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Fatty acids naming

A pentaacyl lipid A is also found in R. sphaeroides (Fig. 7) (88). This lipid A has the same distribution of fatty adds as B.fragilis (79) but, as a notable feature, it contains two rare types of fatty acids, namely, A7-14 1 and 14 0(3-oxo), the former being present as a 3-acyloxytetradecanoic acid group amide-linked to GlcN (II), the latter being amide-bound to GlcN(I). [Pg.243]

The benzofuran epoxides 70 are found to be the most reactive epoxides functioning as alkylative agents. Polyunsaturated free fatty acids, namely linoleic, arachidonic, and eicosatrienic acids, and also their methyl esters have been epoxidized using lb <2006HCA2243>. When the reaction is performed in water, it has been found that due to supramolecular organization of fatty acids into a micelle, the C=C bonds closest to the aqueous-micelle interface are most prone to epoxidation. [Pg.656]

Extruded soybean and sunflower diets yielded a Cheddar cheese that had higher concentrations of unsaturated fatty acids while maintaining flavor, manufacturing, and storage characteristics similar to that of control cheese (Lightfield et al., 1993). It is also beneficial from a safety point of view as the accumulation of fatty acids, namely C12, C14, C18 l, and C18 2, enhanced the safety of cheeses against Listeria monocytogenes and Salmonella typhimurium (Schaffer et al., 1995). [Pg.173]

Fatty Acid Names Are Based on Their Parent Hydrocarbons... [Pg.327]

The synthesis of an iso-anteiso pair of 5,9-21 2 fatty acids, namely the 19-methyleicosa-5,9-dienoic acid (16) and 18-methyleicosa-5,9-dienoic acid (17), prominent constituents of the phospholipids of the sponge... [Pg.84]

Explain the consequences of limiting oxaloacetic acid concentrations on the oxidation of fatty acids. Name and identify the structures of the hetone bodies. [Pg.385]

Thus, in considering two important sources of n-3 fatty acids, namely, MO and SBO, although n-3 fatty acids, especially DHA, are located primarily in the sn-2 position in MO, they are mainly in the sn-1 and sn-3 positions of SBO (Table 2) (6). These differences undoubtedly have a definite influence on their assimilation, absorption, and health benefits as well as reactions in which they are involved. [Pg.310]

Trace amounts of long chain saturated fatty acids, namely, stearic (18 0), arachidic (20 0), behenic (22 0) and lignoceric (24 0) acids, present in the seed oil, have not been quantitated. [Pg.136]

Fig. 2. Reaction sequences implicated in the oxidative degradation of unsaturated fatty acids. Names of enzymes implicated in the oxidation of only unsaturated fatty acids are shown in blocks. Fig. 2. Reaction sequences implicated in the oxidative degradation of unsaturated fatty acids. Names of enzymes implicated in the oxidation of only unsaturated fatty acids are shown in blocks.
Commercially available serum albumins (whether Cohn fraction V or crystalline BSA) contain variable and inconsistent amounts of free fatty acids (0.08-2.4 mol/mol albumin). These fatty acids are entirely (99%) removed by charcoal defatting (Chen, 1967). Differences in free fatty acids in serum albumin have been attributed to variations in the levels of free fatty acids in plasma. Analysis of free fatty acids in human serum (Saifer et aL, 1961) showed a complex composition of 43 different fatty acids, 26 of which were identified. Eight fatty acids—namely oleic, palmitic, linoleic, arachidonic, palmitoleic, myristic, linolenic, and stearic acids—constituted 90% of the total. A similar fatty acid distribution was shown in BSA (Fuller-Noel and Hunter, 1972). The presence of fatty acids in BSA imparts a conformational stability to the molecule, which assumes a more compact conformation as shown by a decreased reactivity of amino groups with fluorodinitrobenzene (Green, 1963) or with trinitrobenzene sulfonic acid (Andersson et aL, 1971) and a decrease in the availability of the disulfide bonds to reduction with j3-mercaptoetha-... [Pg.238]

Castor-oil, from the seeds of Ricinua communis and R. Europsoap material It is obtained largely from the East and West Indies, and also from North America. Castor-oil is supposed to contain three fatty acids, namely, ridn oleicy Tnargariticy and elaiodic acids. When treated with hyponitrous acid, a solid fatty mass is produced, which is called Although not soluble... [Pg.27]

In a more comprehensive ongoing investigation [117], fatty acid-based monomers with acrylate functionality were prepared under mild and green conditions by direct esterification of unsaturated fatty acids, namely 10-undecenoic (Cll l), oleic (C18 l) and linoleic (Cl 8 2) acids, with 2-hydroxyethyl methacrylate (HEMA) inthe presence of N,N -dicyclohexylcarbodiimide and 4-dimethylaminopyridine. Scheme 4 4 shows the structure of these novel monomers, whose additional originality is that they were synthesised directly from the corresponding fatty acid. [Pg.62]

Fatty acids are long-chain carbo>ylic acids, usually of 12 or more carbon atoms, isolated from saponification of fats and oils (esters of glycerol). Draw fhe strucfure of each of the fatty acids named below and also determine its common name ... [Pg.209]

The typical laboratory findings in HAP concern the occurrence in plasma and organ lipids of large amounts of an atypical fatty acid, namely 3,7,11,15-tetra-methylhexadecanoic acid (phytanic acid) which may amount to 20% of total plasma fatty acids. [Pg.352]

This chapter deals with chemical pathways involved in the metabolism of fatty acids, namely, their breakdown, syntheses, and interconversions with other body constituents. A pivotal point in these pathways is the 2-carbon fragment. It is of interest to recall that some of the earhest thoughts on the nature of this fragment were expressed soon after the turn of the century by Knoop, Dakin, Magnus-Levy, and others in connection with their experiments on fatty acid metabolism. In a lecture given at Johns Hopkins Hospital in 1910, Magnus-Levy commented as follows upon the participation of 2-carbon fragments in the synthesis of fatty acids ... [Pg.278]


See other pages where Fatty acids naming is mentioned: [Pg.543]    [Pg.14]    [Pg.329]    [Pg.435]    [Pg.442]    [Pg.186]    [Pg.1197]    [Pg.644]    [Pg.170]    [Pg.250]    [Pg.139]    [Pg.634]    [Pg.307]    [Pg.102]    [Pg.519]    [Pg.35]    [Pg.553]    [Pg.28]    [Pg.54]    [Pg.353]    [Pg.23]    [Pg.432]   
See also in sourсe #XX -- [ Pg.161 ]

See also in sourсe #XX -- [ Pg.161 ]




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Acids naming

Fatty acid common name and formula

Fatty acid names of, table

Fatty acids alternative names

Fatty acids names, properties, sources

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