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Published byKimberly Goodwin Modified over 9 years ago
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Steroids
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Structure of Cholesterol Fundamental framework of steroids is the tetracyclic unit shown. A B CD
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Steroids
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Steroid A/B and B/C Rings Resemble Decalin
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Methyl groups at C-10 and C-13 are “angular” methyl groups Steroid B/ C, and C/D rings are trans fused
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Those on the opposite side of the plane of the ring system are -substituents Substituents on the same side of the steroid ring system as the angular methyl groups are -substituents The A/B rings are usually trans fused in most naturally occurring steroids
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Cholesterol
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Structure of Cholesterol Cholesterol has the fundamental steroid skeleton modified as shown. HO CH 3 H H H
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Structure of Cholesterol Some parts of the cholesterol molecule are isoprenoid. But other parts don't obey the isoprene rule. Also, cholesterol has 27 carbons, which is not a multiple of 5. HO CH 3 H H H
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Biosynthesis of Cholesterol
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Cholesterol is biosynthesized from the triterpene squalene. In the first step, squalene is converted to its 2,3-epoxide.
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Biosynthesis of Cholesterol Cholesterol is biosynthesized from the triterpene squalene. In the first step, squalene is converted to its 2,3-epoxide. O O 2, NADH, enzyme
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Biosynthesis of Cholesterol To understand the second step, we need to look at squalene oxide in a different conformation, one that is in a geometry suitable for cyclization. O
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Biosynthesis of Cholesterol To understand the second step, we need to look at squalene oxide in a different conformation, one that is in a geometry suitable for cyclization. O O
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Biosynthesis of Cholesterol Cyclization is triggered by epoxide ring opening. O H+
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Biosynthesis of Cholesterol Cyclization is triggered by epoxide ring opening. O H+HO +
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Biosynthesis of Cholesterol Loss of a proton is accompanied by a series of hydride shifts and methyl migrations. HO + OH 2 H H H HO H H
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Biosynthesis of Cholesterol The product of this rearrangement is a triterpene called lanosterol. A number of enzyme-catalyzed steps follow that convert lanosterol to cholesterol. HO H H
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Cholesterol Cholesterol is the biosynthetic precursor to a large number of important steroids: Bile acids Vitamin D Corticosteroids Sex hormones
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Vitamin D
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Cholesterol HO CH 3 H H H Cholesterol is the precursor to vitamin D. Enzymes dehydrogenate cholesterol to introduce a second double bond in conjugation with the existing one. The product of this reaction is called 7-dehydrocholesterol.
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7-Dehydrocholesterol HO CH 3 H H Sunlight converts 7-dehydrocholesterol on the skin's surface to vitamin D 3.
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Vitamin D 3 HO H CH 3 Insufficient sunlight can lead to a deficiency of vitamin D 3, interfering with Ca 2+ transport and bone development. Rickets can result.
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Bile Acids
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Cholesterol HO CH 3 H H H Oxidation in the liver degrades the cholesterol side chain and introduces OH groups at various positions on the steroid skeleton. Cholic acid is the most abundant of the bile acids.
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Cholic Acid Salts of cholic acid amides (bile salts), such as sodium taurocholate, act as emulsifying agents to aid digestion. HOHOHOHO CH 3 H H H H OHOHOHOH HOHOHOHOOOH
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Sodium Taurocholate HOHOHOHO CH 3 H H H H OHOHOHOH HOHOHOHOO NHCH 2 CH 2 SO 3 Na
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Corticosteroids
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Cholesterol HO CH 3 H H H Enzymatic degradation of the side chain and oxidation of various positions on the steroid skeleton convert cholesterol to corticosteroids.
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Cortisol Cortisol is the most abundant of the corticosteroids. Enzyme-catalyzed oxidation of cortisol gives cortisone. O CH 3 H H H OHOHOHOH HOHOHOHO O OHOHOHOH
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Cortisone Corticosteroids are involved in maintaining electrolyte levels, in the metabolism of carbohydrates, and in mediating the allergic response. O CH 3 H H H OHOHOHOH O O OHOHOHOH
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Sex Hormones
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Testosterone Testosterone is the main male sex hormone. O H H H H3CH3CH3CH3C H3CH3CH3CH3COH
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Estradiol Estradiol is a female sex hormone involved in regulating the menstrual cycle and in reproduction. HO H H H H3CH3CH3CH3C OH
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Progesterone Supresses ovulation during pregnancy. O H H H H3CH3CH3CH3C H3CH3CH3CH3CO
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Synthetic Steroids
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