Leucanthemum vulgare - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

Leucanthemum vulgare - Unknown
Part: Unknown
Author: Public Domain - WikiMedia

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Internal ID UUID643fca43c3ae9923935600
Scientific name Leucanthemum vulgare
Authority Lam.
First published in Fl. Franç. (Lamarck) 2: 137. 1779 [1778 publ. after 21 Mar 1779]

Description Top

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Synonyms Top

Scientific name Authority First published in
Chrysanthemum montanum Willd. Sp. Pl., ed. 4 [Willdenow] 3(3): 2143. 1803 [Apr-Dec 1803]
Leucanthemum vulgare subsp. incisum Arcang. Arcang.. 1882. 352 1882
Leucanthemum vulgare subsp. praecox Horvatić Horvatić in Acta Bot. Inst. Bot. Univ. Zagreb 10. 1935. 87 1935
Leucanthemum atratum var. heterophyllum (Willd.) Rouy Fl. France 8 (1903) 269 1903
Chrysanthemum montanum var. heterophyllum (Willd.) Koch .
Chrysanthemum leucanthemum subsp. lanceolatum (DC.) E.Mayer E. Mayer in Dela Inst. Biol. Slov. Akad. Znan. 3. 1952. 313 1952
Chrysanthemum lanceolatum Pers. Syn. Pl. [Persoon] 2(2): 460. 1807 [Sept 1807]
Leucanthemum lanceolatum DC. Prodr. [A. P. de Candolle] 6: 47. 1838 [1837 publ. early Jan 1838]

Common names Top

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Language Common/alternative name
English ox-eye daisy
English oxeye daisy
English blossom
Amharic ኣደይ ኣበባ
Arabic أقحوان المروج الشائع
ba Аҡ сәскә
Belarusian Нівянік звычайны
Bulgarian маргаритка
Catalan chrysanthemum leucanthemum
Catalan margaridot
Catalan margarida de prat
Czech kopretina bílá
Welsh llygad-llo mawr
Welsh llygad llo mawr
Danish hvid okseøje
German wiesenmargerite
German chrysanthemum leucanthemum
German margerite
German wiesen-margerite
German wiesen-wucherblume
German magerwiesen-margerite
Esperanto ordinara leŭkanto
Estonian härjasilm
Estonian chrysanthemum leucanthemum
Estonian harilik härjasilm
Basque sanjoan-lore
Persian گل چشمگاوی
Persian لیوکانته موم ولگاره
Persian لیوکانتهموم ولگاره
Finnish ahopäivänkakkara
Finnish chrysanthemum leucanthemum
Finnish päivänkakkara
French grande marguerite
French reine-marguerite
French marguerite commune
frr gewöönelk margerit
frr margerit
Irish nóinín mór
Manx bastag vane
Hebrew חיננית עין שור
Croatian ivančica
Hungarian chrysanthemum leucanthemum
Hungarian chrysanthemum maximum
Hungarian margaréta
Hungarian réti margitvirág
io margrito
Icelandic freyjubrá
Italian chrisanthemum leucanthemum
Italian chrysanthemum leucanthemum
Italian margherita comune
Japanese フランスギク
Georgian მინდვრის გვირილა
kbd Адыгэудзщхьэху
Cornish kaja vras
Lithuanian baltoji ramunė
Lithuanian paprastoji baltagalvė
Latvian parastā pīpene
Malayalam ഓക്സ് ഐ ഡെയ്സി
Norwegian Bokmål prestekrave
Norwegian Bokmål prestekrage
Dutch gewone margriet
Dutch chrysanthemum leucanthemum
Norwegian Nynorsk præstkraga
Norwegian Nynorsk præstkrågå
Norwegian Nynorsk præstkråggå
Norwegian Nynorsk prestekraga
Norwegian Nynorsk prestekrave
Norwegian Nynorsk prestkraga
Norwegian Nynorsk prestkrågå
Norwegian Nynorsk prestkrage
Norwegian Nynorsk prestkragga
Norwegian Nynorsk prestkråggå
Norwegian Nynorsk prestekrage
os Дзедзыкка
Polish chrysanthemum leucanthemum
Polish jastrun wczesny
Polish margerytka
Polish złocień właściwy
Polish jastrun właściwy
Punjab ڈیزی
Portuguese chrysanthemum leucanthemum
Portuguese malmequer bravo
Portuguese malmequer maior
Portuguese malmequer-bravo
Portuguese malmequer-maior
Portuguese margarita maior
Portuguese margarita-maior
Romanian margarete
Romanian margaretă
Russian Поповник
Russian Нивяник обыкновенный
sc margarida
sc chrysantemum leucanthemum
Samogitian baltgalvė
Serbo-Croatian proljetna ivančica
Slovak margaréta biela
Slovenian rana ivanjščica
Slovenian travniška ivanjščina
Slovenian leucanthemum praecox
Slovenian margerita
Slovenian pasja marjetica
Slovenian volovska marjetica
Swedish prästkrage
Turkish beyaz aypapatyası
Turkish Çayir kasimpati
Turkish Çayır kasımpatısı
Turkish chrysanthemum leucanthemum
Turkish chrysanthemum leucantheum
Turkish margarit
Turkish beyaz ay papatyası, margarit, büyük papatya
Ukrainian Королиця звичайна
vep haraganhäč
Chinese 法國菊
Chinese 滨菊
Chinese 法兰西菊
Chinese 濱菊
Chinese 牛眼菊
Chinese 法蘭西菊

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Leucanthemum vulgare subsp. eliasii (Sennen & Pau) Sennen & Pau Sennen & Pau in Bol. Soc. Ibér. Ci. Nat. 28(11). 1929. 34 1929
Leucanthemum vulgare subsp. parviceps (Briq. & Cavill.) Vogt & Greuter Willdenowia 33(1): 42 (2003) (2003)
Leucanthemum vulgare subsp. pujiulae Sennen Bol. Soc. Ibér. Ci. Nat. 28: 33 (1929)
Leucanthemum vulgare subsp. vulgare

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000036932
UNII 744CCZ722D
Florida Plant Atlas 1831
Flora of Alabama 849
Canadensys 3281
USDA Plants LEVU
Tropicos 2700996
INPN 105817
KEW urn:lsid:ipni.org:names:30296198-2
The Plant List gcc-135712
PFAF Leucanthemum vulgare
Open Tree Of Life 371806
Observations.org 6979
NCBI Taxonomy 99072
NBN Atlas NBNSYS0000004464
Nature Serve 2.150433
IPNI 230103-1
iNaturalist 56057
GBIF 5400982
Freebase /m/02qvnf
WisFlora 4055
EPPO CHYLE
EOL 482333
Elurikkus 5461
Elurikkus 672889
Calflora (Californian flora) 4759
USDA GRIN 104402
Wikipedia Leucanthemum_vulgare

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
Targeted Isolation of Antibiofilm Compounds from Halophytic Endophyte Bacillus velezensis 7NPB-3B Using LC-HR-MS-Based Metabolomics Singh S, Nwagwu E, Young L, Kumar P, Shinde PB, Edrada-Ebel R Microorganisms 19-Feb-2024
PMCID:PMC10891937
doi:10.3390/microorganisms12020413
PMID:38399817
Effects of mowing on body size patterns in spider assemblages of mesic meadows Stański T, Stańska M, Hajdamowicz I, Nicewicz Ł, Hiller A Ecol Evol 15-Feb-2024
PMCID:PMC10869948
doi:10.1002/ece3.10892
PMID:38371868
Spider–Plant Interaction: The Role of Extrafloral Nectaries in Spider Attraction and Their Influence on Plant Herbivory and Reproduction de Oliveira Dias KP, Stefani V Plants (Basel) 26-Jan-2024
PMCID:PMC10857052
doi:10.3390/plants13030368
PMID:38337900
Grassland vertical height heterogeneity predicts flower and bee diversity: an UAV photogrammetric approach Torresani M, Rocchini D, Ceola G, de Vries JP, Feilhauer H, Moudrý V, Bartholomeus H, Perrone M, Anderle M, Gamper HA, Chieffallo L, Guatelli E, Gatti RC, Kleijn D Sci Rep 08-Jan-2024
PMCID:PMC10774354
doi:10.1038/s41598-023-50308-9
PMID:38191639
Oleuropein-Rich Jasminum Grandiflorum Flower Extract Regulates the LKB1-PGC-1α Axis Related to the Attenuation of Hepatocellular Lipid Dysmetabolism Hou Y, Zhao X, Wang Y, Li Y, Chen C, Zhou X, Jin J, Ye J, Li D, Gan L, Wu R Nutrients 24-Dec-2023
PMCID:PMC10780778
doi:10.3390/nu16010058
PMID:38201888
Defoliation and fertilisation differentially moderate root trait effects on soil abiotic and biotic properties Liu Y, Cordero I, Bardgett RD J Ecol 25-Oct-2023
PMCID:PMC10952586
doi:10.1111/1365-2745.14215
PMID:38516387
Root litter decomposition is suppressed in species mixtures and in the presence of living roots Heredia‐Acuña C, Semchenko M, De Vries FT J Ecol 13-Oct-2023
PMCID:PMC10976660
doi:10.1111/1365-2745.14207
PMID:38550391
The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.) Thompson V, Harkin C, Stewart AJ PLoS One 04-Oct-2023
PMCID:PMC10602594
doi:10.1371/journal.pone.0291734
PMID:37792900
Allergy patient-specific IgE antibody shows significantly stability during 3 months of storage at multiple temperatures from −80 to 25°C Huang Z, Zhu H, Xiao L, Liu T, Gan H, Lin R, Luo W, Sun B Front Allergy 07-Sep-2023
PMCID:PMC10513756
doi:10.3389/falgy.2023.1239924
PMID:37744695
The great escape: patterns of enemy release are not explained by time, space or climate Xirocostas ZA, Ollerton J, Tamme R, Peco B, Lesieur V, Slavich E, Junker RR, Pärtel M, Raghu S, Uesugi A, Bonser SP, Chiarenza GM, Hovenden MJ, Moles AT Proc Biol Sci 16-Aug-2023
PMCID:PMC10427826
doi:10.1098/rspb.2023.1022
PMID:37583319
Effects of extracts from various parts of invasive Solidago species on the germination and growth of native grassland plant species Perera PC, Chmielowiec C, Szymura TH, Szymura M PeerJ 28-Jul-2023
PMCID:PMC10389070
doi:10.7717/peerj.15676
PMID:37529210
Influences of chemotype and parental genotype on metabolic fingerprints of tansy plants uncovered by predictive metabolomics Dussarrat T, Schweiger R, Ziaja D, Nguyen TT, Krause L, Jakobs R, Eilers EJ, Müller C Sci Rep 19-Jul-2023
PMCID:PMC10356770
doi:10.1038/s41598-023-38790-7
PMID:37468576
Distribution, Effect, and Control of Exotic Plants in Republic of Korea Lim BS, Seok JE, Lim CH, Kim GS, Shin HC, Lee CS Biology (Basel) 06-Jun-2023
PMCID:PMC10294914
doi:10.3390/biology12060826
PMID:37372111
Epipactis bucegensis—A Separate Autogamous Species within the E. helleborine Alliance Anghelescu NE, Balogh M, Balogh L, Kigyossy N, Georgescu MI, Petra SA, Toma F, Peticilă AG Plants (Basel) 25-Apr-2023
PMCID:PMC10180920
doi:10.3390/plants12091761
PMID:37176819
Tanacetum species: Bridging empirical knowledge, phytochemistry, nutritional value, health benefits and clinical evidence Khatib S, Sobeh M, Faraloni C, Bouissane L Front Pharmacol 20-Apr-2023
PMCID:PMC10157496
doi:10.3389/fphar.2023.1169629
PMID:37153781

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 / Enynes
(6E,8E)-hexadeca-1,6,8-trien-10,12,14-triyne 13964097 Click to see CC#CC#CC#CC=CC=CCCCC=C 208.30 unknown https://doi.org/10.1002/CBER.19650980826
Hexadeca-1,6,8-triene-10,12,14-triyne 71359764 Click to see CC#CC#CC#CC=CC=CCCCC=C 208.30 unknown https://doi.org/10.1002/CBER.19650980826
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(1S,2R,3'S,5R)-4-hexa-2,4-diynylidenespiro[3,6-dioxabicyclo[3.1.0]hexane-2,2'-3H-furan]-3'-yl] 2-methylbut-2-enoate 162870098 Click to see CC=C(C)C(=O)OC1C=COC12C3C(O3)C(=CC#CC#CC)O2 312.30 unknown https://doi.org/10.1002/CBER.19650980826
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(3E,5E)-trideca-3,5-dien-7,9,11-triynyl] acetate 13964098 Click to see CC#CC#CC#CC=CC=CCCOC(=O)C 226.27 unknown https://doi.org/10.1002/CBER.19650980826
Trideca-3,5-dien-7,9,11-triynyl acetate 162918169 Click to see CC#CC#CC#CC=CC=CCCOC(=O)C 226.27 unknown https://doi.org/10.1002/CBER.19650980826
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
3,5-Tridecadiene-7,9,11-triyne-1-ol 14443153 Click to see CC#CC#CC#CC=CC=CCCO 184.23 unknown https://doi.org/10.1002/CBER.19650980826
Trideca-3,5-dien-7,9,11-triyn-1-ol 85770432 Click to see CC#CC#CC#CC=CC=CCCO 184.23 unknown https://doi.org/10.1002/CBER.19650980826
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown https://doi.org/10.1007/978-3-540-71095-0_5966
https://doi.org/10.1007/BF00580579
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown https://doi.org/10.1007/978-3-540-71095-0_5966
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
3-[3-(3,4-Dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 348159 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00636588
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1007/BF00636588
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(1S,2S,3'R,4Z,5R)-4-hexa-2,4-diynylidenespiro[3,6-dioxabicyclo[3.1.0]hexane-2,2'-3H-furan]-3'-ol 163191082 Click to see CC#CC#CC=C1C2C(O2)C3(O1)C(C=CO3)O 230.22 unknown https://doi.org/10.1002/CBER.19650980826
(1S,2S,3'R,5R)-4-hexa-2,4-diynylidenespiro[3,6-dioxabicyclo[3.1.0]hexane-2,2'-3H-furan]-3'-ol 163048141 Click to see CC#CC#CC=C1C2C(O2)C3(O1)C(C=CO3)O 230.22 unknown https://doi.org/10.1002/CBER.19650980826
[(2E,5R,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 162983961 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1002/CBER.19650980826
> Organoheterocyclic compounds / Heteroaromatic compounds
2-(Non-1-ene-3,5,7-triyn-1-yl)furan 71403320 Click to see CC#CC#CC#CC=CC1=CC=CO1 180.20 unknown https://doi.org/10.1002/CBER.19650980826
2-[(E)-non-1-en-3,5,7-triynyl]furan 11446685 Click to see CC#CC#CC#CC=CC1=CC=CO1 180.20 unknown https://doi.org/10.1002/CBER.19650980826
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00636588
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00636588
> Phenylpropanoids and polyketides / Flavonoids / Flavones
(5-hydroxy-4-oxo-2-phenylchromen-7-yl) (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxane-2-carboxylate 163036536 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC(=O)C4C(C(C(C(O4)O)O)O)O)O 430.40 unknown https://doi.org/10.1007/BF00636588
(5-Hydroxy-4-oxo-2-phenylchromen-7-yl) 3,4,5,6-tetrahydroxyoxane-2-carboxylate 163036535 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC(=O)C4C(C(C(C(O4)O)O)O)O)O 430.40 unknown https://doi.org/10.1007/BF00636588
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(1S,2R,3S,4S,5S)-2,3,4-trihydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]chromen-4-one 162965225 Click to see C1C(C(C(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O 578.50 unknown https://doi.org/10.1007/BF00579632
5,7-Dihydroxy-2-(4-hydroxyphenyl)-8-[2,3,4-trihydroxy-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexyl]chromen-4-one 162965223 Click to see C1C(C(C(C(C1OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C3=C(C=C(C4=C3OC(=CC4=O)C5=CC=C(C=C5)O)O)O 578.50 unknown https://doi.org/10.1007/BF00579632
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1007/BF00636588
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/10.1007/BF00636588
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1007/BF00636588
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/10.1007/BF00636588
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 154496169 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00580579
3,4,5-Trihydroxy-6-[5-hydroxy-2-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxane-2-carboxylic acid 5387370 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00576106
Apigenin 7-glucuronide 5319484 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1007/BF00576106
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/BF00636588
Vitamin P 5293655 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1007/BF00636588
> Phenylpropanoids and polyketides / Macrolides and analogues
4-Ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 254855 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1007/BF02238350
Hastacine 163587 Click to see CC=C1CC(C(C(=O)OCC2CCN3C2C(CC3)OC1=O)(C)O)C 337.40 unknown https://doi.org/10.1007/BF02238350
Platyphylline 5281742 Click to see CC=C1CC(C(C(=O)OCC2CCN3C2C(CC3)OC1=O)(C)O)C 337.40 unknown https://doi.org/10.1007/BF02238350
https://doi.org/10.1007/978-3-540-71095-0_5966
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1007/978-3-540-71095-0_5966
https://doi.org/10.1007/BF02238350

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