Category: Hormones
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Dihydrotestosterone sulfate
No page at wikipedia – found in a chart
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Androstanetriols
No page at wikipedia – found in a chart
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18-Hydroxyprogesterone
No page at wikipedia – found in a chart
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3α,5α-Tetrahydrocortisol
No page at wikipedia – found in a chart
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11β,17α,21-Trihydroxypregnenolone
No page at wikipedia – found in a chart
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17α,21-Dihydroxypregnenolone
No page at wikipedia – found in a chart
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11β-Hydroxypregnenolone
No page at wikipedia – found in a chart
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20α,22R-Dihydroxycholesterol
20α,22R-Dihydroxycholesterol, or (3β)-cholest-5-ene-3,20,22-triol is an endogenous, metabolic intermediate in the biosynthesis of the steroid hormones from cholesterol. Cholesterol ((3β)-cholest-5-en-3-ol) is hydroxylated by cholesterol side-chain cleavage enzyme (P450scc) to form 22R-hydroxycholesterol, which is subsequently hydroxylated again by P450scc to form 20α,22R-dihydroxycholesterol, and finally the bond between carbons 20 and 22 is cleaved by P450scc to form pregnenolone ((3β)-3-hydroxypregn-5-en-20-one), the precursor to the steroid hormones. CHAUDHURI AC, HARADA Y, SHIMIZU K, GUT M, DORFMAN RI (March 1962). “Biosynthesis of pregnenolone from…
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22R-Hydroxycholesterol
22R-Hydroxycholesterol, or (3β)-cholest-5-ene-3,22-diol is an endogenous, metabolic intermediate in the biosynthesis of the steroid hormones from cholesterol. Cholesterol ((3β)-cholest-5-en-3-ol) is hydroxylated by cholesterol side-chain cleavage enzyme (P450scc) to form 22R-hydroxycholesterol, which is subsequently hydroxylated again by P450scc to form 20α,22R-dihydroxycholesterol, and finally the bond between carbons 20 and 22 is cleaved by P450scc to form pregnenolone ((3β)-3-hydroxypregn-5-en-20-one), the precursor to the steroid hormones. [CHAUDHURI AC, HARADA Y, SHIMIZU K, GUT M, DORFMAN RI (March 1962). “Biosynthesis of pregnenolone…
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Pregnenolone
Not to be confused with Pregnanolone or Pregneninolone. This article is about pregnenolone as a hormone. For its use as a medication or supplement, see Pregnenolone (medication).
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