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Internal ID UUID64400eeb9683b507196937
Scientific name Calophyllum macrocarpum
Authority Hook.f.
First published in Fl. Brit. India 1: 273 (1874)

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Synonyms Top

Scientific name Authority First published in
Calophyllum horstii (Teijsm. & Binn.) Boerl. Cat. Pl. Phan. : 79 (1899)
Calysaccion horstii Teijsm. & Binn. Cat. Hort. Bot. Bogor. (Teijsmann & Binnendijk) 205. 1866

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indo-China
      • Andaman Islands
      • Nicobar Nicobar
      • Thailand
    • Malesia
      • Borneo
      • Malaya
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000581221
Tropicos 100303781
KEW urn:lsid:ipni.org:names:427215-1
The Plant List kew-2693384
Open Tree Of Life 382583
Observations.org 518178
NCBI Taxonomy 271746
IPNI 427215-1
iNaturalist 425537
GBIF 5556376
EOL 5710167
Elurikkus 544055
USDA GRIN 411469

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Widespread ancient whole genome duplications in Malpighiales coincide with Eocene global climatic upheaval Cai L, Xi Z, Amorim AM, Sugumaran M, Rest JS, Liu L, Davis CC New Phytol 21-Jul-2018
PMCID:PMC6265113
doi:10.1111/nph.15357
PMID:30030969
Xanthones and neoflavonoids from two asian species of calophyllum Stephen A. Ampofo, Peter G. Waterman Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84521-5

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 / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
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/10.1016/S0031-9422(00)84521-5
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://doi.org/10.1016/S0031-9422(00)84521-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(2S,3R)-Apetalic acid 40546128 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/10.1016/S0031-9422(00)84521-5
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/10.1016/S0031-9422(00)84521-5
Isoapetalic acid 341189 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/10.1016/S0031-9422(00)84521-5

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