- Question bookุฏู ุฃุณุฆูุฉ ู ู ุงูุฏุงุชุง ุ ู ุด ูู ุงูุฃุณุฆูุฉ ุนูููุง ูู ู ููุฌูุง ุ ุนุงุฏู ุชูุงูู ููุณู ุญููุช ูุชูุฑ ุฎุทุฃ
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- QuizeMono & Disaccharides
- dr.Abdulghani 2026Mono saccharide (to page 30)
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- ุฏ.ุฃูุณ ุงูููุฏูุงูุดุฑุญ ุฒู ู ููุฌ ูููุชูุง
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- ุฏ.ู ุนุงุฐ ููุฏุงูุฏุงุชุง ุงููุฑุจูููุฏุฑุงุช ูุงู ูุฉ ุ ุงูุดุฑุญ ุฒู ู ููุฌูุง
- ุฏ.ู ุญู ูุฏ ุงูุทูููยฒisomer
- VIP lec.ุฏุง ุชูุถูุญ ููููุงุท ุงูู ูู ุฉ ูู ุงูู ุญุงุถุฑุฉ ูุงูู ุงููู ูููู ู ู ุงูู ุงููู ูุญูุธู
๐ Definition
๐ Monosaccharides = simplest form of carbohydrates.
๐ Aldehyde or ketone derivatives of polyhydric alcohols (e.g., glycerol).
๐ Classification
๐ By Number of Carbons:
Trioses (3C): Glyceraldehyde, Dihydroxyacetone
Tetroses (4C): Erythrose, Erythrulose
Pentoses (5C): Ribose, Deoxyribose, Xylulose
Hexoses (6C): Glucose, Galactose, Fructose, Mannose
Heptoses (7C): Rare
๐ฃ By Functional Group:
Aldoses: contain aldehyde group (e.g., Glucose, Galactose)
Ketoses: contain ketone group (e.g., Fructose)
๐ Isomerism
๐ D & L isomerism โ based on asymmetric carbon configuration.
๐ AldoseโKetose isomerism โ e.g., Glucose vs Fructose.
๐ Epimers โ differ at one carbon (not carbonyl), e.g., Glucose vs Galactose (C4).
๐ ฮฑ & ฮฒ isomers โ based on hydroxyl group position at anomeric carbon (C1 in aldoses).
๐ Clinical Importance of Monosaccharides
๐ Pentoses:
Ribose & Deoxyribose โ structure of RNA & DNA.
Ribose โ part of ATP, GTP, NAD, NADP.
Xylulose โ intermediate in uronic acid pathway.
๐ฃ Hexoses (esp. Glucose):
Main energy source (60โ75% of daily calories).
Essential for CNS, skeletal muscle, RBCs, cornea, lens, retina.
Precursor for synthesis: lipids, amino acids, lactose, fructose, ribose.
Formation of glycolipids & glycoproteins.
Produces important compounds: 2,3-BPG (oxygen release), Lactate.
๐ Sugar Derivatives
๐ Sugar acids โ oxidation (e.g., Glucuronic acid).
๐ Sugar alcohols โ reduction (e.g., Sorbitol).
๐ Deoxy-sugars โ oxygen removal (e.g., Deoxyribose).
๐ Amino sugars โ e.g., Glucosamine.
๐ Phosphate esters โ e.g., Glucose-6-phosphate.
๐ Glycosides โ formed by condensation with other molecules.
๐ Definition
๐ Monosaccharides = simplest form of carbohydrates.
๐ Aldehyde or ketone derivatives of polyhydric alcohols (e.g., glycerol).
๐ Classification
๐ By Number of Carbons:
Trioses (3C): Glyceraldehyde, Dihydroxyacetone
Tetroses (4C): Erythrose, Erythrulose
Pentoses (5C): Ribose, Deoxyribose, Xylulose
Hexoses (6C): Glucose, Galactose, Fructose, Mannose
Heptoses (7C): Rare
๐ฃ By Functional Group:
Aldoses: contain aldehyde group (e.g., Glucose, Galactose)
Ketoses: contain ketone group (e.g., Fructose)
๐ Isomerism
๐ D & L isomerism โ based on asymmetric carbon configuration.
๐ AldoseโKetose isomerism โ e.g., Glucose vs Fructose.
๐ Epimers โ differ at one carbon (not carbonyl), e.g., Glucose vs Galactose (C4).
๐ ฮฑ & ฮฒ isomers โ based on hydroxyl group position at anomeric carbon (C1 in aldoses).
๐ Clinical Importance of Monosaccharides
๐ Pentoses:
Ribose & Deoxyribose โ structure of RNA & DNA.
Ribose โ part of ATP, GTP, NAD, NADP.
Xylulose โ intermediate in uronic acid pathway.
๐ฃ Hexoses (esp. Glucose):
Main energy source (60โ75% of daily calories).
Essential for CNS, skeletal muscle, RBCs, cornea, lens, retina.
Precursor for synthesis: lipids, amino acids, lactose, fructose, ribose.
Formation of glycolipids & glycoproteins.
Produces important compounds: 2,3-BPG (oxygen release), Lactate.
๐ Sugar Derivatives
๐ Sugar acids โ oxidation (e.g., Glucuronic acid).
๐ Sugar alcohols โ reduction (e.g., Sorbitol).
๐ Deoxy-sugars โ oxygen removal (e.g., Deoxyribose).
๐ Amino sugars โ e.g., Glucosamine.
๐ Phosphate esters โ e.g., Glucose-6-phosphate.
๐ Glycosides โ formed by condensation with other molecules.