62322-84-3

Usage

Uses

Used in Scientific Research:
11TR-EICOSENOIC ACID is used as a research compound for studying phospholipid membranes, which are essential components of cell membranes and play a crucial role in various cellular processes.
Used in Enzyme Inhibition Studies:
In the field of biochemistry, 11TR-EICOSENOIC ACID is used as an inhibitor of glycerophosphate acyltransferase, cholinephosphotransferase, and ethanolaminephosphotransferase in V79-R cells. This allows researchers to investigate the functions and mechanisms of these enzymes in cellular metabolism and lipid synthesis.

Upstream product

• 506-35-4 behenolic acid 
• 996-82-7 sodium diethylmalonate 
• 5561-99-9 11-eicosenoic acid 
• 143-28-2 oleoyl alcohol 
• 13044-38-7 (Z)-1-bromo-9-octadecene 
• 112-62-9 Methyl oleate 

Downstream Products

• 5557-31-3 9-octadecene 
• 2091-39-6 eicosa-11,14-dienoic acid 
• 69119-90-0 trans-11-eicosenoic acid methyl ester 
• 80380-39-8 (E)-Icos-11-enoic acid 2-((E)-icos-11-enoyloxy)-1-((E)-icos-11-enoyloxymethyl)-ethyl ester 

Relevant academic research and scientific papers

Reducing properties of 1,2-diaryl-1,2-disodiumethanes

1,2-Diphenyl- and 1-phenyl-2-(2-pyridyl)-1,2-disodiumethane efficiently dehalogenate vic-dibromoderivatives, affording the corresponding alkenes. The reaction proceeds rapidly, under mild conditions and is tolerant of a variety of functional groups (alcohol, carboxylic acid, ester and amide). This procedure was successfully extended to similar vic-disubstituted compounds.

1H-Nuclear magnetic resonance spectroscopic studies of saturated, acetylenic and ethylenic triacylglycerols

The 1H-NMR spectroscopic properties of 15 synthetic homologous saturated triacylglycerols of type AAA and 16 mixed saturated triacylglycerols of type ABA and AAB have been studied. Triacylglycerols containing short-chain fatty acids (2:0-6:0) are readily identified. Triacylglycerols containing medium- and long-chain fatty acid components are not differentiated. From the analysis of 19 acetylenic triacylglycerols of type AAA, ABA and AAB (containing positional isomers of acetylenic fatty acids), it is only possible to characterize triacylglycerols with acyl groups containing the acetylenic bond at the Δ2-Δ5 position. 1H-NMR analysis could not confirm the positions (α- or β-acyl) of the acetylenic acids in mixed triacylglycerols. In the study of 22 ethylenic triacylglycerols of type AAA containing positional isomers of (Z)- or (E)-ethylenic acids, molecules containing an ethylenic bond in the Δ2 position of the acyl chains were readily characterized, as the ethylenic protons in the α- and β-acyl chains were fully resolved. Triacylglycerols containing an unsaturated center at the position were characterized by the shifts of the 2-H protons. The spectra of the remaining triacylglycerol molecules were very similar and the position of the ethylenic system could not be determined by this technique.