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Acer tataricum subsp. ginnala

Acer tataricum subsp. ginnala - 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 UUID644006c9588ce141992165
Scientific name Acer tataricum subsp. ginnala
Authority (Maxim.) Wesm.
First published in Bull. Soc. Roy. Bot. Belgique 29: 31. 1890 (1890)

Description Top

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Common names Top

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Language Common/alternative name
Azerbaijani qinnal ağcaqayını
ceb acer tataricum ginnala
Czech javor amurský
Danish ild-løn
German feuer-ahorn
Finnish mongolianvaahtera
French acer tataricum ginnala
Hungarian tűzvörös juhar
Korean 신나무
Latvian ginnalas kļava
mn Гинналийн агч мод
Norwegian Bokmål sibirlønn
Norwegian Nynorsk sibirlønn
Polish klon ginnala
Portuguese acer ginnala
Russian Клён приречный
Albanian acer tataricum ginnala
Swedish ginnalalönn
Vietnamese acer tataricum ginnala
war acer tataricum ginnala
Chinese 茶条
Chinese 华北茶条槭
Chinese 茶条槭
Chinese 苦茶槭
Chinese 桑芽

Varieties (abbr. var.) Top

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No variety added yet.

Forms (abbr. f.) Top

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Germination/Propagation Top

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Start at 4°C for 3 months, then warm to 20°C for another 3 months.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000515184
Cornell Woody Plants 364
Canadensys 9200
Tropicos 50324554
INPN 612608
Flora of Italy 8698
KEW urn:lsid:ipni.org:names:77249729-1
The Plant List kew-2616532
Missouri Botanical Garden 275410
Open Tree Of Life 403798
Observations.org 104638
NCBI Taxonomy 57656
GBIF 4925890
Freebase /m/0bf16c
EPPO ACRGN
USDA GRIN 403019

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 risk factors for insect borer attack in Georgia’s (USA) urban landscapes Williamson ZV, Blaauw BR, Joseph SV PLoS One 26-Feb-2024
PMCID:PMC10896510
doi:10.1371/journal.pone.0299368
PMID:38408102
Environmental factors influencing the diversity and distribution of dictyostelid cellular slime molds in forest and farmland soils of western China Zhang Z, Yang Y, Zhao J, Li Y, Stephenson SL, Qiu J, Liu P Microbiol Spectr 14-Nov-2023
PMCID:PMC10715086
doi:10.1128/spectrum.01732-23
PMID:37962389
Distributional responses to climate change of two maple species in southern China Liu DT, Chen JY, Sun WB Ecol Evol 31-Aug-2023
PMCID:PMC10468973
doi:10.1002/ece3.10490
PMID:37664510
Physiological effects of combined NaCl and NaHCO3 stress on the seedlings of two maple species Xu B, Cao L, Zhang Z, Li X, Zhao X, Wang X, Wang Y, Wu B, Zhou W, Lin C, Gao Y, Rong L Front Plant Sci 11-Jul-2023
PMCID:PMC10367004
doi:10.3389/fpls.2023.1209999
PMID:37496858
Commodity risk assessment of Acer pseudoplatanus plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323731
doi:10.2903/j.efsa.2023.8074
PMID:37427019
Commodity risk assessment of Acer palmatum plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323724
doi:10.2903/j.efsa.2023.8075
PMID:37427020
Commodity risk assessment of Acer campestre plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323733
doi:10.2903/j.efsa.2023.8071
PMID:37427018
Commodity risk assessment of Acer platanoides plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Gardi C, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 06-Jul-2023
PMCID:PMC10323725
doi:10.2903/j.efsa.2023.8073
PMID:37427021
Secondary metabolites from endophytic fungi: Production, methods of analysis, and diverse pharmaceutical potential Singh VK, Kumar A Symbiosis 08-Jun-2023
PMCID:PMC10249938
doi:10.1007/s13199-023-00925-9
PMID:37360552
Adaptation strategies of leaf traits and leaf economic spectrum of two urban garden plants in China Xu L, Zhang N, Wei T, Liu B, Shen L, Liu Y, Liu D BMC Plant Biol 24-May-2023
PMCID:PMC10207826
doi:10.1186/s12870-023-04301-z
PMID:37221486
Ginnalin A and hamamelitannin: the unique gallotannins with promising anti-carcinogenic potential Rippin, Beniwal V, Sharma A, Singh BJ, Ramniwas S, Sak K, Kumar S, Sharma AK Explor Target Antitumor Ther 21-Apr-2023
PMCID:PMC10185439
doi:10.37349/etat.2023.00129
PMID:37205316
Using high-throughput sequencing to investigate the dietary composition of the Korean water deer (Hydropotes inermis argyropus): a spatiotemporal comparison Lee SK, Woo C, Lee EJ, Yamamoto N Sci Rep 23-Dec-2022
PMCID:PMC9789119
doi:10.1038/s41598-022-26862-z
PMID:36564425
Ontogeny influences tree growth response to soil fertility and neighbourhood crowding in an old-growth temperate forest Ren J, Fang S, Wang QW, Liu H, Lin F, Ye J, Hao Z, Wang X, Fortunel C Ann Bot 01-Dec-2022
PMCID:PMC10457036
doi:10.1093/aob/mcac146
PMID:36454654
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Global Trends of Acidity in Rainfall and Its Impact on Plants and Soil Prakash J, Agrawal SB, Agrawal M J Soil Sci Plant Nutr 17-Nov-2022
PMCID:PMC9672585
doi:10.1007/s42729-022-01051-z
PMID:36415481

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 / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1039/CT9222100066
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 53396785 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(80)83034-2
[3,5-Dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 15558211 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.8.72
1,5-Anhydro-3-O,6-O-digalloyl-D-glucitol 53233246 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O 468.40 unknown https://doi.org/10.1248/CPB.8.72
Ginnalin A 5318457 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)O)O)O 468.40 unknown https://doi.org/10.1016/0031-9422(80)83034-2
> Phenylpropanoids and polyketides / Depsides and depsidones
[(2R,3S,4S,5S)-5-[3-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoyl]oxy-3,4-dihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14682443 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[(3S,4S,5S,6R)-6-[[3-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoyl]oxymethyl]-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 14682439 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[(3S,4S,5S,6R)-6-[[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxymethyl]-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 14682435 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 620.50 unknown https://doi.org/10.1248/CPB.38.1902
[5-[[(2R,3S,4S,5S)-5-[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-3,4-dihydroxyoxan-2-yl]methoxycarbonyl]-2,3-dihydroxyphenyl] 3,4,5-trihydroxybenzoate 14682441 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[5-[[5-[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-3,4-dihydroxyoxan-2-yl]methoxycarbonyl]-2,3-dihydroxyphenyl] 3,4,5-trihydroxybenzoate 14682440 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[5-[3-[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoyl]oxy-3,4-dihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14682442 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[5-[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-3,4-dihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14682436 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 620.50 unknown https://doi.org/10.1248/CPB.38.1902
[6-[[3-[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy-4,5-dihydroxybenzoyl]oxymethyl]-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 14682438 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 772.60 unknown https://doi.org/10.1248/CPB.38.1902
[6-[[3,4-Dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxymethyl]-4,5-dihydroxyoxan-3-yl] 3,4,5-trihydroxybenzoate 14682434 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 620.50 unknown https://doi.org/10.1248/CPB.38.1902
1,5-Anhydro-2-O-[5-(galloyloxy)-3,4-dihydroxybenzoyl]-6-O-galloyl-D-glucitol 14682437 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)OC(=O)C3=CC(=C(C(=C3)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O 620.50 unknown https://doi.org/10.1248/CPB.38.1902
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2R,3S,4R,5R,6S)-2-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-[4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoate 163014633 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC=C(C=C6)OC7C(C(C(C(O7)CO)O)O)O)O)O)O)O)O 902.80 unknown https://doi.org/10.1248/CPB.38.1902
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
CID 115063 115063 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1248/CPB.38.1902
Davidiin 14682455 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C(C=C4C(=O)O1)O)O)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 938.70 unknown https://doi.org/10.1248/CPB.38.1902
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1039/CT9222100066
Geraniin 3001497 Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O 952.60 unknown https://doi.org/10.1248/CPB.38.1902

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