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Acer pycnanthum

Acer pycnanthum - Unknown
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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 UUID644006c34ef6d129410316
Scientific name Acer pycnanthum
Authority K.Koch
First published in Ann. Mus. Bot. Lugduno-Batavi 1: 250 (1864)

Description Top

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Acer pycnanthum, also known as the Japanese red maple, is a species of maple tree native to Japan and introduced to Korea. It typically grows to be about 20 meters tall, but can reach up to 30 meters. This tree is commonly found in relict mountain wetlands and blooms in April before its leaves emerge. Despite being considered Vulnerable in its natural habitat, it is often used as a street tree and is the official tree of several Japanese municipalities and Aichi Prefecture. The tree is dioecious, with separate male and female flowers, and has grey bark with a shaggy appearance. Its leaves are shallowly lobed and turn yellow, orange, red, and purple in the autumn. It is similar to the smaller Acer rubrum. A. pycanthum is suitable for USDA hardiness zone 5 and prefers full sun to partial shade. It is hardy in all of the UK and northern Europe, but can be susceptible to aphids and verticillium wilt.

Synonyms Top

Scientific name Authority First published in
Acer rubrum var. pycnanthum (Koch) Makino

Common names Top

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Language Common/alternative name
English hananoki maple
Japanese ハナノキ
Japanese ハナカエデ
Japanese 花の木
Chinese 花之木
Chinese 日本红枫

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-0000514942
Tropicos 200187
KEW urn:lsid:ipni.org:names:781471-1
The Plant List kew-2616307
PaleoBotany 81684
Open Tree Of Life 735109
NCBI Taxonomy 349748
IUCN Red List 193858
IPNI 781471-1
iNaturalist 448022
GBIF 3768230
EPPO ACRPY
EOL 5613113
USDA GRIN 100441
Wikipedia Acer_pycnanthum

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
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
Restoration Contributes to Maintain Ecosystem Services and Bio-Cultural Linkages Between Wetlands and Local Communities: a Case from a Botanical Diversity Hotspot in Japan Saeki I, Li Y Wetlands (Wilmington) 28-Nov-2022
PMCID:PMC9703418
doi:10.1007/s13157-022-01639-2
PMID:36467510
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China 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, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020
Commodity risk assessment of Acer spp. plants from New Zealand Bragard C, Dehnen‐Schmutz K, Di Serio F, Jacques M, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Mosbach‐Schulz O, Gonthier P EFSA J 20-May-2020
PMCID:PMC10464684
doi:10.2903/j.efsa.2020.6105
PMID:37649508
Herbal medicine in the treatment of patients with type 2 diabetes mellitus Pang GM, Li FX, Yan Y, Zhang Y, Kong LL, Zhu P, Wang KF, Zhang F, Liu B, Lu C Chin Med J (Engl) 05-Jan-2019
PMCID:PMC6629308
doi:10.1097/CM9.0000000000000006
PMID:30628962
Pycnalin, a new α-glucosidase inhibitor from Acer pycnanthum. Ogawa A, Miyamae Y, Honma A, Koyama T, Yazawa K, Shigemori H Chem Pharm Bull (Tokyo) 01-Jan-2011
doi:10.1248/CPB.59.672
PMID:21532209

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 / Galloyl esters
[(2R,3R,4R,5S)-3,5-dihydroxy-4-(3,4,5-trihydroxybenzoyl)oxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 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.59.672
[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 53233359 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O 316.26 unknown https://doi.org/10.1248/CPB.59.672
[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/10.1248/CPB.59.672
[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.59.672
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/10.1248/CPB.59.672
Ginnalin B 44512370 Click to see C1C(C(C(C(O1)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O 316.26 unknown https://doi.org/10.1248/CPB.59.672
Ginnalin C 44512371 Click to see C1C(C(C(C(O1)CO)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O 316.26 unknown https://doi.org/10.1248/CPB.59.672

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