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Mallotus metcalfianus

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643fe2659de19828252042
Scientific name Mallotus metcalfianus
Authority Croizat
First published in J. Arnold Arbor. 21: 501 (1940)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 褐毛野桐

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-0000234620
Tropicos 50054185
KEW urn:lsid:ipni.org:names:351614-1
The Plant List kew-118968
Open Tree Of Life 107501
NCBI Taxonomy 463330
IPNI 351614-1
GBIF 5378484
EOL 1154817

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
Chemophenetic Significance of Anomalocalyx uleanus Metabolites Are Revealed by Dereplication Using Molecular Networking Tools de Brito JA, Pinto LD, Chaves CF, Ribeiro da Silva AJ, da Silva MF, Cotinguiba F Molecules 09-Feb-2021
PMCID:PMC7916253
doi:10.3390/molecules26040925
PMID:33572445
Analgesic and Anti-Inflammatory Activities of Leaf Extract of Mallotus repandus (Willd.) Muell. Arg. Hasan MM, Uddin N, Hasan MR, Islam AF, Hossain MM, Rahman AB, Hossain MS, Chowdhury IA, Rana MS Biomed Res Int 31-Dec-2014
PMCID:PMC4297635
doi:10.1155/2014/539807
PMID:25629031
Polyphenols isolated from antiradical extracts of Mallotus metcalfianus. Rivière C, Hong VN, Pieters L, Dejaegher B, Heyden YV, Van MC, Quetin-Leclercq J Phytochemistry 01-Jan-2009
doi:10.1016/J.PHYTOCHEM.2008.10.008
PMID:19062052

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
> Alkaloids and derivatives / Gelsemium alkaloids
7-Ethylidene-3-hydroxy-1'-methoxy-5-methylspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one 163048275 Click to see 370.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4R)-3,5,5-trimethyl-4-[(3R)-3-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one 162941966 Click to see CC1=CC(=O)CC(C1CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 372.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Blumel C glucoside 14135394 Click to see 372.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Byzantionoside B 14135395 Click to see 372.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see 382.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Friedelinol 101341 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-Methoxycarbonylphenyl beta-D-glucopyranoside 7573798 Click to see COC(=O)C1=CC=CC=C1OC2C(C(C(C(O2)CO)O)O)O 314.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-oxa N-2-YL)oxy-chroman-4-one 316844 Click to see 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 26339717 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside 5353915 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 12047524 Click to see 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Afzelin 5316673 Click to see 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Astilbin 119258 Click to see 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Calendoflavobioside 14034827 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Kaempferol-3-O-glucorhamnoside 13915496 Click to see 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Npc318533 5835713 Click to see 432.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Quercetin 3-neohesperidoside 5491657 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 25242967 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)OC(=O)C=CC5=CC=C(C=C5)O)O)O)O)O 608.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-[(2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163194784 Click to see 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[5-hydroxy-2-[(2R,3R)-3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 163188021 Click to see 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 25242966 Click to see 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[4,5-Dihydroxy-6-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74412840 Click to see 608.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[4,5-Dihydroxy-6-[5-hydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74412841 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)OC6C(C(C(C(O6)CO)OC(=O)C=CC7=CC=C(C=C7)O)O)O)O)CO)O 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[4,5-Dihydroxy-6-[5-hydroxy-2-[3-(4-hydroxy-3-methoxyphenyl)-2-(hydroxymethyl)-2,3-dihydro-1,4-benzodioxin-6-yl]-4-oxochromen-7-yl]oxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 162944512 Click to see 772.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008
[6-[2-(3,4-Dihydroxyphenyl)-5-hydroxy-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl] 3-(4-hydroxyphenyl)prop-2-enoate 74412839 Click to see 594.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.10.008

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