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Internal ID UUID64404f7ba401b688826535
Scientific name Urtica circularis
Authority (Hicken) Sorarú
First published in Darwiniana 17: 277 (1972)

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Synonyms Top

Scientific name Authority First published in
Urtica chamaedryoides var. circularis Hauman Anales Mus. Nac. Hist. Nat. Buenos Aires 32: 413 (1923)
Urtica spathulata var. circularis Hicken Apuntes Hist. Nat. 2: 79 (1910)

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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
  • Southern America
    • Brazil
      • Brazil South
    • Southern South America
      • Argentina Northeast
      • Argentina Northwest
      • Paraguay
      • Uruguay
    • Western South America
      • Bolivia

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001143672
Tropicos 33400896
KEW urn:lsid:ipni.org:names:260621-2
The Plant List tro-33400896
Open Tree Of Life 5515413
NCBI Taxonomy 1470438
IPNI 260621-2
GBIF 5670807
EPPO URTCI

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
Anti-Aggregative and Protective Effects of Vicenin-2 on Heat and Oxidative Stress-Induced Damage on Protein Structures Patanè GT, Lombardo L, Putaggio S, Tellone E, Ficarra S, Barreca D, Laganà G, De Luca L, Calderaro A Int J Mol Sci 07-Dec-2023
PMCID:PMC10743203
doi:10.3390/ijms242417222
PMID:38139052
Recent Advances on Natural Aryl-C-glycoside Scaffolds: Structure, Bioactivities, and Synthesis—A Comprehensive Review Liu CF Molecules 01-Nov-2022
PMCID:PMC9654268
doi:10.3390/molecules27217439
PMID:36364266
Antinociceptive activity of the Caesalpinia eriostachys Benth. ethanolic extract, fractions, and isolated compounds in mice Kim H, Lee HJ, Zuo G, Hwang SH, Park JS, Hong JS, Kim KH, Soto Montero S, Yi D, Lee JT, Suh H, Lim SS Food Sci Nutr 07-Apr-2022
PMCID:PMC9281943
doi:10.1002/fsn3.2846
PMID:35844922
Urtica dioica-Derived Phytochemicals for Pharmacological and Therapeutic Applications Taheri Y, Quispe C, Herrera-Bravo J, Sharifi-Rad J, Ezzat SM, Merghany RM, Shaheen S, Azmi L, Prakash Mishra A, Sener B, Kılıç M, Sen S, Acharya K, Nasiri A, Cruz-Martins N, Tsouh Fokou PV, Ydyrys A, Bassygarayev Z, Daştan SD, Alshehri MM, Calina D, Cho WC Evid Based Complement Alternat Med 24-Feb-2022
PMCID:PMC8894011
doi:10.1155/2022/4024331
PMID:35251206
Antinociceptive activity of Cnicus benedictus L. leaf extract: a mechanistic evaluation Ahmadimoghaddam D, Sadeghian R, Ranjbar A, Izadidastenaei Z, Mohammadi S Res Pharm Sci 19-Oct-2020
PMCID:PMC7879793
doi:10.4103/1735-5362.297849
PMID:33628288
Pharmacologic Overview of Chlorogenic Acid and its Metabolites in Chronic Pain and Inflammation Bagdas D, Gul Z, Meade JA, Cam B, Cinkilic N, Gurun MS Curr Neuropharmacol 01-Mar-2020
PMCID:PMC7327949
doi:10.2174/1570159X17666191021111809
PMID:31631820
Structure Identification of ViceninII Extracted from Dendrobium officinale and the Reversal of TGF-β1-Induced Epithelial–Mesenchymal Transition in Lung Adenocarcinoma Cells through TGF-β/Smad and PI3K/Akt/mTOR Signaling Pathways Luo Y, Ren Z, Du B, Xing S, Huang S, Li Y, Lei Z, Li D, Chen H, Huang Y, Wei G Molecules 02-Jan-2019
PMCID:PMC6337427
doi:10.3390/molecules24010144
PMID:30609689
Main Plant Extracts’ Active Properties Effective on Scopolamine-Induced Memory Loss Balmus IM, Ciobica A Am J Alzheimers Dis Other Demen 23-Jun-2017
PMCID:PMC10852862
doi:10.1177/1533317517715906
PMID:28643520
Vicenin-2, a potential anti-inflammatory constituent of Urtica circularis. Marrassini C, Davicino R, Acevedo C, Anesini C, Gorzalczany S, Ferraro G J Nat Prod 24-Jun-2011
doi:10.1021/NP100937E
PMID:21608987

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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP100937E
Vicenin-2 3084407 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP100937E

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