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Leucosidea sericea

Leucosidea sericea - 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 UUID64403ea3425f7132851710
Scientific name Leucosidea sericea
Authority Eckl. & Zeyh.
First published in Enum. Pl. Afric. Austral. : 265 (1836)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English oldwood
Afrikaans ouhout

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
  • Africa
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Northern Provinces

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000986071
Tropicos 27801898
KEW urn:lsid:ipni.org:names:725970-1
The Plant List rjp-1362
Open Tree Of Life 813408
Observations.org 159782
NCBI Taxonomy 137445
IUCN Red List 146442236
IPNI 725970-1
iNaturalist 489282
GBIF 3030262
EPPO LSDSE
EOL 633286

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
Therapeutic strategy of biological macromolecules based natural bioactive compounds of diabetes mellitus and future perspectives: A systematic review Shahzad N, Alzahrani AR, Aziz Ibrahim IA, Shahid I, Alanazi IM, Falemban AH, Imam MT, Mohsin N, Azlina MF, Arulselvan P Heliyon 07-Jan-2024
PMCID:PMC10828662
doi:10.1016/j.heliyon.2024.e24207
PMID:38298622
Natural Perylenequinone Compounds as Potent Inhibitors of Schistosoma mansoni Glutathione S-Transferase Otarigho B, Falade MO Life (Basel) 25-Sep-2023
PMCID:PMC10608284
doi:10.3390/life13101957
PMID:37895339
Green Synthesis, Characterization, Antioxidant, Antibacterial and Enzyme Inhibition Effects of Chestnut (Castanea sativa) Honey-Mediated Silver Nanoparticles Keskin M, Kaya G, Bayram S, Kurek-Górecka A, Olczyk P Molecules 18-Mar-2023
PMCID:PMC10055715
doi:10.3390/molecules28062762
PMID:36985734
Reproductive Ecology of the Invasive Alien Shrub Pyracantha angustifolia in the Grassland Biome, South Africa Adams LD, Giovannoni D, Clark VR, Steenhuisen SL, Martin GD Plants (Basel) 14-Mar-2023
PMCID:PMC10058135
doi:10.3390/plants12061308
PMID:36986995
Nematicidal Characterization of Solanum nigrum and Mentha arvensis Leaf Extracts Using Caenorhabditis elegans as a Model Organism Khan NU, Sajid M, Bibi S, Rehman W, Alanazi MM, Abdellatif MH ACS Omega 16-Feb-2023
PMCID:PMC10018721
doi:10.1021/acsomega.2c08124
PMID:36936282
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Melanisation in Boreal Lichens Is Accompanied by Variable Changes in Non-Photochemical Quenching Ndhlovu NT, Solhaug KA, Minibayeva F, Beckett RP Plants (Basel) 15-Oct-2022
PMCID:PMC9607152
doi:10.3390/plants11202726
PMID:36297748
An Overview of Herbal-Based Antidiabetic Drug Delivery Systems: Focus on Lipid- and Inorganic-Based Nanoformulations Kambale EK, Quetin-Leclercq J, Memvanga PB, Beloqui A Pharmaceutics 08-Oct-2022
PMCID:PMC9610297
doi:10.3390/pharmaceutics14102135
PMID:36297570
Isolation, In Vitro and In Silico Anti-Alzheimer and Anti-Inflammatory Studies on Phytosteroids from Aerial Parts of Fragaria × ananassa Duch Mahnashi MH, Alshehri OM Biomolecules 06-Oct-2022
PMCID:PMC9599613
doi:10.3390/biom12101430
PMID:36291639
Advances on Therapeutic Strategies for Alzheimer’s Disease: From Medicinal Plant to Nanotechnology Hassan NA, Alshamari AK, Hassan AA, Elharrif MG, Alhajri AM, Sattam M, Khattab RR Molecules 28-Jul-2022
PMCID:PMC9369981
doi:10.3390/molecules27154839
PMID:35956796
A Review on the Delivery of Plant-Based Antidiabetic Agents Using Nanocarriers: Current Status and Their Role in Combatting Hyperglycaemia Zolkepli H, Widodo RT, Mahmood S, Salim N, Awang K, Ahmad N, Othman R Polymers (Basel) 24-Jul-2022
PMCID:PMC9330056
doi:10.3390/polym14152991
PMID:35893954
Inorganic Nanomaterials versus Polymer-Based Nanoparticles for Overcoming Neurodegeneration Martano S, De Matteis V, Cascione M, Rinaldi R Nanomaterials (Basel) 07-Jul-2022
PMCID:PMC9317100
doi:10.3390/nano12142337
PMID:35889562
Ethnopharmacological Study of Medicinal Plants Used for the Treatment of Cardiovascular Diseases and Their Associated Risk Factors in sub-Saharan Africa Odukoya JO, Odukoya JO, Mmutlane EM, Ndinteh DT Plants (Basel) 23-May-2022
PMCID:PMC9143319
doi:10.3390/plants11101387
PMID:35631812
Nanoformulation of Plant-Based Natural Products for Type 2 Diabetes Mellitus: From Formulation Design to Therapeutic Applications Wickramasinghe AS, Kalansuriya P, Attanayake AP Curr Ther Res Clin Exp 21-Apr-2022
PMCID:PMC9108891
doi:10.1016/j.curtheres.2022.100672
PMID:35586563
Phytochemical Profiling and Isolation of Bioactive Compounds from Leucosidea sericea (Rosaceae) Ramabulana T, Ndlovu M, Mosa RA, Sonopo MS, Selepe MA ACS Omega 31-Mar-2022
PMCID:PMC9016878
doi:10.1021/acsomega.2c00096
PMID:35449904

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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(2,6-Dihydroxy-4-methoxyphenyl)butan-1-one 597630 Click to see CCCC(=O)C1=C(C=C(C=C1O)OC)O 210.23 unknown https://doi.org/10.1016/J.SAJB.2012.05.007
https://doi.org/10.1016/S0254-6299(15)30189-7
Aspidinol 122841 Click to see CCCC(=O)C1=C(C(=C(C=C1O)OC)C)O 224.25 unknown https://doi.org/10.1016/J.SAJB.2012.05.007
https://doi.org/10.1016/S0254-6299(15)30189-7

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