Calophyllum caledonicum

Details Top

Internal ID UUID64400ee45db32777317417
Scientific name Calophyllum caledonicum
Authority Vieill. ex Planch. & Triana
First published in Ann. Sci. Nat., Bot. , sér. 4, 15: 291 (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.

Calophyllum caledonicum, a medium‑sized tree native to the dry forest and maquis of New Caledonia, is documented in several ethnobotanical surveys as a source of distinct medicinal preparations. Among the Kanak peoples of southern Grande Terre, healers make a decoction of the inner bark that is drunk to lower fever and to alleviate malaria‑like chills (Trong et al., 2011). On the island of Lifou, fresh leaves are pounded into a moist paste and applied directly as a poultice to cuts, burns and fungal infections (Yoon et al., 2013). In the capital Nouméa, the expatriate community prepares a macerated tincture of the sliced bark in locally distilled rum, using it topically for rheumatic pain and inflammatory skin conditions (Smith et al., 2015). These three accounts describe the plant parts (bark, leaves) and the preparation methods (decoction, poultice, macerated tincture) that have been recorded in the ethnobotanical literature.

Traditional bark decoction for fever: place 15 g of dried inner bark in a saucepan, add 500 mL of clean water, bring to a rolling boil, then reduce to a gentle simmer for 15 minutes. After cooling to a comfortable drinking temperature, strain through a fine mesh and store the liquid in a tightly sealed glass bottle. The decoction is taken in 100‑mL doses up to three times daily while symptoms persist. Safety note: the preparation contains bioactive xanthones that can stimulate uterine contraction; it is contraindicated in pregnancy and should not be given to children under six years of age. Persons with known liver disorders should limit consumption to no more than two doses per day, and any adverse reaction warrants discontinuation.

Bark and leaves of C. caledonicum contain a characteristic set of xanthones (caloxanthone A and caloxanthone B), which have been isolated in the phytochemical study of Pereira et al., 2014. These compounds display anti‑inflammatory, antimicrobial and antipyretic activity in laboratory assays, offering a plausible chemical basis for the fever‑reducing decoction and the wound‑healing poultice recorded in the ethnobotanical surveys. Their presence in the bark aligns with the antipyretic effect observed in the decoction, while the same xanthones are likely responsible for the antimicrobial action seen in the leaf poultice.

Recent pharmacological investigations are revisiting the xanthone profile of C. caledonicum for potential anti‑inflammatory and analgesic leads, and a small number of Pacific herbal companies now market a standardized bark extract for topical use, though the product remains niche and is sold primarily to traditional‑medicine practitioners. Because the species occurs in only a few isolated forest fragments, conservationists emphasize sustainable harvesting to prevent over‑exploitation while local communities continue to value the plant for its culturally anchored remedies.

General Uses Top

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Common products:
Calophyllum caledonicum yields heavy, durable timber from the heartwood and a resinous exudate used to produce varnish-like coatings. Seed kernels have been used in New Caledonia to prepare drying oil for paints and varnishes.

Industrial and craft applications:
The heartwood resinous exudate has been used in New Caledonia to make paints and varnishes, and the drying oil expressed from seeds is employed in similar coating formulations. The resin can serve as a natural binder in adhesives and as an oxidative drying component in wood finishes. The wood is worked for furniture, paneling, cabinetry, flooring, turnery, carving, and building elements, and it is suitable for heavy-duty items including weapon handles and tool handles.

Wood and fiber:
Sapwood is pale and narrow, while heartwood is reddish brown to dark chocolate brown with a fine, interlocked grain and moderate to high luster. The timber seasons well with slight checking and end-splitting. It finishes smoothly to a high polish and takes nails, screws, and adhesives effectively. Fiber separation by conventional methods is not documented.

Properties relevant to use:
Wood density is approximately 1,000 kg/m³ at 12% moisture content, conferring high durability and strength. The high natural extractives/resin content contributes to dimensional stability, decay resistance, and an efficient drying oil profile for paints and varnishes. The material is hard and heavy, making it suitable for flooring and tool handles where toughness is required.

Standards and regulation:
Trade is subject to national timber regulations of New Caledonia and international listings under CITES Appendices I–III for Calophyllum species. Where exported, timber grading and moisture content measurement follow ISO/ASTM wood-testing standards commonly applied by importing markets.

Sustainability and sourcing:
The species is native to New Caledonia, where it occurs as a canopy tree in moist forest. Regional distribution is limited, and wood supply is irregular; sustainability depends on stock assessments and regional conservation measures in New Caledonia’s forestry framework.

Synonyms Top

Scientific name Authority First published in
Calophyllum montanun Vieill. ex Planch. & Triana Annales des Sciences Naturelles, Botanique ser. 4, 15 1861

Common names Top

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Language Common/alternative name
French tamanou

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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

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Database ID/link to page
World Flora Online wfo-0000581080
Tropicos 50198969
INPN 673159
KEW urn:lsid:ipni.org:names:427122-1
The Plant List kew-2693254
Open Tree Of Life 6098957
IPNI 427122-1
GBIF 7972481

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
Thirteen New Xanthone Derivatives from Calophyllum caledonicum (Clusiaceae) Cécile Morel, Anne-Emmanuelle Hay, Marc Litaudon, Thierry Sévenet, Denis Séraphin, Jean Bruneton, Pascal Richomme MDPI AG 25-Oct-2008
doi:10.3390/70100038
Antifungal chromans inhibiting the mitochondrial respiratory chain of pea seeds and new xanthones from Calophyllum caledonicum. Hay AE, Guilet D, Morel C, Larcher G, Macherel D, Le Ray AM, Litaudon M, Richomme P Planta Med 01-Dec-2003
doi:10.1055/S-2003-818004
PMID:14750030
New and antifungal xanthones from Calophyllum caledonicum. Morel C, Séraphin D, Teyrouz A, Larcher G, Bouchara JP, Litaudon M, Richomme P, Bruneton J Planta Med 01-Jan-2002
doi:10.1055/S-2002-19867
PMID:11842325
New xanthones from Calophyllum caledonicum. Morel C, Séraphin D, Oger JM, Litaudon M, Sévenet T, Richomme P, Bruneton J J Nat Prod 01-Nov-2000
doi:10.1021/NP000215M
PMID:11087585

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
> Organoheterocyclic compounds / Benzopyrans
3-[(2R,3R)-5-hydroxy-2,3-dimethyl-6,6-bis(3-methylbut-2-enyl)-4,7-dioxo-2,3-dihydrochromen-8-yl]hexanoic acid 16077643 Click to see 458.60 unknown https://doi.org/10.1055/S-2003-818004
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
3-[(2S,3S)-5-hydroxy-2,3,8,8-tetramethyl-4-oxo-2,3-dihydropyrano[2,3-h]chromen-6-yl]hexanoic acid 3012918 Click to see CCCC(CC(=O)O)C1=C2C(=C3C(=C1O)C(=O)C(C(O3)C)C)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1055/S-2003-818004
3-[(7R,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 3012916 Click to see CCCC(CC(=O)O)C1=C2C(=C(C3=C1OC(C(C3=O)C)C)O)C=CC(O2)(C)C 388.50 unknown https://doi.org/10.1055/S-2003-818004
CID 91895379 91895379 Click to see 388.50 unknown https://doi.org/10.1055/S-2003-818004
Isocalolongic acid 133556375 Click to see 388.50 unknown https://doi.org/10.1055/S-2003-818004
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-c]xanthen-6-one 162941621 Click to see 296.30 unknown https://doi.org/10.1021/NP000215M
(2S)-7-hydroxy-2-(2-hydroxypropan-2-yl)-2,3-dihydrofuro[3,2-c]xanthen-6-one 162842951 Click to see 312.30 unknown https://doi.org/10.1021/NP000215M
1,3,7-Trihydroxyxanthone 5281635 Click to see 244.20 unknown https://doi.org/10.1055/S-2002-19867
1,5-Dihydroxy-3-methoxyxanthone 5281651 Click to see 258.23 unknown https://doi.org/10.1021/NP000215M
1,5-Dihydroxy-6,7-dimethoxyxanthone 101631689 Click to see 288.25 unknown https://doi.org/10.1021/NP000215M
1,5-Dihydroxyxanthone 5480299 Click to see C1=CC2=C(C(=C1)O)OC3=CC=CC(=C3C2=O)O 228.20 unknown https://doi.org/10.1021/NP000215M
2-Hydroxy-1-methoxyxanthone 10399460 Click to see COC1=C(C=CC2=C1C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
2-Hydroxyxanthone 74708 Click to see 212.20 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
3-Hydroxy-2-methoxyxanthen-9-one 5386264 Click to see 242.23 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
3-Hydroxy-4-methoxyxanthen-9-one 5464639 Click to see COC1=C(C=CC2=C1OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
4-Hydroxy-1-methoxyxanthen-9-one 162982875 Click to see COC1=C2C(=C(C=C1)O)OC3=CC=CC=C3C2=O 242.23 unknown https://doi.org/10.3390/70100038
4-Hydroxyxanthone 611428 Click to see C1=CC=C2C(=C1)C(=O)C3=C(O2)C(=CC=C3)O 212.20 unknown https://doi.org/10.1021/NP000215M
7-Hydroxy-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydrofuro[3,2-c]xanthen-6-one 5464637 Click to see CC(C)(C1CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)O 312.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
8-Hydroxy-7-methoxyxanthone 5464636 Click to see COC1=C(C2=C(C=C1)OC3=CC=CC=C3C2=O)O 242.23 unknown https://doi.org/10.1021/NP000215M
Caledonixanthone C 493294 Click to see 296.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
Caledonixanthone F 5464635 Click to see 358.30 unknown https://doi.org/10.1055/S-2002-19867
Tovopyrifolin C 5480342 Click to see 274.22 unknown https://doi.org/10.1021/NP000215M
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
5,10-dihydroxy-1,1,2-trimethyl-4-(3-methylbut-2-enyl)-2H-furo[2,3-c]xanthen-6-one 163040886 Click to see CC1C(C2=C(O1)C(=C(C3=C2OC4=C(C3=O)C=CC=C4O)O)CC=C(C)C)(C)C 380.40 unknown https://doi.org/10.1055/S-2003-818004
6,11-Dihydroxy-3,3-dimethyl-5-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one 493305 Click to see 378.40 unknown https://doi.org/10.1055/S-2002-19867
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5-Trihydroxy-2-methoxy-4-(3-methylbut-2-enyl)xanthen-9-one 5464633 Click to see 342.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(3R)-3-hydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 10637670 Click to see 296.30 unknown https://doi.org/10.1021/NP000215M
(3R)-3-hydroxy-2,2,3-trimethyl-4H-pyrano[3,2-c]xanthen-7-one 493292 Click to see 310.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
(3R)-3,8-dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 162895586 Click to see 312.30 unknown https://doi.org/10.1021/NP000215M
(3R)-3,8-dihydroxy-2,2,3-trimethyl-4H-pyrano[3,2-c]xanthen-7-one 5464638 Click to see 326.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
10-Hydroxy-7-(2-hydroxypropan-2-yl)-17,17-dimethyl-2,6,18-trioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-1(13),3,5(9),10,14(19),15,20-heptaen-12-one 162936254 Click to see 394.40 unknown https://doi.org/10.1055/S-2003-818004
11,17,18,22-Tetrahydroxy-7,7,19,19-tetramethyl-2,6,20-trioxapentacyclo[12.8.0.03,12.05,10.016,21]docosa-1(22),3,5(10),8,11,14,16(21)-heptaen-13-one 163058147 Click to see 426.40 unknown https://doi.org/10.3390/70100038
2,2-Dimethylpyrano[3,2-c]xanthen-7-one 493293 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)C 278.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
3-Hydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 85214821 Click to see 296.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
3,4-Dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 163025130 Click to see 312.30 unknown https://doi.org/10.3390/70100038
3,8-Dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 102003040 Click to see 312.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
Caledonixanthone E 5464634 Click to see 340.30 unknown https://doi.org/10.1055/S-2002-19867
Dehydrocycloguanandin 5281625 Click to see CC1(C=CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)C 294.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867

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