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Cladanthus arabicus

Cladanthus arabicus - 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 UUID643fcaa88be6a259371310
Scientific name Cladanthus arabicus
Authority (L.) Cass.
First published in Bull. Sci. Soc. Philom. Paris (1816); et in Dict. Sc. Nat. i

Description Top

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Synonyms Top

Scientific name Authority First published in
Cladanthus maroccanus Gand. Bull. Soc. Bot. France 60: 23 (1913)
Chamaemelum proliferum Moench Suppl. Meth. : 257 (1802)
Anthemis sessilis Salisb. Prodr. Stirp. Chap. Allerton : 204 (1796)
Cladanthus ifniensis Caball. Trab. Mus. Nac. Ci. Nat., Ser. Bot. n.° 28, 25 (1935)
Anthemis arabica L. Sp. Pl. : 896 (1753)
Anthemis prolifera Pers. Syn. Pl. 2(2): 467 (1807)
Cladanthus proliferus DC. Prodr. 6: 18 (1838)
Chamaemelum cladanthus E.H.L.Krause Deutschl. Fl. (Sturm), ed. 2. 13: 218 (1905)

Common names Top

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Language Common/alternative name
Swedish grenkulla
Chinese 金凤菊

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Germany
    • Northern Europe
      • Great Britain
    • Southeastern Europe
      • Sicilia
    • Southwestern Europe
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000040208
Tropicos 2717358
INPN 610631
KEW urn:lsid:ipni.org:names:196234-1
The Plant List gcc-138882
Open Tree Of Life 984748
Observations.org 116588
NCBI Taxonomy 99040
NBN Atlas NBNSYS0200003576
IPNI 196234-1
iNaturalist 512465
GBIF 3110771
EPPO CFAAR
Elurikkus 730458
CMAUP NPO28345

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
Antimicrobial activity in Asterceae: The selected genera characterization and against multidrug resistance bacteria Gou J, Lu Y, Xie M, Tang X, Chen L, Zhao J, Li G, Wang H Heliyon 31-Mar-2023
PMCID:PMC10161380
doi:10.1016/j.heliyon.2023.e14985
PMID:37151707
Overview of Bioactive Fungal Secondary Metabolites: Cytotoxic and Antimicrobial Compounds Conrado R, Gomes TC, Roque GS, De Souza AO Antibiotics (Basel) 11-Nov-2022
PMCID:PMC9687038
doi:10.3390/antibiotics11111604
PMID:36421247
A Quantitative Study on the Ethnobotanical Knowledge about Wild Edible Plants among the Population of Messiwa Ghanimi R, Ouhammou A, Babahmad RA, Cherkaoui M Ethiop J Health Sci 01-Nov-2022
PMCID:PMC9692160
doi:10.4314/ejhs.v32i6.22
PMID:36475263
Chemical Composition and Antimicrobial Potential of Essential Oil of Acritopappus confertus (Gardner) R.M.King & H.Rob. (Asteraceae) da Cruz RP, Castro JW, Leite DO, de Carvalho NK, Almeida-Bezerra JW, Pereira RL, Rodrigues FF, Bezerra JJ, Costa AR, Mori E, de Farias PA, Coutinho HD, Morais-Braga MF, Iriti M, da Costa JG, Rodrigues FF Pharmaceuticals (Basel) 17-Oct-2022
PMCID:PMC9611346
doi:10.3390/ph15101275
PMID:36297389
Ethnobotanical study on wild edible plants traditionally used by Messiwa people, Morocco Ghanimi R, Ouhammou A, Ahouach A, Cherkaoui M J Ethnobiol Ethnomed 15-Mar-2022
PMCID:PMC8922891
doi:10.1186/s13002-022-00500-4
PMID:35292058
Considerations and Caveats in Combating ESKAPE Pathogens against Nosocomial Infections Ma Y, Wang C, Li Y, Li J, Wan Q, Chen J, Tay FR, Niu L Adv Sci (Weinh) 05-Dec-2019
PMCID:PMC6947519
doi:10.1002/advs.201901872
PMID:31921562
Antimicrobial, Antioxidant, and Immunomodulatory Properties of Essential Oils: A Systematic Review Valdivieso-Ugarte M, Gomez-Llorente C, Plaza-Díaz J, Gil Á Nutrients 15-Nov-2019
PMCID:PMC6893664
doi:10.3390/nu11112786
PMID:31731683
Assessment of the Food Habits of the Moroccan Dorcas Gazelle in M’Sabih Talaa, West Central Morocco, Using the trnL Approach Ait Baamrane MA, Shehzad W, Ouhammou A, Abbad A, Naimi M, Coissac E, Taberlet P, Znari M PLoS One 27-Apr-2012
PMCID:PMC3338736
doi:10.1371/journal.pone.0035643
PMID:22558187
ChemInform Abstract: Constituents of Cladanthus Arabicus. M. WICHLACZ, W. M. DANIEWSKI, W. DANIEKIEWICZ, M. GUMULKA, B. DROZDZ, H. GRABARCZYK Wiley 11-Nov-2011
doi:10.1002/CHIN.199516211
Sesquiterpenes of Cladanthus arabicus Wo̵dzimierz M. Daniewsk, Witold Danikiewicz, Maria Gumuk̵a, Elżbieta Pankowska, Janusz Krajewski, Halina Grabarczyk, Monika Wicha̵cz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90862-8

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 / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3-(3,4-Dimethoxyphenyl)propyl 3-(3,4-dimethoxyphenyl)propanoate 9977571 Click to see COC1=C(C=C(C=C1)CCCOC(=O)CCC2=CC(=C(C=C2)OC)OC)OC 388.50 unknown https://doi.org/10.1002/CHIN.199516211
https://doi.org/10.1016/S0031-9422(00)90862-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see CCCCCCCCCCCCCCCCCCCC(CCCCCCCCC)O 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C=C)C 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)OC(=O)C)C 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(=O)C2(C)C)C 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCC(C2(C)C)O)C 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimaric Acid 221580 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see CC1CCC2C(C1)C2(C)C 138.25 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see CC1(CC2(CCC1C2)C)C 138.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see CC(=O)OC1CC2CCC1(C2(C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-beta-Phellandrene 442484 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(5-acetyloxy-3,6,10-trimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-9-yl) acetate 75111168 Click to see CC1C2CC(C(=CCC(C(=CC2OC1=O)C)OC(=O)C)C)OC(=O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)90862-8
[(3R,3aS,5S,6E,9S,10E,11aS)-5-acetyloxy-3,6,10-trimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-9-yl] acetate 45360229 Click to see CC1C2CC(C(=CCC(C(=CC2OC1=O)C)OC(=O)C)C)OC(=O)C 350.40 unknown https://doi.org/10.1016/S0031-9422(00)90862-8
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3R,3aS,6S,6aS,9aR,9bS)-3,6,9-trimethyl-3,3a,4,5,6,6a,9a,9b-octahydroazuleno[4,5-b]furan-2,7-dione 10977807 Click to see CC1CCC2C(C(=O)OC2C3C1C(=O)C=C3C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)90862-8
Cichoralexin 5315718 Click to see CC1CCC2C(C(=O)OC2C3C1C(=O)C=C3C)C 248.32 unknown https://doi.org/10.1016/S0031-9422(00)90862-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1002/CHIN.199516211
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown https://doi.org/10.1002/CHIN.199516211
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database

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