Calophyllum calaba - Unknown
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Internal ID UUID64400ee3f2140883438565
Scientific name Calophyllum calaba
Authority L.
First published in Sp. Pl. : 514 (1753)

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Synonyms Top

Scientific name Authority First published in
Calophyllum burmanni Wight Ill. Ind. Bot. 1: 129 (1840)
Calophyllum burmanni var. parvifolium Wight Icon. Pl. Ind. Orient. 1: t. 107 1839
Calophyllum retusum Wall. ex Planch. & Triana Numer. List [Wallich] n. 4848. 1831; Planch. & Triana, in Ann. Sc. Nat. Ser. IV. xv. (1861) 265.

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Calophyllum calaba var. australianum (F.Muell. ex Vesque) P.F.Stevens J. Arnold Arbor. 61: 269 (1980)
Calophyllum calaba var. bracteatum (Wight) P.F.Stevens J. Arnold Arbor. 61: 261 (1980)
Calophyllum calaba var. cuneatum (Symington ex M.R.Hend. & Wyatt-Sm.) P.F.Stevens J. Arnold Arbor. 61: 267 (1980)
Calophyllum calaba var. worthingtonii P.F.Stevens J. Arnold Arbor. 61(2): 260. 1980

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000581073
Tropicos 7800683
INPN 779750
KEW urn:lsid:ipni.org:names:427119-1
The Plant List kew-2693247
Open Tree Of Life 736767
NCBI Taxonomy 883767
IPNI 427119-1
GBIF 5421070
Freebase /m/010xftd9
EPPO CMUCA
USDA GRIN 8628
Wikipedia Calophyllum_calaba

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
Cytotoxic Metabolites from Calophyllum tacamahaca Willd.: Isolation and Detection through Feature-Based Molecular Networking Gerometta E, Herbette G, Garayev E, Marvilliers A, Naubron JV, Di Giorgio C, Campos PE, Clerc P, Ledoux A, Frederich M, Baghdikian B, Grondin I, Gauvin-Bialecki A Metabolites 23-Apr-2023
PMCID:PMC10222348
doi:10.3390/metabo13050582
PMID:37233623
Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India? Kumar BM Agrofor Syst 07-Apr-2023
PMCID:PMC10081327
doi:10.1007/s10457-023-00821-7
PMID:37193256
A Refined Methodology for Defining Plant Communities Using Postagricultural Data from the Neotropics Myster RW ScientificWorldJournal 12-Mar-2012
PMCID:PMC3317650
doi:10.1100/2012/365409
PMID:22536137
Microthia, Holocryphia and Ursicollum, three new genera on Eucalyptus and Coccoloba for fungi previously known as Cryphonectria Gryzenhout M, Myburg H, Hodges CS, Wingfield BD, Wingfield MJ Stud Mycol 01-Jan-2006
PMCID:PMC2104726
doi:10.3114/sim.55.1.35
PMID:18490970
Composition of fatty acids triacylglycerols and unsaponifiable matter in Calophyllum calaba L. oil from Guadeloupe. Crane S, Aurore G, Joseph H, Mouloungui Z, Bourgeois P Phytochemistry 01-Aug-2005
doi:10.1016/J.PHYTOCHEM.2005.06.009
PMID:16045947
Bark acids of seven Calophyllum species (Guttiferae) Upasiri Samaraweera, Subramaniam Sotheeswaran, M. Uvais S. Sultanbawa, Sinnathamby Balasubramaniam Royal Society of Chemistry (RSC) 26-Apr-2004
doi:10.1039/P19830000703
Chemical investigation of ceylonese plants. Part I. Extractives of Calophyllum calaba L. and Calophyllum bracteatum Thw. (Guttiferae) R. Somanathan, M. U. S. Sultanbawa Royal Society of Chemistry (RSC) 23-Apr-2004
doi:10.1039/P19720001935
Calocalabaxanthone, the putative isoprenyl precursor of calabaxanthone from Calophyllum calaba Vijaya Kumar, Subramaniam Sotheeswaran, Sivagnanasundram Surendrakumar, Sinnathamby Balasubramaniam Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)83202-0
Xanthones from roots of three calophyllum species H.Ranjith W. Dharmaratne, Subramaniam Sotheeswaran, Sinnathamby Balasubramaniam, Johannes Reisch Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81183-8
Terpenoid and biflavonoid constituents of Calophyllum calaba and Garcinia spicata from Sri Lanka A.A.Leslie Gunatilaka, A.M.Y.Jasmin De Silva, Subramaniam Sotheeswaran, Sinnathamby Balasubramaniam, Mohamed I.M. Wazeer Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80326-X

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(2R)-2-[(E)-dec-1-enyl]tetradecanoic acid 154497087 Click to see CCCCCCCCCCCCC(C=CCCCCCCCC)C(=O)O 366.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Gondoic Acid 5282768 Click to see CCCCCCCCC=CCCCCCCCCCC(=O)O 310.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Erucic Acid 5281116 Click to see CCCCCCCCC=CCCCCCCCCCCCC(=O)O 338.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
Nervonic Acid 5281120 Click to see CCCCCCCCC=CCCCCCCCCCCCCCC(=O)O 366.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.06.009
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3S,4aR,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol 11876268 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1039/P19720001935
(4aS,6aR,6aS,8aR,12aR,14aS,14bR)-4,4,6a,6a,8a,11,11,14b-octamethyl-2,4a,5,6,8,9,10,12,12a,13,14,14a-dodecahydro-1H-picen-3-one 11877464 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1039/P19720001935
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-octadecahydro-3(2H)-picenone 500344 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(=O)CCC5(C4CCC3(C2C1)C)C)(C)C)C)C)C 424.70 unknown https://doi.org/10.1039/P19720001935
Epitaraxerol 344467 Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C 426.70 unknown https://doi.org/10.1039/P19720001935
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
5'-hydroxy-1',1',4'a,6,7,7',8'a-heptamethylspiro[3H-furo[3,2-c]pyran-2,8'-5,9,10,10a-tetrahydro-4bH-phenanthrene]-2',4-dione 162958386 Click to see CC1=CC(C2C(C13CC4=C(O3)C(=C(OC4=O)C)C)(CCC5C2(C=CC(=O)C5(C)C)C)C)O 438.60 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4R,4aS,6aS,6aS,6bR,8aS,12aS,14aS,14bS)-8a-(hydroxymethyl)-4,4a,6a,6b,11,11,14a-heptamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol 162979969 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C)O 444.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
2,2,6a,6a,8a,9,14a-heptamethyl-10-oxo-3,4,5,6,6b,7,8,9,11,12,12a,13,14,14b-tetradecahydro-1H-picene-4a-carbaldehyde 586214 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
Canophyllal 12302400 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C=O)C)C)C)C 440.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
Canophyllol 7330581 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
CID 12082783 12082783 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C(=O)O)C)C)C)C)O 458.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
D:A-Friedooleanan-3-one, 28-hydroxy- 623591 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)CO)C)C)C)C 442.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9S,10S,13R,14S,17S)-17-[(2R,5R)-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 162965374 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1039/P19720001935
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/10.1039/P19720001935
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
3-(5-Hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)-3-phenylpropanoic acid 12302861 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)O)C4=CC=CC=C4)(C)C)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
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/10.1039/P19830000703
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/10.1039/P19830000703
Isochapelieric acid 133556240 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)O)C4=CC=CC=C4)(C)C)O)C 422.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
methyl (3R)-3-[(7S,8R)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]-3-phenylpropanoate 163068523 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)OC)C4=CC=CC=C4)(C)C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
methyl (3R)-3-[(7S,8S)-5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl]-3-phenylpropanoate 163068521 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)OC)C4=CC=CC=C4)(C)C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
Methyl 3-(5-hydroxy-2,2,7,8-tetramethyl-6-oxo-7,8-dihydropyrano[3,2-g]chromen-10-yl)-3-phenylpropanoate 74977400 Click to see CC1C(OC2=C(C1=O)C(=C3C=CC(OC3=C2C(CC(=O)OC)C4=CC=CC=C4)(C)C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-4-(8-hydroxy-4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 162893765 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC)C(=O)O 342.30 unknown https://doi.org/10.1039/P19720001935
1,5,6-Trihydroxyxanthone 5281652 Click to see C1=CC(=C2C(=C1)OC3=C(C2=O)C=CC(=C3O)O)O 244.20 unknown https://doi.org/10.1039/P19720001935
1,8-Dimethoxy-2-hydroxyxanthone 493307 Click to see COC1=CC=CC2=C1C(=O)C3=C(O2)C=CC(=C3OC)O 272.25 unknown https://doi.org/10.1039/P19720001935
2,8-Dihydroxy-1-methoxyxanthone 5464640 Click to see COC1=C(C=CC2=C1C(=O)C3=C(C=CC=C3O2)O)O 258.23 unknown https://doi.org/10.1039/P19720001935
4-(8-Hydroxy-4-methoxy-9-oxoxanthen-3-yl)-2-methylbutanoic acid 12315435 Click to see CC(CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)OC)C(=O)O 342.30 unknown https://doi.org/10.1039/P19720001935
6-(3,3-Dimethylallyl)-1,5-dihydroxyxanthone 5281624 Click to see CC(=CCC1=C(C2=C(C=C1)C(=O)C3=C(C=CC=C3O2)O)O)C 296.30 unknown https://doi.org/10.1039/P19720001935
Buchanaxanthone 5481840 Click to see COC1=C(C=CC2=C1OC3=CC=CC(=C3C2=O)O)O 258.23 unknown https://doi.org/10.1039/P19720001935
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Trapezifolixanthone 188341 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=CC=C4O)O)C=CC(O2)(C)C)C 378.40 unknown https://doi.org/10.1016/S0031-9422(00)81183-8
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
1,3-Dihydroxy-7-methoxy-2,8-bis(3-methylbut-2-enyl)xanthen-9-one 163035388 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)OC)C 394.50 unknown https://doi.org/10.1016/S0031-9422(00)81183-8
https://doi.org/10.1016/0031-9422(82)83202-0
Calabaxanthone 341188 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C4=C(C=C3O2)OC(C=C4)(C)C)O)OC)C 392.40 unknown https://doi.org/10.1016/S0031-9422(00)81183-8
https://doi.org/10.1039/P19720001935
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown https://doi.org/10.1039/P19720001935
Jacareubin 5281644 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)C 326.30 unknown https://doi.org/10.1039/P19720001935
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1016/S0031-9422(00)80326-X

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