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Plagius flosculosus

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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 UUID643fca6ebc93a175416659
Scientific name Plagius flosculosus
Authority (L.) S.Alavi & V.H.Heywood
First published in 273 1976

Description Top

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Synonyms Top

Scientific name Authority First published in
Plagius allionii L'Hér. ex DC. Prodr. 6: 135 (1838)
Tanacetum chrysanthemoides Gaertn. Fruct. Sem. Pl. ii. 396. t. 165
Cotula grandis Jacq. Observ. Bot. 4: 4 (1771)
Chrysanthemum flosculosum L. Sp. Pl. : 890 (1753)
Balsamita ageratifolia Desf. Actes Soc. Hist. Nat. Paris 1: t. 2 (1792)
Chrysocoma denticulata Jacq. Pl. Hort. Schoenbr. 3: 62 (1798)
Balsamita corymbosa Salzm. Flora 4: 112 (1821)
Leucanthemum flosculosum (L.) P.Giraud Ann. Univ. Grenoble, Sect. Sci.-Méd. 11: 201 (1935)
Plagius ageratifolius L.Herit. ex DC. Prodr. 6: 135 (1838)
Tanacetum virgatum Loisel. Fl. Gall. 2: 551 (1807)
Plagius virgatus DC. Prodr. 6: 135 (1838)
Matricaria rigida Desr. Encycl. 3: 787 (1792)

Common names Top

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Language Common/alternative name
Estonian sardiinia kaldkakar
French marguerite à feuilles d'agératum

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000038321
Tropicos 2703012
INPN 113791
Flora of Italy 5690
KEW urn:lsid:ipni.org:names:238672-1
The Plant List gcc-137050
Open Tree Of Life 614002
Observations.org 125521
NCBI Taxonomy 133260
IUCN Red List 164028
IPNI 238672-1
iNaturalist 203012
GBIF 5393702
EPPO PGVFL

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
HIV-1 Integrase Inhibition Activity by Spiroketals Derived from Plagius flosculosus, an Endemic Plant of Sardinia (Italy) and Corsica (France) Sanna C, D’Abrosca B, Fiorentino A, Giammarino F, Vicenti I, Corona A, Caredda A, Tramontano E, Esposito F Pharmaceuticals (Basel) 08-Aug-2023
PMCID:PMC10457970
doi:10.3390/ph16081118
PMID:37631033
Phylogeography and colonization pattern of subendemic round-leaved oxeye daisy from the Dinarides to the Carpathians Konowalik K Sci Rep 30-Sep-2022
PMCID:PMC9525303
doi:10.1038/s41598-022-19619-1
PMID:36180475
The Endemic Vascular Flora of Sardinia: A Dynamic Checklist with an Overview of Biogeography and Conservation Status Fois M, Farris E, Calvia G, Campus G, Fenu G, Porceddu M, Bacchetta G Plants (Basel) 23-Feb-2022
PMCID:PMC8912449
doi:10.3390/plants11050601
PMID:35270071
So Uncommon and so Singular, but Underexplored: An Updated Overview on Ethnobotanical Uses, Biological Properties and Phytoconstituents of Sardinian Endemic Plants Sanna C, Maxia A, Fenu G, Loi MC Plants (Basel) 29-Jul-2020
PMCID:PMC7465485
doi:10.3390/plants9080958
PMID:32751394
Antitumor Potential and Phytochemical Profile of Plants from Sardinia (Italy), a Hotspot for Biodiversity in the Mediterranean Basin Cappadone C, Mandrone M, Chiocchio I, Sanna C, Malucelli E, Bassi V, Picone G, Poli F Plants (Basel) 24-Dec-2019
PMCID:PMC7020228
doi:10.3390/plants9010026
PMID:31878127
Inhibiting NF-κB Activation by Small Molecules As a Therapeutic Strategy Gupta SC, Sundaram C, Reuter S, Aggarwal BB Biochim Biophys Acta 21-May-2010
PMCID:PMC2955987
doi:10.1016/j.bbagrm.2010.05.004
PMID:20493977
Endogenous levels of Echinacea alkylamides and ketones are important contributors to the inhibition of prostaglandin E2 and nitric oxide production in cultured macrophages LaLone CA, Rizshsky L, Hammer KD, Wu L, Solco AK, Yum M, Nikolau BJ, Wurtele ES, Murphy PA, Kim M, Birt DF J Agric Food Chem 14-Oct-2009
PMCID:PMC2777644
doi:10.1021/jf901202y
PMID:19807154
Biosynthesis and Function of Polyacetylenes and Allied Natural Products Minto RE, Blacklock BJ Prog Lipid Res 13-Mar-2008
PMCID:PMC2515280
doi:10.1016/j.plipres.2008.02.002
PMID:18387369
Polyacetylenverbindungen, CIII. Über die Polyine aus <i>Chrysanthemum serotinum</i> L. Ferdinand Bohlmann, Hans‐Günther Kapteyn Wiley 08-Jun-2007
doi:10.1002/CBER.19660990609
Cytotoxic diacetylenic spiroketal enol ethers from Plagius flosculosus. Casu L, Bonsignore L, Pinna M, Casu M, Floris C, Gertsch J, Cottiglia F J Nat Prod 01-Feb-2006
doi:10.1021/NP0504513
PMID:16499337
Ein neues sesquiterpen aus Chrysanthemum flosculosum L. F. Bohlmann, Nagabhushan Rao Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)84571-8
Über ein neues terpenderivat aus chrysanthemum flosculosum L. F. Bohlmann, M. Grenz Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)88177-6

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
Phenylheptatriyne 77981 Click to see CC#CC#CC#CC1=CC=CC=C1 164.20 unknown https://doi.org/10.1016/S0040-4039(01)88177-6
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(6R)-6-hydroxy-2-methyl-6-[(1S)-4-methylcyclohex-3-en-1-yl]hept-2-en-4-one 101316894 Click to see CC1=CCC(CC1)C(C)(CC(=O)C=C(C)C)O 236.35 unknown https://doi.org/10.1016/S0040-4039(01)84571-8
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl) acetate 327392 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1021/NP0504513
(2E,5S,7S)-2-hexa-2,4-diynylidene-7-methoxy-1,6-dioxaspiro[4.4]non-3-ene 163007657 Click to see CC#CC#CC=C1C=CC2(O1)CCC(O2)OC 230.26 unknown https://doi.org/10.1021/NP0504513
(2Z,5S,7R)-2-hexa-2,4-diynylidene-7-methoxy-1,6-dioxaspiro[4.4]non-3-ene 163007656 Click to see CC#CC#CC=C1C=CC2(O1)CCC(O2)OC 230.26 unknown https://doi.org/10.1021/NP0504513
(3-Chloro-2-hexa-2,4-diynylidene-4-hydroxy-1,6-dioxaspiro[4.4]non-7-en-9-yl) acetate 73035667 Click to see CC#CC#CC=C1C(C(C2(O1)C(C=CO2)OC(=O)C)O)Cl 308.71 unknown https://doi.org/10.1021/NP0504513
(5R)-2-[(E)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3-ene 44575220 Click to see CC#CC#CC=C1C=CC2(O1)CCCO2 200.23 unknown https://doi.org/10.1002/CBER.19660990609
https://doi.org/10.1021/NP0504513
(5R)-2-[(E)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene 44575221 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown https://doi.org/10.1021/NP0504513
(5R)-2-[(Z)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene 44575223 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown https://doi.org/10.1021/NP0504513
[(2E,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 92269933 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1021/NP0504513
[(2E,5S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 14167380 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1021/NP0504513
[(2Z,5S,9S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 163194702 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1021/NP0504513
[(2Z,5S)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate 44575224 Click to see CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown https://doi.org/10.1021/NP0504513
2-(2,4-Hexadiynylidene)-1,6-dioxaspiro[4.4]non-3-ene 103031 Click to see CC#CC#CC=C1C=CC2(O1)CCCO2 200.23 unknown https://doi.org/10.1002/CBER.19660990609
https://doi.org/10.1021/NP0504513
2-Hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene 327390 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 198.22 unknown https://doi.org/10.1021/NP0504513
2-Hexa-2,4-diynylidene-7-methoxy-1,6-dioxaspiro[4.4]non-3-ene 73023198 Click to see CC#CC#CC=C1C=CC2(O1)CCC(O2)OC 230.26 unknown https://doi.org/10.1021/NP0504513
Flosculin B 11615555 Click to see CC#CC#CC=C1C=CC2(O1)CCC(O2)OC 230.26 unknown https://doi.org/10.1021/NP0504513
Flosculin C 11593812 Click to see CC#CC#CC=C1C=CC2(O1)CCC(O2)OC 230.26 unknown https://doi.org/10.1021/NP0504513
Flosculins A 11630937 Click to see CC#CC#CC=C1C(C(C2(O1)C(C=CO2)OC(=O)C)O)Cl 308.71 unknown https://doi.org/10.1021/NP0504513
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(5E)-5-ethylidene-3,6,6-trimethylpyran-2-one 14606175 Click to see CC=C1C=C(C(=O)OC1(C)C)C 166.22 unknown https://doi.org/10.1016/S0040-4039(01)88177-6

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