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Ceratolimon feei

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440105fa095b233044999
Scientific name Ceratolimon feei
Authority (Girard) M.B.Crespo & M.D.Lledó
First published in Bot. J. Linn. Soc. 132: 170 (2000)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Bubania feei Girard Mém. Sect. Sci. Acad. Sci. Montpellier 1: 185 (1848)
Limoniastrum feei Batt. Fl. Algérie , Dicot.: 726 (1890)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Ceratolimon feei var. grandiflorum (Maire & Wilczek) M.B.Crespo & M.D.Lledó Bot. J. Linn. Soc. 132: 171 (2000)
Ceratolimon feei var. feei

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000596392
Tropicos 100309232
KEW urn:lsid:ipni.org:names:1013533-1
The Plant List kew-2711125
Open Tree Of Life 166732
NCBI Taxonomy 114144
IPNI 1013533-1
iNaturalist 831199
GBIF 7298153
EOL 5490785

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
Electrochemical Characterization of the Antioxidant Properties of Medicinal Plants and Products: A Review Ziyatdinova G, Kalmykova A Molecules 02-Mar-2023
PMCID:PMC10004803
doi:10.3390/molecules28052308
PMID:36903553
An expanded molecular phylogeny of Plumbaginaceae, with emphasis on Limonium (sea lavenders): Taxonomic implications and biogeographic considerations Koutroumpa K, Theodoridis S, Warren BH, Jiménez A, Celep F, Doğan M, Romeiras MM, Santos‐Guerra A, Fernández‐Palacios JM, Caujapé‐Castells J, Moura M, Menezes de Sequeira M, Conti E Ecol Evol 06-Dec-2018
PMCID:PMC6308857
doi:10.1002/ece3.4553
PMID:30619554
Limoniastrum guyonianum aqueous gall extract induces apoptosis in human cervical cancer cells involving p16INK4A re-expression related to UHRF1 and DNMT1 down-regulation Krifa M, Alhosin M, Muller CD, Gies JP, Chekir-Ghedira L, Ghedira K, Mély Y, Bronner C, Mousli M J Exp Clin Cancer Res 20-May-2013
PMCID:PMC3695779
doi:10.1186/1756-9966-32-30
PMID:23688286
Analysis and isolation of saponins from Limoniastrum feei by LC-UV N. Belboukhari, A. Cheriti Springer Science and Business Media LLC 16-Nov-2009
doi:10.1007/S10600-009-9455-2

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 / Prenol lipids / Triterpenoids
[(2S,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bR)-10,11-dihydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-2-yl]methyl acetate 163195385 Click to see 516.80 unknown https://doi.org/10.1007/S10600-009-9455-2
[10,11-Dihydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicen-2-yl]methyl acetate 162846545 Click to see 516.80 unknown https://doi.org/10.1007/S10600-009-9455-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
[(2R,3R,4S,5R,6R)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-6-[3,3-dimethyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-6,16-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl acetate 162982573 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)COC(=O)C)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(C)(C)COC8C(C(C(C(O8)CO)O)O)O)O 975.10 unknown https://doi.org/10.1007/S10600-009-9455-2
[6-[[6-[3,3-Dimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-6,16-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl acetate 162982572 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(C(O6)COC(=O)C)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(C)(C)COC8C(C(C(C(O8)CO)O)O)O)O 975.10 unknown https://doi.org/10.1007/S10600-009-9455-2

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