Literature DB >> 500728

Characterization of the lipoidal derivatives of pregnenolone prepared by incubation of the steroid with adrenal mitochondria.

S Mellon-Nussbaum, L Ponticorvo, S Lieberman.   

Abstract

Using mass spectrometric, radioisotopic, chromatographic and chemical techniques, five fatty acid esters of 3 beta-hydroxy-5-pregnen-20-one (pregnenolone) have been identified as components of the lipoidal derivatives biosynthesized in vitro with bovine adrenal mitochondria. The five compounds are: pregnenolone arachidonate, pregnenolone linoleate, pregnenolone oleate, pregnenolone palmitate, and pregnenolone stearate. The distribution of the fatty acids among these five esters is different from the previously reported (Cmelik, S.H.W., and Ley, H. (1977) Comp. Biochem. Physiol. 56B, 267-270) fatty acid composition of these organelles.

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Year:  1979        PMID: 500728

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  2 in total

1.  Cellular pregnenolone esterification by acyl-CoA:cholesterol acyltransferase.

Authors:  Maximillian A Rogers; Jay Liu; Mark M Kushnir; Elena Bryleva; Alan L Rockwood; A Wayne Meikle; David Shapiro; Boris L Vaisman; Alan T Remaley; Catherine C Y Chang; Ta-Yuan Chang
Journal:  J Biol Chem       Date:  2012-04-02       Impact factor: 5.157

2.  Long-lived testosterone esters in the rat.

Authors:  W Borg; C H Shackleton; S L Pahuja; R B Hochberg
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

  2 in total

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