1966
DOI: 10.1002/recl.19660851210
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Specificity in the enzymic conversion of polyunsaturated fatty acids into prostaglandins

Abstract: The enzyme specificity in the biosynthesis of prostaglandins has been investigated by incubation of a particulate fraction of sheep vesicular glands with w6 tri-and tetraenoic CIS-CZZ fatty acids and isomers of w6 eicosatrienoic acid (20 : 3 06). The chemical synthesis of the various substrate fatty acids is described. The tetraenoic fatty acids were converted into a series of prostaglandin Ez homologues and the trienoic fatty acids into a series of prostaglandin El homologues. The only isomer of 20 : 3 w6 whi… Show more

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Cited by 129 publications
(3 citation statements)
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“…Figure 2 b shows further structural characterization from DRIFT, which clearly confirmed the existence of triazine units and C=O bonds in the OCT in the following details. The peaks at 1017 and 808 cm –1 match well with the C=C bending of benzene units 35 , 36 and the C–H in-plane bending vibrations of the benzene rings, 36 respectively. The characteristic bonds for the triazine unit were found at 1537 cm –1 (C–N stretching mode) 31 , 37 and 1358 cm –1 (in-plane ring stretching vibrations), 37 , 38 confirming the successful formation of triazine rings in our experiments.…”
Section: Resultsmentioning
confidence: 56%
“…Figure 2 b shows further structural characterization from DRIFT, which clearly confirmed the existence of triazine units and C=O bonds in the OCT in the following details. The peaks at 1017 and 808 cm –1 match well with the C=C bending of benzene units 35 , 36 and the C–H in-plane bending vibrations of the benzene rings, 36 respectively. The characteristic bonds for the triazine unit were found at 1537 cm –1 (C–N stretching mode) 31 , 37 and 1358 cm –1 (in-plane ring stretching vibrations), 37 , 38 confirming the successful formation of triazine rings in our experiments.…”
Section: Resultsmentioning
confidence: 56%
“…A full chemical synthesis of this fatty acid was described [5]. When used in the early studies of prostaglandin biosynthesis, this fatty acid proved to be an approximately 6.5 times poorer substrate than 20:4n-6, as judged by the yield of prostaglandins (determined by absorbance at 278 nm after alkali treatment) after 30 min incubation of fatty acids with the particulate enzyme fraction of sheep vesicular glands [6]. Whilst the publication describing the synthesis of 18:4n-6 is occasionally cited, it is usually because of another synthesis described in the same paper, namely that of 20:4n-6.…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, the influence of polyunsaturated fatty acids (PUFA) on elastin and collagen seemed to be more subtle. Their action has been associated with that of prostaglandins (PG) (Struyk et al, 1966;Vergroesen, 1972). Coronary flow was stimulated by PGFi and PGF2, while with certain cation ratios (K-Ca) PCFi^ and PGF2a could stimulate the contractile force in isolated frog and rat heart (Vergroesen and De Boer, 1968).…”
Section: Collagenmentioning
confidence: 99%