Fatty acid derivatives, novel

Nobmann P, Smith A, Dunne J, Henehan G and Bourke P. 2009. The antimicrobial efficacy and structure activity relationship of novel carbohydrate fatty acid derivatives against Listeria spp. and food spoilage microorganisms. Int J Food Microbiol 128(3) 440—445. 

Novel Fatty-Acid Derivatives Found in Plants That Have Industrial Uses... 

The fatty acid-derived alkaloids halichlorine (112) [99,100], pinnaic acid (113), and tauropinnaic acid (114) [101,102] have novel structures and unique anti-inflammatory activity. 

Mechoulam, R. Beuer, A. Hanus, L. Devane, W.A. Fatty Acid Derivatives and Pharmaceutical Compositions Containing Same 1997 US 5,618,955 Mechoulam, R. Lander, N. Dikstein, S. Shalita, B. Novel Tetrahydrocannabinol Type Compounds 1979 US 4,179,517... 

Lie Ken Jie, M.SE., Pasha, M.K., and Alam, M.S. (1998) S3m-thesis of Novel Triazole Fatty Acid Derivatives from Acetylenic Fatty Ester, Chem. Phys. Lipids 97,71-78. 

Lie Ken lie, M.S.F., andM.S. K. Syed-RahmatuUah, Synthesis and Properties of a Novel 1-Pyrroline Fatty Acid Derivative from Methyl Isoricinoleate, J. Chem. Soc. Perkin Trans. I, 421 24 (1991). 

Olestra is a zero-calorie commercial fat substitute with the look and feel of natural fats. It Is a synthetic compound whose structure involves a novel combination of natural components. The core of olestra Is derived from sucrose, ordinary table sugar. Six to eight of the hydroxyl groups on the sucrose framework have long-chain carboxylic acids (fatty acids) appended to them by ester linkages. These fatty acids are from Cs to C22 in length. In the industrial synthesis of olestra, these fatty acids derive from... 

In this study, lipoxygenase was successfully entrapped by a novel immobilization method within a calcium-alginate silicate gel matrix. The entrapped lipoxygenase had stability better than LOX immobilized by other methods. The immobilized preparation also was reusable. This procedure should enhance the potential of LOX as a biocatalysts in the preparation of oxygenated fatty acid derivatives that have unique chemical and physical properties. 

T.A. Isbell, Developmeta of meadowfoam as an industrial crop through novel fatty acid derivatives, Lipid Technology, 1997, 9, 140-144. T.A. Isbell, Lipid Synthesis and Manufacture (ed. F.D. Gunstone) Sheffield Academic Press, Sheffield (1999) pp.401-421. E.C. Leonard, Sources and commercial applications of high-erucic vegetable oils. Lipid Technology, 1994, 6, 79-83. 

Buisman, G.J.H., Overeem, A., Cuperus, F.P., 1999, Synthesis of Epoxidized Novel fatty Acids for Use in Pain Applications. In Knothe, G., Derksen, J.T.P. (Eds), Recent Developments in the Synthesis of Fatty Acid Derivatives. AOCS Press, Champaign, IL, USA,pp. 128-140. 

Ratnayake, W. M. N. Timmins, A. Ohshima, T. Ackman, R. G. Mass spectra of fatty acid derivatives, of isopropylidenes of novel glyceryl ethers of cod muscle and of phenolic acetates obtained with the Finnigan MAT ion trap detector. Lipids. 1986, 27, 518-524. 

B, a novel taurine conjugated fatty acid derivative from a Japanese marine sponge, Ircinia sp. Tetrahedron, 62, 5682—5685. 

Recently, a novel class of prostaglandin derivatives, PG-1,15-lactones (Fig. 1) of both E [16] and F [17] series, has been reported to occur in the opisthobranch mollusc Tethys fimbria, along with smaller amounts of some of the corresponding PGs. Some lactones were present mainly in the mucous secretion and dorsal appendages known as cerata, while others were more abundant in the mantle. Fatty acid esters of PGF-1,15-lactones (C9 and Cu) were found only in T. fimbria eggmasses and reproductive glands (ovotestis). The structural variety of the lactones and the data on their distribution in the body... 

Scheme 2 shows the biosynthesis ofN-(3-oxooctanoyl)-L-homoserine lactone by Tral protein from Agrobacterium using 3-oxooctanoyl-ACP, derived from fatty acid metabolism, as a substrate [29, 33]. Recently, the first crystal structure of a LuxI protein homologue [34] has provided new insights into the function of AHL synthases which will aid the design of novel inhibitors of AHL biosynthesis. 

Fang X, Jin F, Jin H, von Sonntag C (1998) Reaction of the superoxide radical with the A/-centered radical derived from N-acetyltryptophan methyl ester. J Chem Soc Perkin Trans 2 259-263 Ferreri C, Costantino C, Landi L, Mulazzani QG, Chatgilialoglu C (1999) The thiyl radical-mediated isomerisation of c/s-monounsaturated fatty acid residues in phospholipids a novel path of membrane damage Chem Commun 407-408... 

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