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Anthemis auriculata

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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 UUID643fc5d1a51c0362605317
Scientific name Anthemis auriculata
Authority Boiss.
First published in Diagn. Pl. Orient. 4: 5 (1844)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthemis sismondaeana Clem. Mem. Reale Accad. Sci. Torino , ser. 2, 16: 297 (1857)
Anthemis metallorum Heldr.

Common names Top

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Language Common/alternative name
Bulgarian уховидно подрумче

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Southeastern Europe
      • Albania
      • Bulgaria
      • Greece
      • Turkey-in-Europe
      • Yugoslavia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000000365
Tropicos 2700060
KEW urn:lsid:ipni.org:names:177167-1
The Plant List gcc-100345
Open Tree Of Life 1025394
Observations.org 114554
NCBI Taxonomy 589720
IPNI 177167-1
GBIF 3122487
CMAUP NPO20111

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
Asteraceae Plants as Sources of Compounds Against Leishmaniasis and Chagas Disease Moraes Neto RN, Setúbal RF, Higino TM, Brelaz-de-Castro MC, da Silva LC, Aliança AS Front Pharmacol 08-May-2019
PMCID:PMC6530400
doi:10.3389/fphar.2019.00477
PMID:31156427
Zingiber Officinale Roscoe and Echinops Kebericho Mesfin Showed Antiplasmodial Activities against Plasmodium Berghei in a Dose-dependent Manner in Ethiopia Biruksew A, Zeynudin A, Alemu Y, Golassa L, Yohannes M, Debella A, Urge G, De Spiegeleer B, Suleman S Ethiop J Health Sci 01-Sep-2018
PMCID:PMC6308778
doi:10.4314/ejhs.v28i5.17
PMID:30607081
Disentangling the role of floral sensory stimuli in pollination networks Kantsa A, Raguso RA, Dyer AG, Olesen JM, Tscheulin T, Petanidou T Nat Commun 12-Mar-2018
PMCID:PMC5847531
doi:10.1038/s41467-018-03448-w
PMID:29531220
Computer-Aided Drug Design Using Sesquiterpene Lactones as Sources of New Structures with Potential Activity against Infectious Neglected Diseases Herrera Acevedo C, Scotti L, Feitosa Alves M, Formiga Melo Diniz MD, Scotti MT Molecules 03-Jan-2017
PMCID:PMC6155652
doi:10.3390/molecules22010079
PMID:28054952
Efficacy of some natural compounds as antifungal agents Vengurlekar S, Sharma R, Trivedi P Pharmacogn Rev 01-Jul-2012
PMCID:PMC3459460
doi:10.4103/0973-7847.99942
PMID:23055634
Inhibiting enoyl-ACP reductase (FabI) across pathogenic microorganisms by linear sesquiterpene lactones from Anthemis auriculata. Karioti A, Skaltsa H, Zhang X, Tonge PJ, Perozzo R, Kaiser M, Franzblau SG, Tasdemir D Phytomedicine 01-Dec-2008
doi:10.1016/J.PHYMED.2008.02.018
PMID:18424102
Sesquiterpene lactones as chemotaxonomic markers in genus Anthemis. Staneva JD, Todorova MN, Evstatieva LN Phytochemistry 01-Feb-2008
doi:10.1016/J.PHYTOCHEM.2007.07.021
PMID:17850834
Anthecularin: a novel sesquiterpene lactone from Anthemis auriculata with antiprotozoal activity. Karioti A, Skaltsa H, Linden A, Perozzo R, Brun R, Tasdemir D J Org Chem 12-Oct-2007
doi:10.1021/JO701751W
PMID:17880246
Linear sesquiterpene lactones from Anthemis auriculata and their antibacterial activity. Theodori R, Karioti A, Rancić A, Skaltsa H J Nat Prod 01-Apr-2006
doi:10.1021/NP058084I
PMID:16643047

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1021/NP058084I
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids
[(1R,2R,6S,10R,11R,13S,14R,15R)-13-acetyloxy-8-formyl-1-hydroxy-4,12,12,15-tetramethyl-5-oxo-14-tetracyclo[8.5.0.02,6.011,13]pentadeca-3,8-dienyl] 2-(methylamino)benzoate 162901456 Click to see CC1C(C2(C(C2(C)C)C3C1(C4C=C(C(=O)C4CC(=C3)C=O)C)O)OC(=O)C)OC(=O)C5=CC=CC=C5NC 521.60 unknown https://doi.org/10.1021/NP058084I
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4S)-3-methylidene-4-[(E)-3-methyl-4-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]but-2-enyl]oxolan-2-one 162997535 Click to see CC1CC(OC1=O)CC(=CCC2COC(=O)C2=C)C 264.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
(4S)-4-[(1R,2E)-1-hydroxy-3,7-dimethyl-5-oxoocta-2,6-dienyl]-3-methylideneoxolan-2-one 49799789 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)O)C)C 264.32 unknown https://doi.org/10.1021/NP058084I
(4S)-4-[(2E)-3,7-dimethyl-5-oxoocta-2,6-dienyl]-3-methylideneoxolan-2-one 12050675 Click to see CC(=CC(=O)CC(=CCC1COC(=O)C1=C)C)C 248.32 unknown https://doi.org/10.1021/NP058084I
[(1R,2E)-3,7-dimethyl-1-[(3S)-4-methylidene-5-oxooxolan-3-yl]-5-oxoocta-2,6-dienyl] acetate 49799790 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)OC(=O)C)C)C 306.40 unknown https://doi.org/10.1021/NP058084I
[(1S)-3,7-dimethyl-1-[(3S)-4-methylidene-5-oxooxolan-3-yl]-5-oxoocta-2,6-dienyl] acetate 163035026 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)OC(=O)C)C)C 306.40 unknown https://doi.org/10.1021/NP058084I
[3,7-Dimethyl-1-(4-methylidene-5-oxooxolan-3-yl)-5-oxoocta-2,6-dienyl] acetate 72993757 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)OC(=O)C)C)C 306.40 unknown https://doi.org/10.1021/NP058084I
4-(1-Hydroxy-3,7-dimethyl-5-oxoocta-2,6-dienyl)-3-methylideneoxolan-2-one 73069239 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)O)C)C 264.32 unknown https://doi.org/10.1021/NP058084I
4-(3,7-Dimethyl-5-oxoocta-2,6-dienyl)-3-methylideneoxolan-2-one 73154518 Click to see CC(=CC(=O)CC(=CCC1COC(=O)C1=C)C)C 248.32 unknown https://doi.org/10.1021/NP058084I
Acetoxyanthecotulide 11522381 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)OC(=O)C)C)C 306.40 unknown https://doi.org/10.1021/NP058084I
Anthecotulide 11962174 Click to see CC(=CC(=O)CC(=CCC1COC(=O)C1=C)C)C 248.32 unknown https://doi.org/10.1016/J.PHYMED.2008.02.018
https://doi.org/10.1021/NP058084I
Hydroxyanthecotulide 11708731 Click to see CC(=CC(=O)CC(=CC(C1COC(=O)C1=C)O)C)C 264.32 unknown https://doi.org/10.1021/NP058084I
https://doi.org/10.1016/J.PHYMED.2008.02.018
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6aR,6bR,8aR,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-ol 441686 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
(3S,4aR,6aS,6aR,6bR,8aR,12S,12aS,14aR,14bR)-4,4,6a,6b,8a,12,12a,14b-octamethyl-11-methylidene-2,3,4a,5,6,6a,7,8,9,10,12,13,14,14a-tetradecahydro-1H-picen-3-ol 162953395 Click to see CC1C(=C)CCC2(C1(C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1021/NP058084I
4,4,6a,6b,8a,12,12a,14b-octamethyl-11-methylidene-2,3,4a,5,6,6a,7,8,9,10,12,13,14,14a-tetradecahydro-1H-picen-3-ol 162953394 Click to see CC1C(=C)CCC2(C1(C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C)C 440.70 unknown https://doi.org/10.1021/NP058084I
> Organoheterocyclic compounds / Furofurans
(1S,6S,10S,11R)-3,13-dimethyl-8,15-dioxatetracyclo[9.3.1.01,6.06,10]pentadeca-2,13-dien-7-one 101544815 Click to see CC1=CC23C=C(CC(O2)C4C3(CC1)C(=O)OC4)C 246.30 unknown https://doi.org/10.1021/JO701751W
3,13-Dimethyl-8,15-dioxatetracyclo[9.3.1.01,6.06,10]pentadeca-2,13-dien-7-one 73409841 Click to see CC1=CC23C=C(CC(O2)C4C3(CC1)C(=O)OC4)C 246.30 unknown https://doi.org/10.1021/JO701751W
Anthecularin 23651215 Click to see CC1=CC23C=C(CC(O2)C4C3(CC1)C(=O)OC4)C 246.30 unknown https://doi.org/10.1016/J.PHYMED.2008.02.018
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4R)-4-[(E,3S)-3-hydroxy-3-methyl-4-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]but-1-enyl]-3-methylideneoxolan-2-one 163106413 Click to see CC1CC(OC1=O)CC(C)(C=CC2COC(=O)C2=C)O 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
(4S)-3-methylidene-4-[[(2R,3S)-3-methyl-3-[[(2S,4R)-4-methyl-5-oxooxolan-2-yl]methyl]oxiran-2-yl]methyl]oxolan-2-one 163105247 Click to see CC1CC(OC1=O)CC2(C(O2)CC3COC(=O)C3=C)C 280.32 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
(4S)-3-methylidene-4-[3-[[(2S,4R)-4-methyl-5-oxooxolan-2-yl]methyl]-2-oxobut-3-enyl]oxolan-2-one 163103976 Click to see CC1CC(OC1=O)CC(=C)C(=O)CC2COC(=O)C2=C 278.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
(4S)-4-[(2R)-2-hydroperoxy-3-[[(2S,4R)-4-methyl-5-oxooxolan-2-yl]methyl]but-3-enyl]-3-methylideneoxolan-2-one 163105879 Click to see CC1CC(OC1=O)CC(=C)C(CC2COC(=O)C2=C)OO 296.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP058084I
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP058084I
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1021/NP058084I
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/10.1021/NP058084I
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-galactoside 5291488 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP058084I
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP058084I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Pectolinarigenin 5320438 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC)O 314.29 unknown https://doi.org/10.1021/NP058084I
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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