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Internal ID UUID643fd318c6b53061779834
Scientific name Artemisia sylvatica
Authority Maxim.
First published in Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 161 (1859)

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Synonyms Top

Scientific name Authority First published in
Artemisia nutantiflora Komarov Izv. Bot. Sada Akad. Nauk S.S.S.R. 30: 219 (1932)
Artemisia ussuriensis Poljakov Fl. URSS xxvi. 446 (1961)

Common names Top

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Language Common/alternative name
Chinese 白蒿
Chinese 白沙蒿
Chinese 火绒蒿
Chinese 阴地蒿
Chinese 山艾叶
Chinese 林下艾
Chinese 林地蒿
Chinese 白脸蒿
Chinese 茶绒蒿
Chinese 陰地蒿

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 North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Khabarovsk
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000129175
Tropicos 2726870
KEW urn:lsid:ipni.org:names:180179-1
The Plant List gcc-90117
Open Tree Of Life 723285
Observations.org 146739
NCBI Taxonomy 637489
IPNI 180179-1
iNaturalist 866140
GBIF 3120887
EPPO ARTSY
PFAF Artemisia sylvatica

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
Biodiversity and Spatiotemporal Distribution of Spontaneous Vegetation in Tangdao Bay National Wetland Park, Qingdao City, China Xu Y, Zhang X, Liu X, Zhang Z Int J Environ Res Public Health 16-Sep-2022
PMCID:PMC9517414
doi:10.3390/ijerph191811665
PMID:36141939
An overview on natural farnesyltransferase inhibitors for efficient cancer therapy Dai X, Sun Y, Zhang T, Ming Y, Hongwei G J Enzyme Inhib Med Chem 20-Apr-2020
PMCID:PMC7191900
doi:10.1080/14756366.2020.1732366
PMID:32308053
Raging the War Against Inflammation With Natural Products Attiq A, Jalil J, Husain K, Ahmad W Front Pharmacol 07-Sep-2018
PMCID:PMC6137277
doi:10.3389/fphar.2018.00976
PMID:30245627
Oxidopyrylium [5+2] Cycloaddition Chemistry: Historical Perspective and Recent Advances (2008–2018) Bejcek LP, Murelli RP Tetrahedron 05-Apr-2018
PMCID:PMC6238658
doi:10.1016/j.tet.2018.04.006
PMID:30455508
Mycosphaerellaceae – Chaos or clarity? Videira SI, Groenewald JZ, Nakashima C, Braun U, Barreto RW, de Wit PJ, Crous PW Stud Mycol 28-Sep-2017
PMCID:PMC5693839
doi:10.1016/j.simyco.2017.09.003
PMID:29180830
Sesquiterpene Lactones from Artemisia Genus: Biological Activities and Methods of Analysis Ivanescu B, Miron A, Corciova A J Anal Methods Chem 01-Oct-2015
PMCID:PMC4606394
doi:10.1155/2015/247685
PMID:26495156
Inhibiting NF-κB Activation by Small Molecules As a Therapeutic Strategy Gupta SC, Sundaram C, Reuter S, Aggarwal BB Biochim Biophys Acta 21-May-2010
PMCID:PMC2955987
doi:10.1016/j.bbagrm.2010.05.004
PMID:20493977
Anti-Inflammatory properties of Salograviolide A purified from Lebanese plant Centaurea ainetensis Al-Saghir J, Al-Ashi R, Salloum R, Saliba NA, Talhouk RS, Homaidan FR BMC Complement Altern Med 23-Sep-2009
PMCID:PMC2761300
doi:10.1186/1472-6882-9-36
PMID:19775456
Coumarins of species of the genus Artemisia O. A. Konovalova, K. S. Rybalko, A. I. Shretev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00570201
Inhibitors of inducible nitric oxide synthase expression from Artemisia iwayomogi. Ahn H, Kim JY, Lee HJ, Kim YK, Ryu JH Arch Pharm Res 01-Apr-2003
doi:10.1007/BF02976959
PMID:12735688
Sesquiterpene lactones of Artemisia carruthii T.A. Geissman, T.S. Griffin Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(72)80059-1
Sesquiterpene Lactones, Inhibitors of Farnesyl Protein Transferase, Isolated from the Flower of Artemisia sylvatica Seung-Ho Lee, Hyun-Mi Kang, Ho-Chul Song, Heesoon Lee, Un Chul Lee, Kwang-Hee Son, Sung-Hoon Kim, Byoung-Mog Kwon Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4020(00)00394-X
Arteminolide, an Inhibitor of Farnesyl Transferase from Artemisia sylvatica. Lee SH, Kim MJ, Bok SH, Lee H, Kwon BM, Shin J, Seo Y J Org Chem 02-Oct-1998
doi:10.1021/JO980919P
PMID:11672343

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 / Sesterterpenoids
[(1'R,2'R,3aR,4S,5'S,9'S,9aS,9bR,10'S,11'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxospiro[4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] 3-methylbutanoate 100929405 Click to see CC1=C2C(C3C(C(C1)OC(=O)CC(C)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3)C(=CC2=O)C 590.70 unknown https://doi.org/10.1021/JO980919P
[(1'S,2'R,3R,3aR,4S,5'R,9'S,9aR,9bR,11'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxospiro[4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] acetate 163193249 Click to see CC1=C2C(C3C(C(C1)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3)C(=CC2=O)C 548.60 unknown https://doi.org/10.1016/S0040-4020(00)00394-X
[(1'S,2'R,3R,3aR,4S,5'S,9'S,9aS,9bR,10'S,11'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxospiro[4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] acetate 163006036 Click to see CC1=C2C(C3C(C(C1)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3)C(=CC2=O)C 548.60 unknown https://doi.org/10.1016/S0040-4020(00)00394-X
[(2'S,3aR,5'R,9'S,9aS,9bR,10'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxospiro[4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] acetate 102005656 Click to see CC1=C2C(C3C(C(C1)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3)C(=CC2=O)C 548.60 unknown https://doi.org/10.1016/S0040-4020(00)00394-X
[(2'S,3S,3aR,5'R,9'S,9aS,9bR,10'S)-2'-hydroxy-2',6,9,11'-tetramethyl-6'-methylidene-2,7,7'-trioxospiro[4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-3,15'-8-oxatetracyclo[9.2.2.01,10.05,9]pentadec-12-ene]-4-yl] acetate 102005655 Click to see CC1=C2C(C3C(C(C1)OC(=O)C)C4(CC56C=CC4(C5C7C(CCC6(C)O)C(=C)C(=O)O7)C)C(=O)O3)C(=CC2=O)C 548.60 unknown https://doi.org/10.1016/S0040-4020(00)00394-X
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Rupicolin A 3082541 Click to see CC1=CCC2(C1C3C(C(C=C2C)O)C(=C)C(=O)O3)O 262.30 unknown https://doi.org/10.1016/0031-9422(72)80059-1
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
[(3aR,4S,9aS,9bR)-6,9-dimethyl-3-methylidene-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] acetate 13918464 Click to see CC1=C2C(C3C(C(C1)OC(=O)C)C(=C)C(=O)O3)C(=CC2=O)C 302.32 unknown https://doi.org/10.1016/S0040-4020(00)00394-X
5-(3-Methoxy-2-methyl-5-oxocyclopenten-1-yl)-3-methylidene-4-(3-oxobutyl)oxolan-2-one 14527155 Click to see CC1=C(C(=O)CC1OC)C2C(C(=C)C(=O)O2)CCC(=O)C 292.33 unknown https://doi.org/10.1007/BF02976959
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 unknown https://doi.org/10.1007/BF00570201

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