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Calophyllum venulosum

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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 UUID64400ef418d1a237542330
Scientific name Calophyllum venulosum
Authority Zoll.
First published in Syst. Verz. Ind. Archip. 2: 149 (1854)

Description Top

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Synonyms Top

Scientific name Authority First published in
Calophyllum auriculatum Merr. Philipp. J. Sci., C 4: 291 (1909)
Calophyllum ijzermanni Boerl. & Koord.-Schum. Syst. Verz. 2: 39 (1911)
Calophyllum javanicum Miq. Pl. Jungh. : 292 (1854)

Common names Top

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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 venulosum var. tenuivenium (M.R.Hend. & Wyatt-Sm.) P.F.Stevens J. Arnold Arbor. 61: 483 (1980)

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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000581383
Tropicos 100303896
KEW urn:lsid:ipni.org:names:427330-1
The Plant List kew-2693533
Open Tree Of Life 415311
NCBI Taxonomy 667336
IPNI 427330-1
GBIF 6032506
EOL 5710312
USDA GRIN 414429

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)!
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Title Authors Publication Released IDs
A Review on the Phytochemistry, Pharmacology, and Pharmacokinetics of Amentoflavone, a Naturally-Occurring Biflavonoid Yu S, Yan H, Zhang L, Shan M, Chen P, Ding A, Li SF Molecules 16-Feb-2017
PMCID:PMC6155574
doi:10.3390/molecules22020299
PMID:28212342
Biflavonoids of <i>Calophyllum venulosum</i> Shu-Geng Cao, Keng-Yeow Sim, Swee-Hock Goh American Chemical Society (ACS) 26-Jul-2002
doi:10.1021/NP970303F
Minor methylated pyranoamentoflavones from Calophyllum venulosum. Cao SG, Sim KY, Goh SH Nat Prod Lett 01-Jan-2001
doi:10.1080/10575630108041295
PMID:11841112

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
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
10-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 21582613 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)OC(=CC3=O)C7=CC=C(C=C7)O)O)C 604.60 unknown https://doi.org/10.1080/10575630108041295
https://doi.org/10.1021/NP970303F
5-Hydroxy-10-[2-hydroxy-5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)phenyl]-8-(4-methoxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 10532086 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)O)OC(=CC3=O)C7=CC=C(C=C7)OC)O)C 632.60 unknown https://doi.org/10.1021/NP970303F
5-Hydroxy-10-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-8-(4-hydroxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 10556017 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)OC)OC(=CC3=O)C7=CC=C(C=C7)O)O)C 632.60 unknown https://doi.org/10.1021/NP970303F
5-Hydroxy-10-[5-(5-hydroxy-7-methoxy-4-oxochromen-2-yl)-2-methoxyphenyl]-8-(4-methoxyphenyl)-2,2-dimethylpyrano[3,2-g]chromen-6-one 10580051 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)OC)O)OC)OC(=CC3=O)C7=CC=C(C=C7)OC)O)C 646.60 unknown https://doi.org/10.1021/NP970303F
8-[5-(5,7-Dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-2-(4-hydroxyphenyl)chromen-4-one 10722564 Click to see CC(=C)C(CC1=C(C2=C(C(=C1O)C3=C(C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)O)OC(=CC2=O)C6=CC=C(C=C6)O)O)O 622.60 unknown https://doi.org/10.1021/NP970303F
8-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-6-[(2R)-2-hydroxy-3-methylbut-3-enyl]-2-(4-hydroxyphenyl)chromen-4-one 162923141 Click to see CC(=C)C(CC1=C(C2=C(C(=C1O)C3=C(C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)O)OC(=CC2=O)C6=CC=C(C=C6)O)O)O 622.60 unknown https://doi.org/10.1021/NP970303F
8-[5-(5,7-dihydroxy-4-oxochromen-2-yl)-2-hydroxyphenyl]-5,7-dihydroxy-6-[(2S)-2-hydroxy-3-methylbut-3-enyl]-2-(4-hydroxyphenyl)chromen-4-one 162923140 Click to see CC(=C)C(CC1=C(C2=C(C(=C1O)C3=C(C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)O)OC(=CC2=O)C6=CC=C(C=C6)O)O)O 622.60 unknown https://doi.org/10.1021/NP970303F
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/10.1080/10575630108041295
https://doi.org/10.1021/NP970303F
Biflavonoid-flavone base + 3O and flavone base + 3O + 1Prenyl 10555648 Click to see CC(=CCC1=C(C2=C(C(=C1O)C3=C(C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)O)OC(=CC2=O)C6=CC=C(C=C6)O)O)C 606.60 unknown https://doi.org/10.1021/NP970303F

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