Scientific name	Authority	First published in
Achillea sericea	Vis. ex Rchb.	Fl. Germ. Excurs. ii. 228
Achillea clavennae f. velebitica	Bjelčić	Acta Bot. Croat. 43: 76 (1984) (1984)
Achillea clavennae f. volujakensis	Bjelčić & E.Mayer	Acta Bot. Croat. 43: 76 (1984) (1984)
Achillea visianii	Dalla Torre	Alpenfl. 224 (1899) (1899)
Achillea clavennae var. visianii	Beck
Achillea argentea	Salisb.	Prodr. Stirp. Chap. Allerton : 204 (1796)
Achillea argentea	Vis.	Flora 12(1, Ergänzungsbl.): 22. 1829
Achillea capitata	Willd.	Tract. Ach. 17.
Achillea millii	Heldr. ex Boiss.	Fl. Orient. , Suppl.: 296 (1888)
Achillea intercedens	Dalla Torre	Alpenfl. 224 (1899) (1899)
Achillea clavennae var. intercedens	Heimerl	Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 48: 152 (1884)
Achillea tyrolensis	Wender.	Flora 9(1): 353 (1826)
Ptarmica clavennae	DC.	Prodr. 6: 21 (1838)
Chamaemelum clavennae	E.H.L.Krause	Deutschl. Fl. (Sturm), ed. 2. 13: 213 (1905)

Common names Top

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Filter by language:

Language	Common/alternative name
English	silvery yarrow
German	bittere schafgarbe
German	almwermut
German	steinraute
German	weiße schafgarbe
German	weißer speik
Persian	بومادران سیمین
Croatian	bijeli stolisnik
Slovenian	planinski rman
Slovenian	planinski pelin

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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No forms added yet.

Germination/Propagation Top

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Maintain seeds at a constant 10°C.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Europe click to expand
- Middle Europe
  - Austria
  - Germany
  - Switzerland
- Southeastern Europe
  - Albania
  - Italy
  - Yugoslavia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000005461
USDA Plants	ACCL3
Tropicos	100393315
Flora of Italy	5637
KEW	urn:lsid:ipni.org:names:173892-1
The Plant List	gcc-105259
Open Tree Of Life	768363
Observations.org	113850
NCBI Taxonomy	282726
IPNI	173892-1
iNaturalist	55650
GBIF	3120117
Freebase	/m/0xp_gpr
EPPO	ACHCL
EOL	6172909
Elurikkus	730593
USDA GRIN	1261
Wikipedia	Achillea_clavennae

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

Traditional medicinal plants in South Tyrol (northern Italy, southern Alps): biodiversity and use

Petelka J, Plagg B, Säumel I, Zerbe S

J Ethnobiol Ethnomed

26-Nov-2020

PMCID:	PMC7690129
doi:	10.1186/s13002-020-00419-8
PMID:	33243238

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

Antimicrobial Properties of Plant Essential Oils against Human Pathogens and Their Mode of Action: An Updated Review

Swamy MK, Akhtar MS, Sinniah UR

Evid Based Complement Alternat Med

20-Dec-2016

PMCID:	PMC5206475
doi:	10.1155/2016/3012462
PMID:	28090211

Volatile oils: Potential agents for the treatment of respiratory infections

Pasdaran A, Pasdaran A, Sheikhi D

The Microbiology of Respiratory System Infections

05-Aug-2016

PMCID:	PMC7149900
doi:	10.1016/B978-0-12-804543-5.00016-6

Efficacy of cinnamon bark oil and cinnamaldehyde on anti-multidrug resistant Pseudomonas aeruginosa and the synergistic effects in combination with other antimicrobial agents

Utchariyakiat I, Surassmo S, Jaturanpinyo M, Khuntayaporn P, Chomnawang MT

BMC Complement Altern Med

01-Jun-2016

PMCID:	PMC4888607
doi:	10.1186/s12906-016-1134-9
PMID:	27245046

In vitro anti-oxidant, cytotoxic and pro-apoptotic effects of Achillea teretifolia Willd extracts on human prostate cancer cell lines

Bali EB, Açık L, Elçi P, Sarper M, Avcu F, Vural M

Pharmacogn Mag

01-Oct-2015

PMCID:	PMC4653342
doi:	10.4103/0973-1296.166060
PMID:	26664020

A DNA Barcoding Approach to Characterize Pollen Collected by Honeybees

Galimberti A, De Mattia F, Bruni I, Scaccabarozzi D, Sandionigi A, Barbuto M, Casiraghi M, Labra M

PLoS One

08-Oct-2014

PMCID:	PMC4190116
doi:	10.1371/journal.pone.0109363
PMID:	25296114

The Volatile Compounds and Bioactivity of Achillea sieheana Stapf. (Asteraceae)

Albayrak S

Iran J Pharm Res

01-Jan-2013

PMCID:	PMC3813214
PMID:	24250570

Antiproliferative effect of flavonoids and sesquiterpenoids from Achillea millefolium s.l. on cultured human tumour cell lines.

Csupor-Löffler B, Hajdú Z, Zupkó I, Réthy B, Falkay G, Forgo P, Hohmann J

Phytother Res

01-May-2009

doi:	10.1002/PTR.2697
PMID:	19107850

An examination of antibacterial and antifungal properties of constituents described in traditional Ulster cures and remedies

Woods-Panzaru S, Nelson D, McCollum G, Ballard LM, Millar BC, Maeda Y, Goldsmith CE, Rooney PJ, Loughrey A, Rao JR, Moore JE

Ulster Med J

01-Jan-2009

PMCID:	PMC2629014
PMID:	19252724

Cytotoxic constituents of Achillea clavennae from Montenegro.

Trifunović S, Vajs V, Juranić Z, Zizak Z, Tesević V, Macura S, Milosavljević S

Phytochemistry

01-May-2006

doi:	10.1016/J.PHYTOCHEM.2006.02.026
PMID:	16616262

Antibacterial activity of Achillea clavennae essential oil against respiratory tract pathogens.

Skocibusić M, Bezić N, Dunkić V, Radonić A

Fitoterapia

01-Dec-2004

doi:	10.1016/J.FITOTE.2004.05.009
PMID:	15567252

Phytochemical Profile Top

Add a new one!

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
> Lignans, neolignans and related compounds / Furanoid lignans
Episesamin	5204	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)-	6549	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	https://doi.org/10.1016/J.FITOTE.2004.05.009
Myrcene	31253	Click to see CC(=CCCC(=C)C=C)C	136.23	unknown	https://doi.org/10.1016/J.FITOTE.2004.05.009
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
Camphene	6616	Click to see CC1(C2CCC(C2)C1=C)C	136.23	unknown	https://doi.org/10.1016/J.FITOTE.2004.05.009
Camphor	2537	Click to see CC1(C2CCC1(C(=O)C2)C)C	152.23	unknown	https://doi.org/10.1016/J.FITOTE.2004.05.009
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5R)-5-[(2R,5R)-2,5-dihydroxy-6-methylhept-6-en-2-yl]-2-methylcyclohex-2-en-1-one	154496340	Click to see CC1=CCC(CC1=O)C(C)(CCC(C(=C)C)O)O	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(5R)-5-[(E,2R)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-2-methylcyclohex-2-en-1-one	162965196	Click to see CC1=CCC(CC1=O)C(C)(CC=CC(C)(C)O)O	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(5R)-5-[(E,2R)-6-hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl]-2-methylcyclohex-2-en-1-one	162909534	Click to see CC1=CCC(CC1=O)C(C)(CC=CC(C)(C)OO)O	268.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
5-(2,5-Dihydroxy-6-methylhept-6-en-2-yl)-2-methylcyclohex-2-en-1-one	85585508	Click to see CC1=CCC(CC1=O)C(C)(CCC(C(=C)C)O)O	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
5-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-2-methylcyclohex-2-en-1-one	75144793	Click to see CC1=CCC(CC1=O)C(C)(CC=CC(C)(C)O)O	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
5-(6-Hydroperoxy-2-hydroxy-6-methylhept-4-en-2-yl)-2-methylcyclohex-2-en-1-one	162909533	Click to see CC1=CCC(CC1=O)C(C)(CC=CC(C)(C)OO)O	268.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
Indicumenone	46173956	Click to see CC1=CCC(CC1=O)C(C)(CC=CC(C)(C)O)O	252.35	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(11-Chloro-2,12-dihydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-3-yl) acetate	162996535	Click to see CC(=O)OC1CC2C(C3C(C(C4C3(C1(C)O)O4)O)(C)Cl)OC(=O)C2=C	372.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(12-Chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-3-yl) acetate	162846245	Click to see CC(=O)OC1CC2C(C3C(C(C4C3(C1(C)O)O4)Cl)(C)O)OC(=O)C2=C	372.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(1R,2R,5S,9S,10R,11R,12R,13S)-11-chloro-2,12-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one	162971086	Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)Cl)O)OC(=O)C2=C)O	314.76	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(1R,2R,5S,9S,10S,11S,12S,13R)-12-chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one	76853548	Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)O)Cl)OC(=O)C2=C)O	314.76	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(1S,2R,5S,9S,10S,11R,12R,13S)-12-chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one	76853527	Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)O)Cl)OC(=O)C2=C)O	314.76	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
(3aS,4R,6aS,9aR,9bS)-4,6a-dihydroxy-6,9-dimethyl-3-methylidene-4,7,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-2-one	162912238	Click to see CC1=CCC2(C1C3C(C(C=C2C)O)C(=C)C(=O)O3)O	262.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
[(1R,2R,3R,5S,9S,10R,11R,12R,13S)-11-chloro-2,12-dihydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-3-yl] acetate	162996536	Click to see CC(=O)OC1CC2C(C3C(C(C4C3(C1(C)O)O4)O)(C)Cl)OC(=O)C2=C	372.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
[(1S,2R,3R,5S,9S,10S,11R,12R,13S)-12-chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-3-yl] acetate	162846246	Click to see CC(=O)OC1CC2C(C3C(C(C4C3(C1(C)O)O4)Cl)(C)O)OC(=O)C2=C	372.80	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
[(1S,2R,3R,5S,9S,10S,11R,13S,14R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,15-trioxapentacyclo[8.5.0.01,14.05,9.011,13]pentadecan-3-yl] acetate	11631405	Click to see CC(=O)OC1CC2C(C3C4(C(O4)C5C3(C1(C)O)O5)C)OC(=O)C2=C	336.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
[(1S,2R,3R,5S,9S,10S,11R)-2-hydroxy-2,11-dimethyl-6-methylidene-7-oxo-8,12,13-trioxatetracyclo[9.2.2.01,10.05,9]pentadec-14-en-3-yl] acetate	85471523	Click to see CC(=O)OC1CC2C(C3C4(C=CC3(C1(C)O)OO4)C)OC(=O)C2=C	336.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
11-Chloro-2,12-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one	14137584	Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)Cl)O)OC(=O)C2=C)O	314.76	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
12-Chloro-2,11-dihydroxy-2,11-dimethyl-6-methylidene-8,14-dioxatetracyclo[8.4.0.01,13.05,9]tetradecan-7-one	75058626	Click to see CC1(CCC2C(C3C14C(O4)C(C3(C)O)Cl)OC(=O)C2=C)O	314.76	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
Artecanin	442147	Click to see CC1(CCC2C(C3C14C(O4)C5C3(O5)C)OC(=O)C2=C)O	278.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
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/J.PHYTOCHEM.2006.02.026
Rupicolin B	3082542	Click to see CC1=CCC2(C1C3C(C(CC2=C)O)C(=C)C(=O)O3)O	262.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
3-(hydroxymethyl)-6-(1H-indol-3-ylmethylidene)-3-methoxypiperazine-2,5-dione	72501042	Click to see COC1(C(=O)NC(=CC2=CNC3=CC=CC=C32)C(=O)N1)CO	301.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Isofraxidin	5318565	Click to see COC1=C(C(=C2C(=C1)C=CC(=O)O2)OC)O	222.19	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Centaureidin	5315773	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	360.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026 https://doi.org/10.1002/PTR.2697
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin	5320351	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC	388.40	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
Casticin	5315263	Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O	374.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026
Penduletin	5320462	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC	344.30	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2006.02.026

Biological Material Top

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Achillea clavennae

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top