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Acer pictum subsp. mono

Acer pictum subsp. mono - 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 UUID644006c134e87604929293
Scientific name Acer pictum subsp. mono
Authority (Maxim.) H.Ohashi
First published in J. Jap. Bot. 68(6): 321 (1993):.

Description Top

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Common names Top

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Language Common/alternative name
Azerbaijani xırdayarpaq ağcaqayın
ceb acer mono
Armenian Թխկի մանրատերև
Japanese イタヤカエデ
Korean 고로쇠나무
Latvian sīklapu kļava
Russian Клён мелколистный
Swedish acer mono
Vietnamese acer mono
war acer mono
Chinese 五角枫
Chinese 五角槭
Chinese 色木槭
Chinese 地锦槭
Chinese 水色树

Varieties (abbr. var.) 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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000514866
UNII YU83YF4ZL4
Tropicos 50161666
KEW urn:lsid:ipni.org:names:976224-1
Missouri Botanical Garden 292149
Open Tree Of Life 1050917
Observations.org 134680
NCBI Taxonomy 47963
IPNI 976223-1
GBIF 6359081
Freebase /m/09v5fjt
USDA GRIN 403929
Wikipedia Acer_pictum_subsp._mono
CMAUP NPO12148.2

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
Exploration for Asian longhorned beetle parasitoids in Korea using an improved sentinel log trap Lee S, Park DY, Wang X, Duan JJ, Gould JR, Kim IK, Lee S Parasite 12-Dec-2023
PMCID:PMC10714676
doi:10.1051/parasite/2023062
PMID:38084938
Dynamics of the natural enemy community of Hyphantria cunea (Lepidoptera: Erebidae) in Dandong, China Zhang X, Yang L, Chen C, Shi J, Zhang Y, Sun S J Insect Sci 28-Nov-2023
PMCID:PMC10684046
doi:10.1093/jisesa/iead105
PMID:38016005
The Composition of Fatty Acids in Bee Pollen, Royal Jelly, Buckthorn Oil and Their Mixtures with Pollen Preserved for Storage Čeksterytė V, Bliznikas S, Jaškūnė K Foods 23-Aug-2023
PMCID:PMC10487168
doi:10.3390/foods12173164
PMID:37685097
Forest Type and Climate Outweigh Soil Bank in Shaping Dynamic Changes in Macrofungal Diversity in the Ancient Tree Park of Northeast China Zhu Z, Liu X, Hsiang T, Ji R, Liu S J Fungi (Basel) 17-Aug-2023
PMCID:PMC10455530
doi:10.3390/jof9080856
PMID:37623627
Effect of Exogenous Plant Growth Regulators and Rejuvenation Measures on the Endogenous Hormone and Enzyme Activity Responses of Acer mono Maxim in Cuttage Rooting Zhou X, Li R, Shen H, Yang L Int J Mol Sci 25-Jul-2023
PMCID:PMC10418764
doi:10.3390/ijms241511883
PMID:37569257
Patterns and drivers of soil surface‐dwelling Oribatida diversity along an altitudinal gradient on the Changbai Mountain, China Lin Y, Wu H, Liu D, Li Y, Kang Y, Zhang Z, Wang W Ecol Evol 19-May-2023
PMCID:PMC10196937
doi:10.1002/ece3.10105
PMID:37214606
Species asynchrony stabilizes productivity over 20 years in Northeast China Jia B, He J, Wang X Ecol Evol 03-May-2023
PMCID:PMC10156448
doi:10.1002/ece3.9991
PMID:37153024
Effects of seasonal changes on the carbon dynamics in mixed coniferous forests Gao T, Song X, Ren Y, Liu H, Meng Y, Dong X PLoS One 20-Apr-2023
PMCID:PMC10118155
doi:10.1371/journal.pone.0267365
PMID:37079645
A large‐scale field experiment of artificially caused landslides with replications revealed the response of the ground‐dwelling beetle community to landslides Furusawa J, Makoto K, Utsumi S Ecol Evol 24-Mar-2023
PMCID:PMC10037431
doi:10.1002/ece3.9939
PMID:36969925
Comparison of various chemometric methods on visible and near-infrared spectral analysis for wood density prediction among different tree species and geographical origins Li Y, Via BK, Han F, Li Y, Pei Z Front Plant Sci 10-Mar-2023
PMCID:PMC10036815
doi:10.3389/fpls.2023.1121287
PMID:36968398
Soil water content and nitrogen differentially correlate with multidimensional leaf traits of two temperate broadleaf species Jin MY, Johnson DJ, Jin GZ, Guo QX, Liu ZL Plant Divers 07-Mar-2023
PMCID:PMC10772124
doi:10.1016/j.pld.2023.03.001
PMID:38197009
Winter dynamics of functional diversity and redundancy of riffle and pool macroinvertebrates after defoliation in a temperate forest stream Wang L, Xia L, Li J, Wan L, Yang H Front Microbiol 06-Mar-2023
PMCID:PMC10025292
doi:10.3389/fmicb.2023.1105323
PMID:36950171
Effects of arbuscular mycorrhizal fungus inoculation on the growth and nitrogen metabolism of Catalpa bungei C.A.Mey. under different nitrogen levels Chen W, Mou X, Meng P, Chen J, Tang X, Meng G, Xin K, Zhang Y, Wang C Front Plant Sci 23-Feb-2023
PMCID:PMC9996104
doi:10.3389/fpls.2023.1138184
PMID:36909441
Does diet or macronutrients intake drive the structure and function of gut microbiota? Li Y, Yan Y, Fu H, Jin S, He S, Wang Z, Dong G, Li B, Guo S Front Microbiol 13-Feb-2023
PMCID:PMC9970161
doi:10.3389/fmicb.2023.1126189
PMID:36860485
Effects of Bee Pollen Derived from Acer mono Maxim. or Phellodendron amurense Rupr. on the Lipid Composition of Royal Jelly Secreted by Honeybees Zhou E, Wang Q, Li X, Zhu D, Niu Q, Li Q, Wu L Foods 02-Feb-2023
PMCID:PMC9914857
doi:10.3390/foods12030625
PMID:36766159

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 / Diterpenoids
(1R,8S,10S)-4-methoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[6.6.2.01,10.02,7]hexadeca-2,4,6-trien-3-ol 21632855 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)CO3)O)OC 330.50 unknown via CMAUP database
(3S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthrene-3,6-diol 92966440 Click to see CC(C)C1=C(C=C2C(=C1)CCC3C2(CC(CC3(C)C)O)C)O 302.50 unknown via CMAUP database
(4aR)-1,1-Dimethyl-5,6-dimethoxy-7-isopropyl-1,3,4,10aalpha-tetrahydrophenanthrene-4abeta(2H)-carboxylic acid methyl ester 10761833 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3C2(CCCC3(C)C)C(=O)OC)OC)OC 372.50 unknown via CMAUP database
11-Hydroxysugiol 10403490 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O)O 316.40 unknown via CMAUP database
6alpha-Hydroxydemethylcryptojaponol 76326386 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C(C3C2(CCCC3(C)C)C)O)O)O 332.40 unknown via CMAUP database
Arucatriol 102239782 Click to see CC(C)C1=C(C(=C2C(=C1)C(=CC3=C2C(=O)CCC3(C)C)O)O)O 314.40 unknown via CMAUP database
Carnosic acid 65126 Click to see CC(C)C1=C(C(=C2C(=C1)CCC3C2(CCCC3(C)C)C(=O)O)O)O 332.40 unknown via CMAUP database
Salvicanol 101607178 Click to see CC(C)C1=C(C(=C2CC3(CCCC(C3CCC2=C1)(C)C)O)O)OC 332.50 unknown via CMAUP database
Sugiol 94162 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCCC3(C)C)C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Clovanediol 15599878 Click to see CC1(CC(C23C1CCC(C2)(C(CC3)O)C)O)C 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
16-Hydroxycarnosol 12966869 Click to see CC(CO)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 346.40 unknown via CMAUP database
7-Ethoxyrosmanol 23243693 Click to see CCOC1C2C3C(CCCC3(C4=C(C(=C(C=C14)C(C)C)O)O)C(=O)O2)(C)C 374.50 unknown via CMAUP database
7-O-Methylrosmanol 23243692 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)OC)O)O 360.40 unknown via CMAUP database
Carnosol 442009 Click to see CC(C)C1=C(C(=C2C(=C1)C3CC4C2(CCCC4(C)C)C(=O)O3)O)O 330.40 unknown via CMAUP database
Galdosol 13966127 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)C3C4C2(CCCC4(C)C)C(=O)O3)O)O 344.40 unknown via CMAUP database
Isorosmanol 13820511 Click to see CC(C)C1=C(C(=C2C(=C1)C3C(C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown via CMAUP database
Rosmanol 13966122 Click to see CC(C)C1=C(C(=C2C(=C1)C(C3C4C2(CCCC4(C)C)C(=O)O3)O)O)O 346.40 unknown via CMAUP database
Rosmaquinone 23243691 Click to see CC(C)C1=CC2=C(C(=O)C1=O)C34CCCC(C3C(C2O)OC4=O)(C)C 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
5-Hydroxy-7-(beta-D-glucopyranosyloxy)chromone 44583907 Click to see C1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1021/NP0497907
5-Hydroxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 163096285 Click to see C1=COC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O 340.28 unknown https://doi.org/10.1021/NP0497907
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP0497907
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP0497907
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP0497907
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP0497907
> 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/10.1021/NP0497907
> 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/10.1021/NP0497907
Quercitrin 5280459 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/10.1021/NP0497907
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-Hydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 282013 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/NP0497907
Eriodictyol-7-O-glucoside 13254473 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/NP0497907
Miscanthoside 13254471 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1021/NP0497907
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown https://doi.org/10.1021/NP0497907

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