Acyl ghrelin has a 28-amino acid sequence with O-n-octanoyl acid modification at the serine 3 position, whereas des-acyl ghrelin has no octanoyl acid modification. Although these peptides exert different physiological functions, no previous studies have shown the different localization of acyl ghrelin and des-acyl ghrelin in the stomach. Here we have developed an antibody specific for des-acyl ...

Ci4~ i6 branched chain fatty acids have other biological effects, such as platelet aggregation inhibition effect reported by Omura et al.3) On such research background, we have prepared a homologous series of 1-monoglycerides derived from C1 1 ^,20 isoor owtewo-branched chain fatty acids to examine their biological effects. The synthetic scheme adopted here is shown in Fig. 1. Racemic 1,2-isopr...

1-β-O-Acyl-glucuronides (AGs) are common metabolites of carboxylic acid-containing xenobiotics, including, e.g., many nonsteroidal anti-inflammatory drugs (NSAIDs). They concern to regulatory authorities because the association these with hepatotoxicity that has resulted in drug withdrawal. One factor assessing potential risk posed by AGs is rate transacylation biosynthetic 1-β-O-acyl form 2-, ...

The aliphatic carboxylic group was efficiently reduced to the methyl group by HSiEt(3) in the presence of catalytic amounts of B(C(6)F(5))(3). To the best of our knowledge, this is the first example of a direct exhaustive reduction of aliphatic carboxylic function. Aliphatic aldehydes, acyl chlorides, anhydrides, and esters also underwent complete reduction under similar reaction conditions. Ar...

Mouse peritoneal macrophages take up acetylated human low density lipoprotein by receptor-mediated endocytosis, hydrolyze its cholesteryl esters in lysosomes, and re-esterify the cholesterol in the cytoplasm. The re-esterified cholesterol accumulates as cytoplasmic lipid droplets that resemble the droplets seen in “foam cells” of atherosclerotic lesions. In the present studies, we have investig...

Several novel N-(4,5-diphenylthiazol-2-yl)-N'-aryl or alkyl (thio)ureas and N-(4,5-diphenylthiazol-2-yl)alkanamides were prepared as potential acyl-CoA: cholesterol O-acyltransferase (ACAT) inhibitors. Synthesis was accomplished by reaction of 2-amino-4,5-diphenylthiazole with the suitable isocyanate, isothiocyanate or acyl chloride. Some analogues without the 5-phenyl substituent or both the p...

It is shown that acyl-CoA binding protein (ACBP), in contrast with fatty acid binding protein (FABP), stimulates the synthesis of long-chain acyl-CoA esters by mitochondria. ACBP effectively opposes the product feedback inhibition of the long-chain acyl-CoA synthetase by sequestration of the synthesized acyl-CoA esters. Feedback inhibition of microsomal long-chain acyl-CoA synthesis could not b...

In the course of W-tracer studies on the biological synthesis of lecithin in lung tissue slices, the ratio of fatty acid activity to glycerol activity in lecithin was higher than in the triglyceride fraction. It was suggested that the observed isotope distributions could be due to turnover of the fatty acid portion of lecithin without a corresponding synthesis and breakdown of the remainder of ...

Hydroxymethylstearates were made by hydroformylation or oxo reaction of monoand polyunsaturated fats and esters with either rhodium-triphenylphosphine or cobalt carbonyl catalysts. Rhodium-oxo products were hydrogenated with nickel catalyst, whereas, cobalt-oxo products were heated directly under hydrogen pressure. Hydroxymethyl fatty alcohols also were prepared by a two-step copper-cmomite hyd...