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Acer triflorum

Acer triflorum - Unknown
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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 UUID644006ca7c3bf896634071
Scientific name Acer triflorum
Authority Kom.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 18: 430 (1901)

Description Top

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Synonyms Top

Scientific name Authority First published in
Acer leiopodum (Hand.-Mazz.) W.P.Fang & S.Chow Acta Phytotax. Sin. 11: 186 (1966)
Acer triflorum var. leiopodum Hand.-Mazz.
Acer triflorum subsp. leiopodum (Hand.-Mazz.) A.E.Murray Kalmia 8: 11 (1977)
Acer triflorum f. subcoriaceum (Kom.) S.L.Tung Bull. Bot. Res., Harbin 5(1): 104 (1985)
Crula triflora Nieuwl. Amer. Midl. Naturalist 2: 114 (1911)
Acer triflorum var. subcoriaceum Kom. Trudy Imp. S.-Peterburgsk. Bot. Sada 22: 730 1904

Common names Top

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Language Common/alternative name
English chosen maple
Spanish arce florado
Arabic قيقب ثلاثي الأزهار
Bulgarian трицветен явор
German dreiblütiger ahorn
Persian افرای سهگل
Finnish huntuvaahtera
French Érable à trois fleurs
Hungarian háromvirágú juhar
Korean 복자기
Korean 나도박달
Korean 나도박달나무
Korean 복자기나무
Latvian trīsziedu kļava
Russian Клён трёхцветковый
Serbian Троцветни јавор
Chinese 拧筋槭
Chinese 伞花槭
Chinese 三花槭
Chinese 三花枫

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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.
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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000515234
Cornell Woody Plants 375
UConn 26
Tropicos 200288
KEW urn:lsid:ipni.org:names:781544-1
The Plant List kew-2616582
Missouri Botanical Garden 275421
Open Tree Of Life 456199
NCBI Taxonomy 134799
IUCN Red List 193885
IPNI 781544-1
iNaturalist 333997
GBIF 7263031
Freebase /m/026szw4
EPPO ACRTF
EOL 2889019
USDA GRIN 1242
Wikipedia Acer_triflorum
CMAUP NPO2801

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
Transcriptomic and metabolic analysis unveils the mechanism behind leaf color development in Disanthus cercidifolius var. longipes Tian X, Xiang G, Lv H, Zhu L, Peng J, Li G, Mou C Front Mol Biosci 06-Feb-2024
PMCID:PMC10876866
doi:10.3389/fmolb.2024.1343123
PMID:38380429
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
Cyanidin-3-O-glucoside Contributes to Leaf Color Change by Regulating Two bHLH Transcription Factors in Phoebe bournei Wang L, Wang Q, Fu N, Song M, Han X, Yang Q, Zhang Y, Tong Z, Zhang J Int J Mol Sci 14-Feb-2023
PMCID:PMC9960835
doi:10.3390/ijms24043829
PMID:36835240
Characterization of the Complete Chloroplast Genome and Phylogenetic Implications of Euonymus microcarpus (Oliv.) Sprague Li H, Chen M, Wang Z, Hao Z, Zhao X, Zhu W, Liu L, Guo W Genes (Basel) 13-Dec-2022
PMCID:PMC9778254
doi:10.3390/genes13122352
PMID:36553619
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
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
Can Different Forest Structures Lead to Different Levels of Therapeutic Effects? A Systematic Review and Meta-Analysis Kim E, Park S, Kim S, Choi Y, Cho J, Cho SI, Chun HR, Kim G Healthcare (Basel) 23-Oct-2021
PMCID:PMC8623963
doi:10.3390/healthcare9111427
PMID:34828474
Spatial patterns and associations of tree species at different developmental stages in a montane secondary temperate forest of northeastern China Liu J, Bai X, Yin Y, Wang W, Li Z, Ma P PeerJ 03-Jun-2021
PMCID:PMC8180193
doi:10.7717/peerj.11517
PMID:34141481
In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH Animals (Basel) 04-Apr-2021
PMCID:PMC8066825
doi:10.3390/ani11041020
PMID:33916571
Medicinal plants: Treasure for antiviral drug discovery Ali SI, Sheikh WM, Rather MA, Venkatesalu V, Muzamil Bashir S, Nabi SU Phytother Res 16-Feb-2021
PMCID:PMC8013762
doi:10.1002/ptr.7039
PMID:33590931
Complete chloroplast genome sequence of Acer nikoense (Sapindaceae) Fu Q, Yu X, Xia X, Zheng Y, Zhang C Mitochondrial DNA B Resour 03-Aug-2020
PMCID:PMC7782346
doi:10.1080/23802359.2020.1797574
PMID:33458080
Complete chloroplast genome sequence of Acer sutchuenense subsp. tienchuanenge (Sapindaceae) Zhang W, Xia X, Chen D, Li J, He W, Ma W, Wu B, Zheng Y, Zhang C Mitochondrial DNA B Resour 20-Jul-2020
PMCID:PMC7781949
doi:10.1080/23802359.2020.1791002
PMID:33457988

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
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
Neral 643779 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1S,2S,4R)-Limonene-1,2-diol 441246 Click to see CC(=C)C1CCC(C(C1)O)(C)O 170.25 unknown via CMAUP database
2-[(1R)-4-methylcyclohex-3-en-1-yl]prop-2-enal 92467550 Click to see CC1=CCC(CC1)C(=C)C=O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1248/CPB.42.960
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.42.960
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/CPB.42.960
Pyracrenic acid 6439576 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C=CC6=CC(=C(C=C6)O)O)C)C(=O)O 618.80 unknown https://doi.org/10.1248/CPB.42.960
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/CPB.42.960
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxy-trans-cinnamic acid tetracosyl ester 5320239 Click to see CCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 516.80 unknown https://doi.org/10.1248/CPB.42.960
Docosyl caffeate 5316952 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 488.70 unknown https://doi.org/10.1248/CPB.42.960
Hexacosanyl caffeate 15719485 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)O 544.80 unknown https://doi.org/10.1248/CPB.42.960
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2R,3S,4S,5R,6S)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-[(5R)-5-hydroxy-7-(4-hydroxyphenyl)heptyl]phenoxy]oxane-3,4,5-triol 10393688 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)CCCCC(CCC4=CC=C(C=C4)O)O)O)O)O)O)(CO)O 594.60 unknown https://doi.org/10.1248/CPB.42.960
(2S,3R,4S,5S,6R)-2-[4-[(5R)-5-hydroxy-7-(4-hydroxyphenyl)heptyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10253797 Click to see C1=CC(=CC=C1CCC(CCCCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 462.50 unknown https://doi.org/10.1248/CPB.42.960
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[4-[5-hydroxy-7-(4-hydroxyphenyl)heptyl]phenoxy]oxane-3,4,5-triol 85130655 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)CCCCC(CCC4=CC=C(C=C4)O)O)O)O)O)O)(CO)O 594.60 unknown https://doi.org/10.1248/CPB.42.960
2-[4-[5-Hydroxy-7-(4-hydroxyphenyl)heptyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163020414 Click to see C1=CC(=CC=C1CCC(CCCCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O 462.50 unknown https://doi.org/10.1248/CPB.42.960
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Isokaempferide 5280862 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Penduletin 5320462 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC 344.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Calycopterin 10429470 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 374.30 unknown via CMAUP database
Xanthomicrol 73207 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=C(C=C3)O)OC)OC 344.30 unknown via CMAUP database

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