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TASHKENT MEDICAL ACADEMY Department of Bioorganic and Biological Chemistry Bioorganic chemistry I COURSE SUBJECT : Carbohydrates. Structure and chemical properties of monosaccharides. LECTURE №12 LECTURER : PROFESSOR A.D.DZHURAEV
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PURPOSE OF LECTURES: Generate knowledge stereochemically structure, tautomeric forms and the most important properties of monosaccharides as a basis for understanding their metabolic-cal reactions in the body, and also to study the structural organization of the polysaccharides.
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The questions of: Classification of carbohydrates and mono- saccharides Stereoisomers of monosaccharides Ring-chain tautomerism and mutarotatsii phenomenon in solutions of monosaccharides Chemical reactions of monosaccharides The biological significance of individual members of the monosaccharides
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metabolisms solar energy energy photosynthesis, chlorophyll glikolaldegid
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Triose glyceraldehyde dihydroxyacetone
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TETROZY erythrose treoza eritruloza
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Pentose ribosearabinosexyloselikoza
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KETOPENTOZY D- riuloza D- xylulose
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Hexose allose tulozaidoza mannoseglucose altrose taloza galactose
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ISOMERS GLUCOSE L- glucose D- glucose
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On cyclic hemiacetal colle tollens
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A method of producing mannose 1. From natural sources (the hydrolysis of starch, cellulose, sucrose, etc.) 2. Aldol condensation of Butlerov AM. 3. Oxidation six and five atomic alcohols
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Chemical Properties 1. Oxidation
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2. Restoration polyolhexose
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3. Getting Glycosides -D- glucopyranose O-methyl-a-D- glucopyranoside О-methyl- -D- glucopyranoside
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4. Getting Ethers -D-glucopyranose O-methyl-2,3,4,6-tetramethyl- D-glucopyranose 2,3,4,6-tetramethyl- - D-glucopyranose
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5. The resulting ester -D-glucopyranose 1,2,3,4,6-pentaatsetil-D- glucopyranose
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Value monosaccharides and their derivatives in medicine 6-phosphate -D- glucopyranose 1-phosphate -D- glucopyranose 1,6-phosphate -D- glucopyranose
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Neuraminic acid
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Sialic acid acetylN-acetyl - D-neuraminic acidD-mannosamine
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Value glucuronic acid aspirin salicylic acid elimination of salicylic acid in the form of O-glucuronide
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Education glucuronide body meprotan excretion in the form of N-glucuronide meprotan
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