The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
Chemical Compound Review

Monopalmitin     2,3-dihydroxypropyl hexadecanoate

Synonyms: AGN-PC-007IU8, CPD-8508, AG-F-87684, CHEMBL1078140, CHEBI:69081, ...
 
 
Welcome! If you are familiar with the subject of this article, you can contribute to this open access knowledge base by deleting incorrect information, restructuring or completely rewriting any text. Read more.
 

Disease relevance of palmitic acid glyceryl ester

 

High impact information on palmitic acid glyceryl ester

 

Biological context of palmitic acid glyceryl ester

 

Anatomical context of palmitic acid glyceryl ester

 

Associations of palmitic acid glyceryl ester with other chemical compounds

 

Gene context of palmitic acid glyceryl ester

  • Similarly, except for plasma cholesterol esters, there were no differences in fatty acid composition between mice fed palmitoyl glycerol as the only fat or supplemented with a protective unsaturated fat [11].
 

Analytical, diagnostic and therapeutic context of palmitic acid glyceryl ester

  • The HPLC fraction having the highest activity was analyzed by (1)H-NMR and FAB-MS, and the active compound was identified as 1-monopalmitin [4].

References

  1. Effect of ambient temperature on the toxicity of palmitoyl glycerol in weanling mice. Tove, S.B., Gooding, R., Nyajom, M. J. Nutr. (1985) [Pubmed]
  2. Toxicity of palmitoyl glycerol to mice: hypothermia and reversal of the toxicity. Siddhanti, S.R., Trumbo, P.R., Schnitzer-Polokoff, R., King, M.W., Tove, S.B. J. Nutr. (1987) [Pubmed]
  3. Human neuropathy target esterase catalyzes hydrolysis of membrane lipids. van Tienhoven, M., Atkins, J., Li, Y., Glynn, P. J. Biol. Chem. (2002) [Pubmed]
  4. Inhibitory effect of a bitter melon extract on the P-glycoprotein activity in intestinal Caco-2 cells. Konishi, T., Satsu, H., Hatsugai, Y., Aizawa, K., Inakuma, T., Nagata, S., Sakuda, S.H., Nagasawa, H., Shimizu, M. Br. J. Pharmacol. (2004) [Pubmed]
  5. Toxicity of palmitoyl glycerol to mice: depression of thyroid function. Trumbo, P.R., Meuten, D.J., King, M.W., Tove, S.B. J. Nutr. (1987) [Pubmed]
  6. Interstitial pneumonitis induced by ingestion of palmitoyl glycerol. Schnitzer-Polokoff, R., Kanich, R.E., Tove, S.B. J. Nutr. (1980) [Pubmed]
  7. Toxicity of rac-1(3)-palmitoyl glycerol in weanling mice. Schnitzer-Polokoff, R., Tove, S.B. J. Nutr. (1979) [Pubmed]
  8. Effect of bovine serum albumin on monoacyl- and diacylglycerol 3-phosphate formation in mitochondrial and microsomal fractions of rabbit hearts. Zaror-Behrens, G., Kako, K.J. Lipids (1976) [Pubmed]
  9. Specificity of purified monoacylglycerol lipase, palmitoyl-CoA hydrolase, palmitoyl-carnitine hydrolase, and nonspecific carboxylesterase from rat liver microsomes. Mentlein, R., Suttorp, M., Heymann, E. Arch. Biochem. Biophys. (1984) [Pubmed]
  10. Different selectivities in acylation and methylation pathways of phosphatidylcholine formation in guinea pig and rat livers. Macdonald, G., Thompson, W. Biochim. Biophys. Acta (1975) [Pubmed]
  11. The result of feeding palmitoyl glycerol on lymph and plasma lipids. Trumbo, P., Sutherland-Smith, M., Kitchell, B., Tove, S.B. Lipids (1987) [Pubmed]
 
WikiGenes - Universities