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Rumenic acid, (9Z,11E)-9,11-octadecadienoic acid Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.
Linoleic acid (LA) is an organic compound with the formula HOOC(CH 2) 7 CH=CHCH 2 CH=CH(CH 2) 4 CH 3. Both alkene groups (−CH=CH−) are cis. It is a fatty acid sometimes denoted 18:2 (n−6) or 18:2 cis-9,12. A linoleate is a salt or ester of this acid. [5] Linoleic acid is a polyunsaturated, omega−6 fatty acid.
(9Z,11E,13E)-Octadeca-9,11,13-trienoic acid (α-eleostearic acid). An octadecatrienoic acid is a chemical compound with formula C 18 H 30 O 2, a polyunsaturated fatty acid whose molecule has an 18-carbon unbranched backbone with three double bonds.
Linolelaidic acid is an omega-6 trans fatty acid (TFA) and is a cis–trans isomer of linoleic acid.It is found in partially hydrogenated vegetable oils. It is a white (or colourless) viscous liquid.
9-Hydroxyoctadecadienoic acid (or 9-HODE) has been used in the literature to designate either or both of two stereoisomer metabolites of the essential fatty acid, linoleic acid: 9(S)-hydroxy-10(E),12(Z)-octadecadienoic acid (9(S)-HODE) and 9(R)-hydroxy-10(E),12(Z)-octadecadienoic acid (9(R)-HODE); these two metabolites differ in having their hydroxy residues in the S or R configurations ...
In terms of its structure, it is named all-cis-9,12,15-octadecatrienoic acid. [3] In physiological literature, it is listed by its lipid number, 18:3 (n−3). It is a carboxylic acid with an 18-carbon chain and three cis double bonds. The first double bond is located at the third carbon from the methyl end of the fatty acid chain, known as the ...
To determine σ * Taft studied the hydrolysis of methyl esters (RCOOMe). The use of ester hydrolysis rates to study polar effects was first suggested by Ingold in 1930. [ 6 ] The hydrolysis of esters can occur through either acid and base catalyzed mechanisms , both of which proceed through a tetrahedral intermediate .
15-lipoxygenase 1 (), while best known for converting the 20 carbon polyunsaturated fatty acid, arachidonic acid, into a series of 15-hydroxylated arachidonic acid metabolites (see 15-hydroxyicosatetraenoic acid), actually prefers as its substrate the 18 carbon polyunsaturated fatty acid, linoleic acid, over arachidonic acid, converting it to 13-hydroperoxy-9Z,11E-octadecadienoic acid (13-HpODE).