User:Canadamax/sandbox
Hello world.
Some graphs I found
[edit](2011 National Household Survey)[1]
- First Nations (61%)
- Métis (32%)
- Inuit (4%)
- Multiple and non-Canadian North American aboriginals (3%)
 | Graphs are unavailable due to technical issues. Updates on reimplementing the Graph extension, which will be known as the Chart extension, can be found on Phabricator and on MediaWiki.org. |
| Graphs are unavailable due to technical issues. Updates on reimplementing the Graph extension, which will be known as the Chart extension, can be found on Phabricator and on MediaWiki.org. |
| Graphs are unavailable due to technical issues. Updates on reimplementing the Graph extension, which will be known as the Chart extension, can be found on Phabricator and on MediaWiki.org. |
| Graphs are unavailable due to technical issues. Updates on reimplementing the Graph extension, which will be known as the Chart extension, can be found on Phabricator and on MediaWiki.org. |
| Year | Pop. | ±% |
|---|---|---|
| 2011 | 33,470,000 | — |
| 2016 | 36,540,000 | +9.2% |
| 2021 | 39,110,000 | +7.0% |
| 2026 | 41,750,000 | +6.8% |
| 2031 | 44,430,000 | +6.4% |
| 2036 | 47,130,000 | +6.1% |
| 2041 | 49,900,000 | +5.9% |
| 2046 | 52,910,000 | +6.0% |
| 2051 | 56,070,000 | +6.0% |
| 2056 | 59,400,000 | +5.9% |
| 2061 | 63,000,000 | +6.1% |
References
[edit]- ^ "Canadians in Context - Aboriginal Population". Statistics Canada. 2014.
- ^ "Population Projections for Canada - Components of population growth, high-growth scenario - 2009/2010 to 2060/2061" (PDF). Statistics Canada. Catalogue no. 91-520. 2006. Retrieved 8 September 2013.
Hexadecyl
[edit]Hexadecyl is a functional group chain molecule of carbon and hydrogen, with formula C16H33 and with average mass 225.433.[1] It is on the Enzyme Commission number list.
The substance synthesized by Hexadecyl, Carboplatin and polyethylene glycol appears to have increased liposolubility and PEGylation qualities. This may be useful in chemotherapy, specifically non-small cell lung cancer.[2]
Hexadecyl was noted as early as 1982 for its role in radiolabelling.[3] The technique of which it forms a vital part has continued to be useful even as late as 2017.[4] In fact, it is useful to radiolabel exosomes and hydrogels.[5]
Hexadecyl is a bridge molecule important for positron emission tomography.[6]
Hexadecyl platelet-activating factor "has profound effects on the lung".[7]
Hexadecyl and octadecyl groups are favoured by some in the production of Lysophosphatidic acid.[8]
Hexadecyl glyceryl ether is important in the biosynthesis of plasmalogens.[9]
Related compounds
[edit]Category:Hydrocarbon stubs Category:Organic compound stubs Category:Alkene stubs Category:Oxidoreductases Category:EC 1.3.1 Category:Enzymes
References
[edit]- ^ "Hexadecyl". Royal Society of Chemistry. ChemSpider. Retrieved 3 April 2021.
- ^ Lang, Tingting; Li, Nuannuan; Zhang, Jing; Li, Yi; Rong, Rong; Fu, Yuanlei (2021). "Prodrug-based nano-delivery strategy to improve the antitumor ability of carboplatin in vivo and in vitro". Drug Delivery. 28 (1): 1272–1280. doi:10.1080/10717544.2021.1938754. PMC 8238065. PMID 34176381.
- ^ Pool, G. L.; French, M. E.; Edwards, R. A.; Huang, L.; Lumb, R. H. (1982). "Use of radiolabeled hexadecyl cholesteryl ether as a liposome marker". Lipids. 17 (6): 448–452. doi:10.1007/BF02535225. PMID 7050582. S2CID 42583970.
- ^ Manual Kollareth, Denny Joseph; Chang, Chuchun L.; Hansen, Inge H.; Deckelbaum, Richard J. (2018). "Radiolabeled cholesteryl ethers: A need to analyze for biological stability before use". Biochemistry and Biophysics Reports. 13: 1–6. doi:10.1016/j.bbrep.2017.10.007. PMC 5697731. PMID 29188234.
- ^ Lee, Yanick (July 2017). Radiosynthesis of hexadecyl-4-[ 18F]fluorobenzoate for labeling exosomes and chitosan hydrogels (Master's thesis). Université de Montréal.
- ^ "Radioactive cell labeling agent". KR101130737B1. 2012.
- ^ Haroldsen, P. E.; Voelkel, N. F.; Henson, J. E.; Henson, P. M.; Murphy, R. C. (1987). "Metabolism of platelet-activating factor in isolated perfused rat lung". Journal of Clinical Investigation. 79 (6): 1860–1867. doi:10.1172/JCI113028. PMC 424530. PMID 3108322.
- ^ "USPTO 20060264361".
- ^ Wood, Randall; Healy, Kathleen (1970). "Tumor lipids: Biosynthesis of plasmalogens". Biochemical and Biophysical Research Communications. 38 (2): 205–211. doi:10.1016/0006-291x(70)90697-2. PMID 5418699.
Category:Hydrocarbon stubs Category:Organic compound stubs Category:Alkene stubs Category:Oxidoreductases Category:EC 1.3.1 Category:Enzymes
Let's see if I have the hang of things
[edit] | Graphs are unavailable due to technical issues. Updates on reimplementing the Graph extension, which will be known as the Chart extension, can be found on Phabricator and on MediaWiki.org. |
Quantitation of radioactivity by liquid scintillation counting.