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Phebalium clavatum

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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 UUID6440007b4b3cb329669268
Scientific name Phebalium clavatum
Authority C.A.Gardner
First published in J. Roy. Soc. Western Australia 27: 181 (1942)

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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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-0000470226
KEW urn:lsid:ipni.org:names:774702-1
Open Tree Of Life 849344
NCBI Taxonomy 282629
IPNI 774702-1
GBIF 3833541
Wikipedia Phebalium_clavatum

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
Eight new prenylcoumarins from Phebalium clavatum. Colombain M, Girard C, Muyard F, Bévalot F, Tillequin F, Waterman PG J Nat Prod 01-Apr-2002
doi:10.1021/NP0104469
PMID:11975479

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 alcohols
Methyl 2-hydroxy-8-(2-octylcyclopropen-1-yl)octanoate 163048568 Click to see CCCCCCCCC1=C(C1)CCCCCCC(C(=O)OC)O 324.50 unknown https://doi.org/10.1021/NP0104469
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[1-Hexadecanoyloxy-3-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxypropan-2-yl] nonadec-9-enoate 162934538 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)COC2C(C(C(C(O2)CO)O)O)O)O)O)O)OC(=O)CCCCCCCC=CCCCCCCCCC 933.30 unknown https://doi.org/10.1021/NP0104469
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2,3-Diaminobutanoic acid 5316628 Click to see CC(C(C(=O)O)N)N 118.13 unknown https://doi.org/10.1021/NP0104469
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
p-Hydroxycoumaric acid 129671844 Click to see C1C=C(C=CC1(O)O)C=CC(=O)O 182.17 unknown https://doi.org/10.1021/NP0104469
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
3-(2,2-Dimethyl-2H-1-benzopyran-6-yl)-2-propene-1-ol 10398415 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C=CCO)C 216.27 unknown https://doi.org/10.1021/NP0104469
> Organoheterocyclic compounds / Oxolanes
Isooblusilactonc A 6442493 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Methyl 4-hydroxycinnamate 5319562 Click to see COC(=O)C=CC1=CC=C(C=C1)O 178.18 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
9-[(2E,6S)-6-hydroperoxy-3,7-dimethylocta-2,7-dienoxy]furo[3,2-g]chromen-7-one 97043862 Click to see CC(=C)C(CCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)OO 370.40 unknown https://doi.org/10.1021/NP0104469
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
methyl (E,2S)-2-hydroxy-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-3-enoate 162894775 Click to see CC(C=CC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)(C(=O)OC)O 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E,4R)-4-hydroxy-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 162971863 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)OC)O)OC1=O)O)C(=O)OC 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E,4S)-4-hydroxy-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 163188230 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)OC)O)OC1=O)O)C(=O)OC 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E)-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 11109471 Click to see CC(=CCC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)C(=O)OC 304.29 unknown https://doi.org/10.1021/NP0104469
Methyl 2-hydroxy-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-3-enoate 85370531 Click to see CC(C=CC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)(C(=O)OC)O 320.29 unknown https://doi.org/10.1021/NP0104469
Methyl 4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 85402031 Click to see CC(=CCC1=CC2=C(C(=C(C=C2)OC)O)OC1=O)C(=O)OC 304.29 unknown https://doi.org/10.1021/NP0104469
Methyl 4-hydroxy-4-(8-hydroxy-7-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 73088598 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)OC)O)OC1=O)O)C(=O)OC 320.29 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7,8-dihydroxycoumarins
methyl (E,4S)-4-(7,8-dihydroxy-2-oxochromen-3-yl)-4-hydroxy-2-methylbut-2-enoate 162868620 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)O)O)OC1=O)O)C(=O)OC 306.27 unknown https://doi.org/10.1021/NP0104469
Methyl 4-(7,8-dihydroxy-2-oxochromen-3-yl)-4-hydroxy-2-methylbut-2-enoate 85304792 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)O)O)OC1=O)O)C(=O)OC 306.27 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
methyl (E,2R)-2-hydroxy-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-3-enoate 5323530 Click to see CC(C=CC1=CC2=C(C(=C(C=C2)O)OC)OC1=O)(C(=O)OC)O 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E,2S)-2-hydroxy-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-3-enoate 162903194 Click to see CC(C=CC1=CC2=C(C(=C(C=C2)O)OC)OC1=O)(C(=O)OC)O 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E,4S)-4-hydroxy-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 162934011 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)O)OC)OC1=O)O)C(=O)OC 320.29 unknown https://doi.org/10.1021/NP0104469
methyl (E)-4-(7-hydroxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 11119274 Click to see CC(=CCC1=CC2=C(C=C(C=C2)O)OC1=O)C(=O)OC 274.27 unknown https://doi.org/10.1021/NP0104469
methyl (E)-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 10990334 Click to see CC(=CCC1=CC2=C(C(=C(C=C2)O)OC)OC1=O)C(=O)OC 304.29 unknown https://doi.org/10.1021/NP0104469
Methyl 2-hydroxy-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-3-enoate 78385683 Click to see CC(C=CC1=CC2=C(C(=C(C=C2)O)OC)OC1=O)(C(=O)OC)O 320.29 unknown https://doi.org/10.1021/NP0104469
Methyl 4-(7-hydroxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 85405515 Click to see CC(=CCC1=CC2=C(C=C(C=C2)O)OC1=O)C(=O)OC 274.27 unknown https://doi.org/10.1021/NP0104469
Methyl 4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 85357936 Click to see CC(=CCC1=CC2=C(C(=C(C=C2)O)OC)OC1=O)C(=O)OC 304.29 unknown https://doi.org/10.1021/NP0104469
Methyl 4-hydroxy-4-(7-hydroxy-8-methoxy-2-oxochromen-3-yl)-2-methylbut-2-enoate 85296267 Click to see CC(=CC(C1=CC2=C(C(=C(C=C2)O)OC)OC1=O)O)C(=O)OC 320.29 unknown https://doi.org/10.1021/NP0104469
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Luvangetin 343582 Click to see CC1(C=CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)OC)C 258.27 unknown https://doi.org/10.1021/NP0104469
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,7-dihydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 162997366 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(OC4O)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP0104469

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