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Paronychia argentea

Paronychia argentea - 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 UUID64400049ba205187031254
Scientific name Paronychia argentea
Authority Lam.
First published in Fl. Franç. 3: 230 (1779)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Chaetonychia paronychia (L.) Samp. Herb. Port. : 78 (1913)
Ferriera mediterranea Bubani Fl. Pyren. 3: 7 (1901)

Common names Top

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Language Common/alternative name
Spanish illecebrum mauritanicum
Spanish illecebrum maritimum
Arabic داحسية فضية
Arabic رجل الحمامة
Catalan paroníquia argentada
Catalan sanguinària blanca
German silber-mauermiere
Finnish hopeavuohenpolvi
Hebrew אלמוות הכסף
Kabyle latay n lexla
Swedish prasselört

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • Macaronesia
      • Canary Islands
    • Northeast Tropical Africa
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Cyprus
      • East Aegean Islands
      • Palestine
      • Sinai
      • Turkey
  • Europe
    • Southeastern Europe
      • Greece
      • Italy
      • Kriti
      • Sicilia
    • Southwestern Europe
      • Baleares
      • Corse
      • France
      • Portugal
      • Sardegna
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000466806
Tropicos 6302118
INPN 112429
Flora of Italy 749
KEW urn:lsid:ipni.org:names:434984-1
The Plant List kew-2533075
Open Tree Of Life 150973
Observations.org 120419
NCBI Taxonomy 157622
NBN Atlas NBNSYS0200002799
IPNI 434984-1
iNaturalist 208322
GBIF 5528747
EPPO PAYAR
EOL 3014013
USDA GRIN 407974
Wikipedia Paronychia_argentea

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
Complete chloroplast genomes of Cerastium alpinum, C. arcticum and C. nigrescens: genome structures, comparative and phylogenetic analysis Milarska SE, Androsiuk P, Paukszto Ł, Jastrzębski JP, Maździarz M, Larson KW, Giełwanowska I Sci Rep 31-Oct-2023
PMCID:PMC10618263
doi:10.1038/s41598-023-46017-y
PMID:37907682
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
UHPLC-MS Phytochemical Profiling and Insight into Bioactivity of Rabelera holostea (Greater Stitchwort) Extract Katanić Stanković JS, Đorović Jovanović J, Mišić D, Gašić U, Nikles S, Marković Z, Bauer R Molecules 28-Jan-2023
PMCID:PMC9921532
doi:10.3390/molecules28031274
PMID:36770939
An Overview of Hormone-Sensitive Lipase (HSL) Althaher AR ScientificWorldJournal 08-Dec-2022
PMCID:PMC9754850
doi:10.1155/2022/1964684
PMID:36530555
Metabolite Profiling and Biological Activity Assessment of Casuarina equisetifolia Bark after Incorporating Gold Nanoparticles Aboulthana WM, Refaat E, Khaled SE, Ibrahim NE, Youssef AM Asian Pac J Cancer Prev 01-Oct-2022
PMCID:PMC9924326
doi:10.31557/APJCP.2022.23.10.3457
PMID:36308372
Anti-Diabesity Middle Eastern Medicinal Plants and Their Action Mechanisms Saad B, Kmail A, Haq SZ Evid Based Complement Alternat Med 18-Jul-2022
PMCID:PMC9313926
doi:10.1155/2022/2276094
PMID:35899227
Neuroprotective Effects of Quercetin on Ischemic Stroke: A Literature Review Zhang L, Ma J, Yang F, Li S, Ma W, Chang X, Yang L Front Pharmacol 18-May-2022
PMCID:PMC9158527
doi:10.3389/fphar.2022.854249
PMID:35662707
Investigation of Antidiabetic Effect of Pistacia atlantica Leaves by Activity-Guided Fractionation and Phytochemical Content Analysis by LC-QTOF-MS Pekacar S, Deliorman Orhan D Front Pharmacol 25-Feb-2022
PMCID:PMC8913898
doi:10.3389/fphar.2022.826261
PMID:35281888
First Report of Protective Activity of Paronychia argentea Extract against Tobacco Mosaic Virus Infection Abdelkhalek A, Al-Askar AA, Alsubaie MM, Behiry SI Plants (Basel) 11-Nov-2021
PMCID:PMC8620274
doi:10.3390/plants10112435
PMID:34834798
Green Synthesis of Silver Nanoparticles as an Effective Antibiofouling Material for Polyvinylidene Fluoride (PVDF) Ultrafiltration Membrane Alnairat N, Abu Dalo M, Abu-Zurayk R, Abu Mallouh S, Odeh F, Al Bawab A Polymers (Basel) 26-Oct-2021
PMCID:PMC8588217
doi:10.3390/polym13213683
PMID:34771241
Advancing urban ethnopharmacology: a modern concept of sustainability, conservation and cross-cultural adaptations of medicinal plant lore in the urban environment Dutta T, Anand U, Saha SC, Mane AB, Prasanth DA, Kandimalla R, Proćków J, Dey A Conserv Physiol 16-Sep-2021
PMCID:PMC8448427
doi:10.1093/conphys/coab073
PMID:34548925
Traditional medicines and their common uses in central region of Syria: Hama and Homs – an ethnomedicinal survey Khatib C, Nattouf A, Hasan Agha MI Pharm Biol 24-Jun-2021
PMCID:PMC8231352
doi:10.1080/13880209.2021.1936078
PMID:34165371
Metabolic and Epigenetics Action Mechanisms of Antiobesity Medicinal Plants and Phytochemicals Saad B, Ghareeb B, Kmail A Evid Based Complement Alternat Med 09-Jun-2021
PMCID:PMC8208872
doi:10.1155/2021/9995903
PMID:34211580
The Combined Effect of Mediterranean Shrubland Pasture and the Dietary Administration of Sage By-Products on the Antioxidant Status of Segureña Ewes and Lambs Jordán MJ, Martínez-Conesa C, Bañón S, Otal J, Quílez M, García-Aledo I, Romero-Espinar P, Sánchez-Gómez P Antioxidants (Basel) 30-Sep-2020
PMCID:PMC7600900
doi:10.3390/antiox9100938
PMID:33008117
Botanical Origin, Pollen Profile, and Physicochemical Properties of Algerian Honey from Different Bioclimatic Areas Homrani M, Escuredo O, Rodríguez-Flores MS, Fatiha D, Mohammed B, Homrani A, Seijo MC Foods 16-Jul-2020
PMCID:PMC7404483
doi:10.3390/foods9070938
PMID:32708524

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 / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5S,6S)-6-[(4aR,5R,6aR,6aS,6bR,8aR,9R,10R,11S,12aR,14bS)-10-[(2S,3R,4R,5R)-5-[(2S,3R,4S,5S,6S)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-5-[(2S,3R,4S,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyloxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-5,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbonyl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 162975336 Click to see CC1C(C(C(C(O1)OC2COC(C(C2O)O)OC3C(CC4(C(C3(C)CO)CCC5(C4CC=C6C5(CC(C7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)C(=O)O)O)O)O)O)C)C)C)O)O)OC9C(C(CO9)(CO)O)O)OC1C(C(C(CO1)O)OC1C(C(CO1)(CO)O)O)O 1355.40 unknown https://doi.org/10.1002/MRC.2113
6-[10-[5-[4-[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-5-[4-[3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-3-hydroxy-6-methyloxan-2-yl]oxy-3,4-dihydroxyoxan-2-yl]oxy-5,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbonyl]oxy-3,4,5-trihydroxyoxane-2-carboxylic acid 162975335 Click to see CC1C(C(C(C(O1)OC2COC(C(C2O)O)OC3C(CC4(C(C3(C)CO)CCC5(C4CC=C6C5(CC(C7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)C(=O)O)O)O)O)O)C)C)C)O)O)OC9C(C(CO9)(CO)O)O)OC1C(C(C(CO1)O)OC1C(C(CO1)(CO)O)O)O 1355.40 unknown https://doi.org/10.1002/MRC.2113
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5S,6R)-2-[[(2R,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 162910178 Click to see CC(=O)OC1C(C(C(OC1OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)CO)O)O 668.60 unknown https://doi.org/10.1002/MRC.2113
[2-[[6-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] acetate 73022638 Click to see CC(=O)OC1C(C(C(OC1OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)CO)O)O 668.60 unknown https://doi.org/10.1002/MRC.2113
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/MRC.2113
3-[6-O-(beta-D-Glucopyranosyl)-beta-D-galactopyranosyloxy]-3',4',5,7-tetrahydroxyflavone 10282712 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1002/MRC.2113
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/MRC.2113
Isorhamnetin 3-galactoside 13245586 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1002/MRC.2113
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1002/MRC.2113
Quercetin-3-gentiobioside 13915961 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O 626.50 unknown https://doi.org/10.1002/MRC.2113
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
7-(beta-D-Glucopyranosyloxy)-4',5-dihydroxy-3',6-dimethoxyflavone 13940619 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)O 492.40 unknown https://doi.org/10.1002/MRC.2113
Jaceoside 11179379 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)OC)O)O 492.40 unknown https://doi.org/10.1002/MRC.2113
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Eupafolin 5317284 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1002/MRC.2113
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
Phloretin + C-Hex, C-Hex 74819290 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 598.50 unknown https://doi.org/10.1002/MRC.2113
Phloretin 3',5'-Di-C-glucoside 10908130 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 598.50 unknown https://doi.org/10.1002/MRC.2113

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