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Cota palaestina

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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 UUID643fd3a0ab0ee645316892
Scientific name Cota palaestina
Authority Reut. ex Unger & Kotschy
First published in Ins. Cypern : 240 (1865)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anthemis syriaca Bornm. Repert. Spec. Nov. Regni Veg. 10: 470 (1912)
Anthemis melanolepis Boiss. Fl. Orient. , Suppl.: 297 (1888)
Anacyclus truncatus J.Gay Fl. Orient. 3: 283 (1875)
Anthemis palestina Reut. ex Boiss. Fl. Orient. 3: 283 (1875)
Anthemis melanolepis var. cypria Eig Palestine J. Bot., Jerusalem Ser. 1: 206 (1938)
Anthemis cota subsp. melanolepis (Boiss.) Holmboe Veg. Cyp.: 181 (1914)
Anthemis libanotica Bornm. Repert. Spec. Nov. Regni Veg. 10: 471 (1912)
Anthemis truncata P.Candargy P. Candargy in Rev. Méd.-Pharm. 5. 1892. 152 1892
Anacyclus anomalus J.Gay ex Boiss. Fl. Orient. 3: 283 (1875)
Anthemis melanolepis var. macrocarpa Eig Palestine J. Bot., Jerusalem Ser. 1: 207 (1938)
Cota syriaca (Bornm.) Holub Folia Geobot. Phytotax. 9(3): 270 (1974)
Anthemis cota f. apiculata Holmboe Veg. Cyp.: 18 (1914)
Anthemis palestina subsp. syriaca (Bornm.) R.Fern. Rev. Biol. 12: 422 (1984): (1984)

Common names Top

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Language Common/alternative name
Arabic كوتا فلسطينية
Hebrew קחוון שחור מוצים
Hebrew קחוון ארצישראלי
Dutch rumian palestyński
Polish rumian palestyński

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
  • Asia-temperate
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000133617
KEW urn:lsid:ipni.org:names:198398-1
The Plant List gcc-94420
Open Tree Of Life 112205
NCBI Taxonomy 589831
IPNI 198398-1
iNaturalist 514831
GBIF 5390639
EPPO ANTPA
EOL 6260308

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
Effect of Plant Essential Oil Formulations on Bemisia tabaci MEAM1 (Gennadius) and Its Parasitoid Eretmocerus hayati (Zolnerowich and Rose) Hassan E, Obaidoon Y, Mostafiz MM, Senior L Plants (Basel) 12-Dec-2023
PMCID:PMC10747523
doi:10.3390/plants12244137
PMID:38140464
Targeting phosphoglycerate kinases by tatridin A, a natural sesquiterpenoid endowed with anti-cancer activity, using a proteomic platform Ferraro G, Voli A, Mozzicafreddo M, Pollastro F, Tosco A, Monti MC Front Mol Biosci 11-Sep-2023
PMCID:PMC10519794
doi:10.3389/fmolb.2023.1212541
PMID:37767160
Medicinal plants of Jordan: Scoping review Abu-Odeh A, Fino L, Al-Absi G, Alnatour D, Al-Darraji M, Shehadeh M, Suaifan G Heliyon 07-Jun-2023
PMCID:PMC10276232
doi:10.1016/j.heliyon.2023.e17081
PMID:37332946
Sesquiterpene Lactones: Promising Natural Compounds to Fight Inflammation Matos MS, Anastácio JD, Nunes dos Santos C Pharmaceutics 30-Jun-2021
PMCID:PMC8309091
doi:10.3390/pharmaceutics13070991
PMID:34208907
A Comparison Study on Traditional Mixtures of Herbal Teas Used in Eastern Mediterranean Area Obón C, Rivera D, Fonollá E, Alcaraz F, Attieh L Front Pharmacol 23-Apr-2021
PMCID:PMC8103161
doi:10.3389/fphar.2021.632692
PMID:33967769
A Systematic Review of Plants With Antibacterial Activities: A Taxonomic and Phylogenetic Perspective Chassagne F, Samarakoon T, Porras G, Lyles JT, Dettweiler M, Marquez L, Salam AM, Shabih S, Farrokhi DR, Quave CL Front Pharmacol 08-Jan-2021
PMCID:PMC7821031
doi:10.3389/fphar.2020.586548
PMID:33488385
Phytochemicals in Helicobacter pylori Infections: What Are We Doing Now? Salehi B, Sharopov F, Martorell M, Rajkovic J, Ademiluyi AO, Sharifi-Rad M, Fokou PV, Martins N, Iriti M, Sharifi-Rad J Int J Mol Sci 10-Aug-2018
PMCID:PMC6121492
doi:10.3390/ijms19082361
PMID:30103451
Anti-Inflammatory and Cytostatic Activities of a Parthenolide-Like Sesquiterpene Lactone from Cota palaestina subsp. syriaca Talhouk RS, Nasr B, Fares MB, Ajeeb B, Nahhas R, Al Aaraj L, Talhouk SN, Ghaddar TH, Saliba NA Evid Based Complement Alternat Med 19-May-2015
PMCID:PMC4452324
doi:10.1155/2015/474597
PMID:26089941
Medicinal plant activity on Helicobacter pylori related diseases Wang YC World J Gastroenterol 14-Aug-2014
PMCID:PMC4130844
doi:10.3748/wjg.v20.i30.10368
PMID:25132753
Monocyclic Phenolic Acids; Hydroxy- and Polyhydroxybenzoic Acids: Occurrence and Recent Bioactivity Studies Khadem S, Marles RJ Molecules 08-Nov-2010
PMCID:PMC6259451
doi:10.3390/molecules15117985
PMID:21060304
Sesquiterpene lactones from Anthemis melanolepis and their antibacterial and cytotoxic activities. Prediction of their pharmacokinetic profile. Saroglou V, Karioti A, Rancic A, Dimas K, Koukoulitsa C, Zervou M, Skaltsa H J Nat Prod 26-Feb-2010
doi:10.1021/NP9004129
PMID:20112996
Capillary electrophoresis as a screening tool for alpha amylase inhibitors in plant extracts Hamdan II, Afifi FU Saudi Pharm J 13-Feb-2010
PMCID:PMC3792626
doi:10.1016/j.jsps.2010.02.004
PMID:24115900
Sesquiterpene Lactones from <i>Anthemis melanolepis</i> Vasiliki Saroglou, Anastasia Karioti, Jörg Heilmann, Zacharias Kypriotakis, Helen Skaltsa Wiley 26-Jan-2007
doi:10.1002/HLCA.200790012

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1021/NP9004129
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3-Hydroxy-4-methoxybenzoic acid 12575 Click to see COC1=C(C=C(C=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1021/NP9004129
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1021/NP9004129
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4aS,8aS)-3,4a,8,8-tetramethyl-4-[(3R)-3-methyl-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxypent-4-enyl]-5,6,7,8a-tetrahydro-1H-naphthalen-2-one 162940885 Click to see CC1=C(C2(CCCC(C2CC1=O)(C)C)C)CCC(C)(C=C)OC3C(C(C(CO3)O)O)O 436.60 unknown https://doi.org/10.1002/HLCA.200790012
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1R,2R,3S,5R,8S,11R)-2,8-dihydroxy-5-methyl-9,14-dimethylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-13-one 162920553 Click to see CC12CCC(C(=C)CC3C(C(C1O2)O)C(=C)C(=O)O3)O 280.32 unknown https://doi.org/10.1021/NP9004129
(1S,2R,3R,5R,8S,11S)-2,8-dihydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-9-en-13-one 162901613 Click to see CC1=CC2C(C(C3C(O3)(CCC1O)C)O)C(=C)C(=O)O2 280.32 unknown https://doi.org/10.1021/NP9004129
(1S,2R,3R,5R,8S,9E,11S)-2,8-dihydroxy-5,9-dimethyl-14-methylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradec-9-en-13-one 163185942 Click to see CC1=CC2C(C(C3C(O3)(CCC1O)C)O)C(=C)C(=O)O2 280.32 unknown https://doi.org/10.1021/NP9004129
1-epi-Tatridin B 7605278 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1021/NP9004129
2,8-Dihydroxy-5-methyl-9,14-dimethylidene-4,12-dioxatricyclo[9.3.0.03,5]tetradecan-13-one 14757918 Click to see CC12CCC(C(=C)CC3C(C(C1O2)O)C(=C)C(=O)O3)O 280.32 unknown https://doi.org/10.1021/NP9004129
4-Hydroxy-6-methyl-3,10-dimethylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2,9-dione 556782 Click to see CC1=CC(C2C(CC(=C)C(=O)CC1)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1021/NP9004129
4,9-dihydroxy-6-methyl-3,10-dimethylidene-4,7,8,9,11,11a-hexahydro-3aH-cyclodeca[b]furan-2-one 4437183 Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1021/NP9004129
anthemin C 46183869 Click to see CC1=CC(C2C(CC(=C)C(=O)CC1)OC(=O)C2=C)O 262.30 unknown https://doi.org/10.1021/NP9004129
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aR,4S,4aR,8S,8aR,9aR)-4,8-dihydroxy-8a-methyl-3,5-dimethylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 162971591 Click to see CC12CC3C(C(C1C(=C)CCC2O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1021/NP9004129
(3aR,4S,5aS,6S,9S,9aS,9bS)-4,6,9-trihydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one 102469273 Click to see CC1(CCC(C2(C1C3C(C(C2)O)C(=C)C(=O)O3)C)O)O 282.33 unknown https://doi.org/10.1002/HLCA.200790012
(3aS,4S,4aS,5R,8R,8aR,9aS)-4,5,8-trihydroxy-5,8a-dimethyl-3-methylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 46881108 Click to see CC1(CCC(C2(C1C(C3C(C2)OC(=O)C3=C)O)C)O)O 282.33 unknown https://doi.org/10.1021/NP9004129
4,5,8-Trihydroxy-5,8a-dimethyl-3-methylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 75053458 Click to see CC1(CCC(C2(C1C(C3C(C2)OC(=O)C3=C)O)C)O)O 282.33 unknown https://doi.org/10.1021/NP9004129
4,6,9-Trihydroxy-5a,9-dimethyl-3-methylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one 14191305 Click to see CC1(CCC(C2(C1C3C(C(C2)O)C(=C)C(=O)O3)C)O)O 282.33 unknown https://doi.org/10.1002/HLCA.200790012
4,8-Dihydroxy-8a-methyl-3,5-dimethylidene-3a,4,4a,6,7,8,9,9a-octahydrobenzo[f][1]benzofuran-2-one 14756430 Click to see CC12CC3C(C(C1C(=C)CCC2O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1021/NP9004129
Deacetyl-beta-cyclopyrethrosin 21629647 Click to see CC12CC3C(C(C1C(=C)CCC2O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1021/NP9004129
Elegalactone A 11108214 Click to see CC12CC3C(C(C1C(=C)CCC2O)O)C(=C)C(=O)O3 264.32 unknown https://doi.org/10.1021/NP9004129
Naphtho(1,2-b)furan-2(3H)-one, decahydro-4,6-dihydroxy-5a-methyl-3,9-bis(methylene)-, (3aR,4S,5aR,6R,9aS,9bR)- 156601 Click to see CC12CC(C3C(C1C(=C)CCC2O)OC(=O)C3=C)O 264.32 unknown https://doi.org/10.1002/HLCA.200790012
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aS,4R,5E,9E,11aS)-3a,4,7,8,11,11a-Hexahydro-4-hydroxy-6,10-dimethyl-3-methylenecyclodeca[b]furan-2(3H)-one 14191561 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)O 248.32 unknown https://doi.org/10.1002/HLCA.200790012
4-Hydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,11,11a-hexahydrocyclodeca[b]furan-2-one 73718740 Click to see CC1=CC(C2C(CC(=CCC1)C)OC(=O)C2=C)O 248.32 unknown https://doi.org/10.1002/HLCA.200790012
4,9-Dihydroxy-6,10-dimethyl-3-methylidene-3a,4,7,8,9,11a-hexahydrocyclodeca[b]furan-2-one 72731791 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1021/NP9004129
tatridin A 14466151 Click to see CC1=CC(C2C(C=C(C(CC1)O)C)OC(=O)C2=C)O 264.32 unknown https://doi.org/10.1021/NP9004129
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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 610148 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1002/HLCA.200790012
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown https://doi.org/10.1002/HLCA.200790012
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
17-Acetyl-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 4920 Click to see CC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 314.50 unknown https://doi.org/10.1021/NP9004129
Progesterone 5994 Click to see CC(=O)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C 314.50 unknown https://doi.org/10.1021/NP9004129
> Organoheterocyclic compounds / Benzofurans
6-Hydroxy-4,4,7a-trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one 14334 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1002/HLCA.200790012
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown https://doi.org/10.1002/HLCA.200790012
> 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/NP9004129
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP9004129
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/NP9004129
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP9004129
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP9004129
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP9004129
> 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/NP9004129
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/10.1021/NP9004129
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown https://doi.org/10.1021/NP9004129

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