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Steroids. Structure of Cholesterol. Fundamental framework of steroids is the tetracyclic unit shown. C. D. A. B. Steroids. Steroid A/B and B/C Rings Resemble Decalin. Steroid B/ C, and C/D rings are trans fused. Methyl groups at C-10 and C-13 are “angular” methyl groups.
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Structure of Cholesterol • Fundamental framework of steroids is the tetracyclic unit shown. C D A B
Steroid B/ C, and C/D rings are trans fused Methyl groups at C-10 and C-13 are “angular” methyl groups
The A/B rings are usually trans fused in most naturally occurring steroids Substituents on the same side of the steroid ring system as the angular methyl groups are b-substituents Thoseon the opposite side of the plane of the ring system are a-substituents
CH3 CH3 CH3 CH3 CH3 H H H HO Structure of Cholesterol • Cholesterol has the fundamental steroid skeleton modified as shown.
Structure of Cholesterol CH3 CH3 CH3 • 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. CH3 CH3 H H H HO
Biosynthesis of Cholesterol • Cholesterol is biosynthesized from the triterpene squalene. In the first step, squalene is converted to its 2,3-epoxide.
Biosynthesis of Cholesterol • Cholesterol is biosynthesized from the triterpene squalene. In the first step, squalene is converted to its 2,3-epoxide. O2, NADH, enzyme O
O 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 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 + H Biosynthesis of Cholesterol • Cyclization is triggered by epoxide ring opening.
O + H Biosynthesis of Cholesterol • Cyclization is triggered by epoxide ring opening. + HO
•• OH2 •• H HO H Biosynthesis of Cholesterol H • Loss of a proton is accompanied by a series of hydride shifts and methyl migrations. + HO H H
H HO H 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.
Cholesterol • Cholesterol is the biosynthetic precursor to a large number of important steroids: • Bile acidsVitamin DCorticosteroidsSex hormones
CH3 CH3 CH3 CH3 CH3 H H H HO Cholesterol • 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.
7-Dehydrocholesterol CH3 CH3 • Sunlight converts 7-dehydrocholesterol on the skin's surface to vitamin D3. CH3 CH3 CH3 H H HO
Vitamin D3 CH3 CH3 • Insufficient sunlight can lead to a deficiency of vitamin D3, interfering with Ca2+ transport and bone development. Rickets can result. CH3 CH3 H HO
CH3 CH3 CH3 CH3 CH3 H H H HO Cholesterol • 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.
O CH3 HO OH CH3 CH3 H H H HO OH H Cholic Acid • Salts of cholic acid amides (bile salts), such as sodium taurocholate, act as emulsifying agents to aid digestion.
O CH3 HO NHCH2CH2SO3Na CH3 CH3 H H H HO OH H Sodium Taurocholate
CH3 CH3 CH3 CH3 CH3 H H H HO Cholesterol • Enzymatic degradation of the side chain and oxidation of various positions on the steroid skeleton convert cholesterol to corticosteroids.
Cortisol O OH CH3 • Cortisol is the most abundant of the corticosteroids. Enzyme-catalyzed oxidation of cortisol gives cortisone. HO OH CH3 H H H O
Cortisone O OH CH3 • Corticosteroids are involved in maintaining electrolyte levels, in the metabolism of carbohydrates, and in mediating the allergic response. O OH CH3 H H H O
OH H3C H3C H H H O Testosterone • Testosterone is the main male sex hormone.
Estradiol OH H3C • Estradiol is a female sex hormone involved in regulating the menstrual cycle and in reproduction. H H H HO
O H3C H3C H H H O Progesterone • Supresses ovulation during pregnancy.