Toxicodendron sylvestre - Unknown
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Internal ID UUID644044a0599c0336318768
Scientific name Toxicodendron sylvestre
Authority (Siebold & Zucc.) Kuntze
First published in Revis. Gen. Pl. 1: 154 (1891)

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Synonyms Top

Scientific name Authority First published in
Rhus sylvestris Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 140 (1845)

Common names Top

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Language Common/alternative name
Arabic سماق سام حرجي
Japanese ヤマハゼ
Russian Токсикодендрон лесной
Chinese 木蜡树根
Chinese 七月倍
Chinese 木蜡树
Chinese 野毛漆
Chinese 野漆疮树
Chinese 山漆树
Chinese 木蜡树叶
Chinese 木蠟樹

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001052328
Tropicos 1301240
KEW urn:lsid:ipni.org:names:71795-1
The Plant List tro-1301240
Open Tree Of Life 301953
NCBI Taxonomy 269722
IUCN Red List 147629430
IPNI 71795-1
iNaturalist 474638
GBIF 4928886
EOL 2888778
USDA GRIN 410070

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
Partial Correspondence between Host Plant-Related Differentiation and Symbiotic Bacterial Community in a Polyphagous Insect Cheng Z, Liu Q, Huang X Animals (Basel) 16-Jan-2024
PMCID:PMC10812459
doi:10.3390/ani14020283
PMID:38254452
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980
Hydroxy Chalcones and Analogs with Chemopreventive Properties Birsa ML, Sarbu LG Int J Mol Sci 26-Jun-2023
PMCID:PMC10341761
doi:10.3390/ijms241310667
PMID:37445844
Molecular evolution and phylogenomic analysis of complete chloroplast genomes of Cotinus (Anacardiaceae) Liu Q, Yang N, Dong W, Zhao L Ecol Evol 29-May-2023
PMCID:PMC10227175
doi:10.1002/ece3.10134
PMID:37261318
Potential of natural flavonols and flavanones in the treatment of ulcerative colitis Li C, Tang Y, Ye Y, Zuo M, Lu Q Front Pharmacol 03-Mar-2023
PMCID:PMC10020211
doi:10.3389/fphar.2023.1120616
PMID:36937890
Complete Chloroplast Genome Sequence of the Western Poison Oak, Toxicodendron diversilobum (Anacardiaceae), from California Huitron Vazquez LI, Aviles PE, Bailon SA, Cabanillas AG, Fernandez A, Galarza JI, Guerrero B, Hernandez AB, Hernandez D, Jarrett K, Li T, Maravillo FJ, Moreno M, Perez A, Rosales NA, Ruegg HF, Valdez J, Bravo KM, Chávez VL, Diaz DI, Enriquez D, Martinez EL, Mendoza Padilla J, Meza J, Nelson SV, Quintero-Ahumada C, Ramirez AM, Hughey JR Microbiol Resour Announc 16-Feb-2023
PMCID:PMC10019264
doi:10.1128/mra.01279-22
PMID:36794956
Taxonomic Review of the Genus Caloptilia Hübner, 1825 (Lepidoptera: Gracillariidae) with Descriptions of Three New Species and Seven Newly Recorded Species from Korea Kim DS, Shin YM, Lee JY, Byun BK Insects 30-Nov-2022
PMCID:PMC9785696
doi:10.3390/insects13121107
PMID:36555017
Variation among the Complete Chloroplast Genomes of the Sumac Species Rhus chinensis: Reannotation and Comparative Analysis Xu Y, Wen J, Su X, Ren Z Genes (Basel) 25-Oct-2022
PMCID:PMC9689920
doi:10.3390/genes13111936
PMID:36360173
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Stepped Geomorphology Shaped the Phylogeographic Structure of a Widespread Tree Species (Toxicodendron vernicifluum, Anacardiaceae) in East Asia Wang L, Li Y, Noshiro S, Suzuki M, Arai T, Kobayashi K, Xie L, Zhang M, He N, Fang Y, Zhang F Front Plant Sci 02-Jun-2022
PMCID:PMC9201781
doi:10.3389/fpls.2022.920054
PMID:35720535
Molecular reassessment of diaporthalean fungi associated with strawberry, including the leaf blight fungus, Paraphomopsis obscurans gen. et comb. nov. (Melanconiellaceae) Udayanga D, Miriyagalla SD, Manamgoda DS, Lewers KS, Gardiennet A, Castlebury LA IMA Fungus 22-Jun-2021
PMCID:PMC8218473
doi:10.1186/s43008-021-00069-9
PMID:34158123
Compatible Mycorrhizal Types Contribute to a Better Design for Mixed Eucalyptus Plantations Qin F, Yu S Front Plant Sci 12-Feb-2021
PMCID:PMC7907608
doi:10.3389/fpls.2021.616726
PMID:33643349
Bacterial ClpP Protease Is a Potential Target for Methyl Gallate Zheng D, Xu Y, Yuan G, Wu X, Li Q Front Microbiol 04-Feb-2021
PMCID:PMC7890073
doi:10.3389/fmicb.2020.598692
PMID:33613462
Flavonoids in myocardial ischemia-reperfusion injury: Therapeutic effects and mechanisms Jia JY, Zang EH, Lv LJ, Li QY, Zhang CH, Xia Y, Zhang L, Dang LS, Li MH Chin Herb Med 28-Oct-2020
PMCID:PMC9476686
doi:10.1016/j.chmed.2020.09.002
PMID:36117755
Evaluation of Nematicidal Activity of Streptomyces yatensis KRA-28 against Meloidogyne incognita Park EJ, Jang HJ, Park CS, Lee SJ, Lee S, Kim KH, Yun BS, Lee SW, Rho MC J Microbiol Biotechnol 27-Mar-2020
PMCID:PMC9728339
doi:10.4014/jmb.1908.08038
PMID:32482935

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 / Triterpenoids
[(3S,6aR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate 5318302 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
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/10.1016/J.BMCL.2009.04.129
beta-Amyrin acetate 92156 Click to see CC(=O)OC1CCC2(C(C1(C)C)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 468.80 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
Glutinol 9932254 Click to see CC1(CCC2(CCC3(C4CC=C5C(C4(CCC3(C2C1)C)C)CCC(C5(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
Cucurbitadienol 14543446 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3(C2CC=C4C3CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methyl-5-oxohept-6-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 44583619 Click to see CC(CCC(=O)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 438.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
(1S,3R,8R,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one 12305362 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
24-Hydroxycycloart-25-en-3-one 15767709 Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C 440.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.BMCL.2009.04.129
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Kaempferol 3-O-(6''-galloyl)-beta-D-glucopyranoside 5491813 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O 600.50 unknown https://doi.org/10.1055/S-2006-960028
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)-2-propen-1-one 5357488 Click to see COC1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)OC)O 284.31 unknown https://doi.org/10.1016/J.BMCL.2009.04.129

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