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Achillea formosa

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fc832df9e9442692103
Scientific name Achillea formosa
Authority (Boiss.) Sch.Bip.
First published in Flora 38: 13. (1855)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anacyclus membranaceus Benth. & Hook.f. Gen. Pl. [Bentham & Hooker f.] 2(1): 419. 1873 [7-9 Apr 1873]

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Achillea formosa subsp. amanica (Rech.f.) Ehrend. & Y.P.Guo Willdenowia 35(1): 51 (2005)
Achillea formosa subsp. formosa (Boiss.) Sch.Bip.

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000020550
KEW urn:lsid:ipni.org:names:173981-1
The Plant List gcc-119873
Open Tree Of Life 4416
NCBI Taxonomy 359922
IPNI 173981-1
iNaturalist 834242
GBIF 3120305

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
Flavonoid Aglycones in the Leaf Exudate of the Genus Leucocyclus (Compositae) Karin M. Valant-Vetschera, Eckhard Wollenweber Walter de Gruyter GmbH 02-Aug-2018
doi:10.1515/ZNC-1989-3-423
Structure-activity relationships of trigeminal effects for artificial and naturally occurring alkamides related to spilanthol Jakob P. Ley, Gerhard Krammer, Jan Looft, Gerald Reinders, Heinz-Jürgen Bertram Elsevier 07-Sep-2007
doi:10.1016/S0167-4501(06)80006-3
Amides from Achillea species and Leucocyclus formosus Harald Greger, Michael Grenz, Ferdinand Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(81)83098-1
Flavonoid pattern and systematics of the genus Leucocyclus Karin Valant-Vetschera Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)82417-6
Flavonoid aglycones from the leaf surfaces of some Achillea species E. Wollenweber, K.M. Valant-Vetschera, S. Ivancheva, B. Kuzmanov Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81506-X

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 / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E)-N-(2-methylpropyl)trideca-2,4-dienamide 11065358 Click to see CCCCCCCCC=CC=CC(=O)NCC(C)C 265.40 unknown https://doi.org/10.1016/0031-9422(81)83098-1
(2E,4E)-N-Isobutylundeca-2,4-dienamide 11075468 Click to see CCCCCCC=CC=CC(=O)NCC(C)C 237.38 unknown https://doi.org/10.1016/S0167-4501(06)80006-3
https://doi.org/10.1016/0031-9422(81)83098-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
6-[(2R,3S,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 163006183 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(O5)CO)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)81506-X
https://doi.org/10.1016/S0031-9422(00)82417-6
6-[3,4-Dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 137832345 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(O5)CO)O)O)O)O 564.50 unknown https://doi.org/10.1016/S0031-9422(00)81506-X
https://doi.org/10.1016/S0031-9422(00)82417-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1515/ZNC-1989-3-423
> 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/10.1515/ZNC-1989-3-423
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown https://doi.org/10.1515/ZNC-1989-3-423
Cirsiliol 160237 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)OC 330.29 unknown https://doi.org/10.1515/ZNC-1989-3-423
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1515/ZNC-1989-3-423
Eupatorin 97214 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown https://doi.org/10.1515/ZNC-1989-3-423
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown https://doi.org/10.1515/ZNC-1989-3-423

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