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Swainsona canescens

Swainsona canescens - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Swainsona canescens - 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 UUID643fd971a6e9b022306258
Scientific name Swainsona canescens
Authority (Benth.) F.Muell.
First published in Fragm.3: 46 (1862)

Description Top

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Synonyms Top

Scientific name Authority First published in
Swainsona canescens var. canescens (Benth.) F.Muell. Contr. New South Wales Natl. Herb. 1(4) 1948
Cyclogyne canescens Benth. J.Lindley, Sketch Veg. Swan R.: 16 (1839)

Common names Top

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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
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • South Australia
      • Western Australia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000185546
Tropicos 13054685
KEW urn:lsid:ipni.org:names:519753-1
The Plant List ild-31811
Open Tree Of Life 347659
NCBI Taxonomy 491199
IPNI 519753-1
GBIF 2943414
EOL 643487
USDA GRIN 35929
Wikipedia Swainsona_canescens

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
Biomarkers and their potential for detecting livestock plant poisonings in Western North America Green BT, Welch KD, Lee ST, Stonecipher CA, Gardner DR, Stegelmeier BL, Davis TZ, Cook D Front Vet Sci 22-Feb-2023
PMCID:PMC9992831
doi:10.3389/fvets.2023.1104702
PMID:36908517
Identification of global inhibitors of cellular glycosylation Sørensen DM, Büll C, Madsen TD, Lira-Navarrete E, Clausen TM, Clark AE, Garretson AF, Karlsson R, Pijnenborg JF, Yin X, Miller RL, Chanda SK, Boltje TJ, Schjoldager KT, Vakhrushev SY, Halim A, Esko JD, Carlin AF, Hurtado-Guerrero R, Weigert R, Clausen H, Narimatsu Y Nat Commun 20-Feb-2023
PMCID:PMC9941569
doi:10.1038/s41467-023-36598-7
PMID:36804936
Exploring the Potential of Chemical Inhibitors for Targeting Post-translational Glycosylation of Coronavirus (SARS-CoV-2) Tripathi N, Goel B, Bhardwaj N, Vishwakarma RA, Jain SK ACS Omega 28-Jul-2022
PMCID:PMC9344791
doi:10.1021/acsomega.2c02345
PMID:35937682
Phylogenetic Comparison of Swainsonine Biosynthetic Gene Clusters among Fungi Neyaz M, Das S, Cook D, Creamer R J Fungi (Basel) 31-Mar-2022
PMCID:PMC9030584
doi:10.3390/jof8040359
PMID:35448590
Traditional Knowledge to Contemporary Medication in the Treatment of Infectious Disease Dengue: A Review Dhiman M, Sharma L, Dadhich A, Dhawan P, Sharma MM Front Pharmacol 14-Mar-2022
PMCID:PMC8963989
doi:10.3389/fphar.2022.750494
PMID:35359838
Do Lipid-based Nanoparticles Hold Promise for Advancing the Clinical Translation of Anticancer Alkaloids? Loh JS, Tan LK, Lee WL, Ming LC, How CW, Foo JB, Kifli N, Goh BH, Ong YS Cancers (Basel) 25-Oct-2021
PMCID:PMC8582402
doi:10.3390/cancers13215346
PMID:34771511
Swainsonine Triggers Paraptosis via ER Stress and MAPK Signaling Pathway in Rat Primary Renal Tubular Epithelial Cells Wang S, Guo Y, Yang C, Huang R, Wen Y, Zhang C, Wu C, Zhao B Front Pharmacol 10-Aug-2021
PMCID:PMC8383073
doi:10.3389/fphar.2021.715285
PMID:34447312
N-tert-Butanesulfinyl imines in the asymmetric synthesis of nitrogen-containing heterocycles Mendes JA, Costa PR, Yus M, Foubelo F, Buarque CD Beilstein J Org Chem 12-May-2021
PMCID:PMC8144919
doi:10.3762/bjoc.17.86
PMID:34093879
Fungal Endophytes as Efficient Sources of Plant-Derived Bioactive Compounds and Their Prospective Applications in Natural Product Drug Discovery: Insights, Avenues, and Challenges Singh A, Singh DK, Kharwar RN, White JF, Gond SK Microorganisms 19-Jan-2021
PMCID:PMC7833388
doi:10.3390/microorganisms9010197
PMID:33477910
Effect of swainsonine on the processing of the asparagine-linked carbohydrate chains of alpha 1-antitrypsin in rat hepatocytes. Evidence for the formation of hybrid oligosaccharides. V Gross, T A Tran-Thi, K Vosbeck, P C Heinrich Elsevier BV 05-Jan-2021
doi:10.1016/S0021-9258(18)32772-8
Emerging paradigms of viral diseases and paramount role of natural resources as antiviral agents Sagaya Jansi R, Khusro A, Agastian P, Alfarhan A, Al-Dhabi NA, Arasu MV, Rajagopal R, Barcelo D, Al-Tamimi A Sci Total Environ 07-Nov-2020
PMCID:PMC7833357
doi:10.1016/j.scitotenv.2020.143539
PMID:33234268
Participation of MicroRNAs in the Treatment of Cancer with Phytochemicals Son SW, Lee HY, Moeng S, Kuh HJ, Choi SY, Park JK Molecules 14-Oct-2020
PMCID:PMC7587345
doi:10.3390/molecules25204701
PMID:33066509
Glycan Mimetics from Natural Products: New Therapeutic Opportunities for Neurodegenerative Disease Wang W, Gopal S, Pocock R, Xiao Z Molecules 16-Dec-2019
PMCID:PMC6943557
doi:10.3390/molecules24244604
PMID:31888221
The study of metabolites from fermentation culture of Alternaria oxytropis Song R, Wang J, Sun L, Zhang Y, Ren Z, Zhao B, Lu H BMC Microbiol 11-Feb-2019
PMCID:PMC6369557
doi:10.1186/s12866-019-1408-8
PMID:30744547
Developmental and loco-like effects of a swainsonine-induced inhibition of α-mannosidase in the honey bee, Apis mellifera Wedd L, Ashby R, Foret S, Maleszka R PeerJ 16-Mar-2017
PMCID:PMC5357340
doi:10.7717/peerj.3109
PMID:28321369

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
> Organoheterocyclic compounds / Indolizidines
(1R,2R,8R,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizine-1,2,8-triol 162927211 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1071/CH9792257
Octahydroindolizine-1,2,8-triol 5363 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1071/CH9792257
Swainsonine 51683 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1016/S0021-9258(18)32772-8
https://doi.org/10.1071/CH9792257

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