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Glochidion obovatum

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 UUID68f8f75d63e8b597479645
Scientific name Glochidion obovatum
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 143 (1845)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Bradleia sinensis Siebold ex Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 128 (1867)
Diasperus obovatus (Siebold & Zucc.) Kuntze Revis. Gen. Pl. 2: 600 (1891)
Phyllanthus obovatus (Siebold & Zucc.) Müll.Arg. Flora 48: 387 (1865)
Phyllanthus sieboldianus T.Kuros. J. Jap. Bot. 91(2): 119. 2016 [20 Apr 2016]

Common names Top

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Language Common/alternative name
Chinese 倒卵叶算盘子
Chinese 神子木

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
KEW urn:lsid:ipni.org:names:77155911-1
NCBI Taxonomy 2902202
IPNI 77155911-1
GBIF 9421807
Open Tree Of Life 1051525
World Flora Online wfo-0000973448
Tropicos 50057076
KEW urn:lsid:ipni.org:names:349541-1
The Plant List kew-90646
NCBI Taxonomy 271530
IPNI 349541-1
iNaturalist 635079
GBIF 3080932
EOL 1143188
USDA GRIN 17654

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Molecular Aspects of Gall Formation Induced by Mites and Insects Desnitskiy AG, Chetverikov PE, Ivanova LA, Kuzmin IV, Ozman-Sullivan SK, Sukhareva SI Life (Basel) 08-Jun-2023
PMCID:PMC10304984
doi:10.3390/life13061347
PMID:37374129
Chemistry and Pharmacology of Bergenin or Its Derivatives: A Promising Molecule Salimo ZM, Yakubu MN, da Silva EL, de Almeida AC, Chaves YO, Costa EV, da Silva FM, Tavares JF, Monteiro WM, de Melo GC, Koolen HH Biomolecules 21-Feb-2023
PMCID:PMC10046151
doi:10.3390/biom13030403
PMID:36979338
Ab-GALFA, A bioassay for insect gall formation using the model plant Arabidopsis thaliana Hirano T, Okamoto A, Oda Y, Sakamoto T, Takeda S, Matsuura T, Ikeda Y, Higaki T, Kimura S, Sato MH Sci Rep 13-Feb-2023
PMCID:PMC9925437
doi:10.1038/s41598-023-29302-8
PMID:36781988
Phenolic constituents from twigs of Aleurites fordii and their biological activities Park KJ, Suh WS, Yoon DH, Kim CS, Kim SY, Lee KR Beilstein J Org Chem 07-Sep-2021
PMCID:PMC8450942
doi:10.3762/bjoc.17.151
PMID:34621396
Recent Progress Regarding the Molecular Aspects of Insect Gall Formation Takeda S, Hirano T, Ohshima I, Sato MH Int J Mol Sci 30-Aug-2021
PMCID:PMC8430891
doi:10.3390/ijms22179424
PMID:34502330
Comparative transcriptome analysis of galls from four different host plants suggests the molecular mechanism of gall development Takeda S, Yoza M, Amano T, Ohshima I, Hirano T, Sato MH, Sakamoto T, Kimura S PLoS One 24-Oct-2019
PMCID:PMC6812778
doi:10.1371/journal.pone.0223686
PMID:31647845
Origin of gall-inducing from leaf-mining in Caloptilia micromoths (Lepidoptera, Gracillariidae) Guiguet A, Ohshima I, Takeda S, Laurans F, Lopez-Vaamonde C, Giron D Sci Rep 01-May-2019
PMCID:PMC6494848
doi:10.1038/s41598-019-43213-7
PMID:31043653
A Novel, Enigmatic Basal Leafflower Moth Lineage Pollinating a Derived Leafflower Host Illustrates the Dynamics of Host Shifts, Partner Replacement, and Apparent Coadaptation in Intimate Mutualisms Luo SX, Yao G, Wang Z, Zhang D, Hembry DH Am Nat 12-Jan-2017
PMCID:PMC6103454
doi:10.1086/690623
PMID:28350503
Genetic Differentiation and Spatial Structure of Phellinus noxius, the Causal Agent of Brown Root Rot of Woody Plants in Japan Akiba M, Ota Y, Tsai IJ, Hattori T, Sahashi N, Kikuchi T PLoS One 29-Oct-2015
PMCID:PMC4626371
doi:10.1371/journal.pone.0141792
PMID:26513585
Active pollination favours sexual dimorphism in floral scent Okamoto T, Kawakita A, Goto R, Svensson GP, Kato M Proc Biol Sci 07-Dec-2013
PMCID:PMC3813343
doi:10.1098/rspb.2013.2280
PMID:24266037
Floral volatiles, pollinator sharing and diversification in the fig–wasp mutualism: insights from Ficus natalensis, and its two wasp pollinators (South Africa) Cornille A, Underhill JG, Cruaud A, Hossaert-McKey M, Johnson SD, Tolley KA, Kjellberg F, van Noort S, Proffit M Proc Biol Sci 30-Nov-2011
PMCID:PMC3297447
doi:10.1098/rspb.2011.1972
PMID:22130605
Glochidioboside, a glucoside of (7S,8R)-dihydrodehydrodiconiferyl alcohol from leaves of glochidion obovatum Yoshio Takeda, Chieko Mima, Toshiya Masuda, Eiji Hirata, Anki Takushi, Hideaki Otsuka Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00362-8

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3R,4S,4aR,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one 12300074 Click to see 328.27 unknown https://doi.org/10.1016/S0031-9422(98)00362-8
Bergenin 66065 Click to see 328.27 unknown https://doi.org/10.1016/S0031-9422(98)00362-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(E)-4-[(1S,4S,6R)-1-hydroxy-2,2,6-trimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]but-3-en-2-one 21603117 Click to see 388.50 unknown https://doi.org/10.1016/S0031-9422(98)00362-8

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