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Calophyllum dispar

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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 UUID64400ee6b87fb869483067
Scientific name Calophyllum dispar
Authority P.F.Stevens
First published in J. Arnold Arbor. 61: 524 (1980)

Description Top

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Synonyms Top

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Common names Top

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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-0000581123
Tropicos 100303713
KEW urn:lsid:ipni.org:names:169557-1
The Plant List kew-2693294
Open Tree Of Life 6098976
Observations.org 518136
IPNI 169557-1
GBIF 7426163
Elurikkus 596074

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
Four New 4-Phenylcoumarins from Calophyllum dispar. Isolation and Hemisynthesis Pascal Richomme, David Guilet, Cécile Morel, Nathalie Noyer, Maryse Cornec, Denis Séraphin, Christian Wiart, A. Hamid A. Hadi, Thierry Sévenet, Jean Bruneton The Japan Institute of Heterocyclic Chemistry 10-Mar-2009
doi:10.3987/COM-98-8338
Cytotoxic coumarins from Calophyllum dispar. Guilet D, Séraphin D, Rondeau D, Richomme P, Bruneton J Phytochemistry 01-Oct-2001
doi:10.1016/S0031-9422(01)00285-0
PMID:11576600
Novel cytotoxic 4-phenylfuranocoumarins from Calophyllum dispar. Guilet D, Hélesbeux JJ, Séraphin D, Sévenet T, Richomme P, Bruneton J J Nat Prod 01-May-2001
doi:10.1021/NP000517O
PMID:11374944

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 / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
5,7-Dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-6-(2-methylbutanoyl)-4-propylchromen-2-one 10045800 Click to see CCCC1=CC(=O)OC2=C1C(=C(C(=C2CC(C(=C)C)O)O)C(=O)C(C)CC)O 388.50 unknown https://doi.org/10.1016/S0031-9422(01)00285-0
5,7-dihydroxy-8-[(2S)-2-hydroxy-3-methylbut-3-enyl]-6-[(2R)-2-methylbutanoyl]-4-propylchromen-2-one 5323548 Click to see CCCC1=CC(=O)OC2=C1C(=C(C(=C2CC(C(=C)C)O)O)C(=O)C(C)CC)O 388.50 unknown https://doi.org/10.1016/S0031-9422(01)00285-0
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5-Hydroxy-6-(2-methylbutanoyl)-4-phenylfuro[2,3-h]chromen-2-one 21592417 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CO2 362.40 unknown https://doi.org/10.1021/NP000517O
5-hydroxy-6-[(2R)-2-methylbutanoyl]-4-phenylfuro[2,3-h]chromen-2-one 162923650 Click to see CCC(C)C(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=CO2 362.40 unknown https://doi.org/10.1021/NP000517O
> Phenylpropanoids and polyketides / Neoflavonoids / Prenylated neoflavonoids
4-Hydroxy-5-(3-methylbutanoyl)-9-phenylfuro[2,3-f]chromen-7-one 10959387 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C=CO3)C(=CC(=O)O2)C4=CC=CC=C4 362.40 unknown https://doi.org/10.1021/NP000517O
5,7-Dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-8-(2-methylbutanoyl)-4-phenylchromen-2-one 100926911 Click to see CCC(C)C(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC(C(=C)C)O)O 422.50 unknown https://doi.org/10.3987/COM-98-8338
5,7-Dihydroxy-6-(2-hydroxy-3-methylbut-3-enyl)-8-(3-methylbutanoyl)-4-phenylchromen-2-one 100926910 Click to see CC(C)CC(=O)C1=C(C(=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)CC(C(=C)C)O)O 422.50 unknown https://doi.org/10.3987/COM-98-8338
5,7-Dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-6-(2-methylbutanoyl)-4-phenylchromen-2-one 10047855 Click to see CCC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC(=O)C=C2C3=CC=CC=C3)O 422.50 unknown https://doi.org/10.3987/COM-98-8338
5,7-Dihydroxy-8-(2-hydroxy-3-methylbut-3-enyl)-6-(2-methylpropanoyl)-4-phenylchromen-2-one 10250877 Click to see CC(C)C(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC(=O)C=C2C3=CC=CC=C3)O 408.40 unknown https://doi.org/10.1016/S0031-9422(01)00285-0
8-acetyl-5-hydroxy-6-(3-methylbutanoyl)-4-phenyl-2H-furo[2,3-h]chromen-2-one 5324448 Click to see CC(C)CC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)C=C(O2)C(=O)C 404.40 unknown https://doi.org/10.1021/NP000517O
disparinol A 6483321 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC(C(=C)C)O)OC(=O)C=C2C3=CC=CC=C3)O 422.50 unknown https://doi.org/10.3987/COM-98-8338
Isodispar B 6483316 Click to see CC(C)CC(=O)C1=C(C=C(C2=C1OC(=O)C=C2C3=CC=CC=C3)O)O 338.40 unknown https://doi.org/10.1016/S0031-9422(01)00285-0
Mammea A/AC cyclo F 5319254 Click to see CCCC(=O)C1=C2C(=C3C(=C1O)C(=CC(=O)O3)C4=CC=CC=C4)CC(O2)C(C)(C)O 408.40 unknown https://doi.org/10.1021/NP000517O
Mammeisin 5281419 Click to see CC(C)CC(=O)C1=C(C2=C(C(=C1O)CC=C(C)C)OC(=O)C=C2C3=CC=CC=C3)O 406.50 unknown https://doi.org/10.3987/COM-98-8338

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