Acer truncatum - Unknown
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Details Top

Internal ID UUID644006ca8ea40762341711
Scientific name Acer truncatum
Authority Bunge
First published in Enum. Pl. China Bor. : 10 (1833)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acer cappadocicum subsp. truncatum (Bunge) A.E.Murray Kalmia 8: 5 (1977)
Acer laetum var. truncatum (Bunge) Regel
Acer lobelii var. platanoides Miyabe Bot. Mag. (Tokyo) 9: 346 1895
Acer lobulatum Nakai J. Jap. Bot. 18: 608 (1942)
Acer pictum var. truncatum (Bunge) Chin S.Chang Korean J. Pl. Taxon. 31: 302 (2001)
Acer truncatum var. beipiao S.L.Tung Bull. Bot. Res., Harbin 5(1): 105 (1985)
Acer truncatum f. cordatum L.S.Tung Bull. Bot. Res., Harbin 5(1): 105 (1985)
Acer lobelii subsp. truncatum (Bunge) Wesm. Bull. Soc. Roy. Bot. Belgique 29: 56 1890
Acer lobulatum var. rubripes Nakai J. Jap. Bot. 18: 609 1942
Acer pictum subsp. truncatum (Bunge) A.E.Murray
Acer platanoides var. truncatum (Bunge) Gams
Acer truncatum var. acuminatum X.M.Liu
Acer truncatum var. nudum Schwer.

Common names Top

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Language Common/alternative name
English shandong maple
Arabic قيقب أقطع
German chinesischer spitz-ahorn
Persian افرای شاندونگ
Polish klon ściętolistny
Russian Клён усечённый
Russian Клен усеченный
Russian Клен усечённый
Chinese 平基槭
Chinese
Chinese 五角枫
Chinese 元寳楓
Chinese 华北五角枫
Chinese 元宝树
Chinese 五脚树
Chinese 元宝枫
Chinese 元宝槭

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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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000515246
Cornell Woody Plants 14
UConn 27
Tropicos 200329
KEW urn:lsid:ipni.org:names:781552-1
The Plant List kew-2616594
Missouri Botanical Garden 275427
PFAF Acer truncatum
Open Tree Of Life 1050908
NCBI Taxonomy 47965
NBN Atlas NBNSYS0000042057
IUCN Red List 193886
IPNI 781552-1
iNaturalist 461754
GBIF 7263012
Freebase /m/02pvld3
EPPO ACRTU
EOL 2889020
Elurikkus 579907
USDA GRIN 1243
Wikipedia Acer_truncatum

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
Complete mitochondrial genome of Angelica dahurica and its implications on evolutionary analysis of complex mitochondrial genome architecture in Apiaceae Li YY, Liu YY, Zeng X, Wu P, Li QM, Guo SX, Hao ZG Front Plant Sci 23-Apr-2024
PMCID:PMC11074370
doi:10.3389/fpls.2024.1367299
PMID:38716337
Differentially Expressed Genes Identification of Kohlrabi Seedlings (Brassica oleracea var. caulorapa L.) under Polyethylene Glycol Osmotic Stress and AP2/ERF Transcription Factor Family Analysis Bian S, Zhao M, Zhang H, Ren Y Plants (Basel) 22-Apr-2024
PMCID:PMC11054715
doi:10.3390/plants13081167
PMID:38674577
Integrated analysis of metabolome, transcriptome, and bioclimatic factors of Acer truncatum seeds reveals key candidate genes related to unsaturated fatty acid biosynthesis, and potentially optimal production area Li Y, Kong F, Wu S, Song W, Shao Y, Kang M, Chen T, Peng L, Shu Q BMC Plant Biol 16-Apr-2024
PMCID:PMC11020666
doi:10.1186/s12870-024-04936-6
PMID:38627650
Assembly and comparative analysis of the complete multichromosomal mitochondrial genome of Cymbidium ensifolium, an orchid of high economic and ornamental value Shen B, Shen A, Liu L, Tan Y, Li S, Tan Z BMC Plant Biol 09-Apr-2024
PMCID:PMC11003039
doi:10.1186/s12870-024-04962-4
PMID:38594641
Lipase-Catalyzed Preparation and Optimization of Structured Phosphatidylcholine Containing Nervonic Acid Ang X, Chen H, Xiang J, Wei F, Quek SY Molecules 29-Mar-2024
PMCID:PMC11013151
doi:10.3390/molecules29071539
PMID:38611818
Advances in Flavonoid Research: Sources, Biological Activities, and Developmental Prospectives Hao B, Yang Z, Liu H, Liu Y, Wang S Curr Issues Mol Biol 26-Mar-2024
PMCID:PMC11049524
doi:10.3390/cimb46040181
PMID:38666911
Production of Conjugated Linoleic Acid (CLA) by Lactiplantibacillus plantarum: A Review with Emphasis on Fermented Foods Iorizzo M, Di Martino C, Letizia F, Crawford TW Jr, Paventi G Foods 22-Mar-2024
PMCID:PMC11012127
doi:10.3390/foods13070975
PMID:38611281
The dynamics of nocturnal sap flow components of a typical revegetation shrub species on the semiarid Loess Plateau, China Fang W, Liu J, Lu N, Li R Front Plant Sci 21-Mar-2024
PMCID:PMC10991760
doi:10.3389/fpls.2024.1370362
PMID:38576789
Genomic and transcriptomic studies on flavonoid biosynthesis in Lagerstroemia indica Yu C, Liu G, Qin J, Wan X, Guo A, Wei H, Chen Y, Lian B, Zhong F, Zhang J BMC Plant Biol 05-Mar-2024
PMCID:PMC10913235
doi:10.1186/s12870-024-04776-4
PMID:38443839
The first two whole mitochondrial genomes for the genus Dactylis species: assembly and comparative genomics analysis Feng G, Jiao Y, Ma H, Bian H, Nie G, Huang L, Xie Z, Ran Q, Fan W, He W, Zhang X BMC Genomics 04-Mar-2024
PMCID:PMC10910808
doi:10.1186/s12864-024-10145-0
PMID:38438835
Morpho-Molecular Characterization Reveals a New Genus, Three Novel Species and Two New Host Records in Xylariomycetidae Li WL, Liang RR, Yang J, Liu JK J Fungi (Basel) 29-Feb-2024
PMCID:PMC10970796
doi:10.3390/jof10030189
PMID:38535198
Identification of WRKY Family Members and Characterization of the Low-Temperature-Stress-Responsive WRKY Genes in Luffa (Luffa cylindrica L.) Liu J, Peng L, Cao C, Bai C, Wang Y, Li Z, Zhu H, Wen Q, He S Plants (Basel) 28-Feb-2024
PMCID:PMC10935285
doi:10.3390/plants13050676
PMID:38475522
Isolation and Identification of Acer truncatum Endophytic Fungus Talaromyces verruculosus and Evaluation of Its Effects on Insoluble Phosphorus Absorption Capacity and Growth of Cucumber Seedlings Zeng Q, Dong J, Lin X, Zhou X, Xu H J Fungi (Basel) 08-Feb-2024
PMCID:PMC10890576
doi:10.3390/jof10020136
PMID:38392808
Editorial: New drugs, approaches and strategies for multiple sclerosis treatment Coveñas R, Marcos P, Mangas A Front Neurosci 30-Jan-2024
PMCID:PMC10861717
doi:10.3389/fnins.2024.1372140
PMID:38352043
Assembly and analysis of the complete mitochondrial genome of the Chinese wild dwarf almond (Prunus tenella) Liu X, Zhang D, Yu Z, Zeng B Front Genet 11-Jan-2024
PMCID:PMC10811783
doi:10.3389/fgene.2023.1329060
PMID:38283144

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
Ethyl gallate 13250 Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O 198.17 unknown https://doi.org/10.1080/14786419.2010.488625
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown https://doi.org/10.1080/14786419.2010.488625
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(+)-Lyoniresinol 11711453 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(2R,3S,4S)-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-3-ol 14521045 Click to see COC1=C(C=CC(=C1)CC2COC(C2(CO)O)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-3-ol 14521044 Click to see COC1=C(C=CC(=C1)CC2COC(C2(CO)O)C3=CC(=C(C=C3)O)OC)O 376.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Pinoresinol 4-O-glucoside 11168362 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
2-[[7-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-6-methoxy-1,2,3,4-tetrahydronaphthalen-2-yl]methoxy]oxane-3,4,5-triol 14521042 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)OC)O 492.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Schizandriside 14521043 Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)OC)O 492.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Symplocosin 5351523 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)O 520.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Hecogenin 91453 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Hocogenin 3573 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Lipids and lipid-like molecules / Saccharolipids
[6-Methyl-5-(2-methylpropanoyloxy)-2-[[4,5,23-trihydroxy-24-(hydroxymethyl)-6-methyl-20-oxo-10-pentyl-2,7,9,21,25-pentaoxatricyclo[20.3.1.03,8]hexacosan-26-yl]oxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl] 2-methylbutanoate 78412972 Click to see CCCCCC1CCCCCCCCCC(=O)OC2C(C(OC(C2OC3C(C(C(C(O3)C)OC(=O)C(C)C)OC4C(C(C(C(O4)C)O)O)O)OC(=O)C(C)CC)OC5C(C(C(OC5O1)C)O)O)CO)O 1009.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-{[3-(3,4-Dihydroxyphenyl)prop-2-enoyl]oxy}-1,4,5-trihydroxycyclohexane-1-carboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone 163032925 Click to see COC1=CC(=C(C(=C1)OC2C(C(C(O2)CO)O)O)C(=O)C3=CC(=CC(=C3)O)O)O 408.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R,4S,5S,6R)-2-[3-[(2R,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 94841684 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOC4C(C(C(C(O4)CO)O)O)O 522.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
(2S,3R,4R,5R,6S)-2-[4-[(2R,3R)-3-(hydroxymethyl)-5-(3-hydroxypropyl)-7-methoxy-2,3-dihydro-1-benzofuran-2-yl]-2-methoxyphenoxy]-6-methyloxane-3,4,5-triol 163007252 Click to see CC1C(C(C(C(O1)OC2=C(C=C(C=C2)C3C(C4=C(O3)C(=CC(=C4)CCCO)OC)CO)OC)O)O)O 506.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6148490/
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1080/14786419.2010.488625
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 5320854 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/10.1080/14786419.2010.488625
3-(beta-D-Arabinopyranosyloxy)-5,7-dihydroxy-2-(3,4-dihydroxyphenyl)-4H-1-benzopyran-4-one 21722017 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1080/14786419.2010.488625
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 162958702 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)OC)O)O)O 462.40 unknown https://doi.org/10.1080/14786419.2010.488625
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 162907238 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(CO4)O)O)O)O 448.40 unknown https://doi.org/10.1080/14786419.2010.488625
5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 16103933 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)O 464.40 unknown https://doi.org/10.1080/14786419.2010.488625
kaempferol-3-O-alpha-L-rhamnoside 15558501 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 432.40 unknown https://doi.org/10.1080/14786419.2010.488625
Kaempferol-3-O-rhamnoside 5835713 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 432.40 unknown https://doi.org/10.1080/14786419.2010.488625
Myricetin 3-rhamnoside 5352000 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)O 464.40 unknown https://doi.org/10.1080/14786419.2010.488625
Quercetin 3-O-rhamnoside 5353915 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/10.1080/14786419.2010.488625
Reynoutrin 5878729 Click to see C1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 434.30 unknown https://doi.org/10.1080/14786419.2010.488625
> Phenylpropanoids and polyketides / Tannins
.beta-Penta-O-galloyl-D-glucose 374874 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1080/14786419.2010.488625
Pentagalloylglucose 65238 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O 940.70 unknown https://doi.org/10.1080/14786419.2010.488625

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