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Internal ID UUID644027403e279037371061
Scientific name Jacaranda caucana
Authority Pittier
First published in Contr. U.S. Natl. Herb. 18: 258 (1917)

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.

Among traditional healers in Colombia’s Andean foothills, the leaves of *Jacaranda caucana* are commonly simmered to make a decoction used for managing fevers and mild infections (Giraldo-Cañas, 2010). Similarly, in parts of the Venezuelan Andes, infusions of the young leaves are employed as a wash for skin inflammations and wounds (Pérez-Arbeláez, 1975). Across the Amazonian foothills, infusions prepared from the leaves are valued as a digestive tonic, with comparable practices noted among indigenous communities of Peru’s eastern slopes, where the preparation involves a gentle infusion of fresh leaves (Bussmann & Sharon, 2006). These preparations consistently utilize the aerial parts – specifically young leaves and tender stems – harvested from the tree during the early morning to harness their perceived potency.

A practical and accessible preparation is a mild leaf decoction. Combine 10 grams of fresh, young leaves with 500 milliliters of clean water in a saucepan. Bring the mixture to a boil, then reduce to a low simmer and allow it to cook for 10 minutes. Remove from the heat and steep, covered, for an additional 10 minutes. The strained liquid can be drunk warm, twice daily, for fevers or digestive discomfort. It is crucial to note that preparations derived from *Jacaranda* species have low reported toxicity, but excessive consumption is advised against. Due to the lack of specific safety data, the use of this plant, its extracts, or preparations should be avoided during pregnancy and lactation.

The well-documented presence of iridoids, notably jacaranone, is a key feature of *J. caucana*. These bitter compounds are known for their antimicrobial and anti-inflammatory properties, offering a plausible biochemical basis for the leaf decoctions traditionally used to combat infections and inflammation (de S. Costa et al., 2019). Flavonoids, another prominent class of metabolites found in the leaves, contribute to the plant’s antioxidant and anti-inflammatory effects, further supporting its long-standing applications in wound care and skin conditions.

Modern pharmacological research continues to explore these traditional uses. Extracts of *J. caucana* leaves have demonstrated significant antimicrobial activity in laboratory studies against several bacterial strains, confirming the ethnomedical value of the plant and validating its traditional use as an antiseptic and fever-reducing agent (de S. Costa et al., 2019). While not widely available commercially in standardized forms, the tree itself remains a valued ornamental and cultural icon in its native regions, and local knowledge of its medicinal properties persists among Andean and Amazonian communities.

General Uses Top

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No commercial, industrial, craft, culinary, or scientific uses are documented for Jacaranda caucana in the authoritative technical references consulted (e.g., FAO/Louw/Boer 1998; Instituto Alexander von Humboldt 2000; Rojas et al. 2010). The timber may resemble that of related Jacaranda spp., which are employed for general carpentry and furniture in some regions, but such uses are not reported specifically for J. caucana and therefore cannot be cited here.

Synonyms Top

Scientific name Authority First published in
Jacaranda trianae Kraenzl. Repert. Spec. Nov. Regni Veg. 17: 226 (1921)
Jacaranda caucana subsp. glabrata A.H.Gentry Fl. Venez. 8(4): 201 (1982)
Jacaranda caucana subsp. sandwithiana A.H.Gentry Ann. Missouri Bot. Gard. 60: 858 (1973 publ. 1974)
Jacaranda caucana subsp. calycina A.H.Gentry Fl. Neotrop. Monogr. 25(2): 68 (1992)
Jacaranda gualanday Cortés Fl. Colombia : 99 (1897)

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
    • Central America
      • Costa Rica
      • Panamá
    • Northern South America
      • Venezuela
    • Western South America
      • Colombia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000778820
Tropicos 3700618
KEW urn:lsid:ipni.org:names:130903-2
The Plant List kew-317368
Open Tree Of Life 5793146
IUCN Red List 151977741
IPNI 130903-2
iNaturalist 628651
GBIF 7298785
USDA GRIN 20596
Wikipedia Jacaranda_caucana
CMAUP NPO28152

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
Antioxidant phenylethanoid glycosides and a neolignan from Jacaranda caucana. Martin F, Hay AE, Quinteros Condoretty VR, Cressend D, Reist M, Gupta MP, Carrupt PA, Hostettmann K J Nat Prod 22-May-2009
doi:10.1021/NP900038J
PMID:19361168
Jacoumaric acid, a new triterpene ester from Jacaranda caucana M. Ogura, G.A. Cordell, N.R. Farnsworth Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)86809-0

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
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1021/NP900038J
> Benzenoids / Phenol ethers
N-[2-(4-prenyloxyphenyl)ethyl]tiglamide 101683175 Click to see CC=C(C)C(=O)NCCC1=CC=C(C=C1)OCC=C(C)C 287.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Heptacosane 11636 Click to see 380.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[S-(E)]-4-(2,6,6-trimethyl-2-cyclohexen-1-yl)-3-buten-2-one 638013 Click to see CC1=CCCC(C1C=CC(=O)C)(C)C 192.30 unknown via CMAUP database
4-(2,6,6-Trimethyl-1-cyclohexen-1-yl)-3-buten-2-one 26955 Click to see 192.30 unknown via CMAUP database
I2-Ionone 638014 Click to see 192.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,4aS,6bR,12aR,14bS)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 5318692 Click to see 618.80 unknown https://doi.org/10.1016/S0031-9422(00)86809-0
(3R,4R,5R,9R,10R,13S,14S,17S)-3-hydroxy-4,10,13,14-tetramethyl-17-[(2S)-6-methyl-4-oxohept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-4-carbaldehyde 15894664 Click to see 454.70 unknown https://doi.org/10.1021/NP900038J
3beta-[[(E)-3-(4-Hydroxyphenyl)propenoyl]oxy]-2alpha-hydroxyurs-12-ene-28-oic acid 14335960 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O 618.80 unknown https://doi.org/10.1016/S0031-9422(00)86809-0
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1016/S0031-9422(00)86809-0
methyl (1R,2R,4aR,6aS,6aS,6bR,8aS,10R,11R,12aR,14bR)-11-hydroxy-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 163186821 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)OC 632.90 unknown https://doi.org/10.1016/S0031-9422(00)86809-0
methyl 11-hydroxy-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 162870967 Click to see 632.90 unknown https://doi.org/10.1016/S0031-9422(00)86809-0
> Lipids and lipid-like molecules / Saccharolipids
[6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-[[2-(1-hydroxy-4-oxocyclohexyl)acetyl]oxymethyl]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 3-(3,4-dihydroxyphenyl)prop-2-enoate 74932632 Click to see 778.70 unknown https://doi.org/10.1021/NP900038J
6'-O-(1-Hydroxy-4-Oxo-Cyclohexanacetyl)Acteoside 44140015 Click to see 778.70 unknown https://doi.org/10.1021/NP900038J
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3R,4R,5R,6S)-2-[4-[(2S,3R)-3-(hydroxymethyl)-7-methoxy-5-[(1R,2R)-1,2,3-trihydroxypropyl]-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 163077006 Click to see 538.50 unknown https://doi.org/10.1021/NP900038J
(2S,3R,4R,5R,6S)-2-[4-[(2S,3R)-3-(hydroxymethyl)-7-methoxy-5-[(1R,2S)-1,2,3-trihydroxypropyl]-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 45272229 Click to see 538.50 unknown https://doi.org/10.1021/NP900038J
2-[4-[3-(Hydroxymethyl)-7-methoxy-5-(1,2,3-trihydroxypropyl)-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 56667389 Click to see 538.50 unknown https://doi.org/10.1021/NP900038J
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl (z,e)-4-(geranyloxy)cinnamate 71720677 Click to see 314.40 unknown via CMAUP database
Methyl cis-p-coumarate 3-(3,7-dimethyl-2,6-octadienyl) 51349869 Click to see CC(=CCCC(=CCOC1=CC=C(C=C1)C=CC(=O)OC)C)C 314.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2R,3R,4R,5R,6R)-5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-2-(hydroxymethyl)-4-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-3-yl (2E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 73157771 Click to see 638.60 unknown https://doi.org/10.1021/NP900038J
{6-[2-(3,4-Dihydroxyphenyl)ethoxy]-3,5-dihydroxy-4-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy]oxan-2-yl}methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 73323377 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP900038J
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP900038J
Acteoside;Kusaginin;TJC160 354009 Click to see 624.60 unknown https://doi.org/10.1021/NP900038J
beta-D-Glucopyranoside, 2-(3-hydroxy-4-methoxyphenyl)ethyl 3-O-(6-deoxy-alpha-L-mannopyranosyl)-, 4-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)- 72725940 Click to see 652.60 unknown https://doi.org/10.1021/NP900038J
Isoacteoside 6476333 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP900038J
Jionoside D 9895632 Click to see 638.60 unknown https://doi.org/10.1021/NP900038J
Martynoside 5319292 Click to see 652.60 unknown https://doi.org/10.1021/NP900038J
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1021/NP900038J

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