Lysimachia monelli - Unknown
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Internal ID UUID644022c0bb5a7674966236
Scientific name Lysimachia monelli
Authority (L.) U.Manns & Anderb.
First published in Willdenowia 39: 52 (2009)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anagallis angustifolia Salisb. Prodr. Stirp. Chap. Allerton : 121 (1796)
Anagallis collina Schousb. Iagttag. Vextrig. Marokko : 64 (1800)
Anagallis fruticosa Vent. Choix Pl. : t. 14 (1803)
Anagallis grandiflora Andrews Bot. Repos. 6: t. 367 (1804)
Anagallis hispanica Samp. Ann. Sci. Nat. (Oporto) 6: 58 (1901)
Anagallis linifolia var. collina (Schousb.) Ball J. Linn. Soc., Bot. 16: 562 1878
Anagallis linifolia var. microphylla Ball J. Linn. Soc., Bot. 16: 562 1878
Anagallis linifolia var. monelli (L.) R.Knuth Pflanzenr. IV, 237: 325 1905
Anagallis linifolia var. rubriflora Batt. Fl. Algérie Dicot.: 723 1890
Anagallis longicaulis Lázaro Ibiza Anales Soc. Esp. Hist. Nat. 29: 166 (1900)
Anagallis monelli L. Sp. Pl. : 148 (1753)
Anagallis monelli subsp. collina (Schousb.) H.Lindb. Acta Soc. Sci. Fenn., Ser. B, Opera Biol. 1(2): 115 1932
Anagallis monelli subsp. linifolia (L.) Maire Cat. Pl. Maroc 3: 562 1934
Anagallis monelli var. microphylla (Ball) Vasc. Mem. Soc. Brot. 21: 232. 1971
Anagallis monelli var. willmoreana Curtis Bot. Mag. 62: t. 3380 1835
Anagallis webbiana Penny ex Loud. Gard. Mag. & Reg. Rural Domest. Improv. 5: 471 (1829)
Anagallis willkommii Sennen Bol. Soc. Ibér. Ci. Nat. 35: 21 (1936)
Anagallis willmoreana Don ex Hook. Bot. Mag. 61: t. 3380 (1834)
Anagallis phillipsii Paxton Paxton's Mag. Bot. 4: 167 (1838)
Anagallis monelli var. lilacina D.Don Brit. Fl. Gard. 7: t. 377 (1837)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Lysimachia monelli subsp. linifolia (L.) Peruzzi Inform. Bot. Ital. 42(1): 383 (2010)
Lysimachia monelli subsp. maritima (Mariz) Carlón, M.Laínz, Moreno Mor., Rodr.Berd. & Ó.Sánchez Doc. Jard. Bot. Atlántico 10: 65 (2014)

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Europe
    • Middle Europe
      • Czechoslovakia
    • Southeastern Europe
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Portugal
      • Sardegna
      • Spain
  • Northern America
    • Southeastern U.S.A.
      • Virginia
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000744203
INPN 610912
Flora of Italy 3824
KEW urn:lsid:ipni.org:names:77100405-1
The Plant List kew-2896585
NCBI Taxonomy 306291
IPNI 77100405-1
GBIF 8076173
Calflora (Californian flora) 13210
USDA GRIN 467245
CMAUP NPO21404
Open Tree Of Life 671287

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
Biosynthesis and Characterization of Silver Nanoparticles from the Extremophile Plant Aeonium haworthii and Their Antioxidant, Antimicrobial and Anti-Diabetic Capacities Essghaier B, Dridi R, Mottola F, Rocco L, Zid MF, Hannachi H Nanomaterials (Basel) 25-Dec-2022
PMCID:PMC9823831
doi:10.3390/nano13010100
PMID:36616010
First Report of the Biosynthesis and Characterization of Silver Nanoparticles Using Scabiosa atropurpurea subsp. maritima Fruit Extracts and Their Antioxidant, Antimicrobial and Cytotoxic Properties Essghaier B, Toukabri N, Dridi R, Hannachi H, Limam I, Mottola F, Mokni M, Zid MF, Rocco L, Abdelkarim M Nanomaterials (Basel) 07-May-2022
PMCID:PMC9104986
doi:10.3390/nano12091585
PMID:35564294
In silico bioprospecting of taraxerol as a main protease inhibitor of SARS-CoV-2 to develop therapy against COVID-19 Mujwar S, Harwansh RK Struct Chem 28-Apr-2022
PMCID:PMC9046011
doi:10.1007/s11224-022-01943-x
PMID:35502321
Antioxidant Activity of Natural Hydroquinones Giner RM, Ríos JL, Máñez S Antioxidants (Basel) 09-Feb-2022
PMCID:PMC8868229
doi:10.3390/antiox11020343
PMID:35204225
Screening for Selective Anticancer Activity of 65 Extracts of Plants Collected in Western Andalusia, Spain Calderón-Montaño JM, Martínez-Sánchez SM, Jiménez-González V, Burgos-Morón E, Guillén-Mancina E, Jiménez-Alonso JJ, Díaz-Ortega P, García F, Aparicio A, López-Lázaro M Plants (Basel) 15-Oct-2021
PMCID:PMC8537044
doi:10.3390/plants10102193
PMID:34686002
Do s genes or deleterious recessives control late-acting self-incompatibility in Handroanthus heptaphyllus (Bignoniaceae)? A diallel study with four full-sib progeny arrays Bianchi MB, Meagher TR, Gibbs PE Ann Bot 23-Feb-2021
PMCID:PMC8103807
doi:10.1093/aob/mcab031
PMID:33619532
DiaNat-DB: a molecular database of antidiabetic compounds from medicinal plants Madariaga-Mazón A, Naveja JJ, Medina-Franco JL, Noriega-Colima KO, Martinez-Mayorga K RSC Adv 28-Jan-2021
PMCID:PMC8694643
doi:10.1039/d0ra10453a
PMID:35424427
Characterization of Metabolites and Transcripts Involved in Flower Pigmentation in Primula vulgaris Li L, Ye J, Li H, Shi Q Front Plant Sci 20-Nov-2020
PMCID:PMC7714730
doi:10.3389/fpls.2020.572517
PMID:33329630
Anatomical and biochemical analyses reveal the mechanism of double-color formation in Paeonia suffruticosa ‘Shima Nishiki’ Zhang X, Zhao M, Guo J, Zhao L, Xu Z 3 Biotech 26-Sep-2018
PMCID:PMC6158150
doi:10.1007/s13205-018-1459-9
PMID:30305991
Visibility vs. biomass in flowers: exploring corolla allocation in Mediterranean entomophilous plants Herrera J Ann Bot 02-Mar-2009
PMCID:PMC2707908
doi:10.1093/aob/mcp046
PMID:19258340
Mutagenic, antimutagenic and antioxidant activities of a new class of beta-glucoside hydroxyhydroquinone from Anagallis monelli growing in Tunisia. Ammar S, Mahjoub MA, Charfi N, Skandarani I, Chekir-Ghedira L, Mighri Z Chem Pharm Bull (Tokyo) 01-Mar-2007
doi:10.1248/CPB.55.385
PMID:17329877

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
> Alkaloids and derivatives / Aporphines
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown via CMAUP database
Lysicamine 122691 Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC 291.30 unknown via CMAUP database
> Alkaloids and derivatives / Aristolactams
Goniopedaline 183523 Click to see COC1=C(C(=C2C3=C1C4=CC=CC=C4C=C3NC2=O)OC)O 295.29 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzylethers
8-Methoxygoniodiol 637248 Click to see COC(C1=CC=CC=C1)C(C2CC=CC(=O)O2)O 248.27 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Goniodiol 8-acetate 10945698 Click to see CC(=O)OC(C1=CC=CC=C1)C(C2CC=CC(=O)O2)O 276.28 unknown via CMAUP database
Goniodiol diacetate 11012583 Click to see CC(=O)OC(C1CC=CC(=O)O1)C(C2=CC=CC=C2)OC(=O)C 318.32 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Styrenes
Goniothalamin 6440856 Click to see C1C=CC(=O)OC1C=CC2=CC=CC=C2 200.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Pinoresinol 73399 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
(1R,5R,7R,8S)-8-hydroxy-7-phenyl-2,6-dioxabicyclo[3.3.1]nonan-3-one 102591096 Click to see C1C2CC(=O)OC1C(C(O2)C3=CC=CC=C3)O 234.25 unknown via CMAUP database
9-Deoxygoniopypyrone 126233 Click to see C1C2CC(=O)OC1C(C(O2)C3=CC=CC=C3)O 234.25 unknown via CMAUP database
Goniothalesdiol A 16079978 Click to see COC(=O)CC1CC(C(C(O1)C2=CC=CC=C2)O)O 266.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-[2,5-Dihydroxy-3-(methylaminomethyl)phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162938739 Click to see CNCC1=C(C(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O)O 331.32 unknown https://doi.org/10.1248/CPB.55.385
Goniothalesacetate 16079979 Click to see CC(=O)OC1C(C(OC1C(CC(=O)OC)OC)C2=CC=CC=C2)O 338.40 unknown via CMAUP database
Zinolol 16216016 Click to see CNCC1=C(C(=CC(=C1)O)OC2C(C(C(C(O2)CO)O)O)O)O 331.32 unknown https://doi.org/10.1248/CPB.55.385
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5Z)-5-[(2S,3R)-2,3-dihydroxy-3-phenylpropylidene]furan-2-one 10998863 Click to see C1=CC=C(C=C1)C(C(C=C2C=CC(=O)O2)O)O 232.23 unknown via CMAUP database
Goniobutenolide A 11770317 Click to see C1=CC=C(C=C1)C(C(C=C2C=CC(=O)O2)O)O 232.23 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(5S,6R,7S,8S)-Goniotriol 26496963 Click to see C1=CC=C(C=C1)C(C(C2C(C=CC(=O)O2)O)O)O 250.25 unknown via CMAUP database
8-Chlorogoniodiol 10988787 Click to see C1C=CC(=O)OC1C(C(C2=CC=CC=C2)Cl)O 252.69 unknown via CMAUP database
Goniodiol 180702 Click to see C1C=CC(=O)OC1C(C(C2=CC=CC=C2)O)O 234.25 unknown via CMAUP database
Goniodiol 7-acetate 126414 Click to see CC(=O)OC(C1CC=CC(=O)O1)C(C2=CC=CC=C2)O 276.28 unknown via CMAUP database
Goniothalamin epoxide 11042149 Click to see C1C=CC(=O)OC1C2C(O2)C3=CC=CC=C3 216.23 unknown via CMAUP database
Goniotriol 125950 Click to see C1=CC=C(C=C1)C(C(C2C(C=CC(=O)O2)O)O)O 250.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database

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