Achillea filipendulina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Achillea filipendulina - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Details Top

Internal ID UUID643fcac770f2d641107668
Scientific name Achillea filipendulina
Authority Lam.
First published in Encycl. 1: 27 (1783)

Description Top

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Achillea filipendulina, also known as yarrow, fernleaf yarrow, milfoil, or nosebleed, is a flowering plant native to central and southwestern Asia. It has fern-like foliage and large, yellow flowers that bloom in mid to late summer. This herbaceous perennial is commonly grown as an ornamental plant in temperate regions and is drought tolerant when established. While the species itself is not as popular, there are many improved cultivars that have gained recognition, such as 'Coronation Gold' and 'Moonshine'. It can be propagated by seed or root division in the spring.

Synonyms Top

Scientific name Authority First published in
Achillea eupatorium M.Bieb. Tabl. Prov. Mer Casp. : 119 (1798)
Tanacetum angulatum Willd. Sp. Pl., ed. 4 , 3: 1811 (1803)
Achillea filicifolia M.Bieb. Fl. Taur.-Caucas. 2: 338 (1808)

Common names Top

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Language Common/alternative name
English fernleaf yarrow
Spanish milenrama dorada
Arabic قيصوم سرخسي
Czech řebříček tužebníkovitý
Danish pragt-røllike
German goldgarbe
Persian بومادران سرخسی
Finnish kultakärsämö
French achillée à feuilles de fougère
French achillée eupatoire
French achillée filipendule
Hungarian sárga cickafark
Hungarian jószagú cickafark
Hungarian páfránylevelű cickafark
Dutch geel duizendblad
Polish krwawnik wiązówkowaty
Slovenian rumeni rman
Swedish praktröllika
tg Бӯмодарони сарахсӣ
Chinese 凤尾蓍

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Turkey
  • Europe
    • Eastern Europe
      • Ukraine
    • Middle Europe
      • Belgium
      • Czechoslovakia
      • Germany
      • Poland
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Italy
      • Romania
    • Southwestern Europe
      • France
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • Northeastern U.S.A.
      • Michigan
      • New York
      • Vermont
    • Southwestern U.S.A.
      • California
      • Utah

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000041091
Canadensys 2764
USDA Plants ACFI
Tropicos 2701617
INPN 79890
Flora of Italy 8381
KEW urn:lsid:ipni.org:names:173972-1
The Plant List gcc-139741
Plantarium 303
Missouri Botanical Garden 277264
Open Tree Of Life 245238
NCBI Taxonomy 282736
NBN Atlas NBNSYS0000034144
Nature Serve 2.154410
IPNI 173972-1
iNaturalist 157924
GBIF 3120284
Freebase /m/02qc621
EPPO ACHFI
EOL 578297
Calflora (Californian flora) 8471
USDA GRIN 1263
Wikipedia Achillea_filipendulina

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
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Searching for Natural Plants with Antimelanogenesis and Antityrosinase Properties for Cosmeceutical or Nutricosmetics Applications: A Systematic Review Tung XY, Yip JQ, Gew LT ACS Omega 06-Sep-2023
PMCID:PMC10515176
doi:10.1021/acsomega.3c02994
PMID:37744793
Chemical Composition and Antiplasmodial Activity of the Essential Oil of Rhododendron subarcticum Leaves from Nunavik, Québec, Canada Séguin JC, Gagnon D, Bélanger S, Richard D, Fernandez X, Boudreau S, Voyer N ACS Omega 01-May-2023
PMCID:PMC10193425
doi:10.1021/acsomega.3c00235
PMID:37214733
Exploiting the bioactive properties of essential oils and their potential applications in food industry Pandey VK, Tripathi A, Srivastava S, Dar AH, Singh R, Farooqui A, Pandey S Food Sci Biotechnol 24-Mar-2023
PMCID:PMC10130317
doi:10.1007/s10068-023-01287-0
PMID:37123062
Production of herbal toothpaste: Physical, organoleptic, phyto-compound, and antimicrobial properties Oluwasina OO, Idris SO, Ogidi CO, Igbe FO Heliyon 28-Feb-2023
PMCID:PMC10009007
doi:10.1016/j.heliyon.2023.e13892
PMID:36923892
The Evanescent Bouquet of Individual Bear Fingerprint Mazzatenta A, Fiorito S, Guadagnini R, Genovese S, Valentini A, Bonadiman F, Guadagnini S, Epifano F, Mollica A Animals (Basel) 06-Jan-2023
PMCID:PMC9854677
doi:10.3390/ani13020220
PMID:36670761
An in vitro Propagation of Aspilia africana (Pers.) C. D. Adams, and Evaluation of Its Anatomy and Physiology of Acclimatized Plants Okello D, Yang S, Komakech R, Rahmat E, Chung Y, Gang R, Kim YG, Omujal F, Kang Y Front Plant Sci 29-Jul-2021
PMCID:PMC8358661
doi:10.3389/fpls.2021.704896
PMID:34394159
Variable Secondary Metabolite Profiles Across Cultivars of Curcuma longa L. and C. aromatica Salisb. Kulyal P, Acharya S, Ankari AB, Kokkiripati PK, Tetali SD, Raghavendra AS Front Pharmacol 30-Jun-2021
PMCID:PMC8278146
doi:10.3389/fphar.2021.659546
PMID:34276362
Achillea Species as Sources of Active Phytochemicals for Dermatological and Cosmetic Applications Strzępek-Gomółka M, Gaweł-Bęben K, Kukula-Koch W Oxid Med Cell Longev 25-Mar-2021
PMCID:PMC8018854
doi:10.1155/2021/6643827
PMID:33833853
Evaluation of the Toxicity of Satureja intermedia C. A. Mey Essential Oil to Storage and Greenhouse Insect Pests and a Predator Ladybird Ebadollahi A, Setzer WN Foods 02-Jun-2020
PMCID:PMC7353542
doi:10.3390/foods9060712
PMID:32498219
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
Isolation and identification of L-asparaginase-producing endophytic fungi from the Asteraceae family plant species of Iran Hatamzadeh S, Rahnama K, Nasrollahnejad S, Fotouhifar KB, Hemmati K, White JF, Taliei F PeerJ 14-Jan-2020
PMCID:PMC6968492
doi:10.7717/peerj.8309
PMID:31976175
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
A new perspective on evaluation of medicinal plant biological activities: The correlation between phytomics and matrix metalloproteinases activities of some medicinal plants Gonulalan EM, Nemutlu E, Demirezer LO Saudi Pharm J 11-Jan-2019
PMCID:PMC6438986
doi:10.1016/j.jsps.2019.01.006
PMID:30976190
The changing face of farmers’ home gardens: a diachronic analysis from Sillian (Eastern Tyrol, Austria) Vogl-Lukasser B, Vogl CR J Ethnobiol Ethnomed 29-Oct-2018
PMCID:PMC6205796
doi:10.1186/s13002-018-0262-3
PMID:30373655

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
2-Methyl-2,4-hexadiene 5367611 Click to see CC=CC=C(C)C 96.17 unknown https://doi.org/10.1007/BF00713327
2-Methylhexa-2,4-diene 520396 Click to see CC=CC=C(C)C 96.17 unknown https://doi.org/10.1007/BF00713327
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2007-969446
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown https://doi.org/10.1055/S-2007-969446
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1S,3R,5S)-3-hydroperoxy-6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptane 13819205 Click to see CC1(C2CC1C(=C)C(C2)OO)C 168.23 unknown https://doi.org/10.1002/ARDP.19943270502
6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptane-3-peroxol 13819203 Click to see CC1(C2CC1C(=C)C(C2)OO)C 168.23 unknown https://doi.org/10.1002/ARDP.19943270502
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,4R)-3-ethenyl-2,5-dimethylhex-5-ene-2,4-diol 162908416 Click to see CC(=C)C(C(C=C)C(C)(C)O)O 170.25 unknown https://doi.org/10.1002/ARDP.19943270502
(3R,4S)-2,5-dimethyl-3-vinyl-hex-5-ene-2,4-diol 5273756 Click to see CC(=C)C(C(C=C)C(C)(C)O)O 170.25 unknown https://doi.org/10.1002/ARDP.19943270502
(3S,4R)-3-ethenyl-4-hydroperoxy-2,5-dimethylhex-5-en-2-ol 10058252 Click to see CC(=C)C(C(C=C)C(C)(C)O)OO 186.25 unknown https://doi.org/10.1002/ARDP.19943270502
(3S,4S)-3-ethenyl-4-hydroperoxy-2,5-dimethylhex-5-en-2-ol 101663663 Click to see CC(=C)C(C(C=C)C(C)(C)O)OO 186.25 unknown https://doi.org/10.1002/ARDP.19943270502
3-Ethenyl-2,5-dimethylhex-5-ene-2,4-diol 21158012 Click to see CC(=C)C(C(C=C)C(C)(C)O)O 170.25 unknown https://doi.org/10.1002/ARDP.19943270502
3-Ethenyl-4-hydroperoxy-2,5-dimethylhex-5-en-2-ol 85106747 Click to see CC(=C)C(C(C=C)C(C)(C)O)OO 186.25 unknown https://doi.org/10.1002/ARDP.19943270502
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
Ascaridole 10545 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown https://doi.org/10.1002/ARDP.19943270502
cis-Isoascaridole 6430795 Click to see CC(C)C12CCC(C=C1)(OO2)C 168.23 unknown https://doi.org/10.1002/ARDP.19943270502
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin 660 Click to see C1CC(=O)OC2=CC=CC=C21 148.16 unknown https://doi.org/10.1007/BF02238223
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1007/BF02238223

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