Literature DB >> 5012318

Studies on the biosynthetic conversion of cholesterol into pregnenolone. Side chain cleavage of a t-butyl analog of 20 -hydroxycholesterol, (20R(-t-butyl-5-pregnene-3 ,20-diol, a compound completely substituted at C-22.

B Luttrell, R B Hochberg, W R Dixon, P D McDonald, S Lieberman.   

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Year:  1972        PMID： 5012318

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


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  5 in total

Review 1.  Cytochrome P450 in adrenocortical mitochondria.

Authors:  F Mitani
Journal:  Mol Cell Biochem       Date:  1979-03-05       Impact factor: 3.396

2.  Discovery and characterization of a terpene biosynthetic pathway featuring a norbornene-forming Diels-Alderase.

Authors:  Zuodong Sun; Cooper S Jamieson; Masao Ohashi; K N Houk; Yi Tang
Journal:  Nat Commun       Date:  2022-05-11       Impact factor: 17.694

3.  Oxidation of cholesterol and cholesterol analogues by mitochondrial preparations of steroid-hormone-producing tissue.

Authors:  J R Arthur; H A Blair; G S Boyd; J I Mason; K E Suckling
Journal:  Biochem J       Date:  1976-07-15       Impact factor: 3.857

4.  Precursors of the neurosteroids.

Authors:  V V Prasad; S R Vegesna; M Welch; S Lieberman
Journal:  Proc Natl Acad Sci U S A       Date:  1994-04-12       Impact factor: 11.205

5.  The stoichiometry of the conversion of cholesterol and hydroxycholesterols to pregnenolone (3beta-hydroxypregn-5-en-20-one) catalysed by adrenal cytochrome P-450.

Authors:  M Shikita; P F Hall
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205
  5 in total

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