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- W2144376473 abstract "Dioctanoylthiophosphatidylcholine, a racemic thiophosphate analog of L-alpha-dioctanoylphosphatidylcholine, has been synthesized and isolated by flash chromatography. In contrast with the didecanoylthiophosphatidylcholine synthesized previously, the analog is easily dispersed on sonication in aqueous media and is rapidly hydrolyzed to produce a free thiol group in the presence of the extracellular phospholipase C from either Bacillus cereus or Clostridium perfringens. When 5,5'-dithiobis (2-nitro-benzoic acid) was included as a thiol reactive chromogenic agent, the resultant measurement of product release, as an increase in absorbance at 412 nm, showed a linear relationship with added enzyme." @default.
- W2144376473 created "2016-06-24" @default.
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- W2144376473 date "1987-08-01" @default.
- W2144376473 modified "2023-09-28" @default.
- W2144376473 title "Synthesis of a thiophosphate analog of dioctanoylphosphatidylcholine: a phospholipase C substrate" @default.
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- W2144376473 doi "https://doi.org/10.1016/s0022-2275(20)38629-6" @default.
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