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Quercus miyagii

Quercus miyagii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fea7d868d3218244120
Scientific name Quercus miyagii
Authority Koidz.
First published in Bot. Mag. (Tokyo) 26: 167 (1912)

Description Top

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Synonyms Top

Scientific name Authority First published in
Quercus yayamensis Koidz. Bot. Mag. (Tokyo) 32: 251. 1918 (1918)
Cyclobalanopsis miyagii Kudô & Masam. Trans. Nat. Hist. Soc. Formosa 20: 161 (1930)
Cyclobalanopsis yayeyamensis Kudô & Masam. Trans. Nat. Hist. Soc. Formosa 20: 161 (1930)

Common names Top

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Language Common/alternative name
Japanese オキナワウラジロガシ

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-0000292037
Tropicos 50279418
KEW urn:lsid:ipni.org:names:359861-1
The Plant List kew-173973
Open Tree Of Life 239489
NCBI Taxonomy 103491
IUCN Red List 78969684
IPNI 359861-1
GBIF 2880493
EOL 1151437
USDA GRIN 30719
Wikipedia Quercus_miyagii

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
Exploring the pharmacological aspects of natural phytochemicals against SARS-CoV-2 Nsp14 through an in silico approach De A, Bhattacharya S, Debroy B, Bhattacharya A, Pal K In Silico Pharmacol 28-Apr-2023
PMCID:PMC10141836
doi:10.1007/s40203-023-00143-7
PMID:37131867
Role of landscape context in Toxoplasma gondii infection of invasive definitive and intermediate hosts on a World Heritage Island Okada S, Shoshi Y, Takashima Y, Sanjoba C, Watari Y, Miyashita T Int J Parasitol Parasites Wildl 29-Aug-2022
PMCID:PMC9465111
doi:10.1016/j.ijppaw.2022.08.010
PMID:36105679
Biogeographic Patterns of Ectomycorrhizal Fungal Communities Associated With Castanopsis sieboldii Across the Japanese Archipelago Matsuoka S, Iwasaki T, Sugiyama Y, Kawaguchi E, Doi H, Osono T Front Microbiol 14-Nov-2019
PMCID:PMC6868053
doi:10.3389/fmicb.2019.02656
PMID:31798567
Predation on endangered species by human-subsidized domestic cats on Tokunoshima Island Maeda T, Nakashita R, Shionosaki K, Yamada F, Watari Y Sci Rep 07-Nov-2019
PMCID:PMC6838317
doi:10.1038/s41598-019-52472-3
PMID:31700052
Mixed-power scaling of whole-plant respiration from seedlings to giant trees Mori S, Yamaji K, Ishida A, Prokushkin SG, Masyagina OV, Hagihara A, Hoque AT, Suwa R, Osawa A, Nishizono T, Ueda T, Kinjo M, Miyagi T, Kajimoto T, Koike T, Matsuura Y, Toma T, Zyryanova OA, Abaimov AP, Awaya Y, Araki MG, Kawasaki T, Chiba Y, Umari M Proc Natl Acad Sci U S A 08-Jan-2010
PMCID:PMC2824365
doi:10.1073/pnas.0902554107
PMID:20080600
Flavan-3-ol and procyanidin glycosides from quercus miyagii Kanji Ishimaru, Gen-Ichiro Nonaka, Itsuo Nishioka Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82371-7

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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
hyperibone K 44575719 Click to see CC(=CCC12CC3C(C(C1=O)(C(=O)C(C2=O)(C3(C)C)CC=C(C)C)C(=O)C4=CC=CC=C4)C=C(C)C)C 500.70 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162935640 Click to see CC1C(C(C(C(O1)OC2CC3=C(C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)OC2C7=CC(=C(C=C7)O)O)O)O)O 724.70 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
(2R,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162927656 Click to see CC1C(C(C(C(O1)OC2C(C3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)C5=C(C=C(C6=C5OC(C(C6)O)C7=CC(=C(C=C7)O)O)O)O)O)O)O 724.70 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
2-(3,4-dihydroxyphenyl)-4-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3,4-dihydro-2H-chromen-8-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162935639 Click to see CC1C(C(C(C(O1)OC2CC3=C(C(=C(C=C3O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)OC2C7=CC(=C(C=C7)O)O)O)O)O 724.70 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
2-(3,4-dihydroxyphenyl)-8-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 162927654 Click to see CC1C(C(C(C(O1)OC2C(C3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)C5=C(C=C(C6=C5OC(C(C6)O)C7=CC(=C(C=C7)O)O)O)O)O)O)O 724.70 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Arecatannin C1 9876038 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Endotelon 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
ent-Epicatechin-(4alpha->6)-ent-epicatechin 13990892 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
ent-Epicatechin-(4alpha->8)-ent-epicatechin 3-gallate 12795889 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
procyanidin B1 3'-O-gallate 72193635 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 730.60 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Procyanidin B3 146798 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
procyanidin B3 3-O-gallate 11331595 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)C7=CC(=C(C=C7)O)O)O 730.60 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Procyanidin B6 474540 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Procyanidin B7 13990893 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Procyanidin trimer T2 13751990 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C(C(=CC(=C34)O)O)C5C(C(OC6=CC(=CC(=C56)O)O)C7=CC(=C(C=C7)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O)C9=CC(=C(C=C9)O)O)O 866.80 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(+)-Catechin 3-glucoside 14104302 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
(2R,3R,4R,5R,6S)-2-[[(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 126970087 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Catechin 3-O-beta-D-glucopyranoside 44257076 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Catechin 3-rhamnoside 21626704 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C=C4)O)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
Epicatechin 3-glucoside 14104301 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 452.40 unknown https://doi.org/10.1016/S0031-9422(00)82371-7
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ponapensin 44430502 Click to see COC1CCCN1C(=O)C2C(C3(C(C2(C4=C(O3)C=C(C=C4OC)OC)O)O)C5=CC=C(C=C5)OC)C6=CC=CC=C6 561.60 unknown https://doi.org/10.1016/S0031-9422(00)82371-7

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