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Magnolia chevalieri

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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 UUID644029a22e3b2787558262
Scientific name Magnolia chevalieri
Authority (Dandy) V.S.Kumar
First published in Kew Bull. 61: 183 (2006)

Description Top

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Synonyms Top

Scientific name Authority First published in
Manglietia chevalieri Dandy J. Bot. 68: 204 (1930)
Manglietia phuthoensis Dandy ex Gagnep. Fl. Indo-Chine , Suppl. 1: 36 (1938)
Magnolia phuthoensis V.S.Kumar Kew Bull. 61(2): 185. 2006

Common names Top

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Language Common/alternative name
English southern peace lotus tree

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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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-0000806084
Tropicos 50302721
KEW urn:lsid:ipni.org:names:77074657-1
The Plant List kew-344355
Open Tree Of Life 3867229
NCBI Taxonomy 2735983
IUCN Red List 191506
IPNI 77074657-1
iNaturalist 439979
GBIF 3153394
EOL 1148563

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
Chemical constituents from the leaves of Manglietia phuthoensis and their effects on osteoblastic MC3T3-E1 cells. Kiem PV, Tri MD, Tuong le VD, Tung NH, Hanh NN, Quang TH, Cuong NX, Minh CV, Choi EM, Kim YH Chem Pharm Bull (Tokyo) 01-Sep-2008
doi:10.1248/CPB.56.1270
PMID:18758099

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
> Benzenoids / Benzene and substituted derivatives / Biphenyls and derivatives
5,5'-Di-2-propenyl-3-methoxy-[1,1'-biphenyl]-2,2'-diol 14282780 Click to see COC1=CC(=CC(=C1O)C2=C(C=CC(=C2)CC=C)O)CC=C 296.40 unknown https://doi.org/10.1248/CPB.56.1270
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
Obovatol 100771 Click to see C=CCC1=CC=C(C=C1)OC2=CC(=CC(=C2O)O)CC=C 282.30 unknown https://doi.org/10.1248/CPB.56.1270
> Lignans, neolignans and related compounds / Lignan glycosides
2-[4-[[5-(4-Hydroxy-3,5-dimethoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 75227842 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)O)OC 582.60 unknown https://doi.org/10.1248/CPB.56.1270
Tortoside B (Manglieside E) 46889358 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)O)OC 582.60 unknown https://doi.org/10.1248/CPB.56.1270
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4R,5S,6R)-2-[(1R)-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-3-en-1-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 102473623 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)O 374.50 unknown https://doi.org/10.1248/CPB.56.1270
(2S,3R,4R,5S,6R)-2-[(1R)-4-[(3R)-3-hydroxybutyl]-3,5,5-trimethylcyclohex-3-en-1-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162899118 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)O 374.50 unknown https://doi.org/10.1248/CPB.56.1270
Tsangane L 3-glucoside 73981648 Click to see CC1=C(C(CC(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)C)CCC(C)O 374.50 unknown https://doi.org/10.1248/CPB.56.1270
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4R,5R,6S)-2-(hydroxymethyl)-6-(2-hydroxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol 102473622 Click to see C=CCC1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 312.31 unknown https://doi.org/10.1248/CPB.56.1270
2-(Hydroxymethyl)-6-(2-hydroxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol 162966853 Click to see C=CCC1=CC(=C(C=C1)O)OC2C(C(C(C(O2)CO)O)O)O 312.31 unknown https://doi.org/10.1248/CPB.56.1270
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(2-hydroxy-5-prop-2-enylphenoxy)oxane-3,4,5-triol 162857050 Click to see C=CCC1=CC(=C(C=C1)O)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 444.40 unknown https://doi.org/10.1248/CPB.56.1270
Manglieside B 25111341 Click to see C=CCC1=CC(=C(C=C1)O)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 444.40 unknown https://doi.org/10.1248/CPB.56.1270
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2S,3R,4S,5S,6R)-2-[2-[(2S)-1-hydroxy-3-(3-hydroxy-5-methoxyphenyl)propan-2-yl]-4-[(E)-3-hydroxyprop-1-enyl]-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162844700 Click to see COC1=CC(=CC(=C1)O)CC(CO)C2=C(C(=CC(=C2)C=CCO)OC)OC3C(C(C(C(O3)CO)O)O)O 522.50 unknown https://doi.org/10.1248/CPB.56.1270
2-[2-[1-Hydroxy-3-(3-hydroxy-5-methoxyphenyl)propan-2-yl]-4-(3-hydroxyprop-1-enyl)-6-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162844699 Click to see COC1=CC(=CC(=C1)O)CC(CO)C2=C(C(=CC(=C2)C=CCO)OC)OC3C(C(C(C(O3)CO)O)O)O 522.50 unknown https://doi.org/10.1248/CPB.56.1270
Manglieside D 102473624 Click to see COC1=CC(=CC(=C1)O)CC(CO)C2=C(C(=CC(=C2)C=CCO)OC)OC3C(C(C(C(O3)CO)O)O)O 522.50 unknown https://doi.org/10.1248/CPB.56.1270

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