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Mundulea chapelieri

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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 UUID643fdb98bc2be961238609
Scientific name Mundulea chapelieri
Authority (Baill.) Du Puy & Labat
First published in Legum. Madagascar: 419 (2002)

Description Top

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Synonyms Top

Scientific name Authority First published in
Millettia chapelieri Baill. Bull. Mens. Soc. Linn. Paris1: 395 (1883)
Mundulea chpelieri (Baill.) Du Puy & Labat

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-0000196351
Tropicos 13074804
KEW urn:lsid:ipni.org:names:20004737-1
The Plant List ild-42921
Open Tree Of Life 3920496
IUCN Red List 69221934
IPNI 20004737-1
GBIF 2933881
EOL 647964

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
Cytotoxic compounds from Mundulea chapelieri from the Madagascar Rainforest. Cao S, Schilling JK, Miller JS, Andriantsiferana R, Rasamison VE, Kingston DG J Nat Prod 01-Mar-2004
doi:10.1021/NP0303815
PMID:15043430

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 / Sesquiterpenoids / Elemane sesquiterpenoids
[5-Ethenyl-2-(2-hydroxypropan-2-yl)-5-methyl-4-prop-1-en-2-ylcyclohexyl] acetate 14138885 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown https://doi.org/10.1021/NP0303815
8alpha-Acetoxyelemol 44566708 Click to see CC(=C)C1CC(C(CC1(C)C=C)OC(=O)C)C(C)(C)O 280.40 unknown https://doi.org/10.1021/NP0303815
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(7S,8S)-5,7-dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one 163033566 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0303815
5,7-Dihydroxy-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one 53484196 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0303815
5,7-Dimethoxy-8-(3-methylbut-2-en-1-yl)-2-phenylchroman-4-one 14033978 Click to see CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=CC=C3)C 352.40 unknown https://doi.org/10.1021/NP0303815
Candidone 157102 Click to see CC(=CCC1=C2C(=C(C=C1OC)OC)C(=O)CC(O2)C3=CC=CC=C3)C 352.40 unknown https://doi.org/10.1021/NP0303815
Mundulinol 10363971 Click to see CC(=CCC1=C2C(=C(C3=C1OC(C(C3=O)O)C4=CC=CC=C4)O)C=CC(O2)(C)C)C 406.50 unknown https://doi.org/10.1021/NP0303815
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
Mundulone 4587968 Click to see CC1(C=CC2=C(O1)C=CC(=C2OC)C3=COC4=C(C3=O)C=C5CC(C(OC5=C4)(C)C)O)C 434.50 unknown https://doi.org/10.1021/NP0303815
Munetone 12312999 Click to see CC1(C=CC2=CC3=C(C=C2O1)OC=C(C3=O)C4=C(C5=C(C=C4)OC(C=C5)(C)C)OC)C 416.50 unknown https://doi.org/10.1021/NP0303815
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(Rac)-Tephrosin 4485131 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1021/NP0303815
5'beta-Rotenone 5102 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1021/NP0303815
CID 303992 303992 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1021/NP0303815
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1021/NP0303815
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1021/NP0303815
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1021/NP0303815

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