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

Add a new one! Suggest a correction!

Filter by language:

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	槭
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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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

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 click to expand
- China
  - China North-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Amur
  - Sakhalin

Links to other databases Top

Suggest others/fix!

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

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

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

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

Genome-Wide Identification of the CBF Gene Family and ICE Transcription Factors in Walnuts and Expression Profiles under Cold Conditions

Zhou H, Ma J, Liu H, Zhao P

Int J Mol Sci

19-Dec-2023

PMCID:	PMC10778614
doi:	10.3390/ijms25010025
PMID:	38203199

High-level production of nervonic acid in the oleaginous yeast Yarrowia lipolytica by systematic metabolic engineering

Su H, Shi P, Shen Z, Meng H, Meng Z, Han X, Chen Y, Fan W, Fa Y, Yang C, Li F, Wang S

Commun Biol

07-Nov-2023

PMCID:	PMC10630375
doi:	10.1038/s42003-023-05502-w
PMID:	37935958

Assembly and comparative analysis of the complete mitochondrial genome of Isopyrum anemonoides (Ranunculaceae)

Yisilam G, Liu Z, Turdi R, Chu Z, Luo W, Tian X

PLoS One

05-Oct-2023

PMCID:	PMC10553351
doi:	10.1371/journal.pone.0286628
PMID:	37796878

Chloroplast genome assembly of Serjania erecta Raldk: comparative analysis reveals gene number variation and selection in protein-coding plastid genes of Sapindaceae

Corvalán LC, Sobreiro MB, Carvalho LR, Dias RO, Braga-Ferreira RS, Targueta CP, Silva-Neto CM, Berton BW, Pereira AM, Diniz-filho JA, Telles MP, Nunes R

Front Plant Sci

26-Sep-2023

PMCID:	PMC10562606
doi:	10.3389/fpls.2023.1258794
PMID:	37822334

The Chemical Composition and Health-Promoting Benefits of Vegetable Oils—A Review

Tian M, Bai Y, Tian H, Zhao X

Molecules

01-Sep-2023

PMCID:	PMC10489903
doi:	10.3390/molecules28176393
PMID:	37687222

Assembly and comparative analysis of the complete mitochondrial genome of Ilex metabaptista (Aquifoliaceae), a Chinese endemic species with a narrow distribution

Zhou P, Zhang Q, Li F, Huang J, Zhang M

BMC Plant Biol

14-Aug-2023

PMCID:	PMC10424370
doi:	10.1186/s12870-023-04377-7
PMID:	37580695

Environmental Stress and Plants 2.0

Parrotta L, Mareri L, Cai G

Int J Mol Sci

04-Aug-2023

PMCID:	PMC10418621
doi:	10.3390/ijms241512413
PMID:	37569788

Acer truncatum leaves extract modulates gut microbiota, improves antioxidant capacity, and alleviates lipopolysaccharide-induced inflammation in broilers

Liu J, Liang S, Qin K, Jia B, Ren Z, Yang X, Yang X

Poult Sci

21-Jul-2023

PMCID:	PMC10432845
doi:	10.1016/j.psj.2023.102951
PMID:	37562124

Differences in the Suitable Distribution Area between Northern and Southern China Landscape Plants

Wang C, Sheng Q, Zhao R, Zhu Z

Plants (Basel)

20-Jul-2023

PMCID:	PMC10385631
doi:	10.3390/plants12142710
PMID:	37514324

Leaf nutrient resorption of two life-form tree species in urban gardens and their response to soil nutrient availability

Hu R, Liu T, Zhang Y, Zheng R, Guo J

PeerJ

19-Jul-2023

PMCID:	PMC10362843
doi:	10.7717/peerj.15738
PMID:	37483974

Whole-genome sequencing and functional annotation of pathogenic Paraconiothyrium brasiliense causing human cellulitis

Liu H, Zhang Y, Chen J

Hum Genomics

17-Jul-2023

PMCID:	PMC10351199
doi:	10.1186/s40246-023-00512-5
PMID:	37461066

Phytochemical Profile Top

Add a new one!

Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

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-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic 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-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	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
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
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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Acer truncatum

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top