Linolenate/linolenic acid

Linolenic acid, monoester with 1,2-propanediol. See Propylene glycol linolenate Linolenic acid, monoester with 1,2,3-propanetriol. See Glyceryl linolenate Linolenic acid, 1,2,3-propanetriyl ester. See Trilinolenin... 

SC—CO2, Supercritical carbon dioxide extraction UAE, ultrasonic assisted extraction. ARA, arachidonic acid C20 4((t)-6) DHAt docosahexaenoic acid C22 6(u)-3) EPA, eicosapentaenoic acid C20 5(u)-3) GLA, y-linolenic acid C18 3((o-6) Linolenic, linolenic acid (C18 3) Oleic, oleic acid (C18 l) Palmitic, palmitic acid (C16 0). 

The linolenic acid series, C H2n-602, with three double bonds. 

The unsaturated fatty acids, linoleic [60-33-3] and linolenic [463-40-17, contain two and three double bonds and are considered beneficial components of the diet. The double bond is an essential ingredient for human nutrition when it is in the correct position on the fat molecule. Humans are unable to insert the double bond at the omega-3 and -6 position. Therefore, fatty acids containing double bonds at these positions are essential in the diet, including linoleic and linolenic acids. They are accordingly described as essential fatty acids (EFA) (23). 

Fig. 2. (a) The basis for prostaglandin nomenclature, where the letters A—F and J define principal families (b) defines the side chains for PG derived from dihomo-y-linolenic acid (c) PG2 derived from arachidonic acid and (d), PG derived from eicosapentaenoic acid. 

Detailed accounts of the biosynthesis of the prostanoids have been pubUshed (14—17). Under normal circumstances arachidonic acid (AA) is the most abundant C-20 fatty acid m vivo (18—21) which accounts for the predominance of the prostanoids containing two double bonds eg, PGE2 (see Fig. 1). Prostanoids of the one and three series are biosynthesized from dihomo-S-linolenic and eicosapentaenoic acids, respectively. Concentrations ia human tissue of the one-series precursor, dihomo-S-linolenic acid, are about one-fourth those of AA (22) and the presence of PGE has been noted ia a variety of tissues (23). The biosynthesis of the two-series prostaglandins from AA is shown ia Eigure 1. These reactions make up a portion of what is known as the arachidonic acid cascade. Other Hpid products of the cascade iaclude the leukotrienes, lipoxins, and the hydroxyeicosatetraenoic acids (HETEs). Collectively, these substances are termed eicosanoids. 

Lipids. Representative fatty acid compositions of the unprocessed triglyceride oils found in the four oilseeds are given in Table 4 (see Fats and FATTY oils). Cottonseed, peanut, and sundower oils are classified as oleic—linoleic acid oils because of the high (>50%) content of these fatty acids. Although the oleic and linoleic acid content of soybean oils is high, it is distinguished from the others by a content of 4—10% of linolenic acid, and hence is called a linolenic acid oil. 

Conjugation as well as geometric and positional isomerization occur when an alkadienoic acid such as linoleic acid is treated with a strong base at an elevated temperature. CycHc fatty acids result from isomerization of linolenic acid ia strong base at about 250°C (58). Conjugated fatty acids undergo the Diels-Alder reaction with many dienophiles including ethylene, propylene, acryUc acid, and maleic anhydride. 

Fig. 35 Fluorescence scan of the dansyl semicadavende denvatives of 1 behenic acid 2 erucic acid, 3 steanc acid, 4 oleic acid, 5 linoleic acid, 6 linolenic acid...

Some fatty acids are not synthesized by mammals and yet are necessary for normal growth and life. These essential fatty aeids include llnoleic and y-linolenic acids. These must be obtained by mammals in their diet (specifically from plant sources). Arachidonic acid, which is not found in plants, can only be synthesized by mammals from linoleic acid. At least one function of the essential fatty acids is to serve as a precursor for the synthesis of eicosanoids, such as... 

Draw the structures of (a) all the possible triacylglycerols that can be formed from glycerol with stearic and arachidonic acid, and (b) all the phosphatidylserine isomers that can be formed from palmitic and linolenic acids. 

Write properly balanced chemical equations for the oxidation to COg and water of (a) myristic acid, (b) stearic acid, (c) a-linolenic acid, and (d) arachidonic acid. 

Organisms differ with respect to formation, processing, and utilization of polyunsaturated fatty acids. E. coli, for example, does not have any polyunsaturated fatty acids. Eukaryotes do synthesize a variety of polyunsaturated fatty acids, certain organisms more than others. For example, plants manufacture double bonds between the A and the methyl end of the chain, but mammals cannot. Plants readily desaturate oleic acid at the 12-position (to give linoleic acid) or at both the 12- and 15-positions (producing linolenic acid). Mammals require polyunsaturated fatty acids, but must acquire them in their diet. As such, they are referred to as essential fatty acids. On the other hand, mammals can introduce double bonds between the double bond at the 8- or 9-posi-tion and the carboxyl group. Enzyme complexes in the endoplasmic reticulum desaturate the 5-position, provided a double bond exists at the 8-position, and form a double bond at the 6-position if one already exists at the 9-position. Thus, oleate can be unsaturated at the 6,7-position to give an 18 2 d5-A ,A fatty acid. 

Linolenic acid Linseed oil, hemp seed oil, perilla oil Holarrihidine holarrhena antidy, senterica... 

CH3CH2CH=CHCH2CH=CHCH2CH=CHCH2CH2CH2CH2CH2CH2CH2COH Linolenic acid, a polyunsaturated fatty acid... 

Linoleic acid, structure of, 1062 Linolenic acid, molecular model of. 1063... 

Linearity, improvement of calibration curves by derivatization 56 Linoleic acid 73 Linolenic acid 73 Linuron 74,108 Lipid amines 284... 

Linoleic and a-linolenic acids are the only fatty acids known to be essential for the complete nutrition of many species of animals, including humans, and are known as the nutritionally essential fatty acids. In most mammals, arachidonic acid can be formed from linoleic acid (Figure 23-4). Double bonds can be intro-... 

Figure 23-1. Structure of some unsaturated fatty acids. Although the carbon atoms in the molecules are conventionally numbered—ie, numbered from the carboxyl terminal—the co numbers (eg, co7 in palmitoleic acid) are calculated from the reverse end (the methyl terminal) of the molecules. The information in parentheses shows, for instance, that a-linolenic acid contains double bonds starting at the third carbon from the methyl terminal, has 18 carbons and 3 double bonds, and has these double bonds at the 9th, 12th, and 15th carbons from the carboxyl terminal. (Asterisks Classified as "essential fatty acids.")...

---