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Achillea cretica

Achillea cretica - 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 UUID643fc7e71e6e3187721516
Scientific name Achillea cretica
Authority L.
First published in Sp. Pl. : 899 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Achillea santolina Lindl. Fl. Graec. 9: 70 (1839)
Achillea sphaciotica Rikli Rikli in Vierteljahrsschr. Naturf. Ges. Zürich 68. 1923. 140 1923
Santolina anthemoides L. Sp. Pl. ed. 2 2: 1180 (1763)
Achillea erioclada DC. Prodr. 7(1): 296 (1838)
Santolina alpina Sieber ex Steud. Nomencl. Bot. 2: 511 (1841)

Common names Top

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Language Common/alternative name
English cretan yarrow
German kretische schafgarbe
Turkish girit civanperçemi

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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No germination or propagation data was added yet.

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-0000018302
Tropicos 2733643
KEW urn:lsid:ipni.org:names:173912-1
The Plant List gcc-117699
Open Tree Of Life 245244
Observations.org 113856
NCBI Taxonomy 282731
NBN Atlas NBNSYS0200001648
IPNI 173912-1
iNaturalist 514835
GBIF 3120369
Elurikkus 730434
Wikipedia Achillea_cretica
CMAUP NPO5368

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
Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK Int J Mol Sci 01-Jan-2023
PMCID:PMC9821772
doi:10.3390/ijms24010739
PMID:36614181
Endometriosis and Phytoestrogens: Friends or Foes? A Systematic Review Bartiromo L, Schimberni M, Villanacci R, Ottolina J, Dolci C, Salmeri N, Viganò P, Candiani M Nutrients 24-Jul-2021
PMCID:PMC8398277
doi:10.3390/nu13082532
PMID:34444692
Potential anti-influenza effective plants used in Turkish folk medicine: A review Sargin SA J Ethnopharmacol 31-Aug-2020
PMCID:PMC7458060
doi:10.1016/j.jep.2020.113319
PMID:32882361
Non-Oxygenated Sesquiterpenes in the Essential Oil of Copaifera langsdorffii Desf. Increase during the Day in the Dry Season de Almeida LF, Portella RD, Bufalo J, Marques MO, Facanali R, Frei F PLoS One 17-Feb-2016
PMCID:PMC4757570
doi:10.1371/journal.pone.0149332
PMID:26886431
Bisabolenes from Achillea cretica Maurizio Bruno, Maria L. Bondi, Maria P. Paternostro, Nelly A. Arnold, Jesús G. Díaz, Werner Herz Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00040-4
Isoorientin 7,3′-dimethyl ether, a new C-glycosylflavone from Achillea cretica Karin Valant, Elisabeth Besson, Jean Chopin Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)85039-4

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
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/10.1016/0031-9422(96)00040-4
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/10.1016/0031-9422(96)00040-4
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/10.1016/0031-9422(96)00040-4
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/10.1016/0031-9422(96)00040-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(5R)-5-[(E,2R)-2-hydroxy-6-oxohept-4-en-2-yl]-2-methylcyclohex-2-en-1-one 101995255 Click to see CC1=CCC(CC1=O)C(C)(CC=CC(=O)C)O 236.31 unknown https://doi.org/10.1016/0031-9422(96)00040-4
5-(2-Hydroxy-6-oxohept-4-en-2-yl)-2-methylcyclohex-2-en-1-one 162908324 Click to see CC1=CCC(CC1=O)C(C)(CC=CC(=O)C)O 236.31 unknown https://doi.org/10.1016/0031-9422(96)00040-4
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3S,4S,6R)-3,4,6-trihydroxy-2-methylidene-6-[(1R)-4-methyl-5-oxocyclohex-3-en-1-yl]heptanoic acid 163025862 Click to see CC1=CCC(CC1=O)C(C)(CC(C(C(=C)C(=O)O)O)O)O 298.33 unknown https://doi.org/10.1016/0031-9422(96)00040-4
(4R,5S)-5-[(2R,5R)-2,5-dihydroxy-6-methylhept-6-en-2-yl]-4-hydroxy-2-methylcyclohex-2-en-1-one 101995257 Click to see CC1=CC(C(CC1=O)C(C)(CCC(C(=C)C)O)O)O 268.35 unknown https://doi.org/10.1016/0031-9422(96)00040-4
(4R,5S)-5-[(E,2R)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-4-hydroxy-2-methylcyclohex-2-en-1-one 101995256 Click to see CC1=CC(C(CC1=O)C(C)(CC=CC(C)(C)O)O)O 268.35 unknown https://doi.org/10.1016/0031-9422(96)00040-4
(E,2S,6R)-6-hydroxy-2-(hydroxymethyl)-6-[(1R)-4-methyl-5-oxocyclohex-3-en-1-yl]hept-3-enoic acid 162944874 Click to see CC1=CCC(CC1=O)C(C)(CC=CC(CO)C(=O)O)O 282.33 unknown https://doi.org/10.1016/0031-9422(96)00040-4
[(E,2R)-7-hydroxy-6-methyl-2-[(1R)-4-methyl-5-oxocyclohex-3-en-1-yl]hept-5-en-2-yl] acetate 101995252 Click to see CC1=CCC(CC1=O)C(C)(CCC=C(C)CO)OC(=O)C 294.40 unknown https://doi.org/10.1016/0031-9422(96)00040-4
[7-Hydroxy-6-methyl-2-(4-methyl-5-oxocyclohex-3-en-1-yl)hept-5-en-2-yl] acetate 163015937 Click to see CC1=CCC(CC1=O)C(C)(CCC=C(C)CO)OC(=O)C 294.40 unknown https://doi.org/10.1016/0031-9422(96)00040-4
3,4,6-Trihydroxy-2-methylidene-6-(4-methyl-5-oxocyclohex-3-en-1-yl)heptanoic acid 163025861 Click to see CC1=CCC(CC1=O)C(C)(CC(C(C(=C)C(=O)O)O)O)O 298.33 unknown https://doi.org/10.1016/0031-9422(96)00040-4
5-(2,5-Dihydroxy-6-methylhept-6-en-2-yl)-4-hydroxy-2-methylcyclohex-2-en-1-one 162908303 Click to see CC1=CC(C(CC1=O)C(C)(CCC(C(=C)C)O)O)O 268.35 unknown https://doi.org/10.1016/0031-9422(96)00040-4
5-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-4-hydroxy-2-methylcyclohex-2-en-1-one 163023571 Click to see CC1=CC(C(CC1=O)C(C)(CC=CC(C)(C)O)O)O 268.35 unknown https://doi.org/10.1016/0031-9422(96)00040-4
6-Hydroxy-2-(hydroxymethyl)-6-(4-methyl-5-oxocyclohex-3-en-1-yl)hept-3-enoic acid 162944873 Click to see CC1=CCC(CC1=O)C(C)(CC=CC(CO)C(=O)O)O 282.33 unknown https://doi.org/10.1016/0031-9422(96)00040-4
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
13-Homo-13-oxa-6a,12a-dehydroelliptone 10501591 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC 408.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
13-Homo-13-oxa-6a,12a-dehydrodeguelin 10092854 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)OC5=CC(=C(C=C5OC4)OC)OC)C 408.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-6-(gamma,gamma-dimethylallyl)-5-hydroxy-3',4'-dimethoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone 44559036 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)OC)O)C 450.50 unknown via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,3'-dihydroxy-4'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone 44559037 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)OC)O)O)C 436.50 unknown via CMAUP database
(2S)-6-(gamma,gamma-dimethylallyl)-5,4'-dihydroxy-3'-methoxy-6'',6''-dimethylpyran[2'',3'':7,8]flavanone 44559077 Click to see CC(=CCC1=C(C2=C(C3=C1OC(C=C3)(C)C)OC(CC2=O)C4=CC(=C(C=C4)O)OC)O)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
7,3'-Di-O-methylisoorientin 25002956 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)C4C(C(C(C(O4)CO)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/0031-9422(80)85039-4
Isoorientin 7,3'-dimethyl ether 74385208 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)C4C(C(C(C(O4)CO)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/0031-9422(80)85039-4
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
Anhydropisatin 11822566 Click to see COC1=CC2=C(C=C1)C3=C(CO2)C4=CC5=C(C=C4O3)OCO5 296.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids
Rotenonone 442819 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4=O)OC)OC 406.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(1)Benzopyrano(3,4-b)furo(2,3-h)(1)benzopyran-6(12H)-one, 1,2-dihydro-8,9-dimethoxy-2-(1-methylethenyl)-, (R)- 99190 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC 392.40 unknown via CMAUP database
(1R)-1beta,2alpha,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 11797541 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1R)-1beta,2beta,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 10694586 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1S)-1alpha,2alpha,7aalpha-Trihydroxy-9,10-dimethoxy-3,3-dimethyl-1,2,13,13aalpha-tetrahydro-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 10789429 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(1S)-1alpha,2beta,7aalpha-Trihydroxy-3,3-dimethyl-9,10-dimethoxy-2,3,13,13aalpha-tetrahydro-1H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 10049103 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)O)C 444.40 unknown via CMAUP database
(2R)-1,2,12,12aalpha-Tetrahydro-6aalpha-methoxy-2alpha-isopropenyl-8,9-dimethoxy-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one 100970024 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC 424.40 unknown via CMAUP database
(2R)-1,2,12,12aalpha-Tetrahydro-6abeta-methoxy-2alpha-isopropenyl-8,9-dimethoxy-[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one 100970021 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC 424.40 unknown via CMAUP database
(6aR)-12,12aalpha-Dihydro-2-acetyl-6aalpha-hydroxy-8,9-dimethoxy[1]benzopyrano[3,4-b]furo[2,3-h][1]benzopyran-6(6aH)-one 10549503 Click to see CC(=O)C1=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
(7aR)-13,13aalpha-Dihydro-7aalpha-methoxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 100970022 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C 424.40 unknown via CMAUP database
(7aS)-13,13aalpha-Dihydro-7abeta-hydroxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 11962145 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown via CMAUP database
(7aS)-13,13aalpha-Dihydro-7abeta-methoxy-9,10-dimethoxy-3,3-dimethyl-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(7aH)-one 100970023 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)OC)OC)OC)C 424.40 unknown via CMAUP database
11-Hydroxytephrosin 155725 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)O)C 426.40 unknown via CMAUP database
12a-Hydroxyrotenonic acid 51136534 Click to see CC(=CCC1=C(C=CC2=C1OC3COC4=CC(=C(C=C4C3(C2=O)O)OC)OC)O)C 412.40 unknown via CMAUP database
alpha-Toxicarol 442826 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)O)C 410.40 unknown via CMAUP database
Deguelin 107935 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown via CMAUP database
Dehydrodeguelin 3083803 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)C 392.40 unknown via CMAUP database
Dehydrotoxicarol 5491616 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=CC(=C(C=C5OC4)OC)OC)O)C 408.40 unknown via CMAUP database
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC)C 394.40 unknown via CMAUP database
Rotenolon II 99189 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown via CMAUP database
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown via CMAUP database
Tephrosin 114909 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
Isobavachromene 5889042 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC=C(C=C3)O)C 322.40 unknown via CMAUP database
Pongachalcone II 10712965 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C(=O)C=CC3=CC(=C(C=C3)O)OC)C 352.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,2-Dimethyl-7-[2-(3,4,5-trimethoxyphenyl)ethenyl]-2H-1-benzopyran 10689330 Click to see CC1(C=CC2=C(O1)C=C(C=C2)C=CC3=CC(=C(C(=C3)OC)OC)OC)C 352.40 unknown via CMAUP database
5-Methoxy-2,2-dimethyl-7-[2-(4-hydroxy-3-methoxyphenyl)ethenyl]-2H-1-benzopyran 10520980 Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC(=C(C=C3)O)OC)C 338.40 unknown via CMAUP database
5-Methoxy-2,2-dimethyl-7-[2-(4-hydroxyphenyl)ethenyl]-2H-1-benzopyran 10542828 Click to see CC1(C=CC2=C(O1)C=C(C=C2OC)C=CC3=CC=C(C=C3)O)C 308.40 unknown via CMAUP database

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