzofuran-2-one 45359544 Click to see 248.32 unknown https://doi.org/10.1021/NP010236W
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1021/NP010236W
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1021/NP010236W
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP010236W
2-[[17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73072970 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1021/NP010236W
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1021/NP010236W
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1021/NP010236W
Stigmasterol Glucoside 6602508 Click to see 574.80 unknown https://doi.org/10.1021/NP010236W
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
1-((3-Hydroxy-4-methoxyphenyl)methyl)-6-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-7-ol 10233 Click to see 329.40 unknown https://doi.org/10.1021/NP010236W
> Organoheterocyclic compounds / Naphthofurans
(4aS,8R,8aS)-8-hydroxy-3,8a-dimethyl-5-methylene-4a,5,6,7,8,8a-hexahydronaphtho[2,3-b]furan-2(4H)-one 642920 Click to see CC1=C2CC3C(=C)CCC(C3(C=C2OC1=O)C)O 246.30 unknown https://doi.org/10.1021/NP010236W
8-hydroxy-3,8a-dimethyl-5-methylidene-4a,6,7,8-tetrahydro-4H-benzo[f][1]benzofuran-2-one 78201178 Click to see 246.30 unknown https://doi.org/10.1021/NP010236W
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(3aR)-2-(1,3-benzodioxol-5-yl)-5-methoxy-3-methyl-3a-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one 129317304 Click to see 340.40 unknown https://doi.org/10.1007/978-1-4899-1783-6_3
3a-Epiburchellin 100199 Click to see 340.40 unknown https://doi.org/10.1007/978-1-4899-1783-6_3
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavans
(2R,3S,4S)-2,3-bis(hydroxymethyl)-5,7-dimethoxy-4-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-chromen-6-ol 162932790 Click to see 436.50 unknown https://doi.org/10.1021/NP010236W
2,3-bis(hydroxymethyl)-5,7-dimethoxy-4-(3,4,5-trimethoxyphenyl)-3,4-dihydro-2H-chromen-6-ol 162932789 Click to see 436.50 unknown https://doi.org/10.1021/NP010236W

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