Pages that link to "Q68750310"

The following pages link to Sterol metabolism. XVI. Cholesterol 20-alpha-hydroperoxide as an intermediate in pregnenolone biosynthesis from cholesterol (Q68750310):

Displaying 17 items.

• Inhibition of cholesterol side-chain cleavage by 22-azacholesterol (Q28321325) (← links)
• Reflections on sterol sidechain cleavage process catalyzed by cytochrome P450(scc). (Q34351373) (← links)
• Precursors of the neurosteroids (Q35162412) (← links)
• Oxidative Stress-Mediated Brain Dehydroepiandrosterone (DHEA) Formation in Alzheimer's Disease Diagnosis (Q35972310) (← links)
• Molecular aspects of the biosynthesis of adrenal steroids (Q37102930) (← links)
• The stoichiometry of the conversion of cholesterol and hydroxycholesterols to pregnenolone (3beta-hydroxypregn-5-en-20-one) catalysed by adrenal cytochrome P-450. (Q37440174) (← links)
• Studies on hydroperoxide-dependent substrate hydroxylation by purified liver microsomal cytochrome P-450 (Q39109680) (← links)
• Transannular dioxygenation of 9,10-dimethyl-1,2-benzanthracene by cytochrome P-450 oxygenase of rat liver (Q39135361) (← links)
• Cholesterol hydroperoxides as substrates for cholesterol-metabolizing cytochrome P450 enzymes and alternative sources of 25-hydroxycholesterol and other oxysterols (Q41527256) (← links)
• Cytochrome P-450 as a microsomal peroxidase in steroid hydroxylations. (Q42173708) (← links)
• Evidence for 20, 22‐epoxycholesterol as an intermediate in side‐chain cleavage of 22R‐OH cholesterol by adrenal cortex mitochondria (Q43728271) (← links)
• Mass spectrometric study of the enzymatic conversion of cholesterol to (22R)-22-hydroxycholesterol, (20R,22R)-20,22-dihydroxycholesterol, and pregnenolone, and of (22R)-22-hydroxycholesterol to the lgycol and pregnenolone in bovine adrenocortical pr (Q45198000) (← links)
• Stereochemical specificity at carbon-20 and -22 of hydroxylated cholesterols for side-chain cleavage by adrenocortical cytochrome P-450scc (Q47958393) (← links)
• Enzymatic formation of (20R,22R)-20,22-dihydroxycholesterol from cholesterol and a mixture of 16O2 and 18O2: Random incorporation of oxygen atoms (Q68935435) (← links)
• Microbial hydroxylations—IX: On the dihydroxylation of 19-norsteroids by Curvularialunata (Q68936414) (← links)
• Metabolic regulation of steroidogenesis in isolated adrenal and adrenocortical carcinoma cells of rat. The incorporation of (20S)-20-[7-3H]hydroxycholesterol into deoxycorticosterone and corticosterone (Q69551736) (← links)
• Biological conversion of 17α-hydroperoxyprogesterone to 11α,17α-dihydroxyprogesterone (Q71585614) (← links)