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Internal ID UUID643fcf9848c80797725517
Scientific name Anacyclus monanthos
Authority Thell.
First published in Mém. Soc. Sci. Nat. Math. Cherbourg 38: 518 (1912)

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Synonyms Top

Scientific name Authority First published in
Anthemis arabica Velen. Sitzungsber. Königl. Böhm. Ges. 1911(11): 11. 1912 [1911 publ 1912]

Common names Top

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Language Common/alternative name
Arabic قنيطسة أحادية السداة

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Anacyclus monanthos subsp. cyrtolepidioides (Pomel) Humphries Bull. Brit. Mus. (Nat. Hist.), Bot. 7(3): 118 (1979)
Anacyclus monanthos subsp. monanthos (L.) Thell.

Varieties (abbr. var.) 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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000091725
Tropicos 2733871
INPN 610702
KEW urn:lsid:ipni.org:names:176324-1
The Plant List gcc-47996
Open Tree Of Life 919824
NCBI Taxonomy 282203
IPNI 176324-1
GBIF 3148584
EOL 6262790
CMAUP NPO27889

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)!
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Title Authors Publication Released IDs
Genome size variation at constant chromosome number is not correlated with repetitive DNA dynamism in Anacyclus (Asteraceae) Vitales D, Álvarez I, Garcia S, Hidalgo O, Nieto Feliner G, Pellicer J, Vallès J, Garnatje T Ann Bot 07-Nov-2019
PMCID:PMC7103019
doi:10.1093/aob/mcz183
PMID:31697800
Diversity of desert rangelands of Tunisia Gamoun M, Belgacem AO, Louhaichi M Plant Divers 20-Aug-2018
PMCID:PMC6224667
doi:10.1016/j.pld.2018.06.004
PMID:30740567
New N-alkylamides from Anacyclus pyrethrum J Boonen, V Sharma, V Dixit, B De Spiegeleer Georg Thieme Verlag KG 05-Aug-2011
doi:10.1055/S-0031-1282578

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Hentriacontanoic acid pentyl ester 21775821 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCC 537.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Amino fatty acids
3-Aminopentanedioic acid 73064 Click to see C(C(CC(=O)O)N)C(=O)O 147.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,4R,5S,6S,9R)-9-bromo-4-[[(1R,4R)-4-bromo-1-hydroxy-3,3-dimethylcyclohexyl]methyl]-6-methyl-11-oxatricyclo[4.3.2.01,5]undecan-10-one 46703590 Click to see CC1(CC(CCC1Br)(CC2CCC34C2C(CCC3Br)(OC4=O)C)O)C 478.30 unknown via CMAUP database
[(1R,4R)-4-bromo-1-[[(1R,4R,5S,6S,9R)-9-bromo-6-methyl-10-oxo-11-oxatricyclo[4.3.2.01,5]undecan-4-yl]methyl]-3,3-dimethylcyclohexyl] acetate 46703591 Click to see CC(=O)OC1(CCC(C(C1)(C)C)Br)CC2CCC34C2C(CCC3Br)(OC4=O)C 520.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
Santonin 221071 Click to see CC1C2CCC3(C=CC(=O)C(=C3C2OC1=O)C)C 246.30 unknown https://doi.org/10.1055/S-0031-1282578
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1055/S-0031-1282578
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(6R,7S,10R,11S,14R)-2,6,10-Trimethyl-14-[(S)-1-hydroxy-1-methyl-3-(3beta-hydroxy-3,7,7-trimethyl-6beta-bromohexahydrooxepin-2beta-yl)propyl]-2,7:6,11:10,14-triepoxy-3-tetradecene 102432674 Click to see CC1(C=CCC2(C(O1)CCC3(C(O2)CCC(O3)C(C)(CCC4C(CCC(C(O4)(C)C)Br)(C)O)O)C)C)C 587.60 unknown via CMAUP database
Aplysiol C 101519535 Click to see CC(=CCCC(C)(C1CCC(O1)(C)C2CCC3C(O2)(CCC(O3)C4(CCC(C(O4)(C)C)Br)C)C)O)C 571.60 unknown via CMAUP database
Aplysiol D 46703589 Click to see CC1(C(CCC(O1)(C)C2CCC3(C(O2)CCC(O3)C4(CCC(O4)C(C)(CC=CC(C)(C)O)O)C)C)Br)C 587.60 unknown via CMAUP database
Aplysiol E 101519536 Click to see CC1(C(CCC(O1)(C)C2CCC3(C(O2)CCC(O3)C4(CCC(O4)C(C)(CC(C5C(O5)(C)C)Cl)O)C)C)Br)C 622.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-2-azaniumyl-5-(carbamoylamino)pentanoate 6992098 Click to see C(CC(C(=O)[O-])[NH3+])CNC(=O)N 175.19 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Aspartic acid and derivatives
D-Aspartic acid 83887 Click to see C(C(C(=O)O)N)C(=O)O 133.10 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Amino acids and derivatives / Kainoids
(6'S)-Isodomoic acid G 17753955 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Domoic acid 5282253 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid A 6442601 Click to see CC(=CCC=C(C)C(=O)O)C1CNC(C1CC(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid B 6442550 Click to see CC(=CCC=C(C)C(=O)O)C1CNC(C1CC(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid C 11301378 Click to see CC(=CCCC(=C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid D 6442551 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Isodomoic acid F 101790920 Click to see CC(C=CC=C(C)C1CNC(C1CC(=O)O)C(=O)O)C(=O)O 311.33 unknown via CMAUP database
Kainic acid 10255 Click to see CC(=C)C1CNC(C1CC(=O)O)C(=O)O 213.23 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1055/S-0031-1282578
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790 790 Click to see C1=NC2=C(N1)C(=O)N=CN2 136.11 unknown via CMAUP database

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