Scientific name	Authority	First published in
Anthemis rotata	Boiss.	Fl. Orient. 3: 318 (1875)
Anthemis pamphylica	Boiss. & Heldr.	Diagn. Pl. Orient. 11: 8 (1849)
Anthemis pseudocotula subsp. rotata	(Boiss.) Eig	Palestine J. Bot., Jerusalem Ser. 1: 197. 1938 (1938)
Anthemis rotata var. auriculata	Pamp.	Arch. Bot. (Forlì) 12(1): 46 (1936)

Common names Top

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Language	Common/alternative name
Hebrew	קחוון מצוי

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

Africa click to expand
- Northern Africa
  - Egypt
  - Libya

Asia-temperate click to expand
- Arabian Peninsula
  - Kuwait
  - Saudi Arabia
  - Yemen
- Western Asia
  - Cyprus
  - East Aegean Islands
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Sinai
  - Turkey

Europe click to expand
- Southeastern Europe
  - Kriti
  - Turkey-in-Europe

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000016673
Tropicos	2733875
KEW	urn:lsid:ipni.org:names:177532-1
The Plant List	gcc-11613
Open Tree Of Life	678116
Observations.org	139806
NCBI Taxonomy	158231
IPNI	177532-1
iNaturalist	492745
GBIF	3122622
EPPO	ANTPS
CMAUP	NPO11798

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

Isolation and Screening of Antibacterial Activity of Actinomycetota from the Medicinal Plant, Anthemis pseudocotula Boiss

Maryam H, Fazel P, Mostafa N

Arch Razi Inst

31-Oct-2023

PMCID:	PMC10998938
doi:	10.22092/ARI.2023.78.5.1638
PMID:	38590676

Green Synthesis of Silver Nanoparticles Using Aerial Part Extract of the Anthemis pseudocotula Boiss. Plant and Their Biological Activity

Ajlouni AW, Hamdan EH, Alshalawi RA, Shaik MR, Khan M, Kuniyil M, Alwarthan A, Ansari MA, Khan M, Alkhathlan HZ, Shaik JP, Adil SF

Molecules

28-Dec-2022

PMCID:	PMC9822267
doi:	10.3390/molecules28010246
PMID:	36615440

Facile synthesis of Tb-decorated graphene oxide: electrochemical stability, hydrogen storage, and corrosion inhibition of Mg AZ13 alloy in 3.5% NaCl medium

Nagarajan P, Cole IS, Kuznetsov A, Manickam S

RSC Adv

24-Dec-2020

PMCID:	PMC8693361
doi:	10.1039/d0ra08766a
PMID:	35423666

Experimental and DFT studies on the ultrasonic energy-assisted extraction of the phytochemicals of Catharanthus roseus as green corrosion inhibitors for mild steel in NaCl medium

Palaniappan N, Cole I, Caballero-Briones F, Manickam S, Justin Thomas KR, Santos D

RSC Adv

03-Feb-2020

PMCID:	PMC9049168
doi:	10.1039/c9ra08971c
PMID:	35498297

Greener synthesis of chemical compounds and materials

Kharissova OV, Kharisov BI, Oliva González CM, Méndez YP, López I

R Soc Open Sci

06-Nov-2019

PMCID:	PMC6894553
doi:	10.1098/rsos.191378
PMID:	31827868

Fine‐scale substrate heterogeneity in green roof plant communities: The constraint of size

Vasl A, Schindler BY, Kadas GJ, Blaustein L

Ecol Evol

30-Sep-2019

PMCID:	PMC6822028
doi:	10.1002/ece3.5517
PMID:	31695868

Fine-scale substrate heterogeneity does not affect arthropod communities on green roofs

Schindler BY, Vasl A, Blaustein L, Gurevich D, Kadas GJ, Seifan M

PeerJ

19-Mar-2019

PMCID:	PMC6430103
doi:	10.7717/peerj.6445
PMID:	30918748

Green Synthesis of Hydrophobic Magnetite Nanoparticles Coated with Plant Extract and Their Application as Petroleum Oil Spill Collectors

Abdullah MM, Atta AM, Allohedan HA, Alkhathlan HZ, Khan M, Ezzat AO

Nanomaterials (Basel)

19-Oct-2018

PMCID:	PMC6215231
doi:	10.3390/nano8100855
PMID:	30347724

Molecular authentication of Anthemis deserti Boiss. (Asteraceae) based on ITS2 region of nrDNA gene sequence

Ajmal Ali M

Saudi J Biol Sci

15-Sep-2018

PMCID:	PMC6319191
doi:	10.1016/j.sjbs.2018.09.003
PMID:	30622420

Morphological and Molecular Revision of the Genus Ozirhincus (Diptera: Cecidomyiidae)—Long-Snouted Seed-Feeding Gall Midges on Asteraceae

Dorchin N, Astrin JJ, Bodner L, Harris KM

PLoS One

02-Jul-2015

PMCID:	PMC4489628
doi:	10.1371/journal.pone.0130981
PMID:	26134526

Floristic diversity and vegetation analysis of Wadi Arar: A typical desert Wadi of the Northern Border region of Saudi Arabia

Osman AK, Al-Ghamdi F, Bawadekji A

Saudi J Biol Sci

18-Feb-2014

PMCID:	PMC4250517
doi:	10.1016/j.sjbs.2014.02.001
PMID:	25473364

New cytotoxic sesquiterpene lactones from Anthemis scrobicularis.

Zaghloul AM, Yusufoglu HS, Salkini MA, Alam A

J Asian Nat Prod Res

01-Jan-2014

doi:	10.1080/10286020.2014.931377
PMID:	25227949

Pharmacological and Phytochemical Appraisal of Selected Medicinal Plants from Jordan with Claimed Antidiabetic Activities

Afifi FU, Kasabri V

Sci Pharm

15-Oct-2013

PMCID:	PMC3867248
doi:	10.3797/scipharm.1212-20
PMID:	24482764

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

Seco-germacranolides from Anthemis pseudocotula

M.Abou El-Ela, J. Jakupovic, F. Bohlmann, A.A. Ahmed, A.Seif El-Din, S. Khafagi, N. Sabri, M. El-Ghazouly

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(90)85221-Z

Phytochemical Profile Top

Add a new one!

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
[(1R,2E,6E)-7-methyl-1-[(3R)-4-methylidene-5-oxooxolan-3-yl]-8-oxoocta-2,6-dienyl] acetate	162817354	Click to see CC(=CCCC=CC(C1COC(=O)C1=C)OC(=O)C)C=O	292.33	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2E,6E,8R)-8-hydroxy-2-methyl-8-[(3R)-4-methylidene-5-oxooxolan-3-yl]octa-2,6-dienal	162971685	Click to see CC(=CCCC=CC(C1COC(=O)C1=C)O)C=O	250.29	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(2E,6E,8R)-8-hydroxy-2,6-dimethyl-8-[(3R)-4-methylidene-5-oxooxolan-3-yl]octa-2,6-dienal	14733724	Click to see CC(=CC(C1COC(=O)C1=C)O)CCC=C(C)C=O	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(4R)-3-methylidene-4-[(E)-3-methyl-4-[(2R,4S)-4-methyl-5-oxooxolan-2-yl]but-2-enyl]oxolan-2-one	38356551	Click to see CC1CC(OC1=O)CC(=CCC2COC(=O)C2=C)C	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(4R)-3-methylidene-4-[(E)-3-methyl-4-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]but-2-enyl]oxolan-2-one	38356536	Click to see CC1CC(OC1=O)CC(=CCC2COC(=O)C2=C)C	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(5S)-3-methylidene-5-[(Z)-2-methyl-4-(4-methylidene-5-oxooxolan-3-yl)but-2-enyl]oxolan-2-one	162817352	Click to see CC(=CCC1COC(=O)C1=C)CC2CC(=C)C(=O)O2	262.30	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
[(1R,2E,6E)-3,7-dimethyl-1-[(3R)-4-methylidene-5-oxooxolan-3-yl]-8-oxoocta-2,6-dienyl] acetate	14733726	Click to see CC(=CC(C1COC(=O)C1=C)OC(=O)C)CCC=C(C)C=O	306.40	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
[(1S,2E,6E)-3,7-dimethyl-1-[(3R)-4-methylidene-5-oxooxolan-3-yl]-8-oxoocta-2,6-dienyl] acetate	163022030	Click to see CC(=CC(C1COC(=O)C1=C)OC(=O)C)CCC=C(C)C=O	306.40	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
[3,7-Dimethyl-1-(4-methylidene-5-oxooxolan-3-yl)-8-oxoocta-2,6-dienyl] acetate	163022029	Click to see CC(=CC(C1COC(=O)C1=C)OC(=O)C)CCC=C(C)C=O	306.40	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
3-Methylidene-4-[3-methyl-4-(4-methyl-5-oxooxolan-2-yl)but-2-enyl]oxolan-2-one	72738651	Click to see CC1CC(OC1=O)CC(=CCC2COC(=O)C2=C)C	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
8-Hydroxy-2,6-dimethyl-8-(4-methylidene-5-oxooxolan-3-yl)octa-2,6-dienal	162893444	Click to see CC(=CC(C1COC(=O)C1=C)O)CCC=C(C)C=O	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
Antheindurolide A	133556391	Click to see CC1CC(OC1=O)CC(=CCC2COC(=O)C2=C)C	264.32	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S,3aR,4S,6E,11aR)-4-hydroxy-10-(hydroxymethyl)-3,6-dimethyl-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-2-one	163004748	Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)O	266.33	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,5R)-3-methyl-5-(2-oxopropyl)oxolan-2-one	92164750	Click to see CC1CC(OC1=O)CC(=O)C	156.18	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(3R,5S)-3-methyl-5-(2-oxopropyl)oxolan-2-one	92245063	Click to see CC1CC(OC1=O)CC(=O)C	156.18	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(3S,5S)-3-methyl-5-(2-oxopropyl)oxolan-2-one	92164749	Click to see CC1CC(OC1=O)CC(=O)C	156.18	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(5R)-3-methylidene-5-[(2R)-2-methyl-4-[(3R)-4-methylidene-5-oxooxolan-3-yl]-3-oxobutyl]oxolan-2-one	162933267	Click to see CC(CC1CC(=C)C(=O)O1)C(=O)CC2COC(=O)C2=C	278.30	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
(5S)-3-methylidene-5-[(2S)-2-methyl-4-[(3R)-4-methylidene-5-oxooxolan-3-yl]-3-oxobutyl]oxolan-2-one	162933265	Click to see CC(CC1CC(=C)C(=O)O1)C(=O)CC2COC(=O)C2=C	278.30	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
3-Methyl-5-(2-oxopropyl)dihydrofuran-2(3h)-one	282175	Click to see CC1CC(OC1=O)CC(=O)C	156.18	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
3-Methylidene-5-[2-methyl-4-(4-methylidene-5-oxooxolan-3-yl)-3-oxobutyl]oxolan-2-one	14733729	Click to see CC(CC1CC(=C)C(=O)O1)C(=O)CC2COC(=O)C2=C	278.30	unknown	https://doi.org/10.1016/0031-9422(90)85221-Z
Achillin	291264	Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C	246.30	unknown	https://doi.org/10.1080/10286020.2014.931377
Desacetoxymatricarin	167683	Click to see CC1C2CCC(=C3C(C2OC1=O)C(=CC3=O)C)C	246.30	unknown	https://doi.org/10.1080/10286020.2014.931377 https://doi.org/10.1016/J.PHYTOCHEM.2007.07.021
> 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/10.1055/S-0028-1097913
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin	5280704	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O	432.40	unknown	https://doi.org/10.1055/S-0028-1097913
Linarin	5317025	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC=C(C=C5)OC)O)O)O)O)O)O)O	592.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin	5281702	Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Hispidulin	5281628	Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O	300.26	unknown	via CMAUP database

Biological Material Top

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Anthemis pseudocotula

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top