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Calophyllum caledonicum

Calophyllum caledonicum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

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)

Description Top

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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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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!
You can also contribute to this by clicking here.
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 CCCC(CC(=O)O)C1=C(C(C(=O)C2=C1OC(C(C2=O)C)C)(CC=C(C)C)CC=C(C)C)O 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,8R)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]hexanoic acid 91895379 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
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
Isocalolongic acid 133556375 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
> 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 CC(C)(C1CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)O 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 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
1,3,5-Trihydroxy-2-methoxyxanthen-9-one 5480342 Click to see COC1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC=C3O)O 274.22 unknown https://doi.org/10.1021/NP000215M
1,5-Dihydroxy-6,7-dimethoxyxanthone 101631689 Click to see COC1=C(C(=C2C(=C1)C(=O)C3=C(C=CC=C3O2)O)O)OC 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 C1=CC=C2C(=C1)C(=O)C3=C(O2)C=CC(=C3)O 212.20 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
3-Hydroxy-2-methoxyxanthen-9-one 5386264 Click to see COC1=C(C=C2C(=C1)C(=O)C3=CC=CC=C3O2)O 242.23 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
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 CC(C)(C1CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)O 296.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
Caledonixanthone F 5464635 Click to see CC(C)(C1CC2=C3C(=C(C(=C2O1)OC)O)C(=O)C4=C(O3)C(=CC=C4)O)O 358.30 unknown https://doi.org/10.1055/S-2002-19867
Gentisein 5281635 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(C=C(C=C3O2)O)O 244.20 unknown https://doi.org/10.1055/S-2002-19867
Mesuaxanthone A 5281651 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)C=CC=C3O)O 258.23 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 CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C(=CC=C4)O)C=CC(O2)(C)C)C 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 CC(=CCC1=C(C(=C(C2=C1OC3=C(C2=O)C=CC=C3O)O)OC)O)C 342.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
> 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 CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)O)C 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 CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)(C)O)C 310.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
(3R)-3,8-dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 162895586 Click to see CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)O)C 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 CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)(C)O)C 326.30 unknown https://doi.org/10.1021/NP000215M
https://doi.org/10.1055/S-2002-19867
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 CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(C5=C(C=C4O3)OC(C5)C(C)(C)O)O)C 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 CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=CC5=C(C(=C4O3)O)OC(C(C5O)O)(C)C)C 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 CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)O)C 296.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
3,4-Dihydroxy-2,2-dimethyl-3,4-dihydropyrano[3,2-c]xanthen-7-one 163025130 Click to see CC1(C(C(C2=C(O1)C3=C(C=C2)C(=O)C4=CC=CC=C4O3)O)O)C 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 CC1(C(CC2=C(O1)C3=C(C=C2)C(=O)C4=C(C=CC=C4O3)O)O)C 312.30 unknown https://doi.org/10.1055/S-2002-19867
https://doi.org/10.1021/NP000215M
Caledonixanthone E 5464634 Click to see CC1(C=CC2=C3C(=C(C(=C2O1)OC)O)C(=O)C4=C(O3)C(=CC=C4)O)C 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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