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Achillea holosericea

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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 UUID643fcc5c43bac327452344
Scientific name Achillea holosericea
Authority Sm.
First published in Fl. Graec. Prodr. 2(1): 194 (1813)

Description Top

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Synonyms Top

Scientific name Authority First published in
Achillea tomentosa Fraas ex Nyman Consp. Fl. Eur. 2: 367 (1879)
Achillea flabelliformis Sibth. & Sm. Fl. Graec. ix. 72.
Achillea flabelliformis Lindl. Fl. Graec. 9(2): 72 (1839)

Common names Top

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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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Hungary
    • Southeastern Europe
      • Albania
      • Greece
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000061832
Tropicos 2701618
KEW urn:lsid:ipni.org:names:174026-1
The Plant List gcc-1885
Open Tree Of Life 921036
Observations.org 128381
NCBI Taxonomy 282740
IPNI 174026-1
iNaturalist 565142
GBIF 3120168
EPPO ACHHO

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
Antimicrobial and anti-aflatoxigenic activities of nanoemulsions based on Achillea millefolium and Crocus sativus flower extracts as green promising agents for food preservatives Abu Safe FA, Badr AN, Shehata MG, El-Sayyad GS BMC Microbiol 07-Oct-2023
PMCID:PMC10559460
doi:10.1186/s12866-023-03033-2
PMID:37805450
Anticancer Potentials of the Lignan Magnolin: A Systematic Review Bhuia MS, Wilairatana P, Chowdhury R, Rakib AI, Kamli H, Shaikh A, Coutinho HD, Islam MT Molecules 23-Apr-2023
PMCID:PMC10180476
doi:10.3390/molecules28093671
PMID:37175081
Medicinal Plants Used Traditionally for Skin Related Problems in the South Balkan and East Mediterranean Region—A Review Tsioutsiou EE, Amountzias V, Vontzalidou A, Dina E, Stevanović ZD, Cheilari A, Aligiannis N Front Pharmacol 05-Jul-2022
PMCID:PMC9294246
doi:10.3389/fphar.2022.936047
PMID:35865952
Contribution to the Orophilous Cushion-Like Vegetation of Central-Southern and Insular Greece Musarella CM, Brullo S, del Galdo GG Plants (Basel) 30-Nov-2020
PMCID:PMC7760968
doi:10.3390/plants9121678
PMID:33266088
Ethnobotanical Study of Medicinal Plants Used in Central Macedonia, Greece Tsioutsiou EE, Giordani P, Hanlidou E, Biagi M, De Feo V, Cornara L Evid Based Complement Alternat Med 01-Apr-2019
PMCID:PMC6463668
doi:10.1155/2019/4513792
PMID:31057648
COPIOUS: A gold standard corpus of named entities towards extracting species occurrence from biodiversity literature Nguyen NT, Gabud RS, Ananiadou S Biodivers Data J 22-Jan-2019
PMCID:PMC6351503
doi:10.3897/BDJ.7.e29626
PMID:30700967
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
The Volatile Compounds and Bioactivity of Achillea sieheana Stapf. (Asteraceae) Albayrak S Iran J Pharm Res 01-Jan-2013
PMCID:PMC3813214
PMID:24250570
Leaf flavonoids of Achillea ligustica and Achillea holosericea Olga Tzakou, Maria Couladis, Verykokidou Evmorfia, Argiris Loukis Elsevier BV 25-Jul-2002
doi:10.1016/0305-1978(95)00044-U
Two highly oxygenated eudesmanes and 10 lignans from Achillea holosericea. Ahmed AA, Mahmoud AA, Ali ET, Tzakou O, Couladis M, Mabry TJ, Gáti T, Tóth G Phytochemistry 01-Apr-2002
doi:10.1016/S0031-9422(01)00442-3
PMID:11937165

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
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Epieudesmin 7000209 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
(+)-Fargesin 5320622 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
(3R,3aR,6S,6aR)-3-(3,4-dimethoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 10454576 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
1,4-Bis(3,4-dimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 234823 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC)OC)OC 386.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
1,4-Bis(3,4,5-trimethoxyphenyl)tetrahydro-1H,3H-furo[3,4-c]furan 99091 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
3-(3,4-Dimethoxyphenyl)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan 5319210 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
6-[(3S,3aR,6R,6aR)-6-(3,4,5-trimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-4-methoxy-1,3-benzodioxole 12697528 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Aschantin 3836321 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Aschantin 122643 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Epiaschantin 10408679 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 400.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Episesartemin A 3732009 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Epiyangambin 10049223 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Kobusin 182278 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)OC 370.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Medioresinol dimethyl ether 169234 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC)OC 416.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Sesartemin 342737 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC)OC 430.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
Yangambin 443028 Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC 446.50 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(4aS,7R)-1,4a-dimethyl-7-(1,2,3-trihydroxypropan-2-yl)-3,4,5,6,7,8-hexahydronaphthalen-2-one 5320341 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(CO)(CO)O 268.35 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
[8a-hydroxy-4a-methyl-1-methylidene-7-(1,2,3-trihydroxypropan-2-yl)-3,4,5,6,7,8-hexahydro-2H-naphthalen-2-yl] acetate 73880597 Click to see CC(=O)OC1CCC2(CCC(CC2(C1=C)O)C(CO)(CO)O)C 328.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
1,4a-Dimethyl-7-(1,2,3-trihydroxypropan-2-yl)-3,4,5,6,7,8-hexahydronaphthalen-2-one 78385391 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(CO)(CO)O 268.35 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
3beta-Acetoxy,5alpha,11,12,13-tetrahydroxy-eudesm-4(15)-ene 636635 Click to see CC(=O)OC1CCC2(CCC(CC2(C1=C)O)C(CO)(CO)O)C 328.40 unknown https://doi.org/10.1016/S0031-9422(01)00442-3
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1016/0305-1978(95)00044-U
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0305-1978(95)00044-U
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Desmethoxycentaureidin 5469524 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O)O 330.29 unknown https://doi.org/10.1016/0305-1978(95)00044-U

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