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Achillea erba-rotta

Achillea erba-rotta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fcffa77cc5286050918
Scientific name Achillea erba-rotta
Authority All.
First published in Auct. Syn. Meth. Stirp. Hort. Regii Taur. : 17 (1773)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ptarmica erba-rotta (All.) DC. Prodr. 6: 22 (1838)
Ptarmica herba-rota DC. Prodr. 6: 22 (1838)

Common names Top

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Language Common/alternative name
English simple leaved milfoil
Arabic أخيليا دولابية
Persian بومادران سادهبرگ
Chinese 单叶蓍

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Achillea erba-rotta subsp. erba-rotta All.
Achillea erba-rotta subsp. moschata (Wulfen) I.Richardson Bot. J. Linn. Soc. 71(4): 271 (1976)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Austria
      • Switzerland
    • Southeastern Europe
      • Italy
    • Southwestern Europe
      • France

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000095159
USDA Plants ACER7
Tropicos 2701615
INPN 79887
Flora of Italy 9844
KEW urn:lsid:ipni.org:names:50869252-1
The Plant List gcc-51344
Open Tree Of Life 245234
NCBI Taxonomy 282734
IPNI 50869252-1
iNaturalist 487757
GBIF 3120266
Freebase /m/0h7n7sk
EPPO ACHER
EOL 6172969
USDA GRIN 1265
Wikipedia Achillea_erba-rotta

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
N-Alkyl dien- and trienamides from the roots of Otanthus maritimus with binding affinity for opioid and cannabinoid receptors. Ruiu S, Anzani N, Orrù A, Floris C, Caboni P, Maccioni E, Distinto S, Alcaro S, Cottiglia F Bioorg Med Chem 15-Nov-2013
doi:10.1016/J.BMC.2013.09.017
PMID:24095014
Essential Oils and Chromosome Numbers From Italian<i>Achillea</i>Species Massimo Maffei, Franco Chialva, Arnaldo Codignola Informa UK Limited 24-Apr-2012
doi:10.1080/10412905.1989.9697751
Hepatoprotective amide constituents from the fruit of Piper chaba: Structural requirements, mode of action, and new amides. Matsuda H, Ninomiya K, Morikawa T, Yasuda D, Yamaguchi I, Yoshikawa M Bioorg Med Chem 15-Oct-2009
doi:10.1016/J.BMC.2009.08.050
PMID:19775895
Piperidinyl amides with insecticidal activity from the maritime plant Otanthus maritimus. Christodoulopoulou L, Tsoukatou M, Tziveleka LA, Vagias C, Petrakis PV, Roussis V J Agric Food Chem 09-Mar-2005
doi:10.1021/JF0481857
PMID:15740019
Leaf exudate flavonoids of Achillea clusiana Tausch and related species Karin M. Valant-Vetschera, Eckhard Wollenweber Elsevier BV 12-May-2003
doi:10.1016/0305-1978(96)88878-8
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
Pyrrolidine and piperidine amides from Achillea Harald Greger, Christa Zdero, Ferdinand Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80494-X
Isobutylamides from the fruit of Zanthoxylum integrifoliolum I Chen Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00175-2
In vitro inhibition of cyclooxygenase and 5-lipoxygenase by alkamides from Echinacea and Achillea species. Müller-Jakic B, Breu W, Pröbstle A, Redl K, Greger H, Bauer R Planta Med 01-Feb-1994
doi:10.1055/S-2006-959404
PMID:8134414

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
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide 73355665 Click to see CCCCCC=CCCC=CC=CC(=O)NCC(C)C 277.40 unknown https://doi.org/10.1016/0031-9422(81)83098-1
https://doi.org/10.1016/J.BMC.2009.08.050
https://doi.org/10.1016/S0031-9422(00)80494-X
https://doi.org/10.1016/J.BMC.2013.09.017
https://doi.org/10.1021/JF0481857
Anacyclin 5281131 Click to see CCCC#CC#CCCC=CC=CC(=O)NCC(C)C 271.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
CID 133682 133682 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)C 275.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
Hazaleamide 6439588 Click to see CCC=CCC=CCCC=CC=CC(=O)NCC(C)C 275.40 unknown https://doi.org/10.1016/S0031-9422(99)00175-2
https://doi.org/10.1016/0031-9422(81)83098-1
https://doi.org/10.1016/S0031-9422(00)80494-X
https://doi.org/10.1021/JF0481857
N-(2-methylpropyl)-2,4-tetradecadiene-8,10-diynamide 441492 Click to see CCCC#CC#CCCC=CC=CC(=O)NCC(C)C 271.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
N-(2-Methylpropyl)tetradeca-2,4,12-triene-8,10-diynamide 71336688 Click to see CC=CC#CC#CCCC=CC=CC(=O)NCC(C)C 269.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
N-(2-methylpropyl)tetradeca-2,4,8-trienamide 86017492 Click to see CCCCCC=CCCC=CC=CC(=O)NCC(C)C 277.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
Tetradeca-2,4,10-triene-8-ynoic acid isobutylamide 86110935 Click to see CCCC=CC#CCCC=CC=CC(=O)NCC(C)C 273.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9-Hydroxy-10,12-octadecadienoic acid 5282945 Click to see CCCCCC=CC=CC(CCCCCCCC(=O)O)O 296.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1S,5S,8R,9S,11R,14R,16S,17R,18R,19S)-10,19-dihydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-3-one 101930090 Click to see CC12CC(=O)CC34C1C5CC67C3C(C(C(C6C4N5C2)O)C(=C)C7)O 327.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> 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/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R)-2-methyl-5-propan-2-ylbicyclo[3.1.0]hex-2-ene 6451618 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697751
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697751
Bicyclo[3.1.0]hex-2-ene, 2-methyl-5-(1-methylethyl)- 17868 Click to see CC1=CCC2(C1C2)C(C)C 136.23 unknown https://doi.org/10.1080/10412905.1989.9697751
Bornyl acetate 6448 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown https://doi.org/10.1080/10412905.1989.9697751
Camphor 2537 Click to see CC1(C2CCC1(C(=O)C2)C)C 152.23 unknown https://doi.org/10.1080/10412905.1989.9697751
Myrtenal 61130 Click to see CC1(C2CC=C(C1C2)C=O)C 150.22 unknown https://doi.org/10.1080/10412905.1989.9697751
Thujone 261491 Click to see CC1C2CC2(CC1=O)C(C)C 152.23 unknown https://doi.org/10.1080/10412905.1989.9697751
trans-Borneol 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Carveol 7438 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown https://doi.org/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1989.9697751
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1989.9697751
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1989.9697751
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown https://doi.org/10.1080/10412905.1989.9697751
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/10412905.1989.9697751
cis-Nerolidol 5320128 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1989.9697751
trans-Nerolidol 5284507 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1080/10412905.1989.9697751
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(S,1Z,6Z)-8-Isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene 91723653 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1080/10412905.1989.9697751
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Jasmone 1549018 Click to see CCC=CCC1=C(CCC1=O)C 164.24 unknown https://doi.org/10.1080/10412905.1989.9697751
> Organoheterocyclic compounds / Pyrrolidines / N-acylpyrrolidines
(2E,4E,10Z)-1-pyrrolidin-1-yltetradeca-2,4,10-trien-8-yn-1-one 21681004 Click to see CCCC=CC#CCCC=CC=CC(=O)N1CCCC1 271.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
https://doi.org/10.1055/S-2006-959404
(2E,4E)-1-(Pyrrolidin-1-yl)tetradeca-2,4-dien-1-one 10923868 Click to see CCCCCCCCCC=CC=CC(=O)N1CCCC1 277.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
1-Pyrrolidin-1-yltetradeca-2,4-dien-1-one 73816696 Click to see CCCCCCCCCC=CC=CC(=O)N1CCCC1 277.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
1-Pyrrolidin-1-yltetradeca-2,4-dien-8,10-diyn-1-one 163031463 Click to see CCCC#CC#CCCC=CC=CC(=O)N1CCCC1 269.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
1-Pyrrolidin-1-yltetradeca-2,4,10-trien-8-yn-1-one 73823902 Click to see CCCC=CC#CCCC=CC=CC(=O)N1CCCC1 271.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
1-Pyrrolidin-1-yltetradeca-2,4,12-trien-8,10-diyn-1-one 163026154 Click to see CC=CC#CC#CCCC=CC=CC(=O)N1CCCC1 267.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
5-((3R,5S)-3,5-Dihydroxy-7-(4-hydroxyphenyl)heptyl)-3-methoxybenzene-1,2-diol 53387512 Click to see COC1=CC(=CC(=C1O)O)CCC(CC(CCC2=CC=C(C=C2)O)O)O 362.40 unknown https://doi.org/10.1016/S0031-9422(00)80494-X
> 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/10.1016/0305-1978(96)88878-8
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/10.1016/0305-1978(96)88878-8
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/0305-1978(96)88878-8
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/10.1016/0305-1978(96)88878-8
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/10.1016/0305-1978(96)88878-8

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