Artemisia keiskeana - Unknown
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Internal ID UUID643fc5eb3b5b2032490991
Scientific name Artemisia keiskeana
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 2: 176 (1866)

Description Top

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Synonyms Top

Scientific name Authority First published in
Artemisia morrisonensis var. minima Pamp. Nuovo Giorn. Bot. Ital., n.s., 34: 682 (1927)

Common names Top

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Language Common/alternative name
Japanese イヌヨモギ
Chinese 臭蒿
Chinese 庵 (艹闾)子
Chinese 庵闾
Chinese 菴蔺(庵蔺)
Chinese 庵蒿
Chinese 菴芦
Chinese 菴闾
Chinese 菴闾子
Chinese 菴𰱩
Chinese 覆闾
Chinese 菴閭

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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
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000001132
Tropicos 2701783
KEW urn:lsid:ipni.org:names:179677-1
The Plant List gcc-101077
Open Tree Of Life 1034915
Observations.org 130218
NCBI Taxonomy 637481
IPNI 179677-1
iNaturalist 709033
GBIF 3121055
EPPO ARTKE

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)!
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Title Authors Publication Released IDs
Research Advances on Health Effects of Edible Artemisia Species and Some Sesquiterpene Lactones Constituents Trendafilova A, Moujir LM, Sousa PM, Seca AM Foods 30-Dec-2020
PMCID:PMC7823681
doi:10.3390/foods10010065
PMID:33396790
Isofraxidin: Synthesis, Biosynthesis, Isolation, Pharmacokinetic and Pharmacological Properties Majnooni MB, Fakhri S, Shokoohinia Y, Mojarrab M, Kazemi-Afrakoti S, Farzaei MH Molecules 27-Apr-2020
PMCID:PMC7248759
doi:10.3390/molecules25092040
PMID:32349420
An rbcL reference library to aid in the identification of plant species mixtures by DNA metabarcoding Bell KL, Loeffler VM, Brosi BJ Appl Plant Sci 10-Mar-2017
PMCID:PMC5357121
doi:10.3732/apps.1600110
PMID:28337390
Description and DNA barcoding of Tipula ( Pterelachisus) recondita sp. n. from the Palaearctic region (Diptera, Tipulidae) Pilipenko VE, Salmela J, Vesterinen EJ Zookeys 08-May-2012
PMCID:PMC3349062
doi:10.3897/zookeys.192.2364
PMID:22639539
Four new coumarin derivatives from Artemisia keiskeana. Kwak JH, Lee KB, Schmitz FJ J Nat Prod 01-Aug-2001
doi:10.1021/NP010103A
PMID:11520232
Artekeiskeanin A: a new coumarin-monoterpene ether from Artemisia keiskeana. Kwak JH, Jang WY, Zee OP, Lee KR Planta Med 01-Oct-1997
doi:10.1055/S-2006-957741
PMID:9342955

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 / Glycerolipids / Glycosylglycerols / Glycosyldiacylglycerols
[2-Octadeca-6,9,12,15-tetraenoyloxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropyl] octadeca-6,9,12,15-tetraenoate 74000084 Click to see CCC=CCC=CCC=CCC=CCCCCC(=O)OCC(COC1C(C(C(C(O1)CO)O)O)O)OC(=O)CCCCC=CCC=CCC=CCC=CCC 771.00 unknown https://doi.org/10.1021/NP010103A
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
7-(8-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6-methoxychromen-2-one 85318069 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)CO 344.40 unknown https://doi.org/10.1021/NP010103A
7-(8-Hydroxy-3,7-dimethylocta-2,6-dienoxy)-6,8-dimethoxychromen-2-one 73118360 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)CCC=C(C)CO 374.40 unknown https://doi.org/10.1021/NP010103A
8-(6-Methoxy-2-oxochromen-7-yl)oxy-2,6-dimethylocta-2,6-dienal 54322219 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)C=O 342.40 unknown https://doi.org/10.1055/S-2006-957741
Artekeiskeanin A 24823845 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)C=O 342.40 unknown https://doi.org/10.1055/S-2006-957741
Artekeiskeanol A 11131723 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)CO 344.40 unknown https://doi.org/10.1021/NP010103A
Artekeiskeanol B 10925981 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1)OC)CCC=C(C)CO 344.40 unknown https://doi.org/10.1021/NP010103A
Artekeiskeanol C 10883271 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)CCC=C(C)CO 374.40 unknown https://doi.org/10.1021/NP010103A
Artekeiskeanol D 11824908 Click to see CC(=CCOC1=C(C=C2C=CC(=O)OC2=C1OC)OC)CCC=C(C)CO 374.40 unknown https://doi.org/10.1021/NP010103A
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1055/S-2006-957741
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1055/S-2006-957741
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2006-957741
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/10.1055/S-2006-957741
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2006-957741
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1055/S-2006-957741
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-2006-957741
> Organic acids and derivatives / Peptidomimetics / Depsipeptides / Cyclic depsipeptides
Tripropeptin E 139588376 Click to see CC(C)CCCCCCCCCCCC1CC(=O)NC(C(=O)N2CCCC2C(=O)N3CCCC3C(=O)NC(C(=O)NC(C(=O)NC(C(=O)N4CCC(C4C(=O)NC(C(=O)O1)C(C(=O)O)O)O)CO)C(C(=O)O)O)CCCN=C(N)N)C(C)O 1182.30 unknown https://doi.org/10.1021/NP010103A
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dracunculin 5319474 Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2 220.18 unknown https://doi.org/10.1055/S-2006-957741
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Fraxidin 3083616 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)OC 222.19 unknown https://doi.org/10.1021/NP010103A
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Daphnoretin 5281406 Click to see COC1=C(C=C2C(=C1)C=C(C(=O)O2)OC3=CC4=C(C=C3)C=CC(=O)O4)O 352.30 unknown https://doi.org/10.1021/NP010103A
Isofraxidin 5318565 Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O 222.19 unknown https://doi.org/10.1021/NP010103A
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1055/S-2006-957741

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