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MONOSACCHARIDE DISACCHARIDE
- is a polyhydroxy aldehyde (aldose), a -Cn(H2O)n - is a carbohydrate that contains a - is a carbohydrate that contains two
polyhydroxy ketone (ketose), or a Or single polyhydroxy aldehyde or monosaccharide units covalently
compound that yields polyhydroxy CnH2nOn polyhydroxy ketone unit. bonded to each other.
aldehydes or polyhydroxy ketones upon
hydrolysis.
- is an atom in a molecule that has - is a molecule whose mirror images - is a molecule whose mirror images - having double or triple can’t be a
four different groups tetrahedrally are not superimposable. is superimposable. chiral center; having two like groups
bonded to it. bonded also; and lastly it needs both,
the substituent are different and the two
“halves” of the ring emanating from the
chiral center are different.
- D-epinephrine is 20x greater than its - is a compounds that have the - is an isomers with atoms of the - is a two dimensional structural
response to L-epinephrine; Building same numbers and kinds of atoms same connectivity that differ only in notation for showing the spatial
blocks of monosaccharides are right- but differ in the way the atoms are the orientation of the atoms in space arrangement of groups about chiral
handed (D-glucose); and Building blocks arranged. (L or D). centers in molecules.
of proteins L-phenylalanine.
D DESIGNATION L DESIGNATION OPTICALLY ACTIVE COMPOUND DEXTROROTATORY COMPOUND
- comes from the Latin word dextro - comes from the Latin word levo - is a compound that rotates the - is a chiral compound that rotates
means “right”. means “left”. plane of polarized light. the plane of polarized light in a
clockwise direction.
- is a chiral compound that rotates - is an isomers that have the same - a.k.a. enantios which means - are stereoisomers whose
the plane of polarized light in a molecular and structural formulas “opposite”, are stereoisomers whose molecules are not mirror images of
counter clockwise direction. but differ in the orientation of atoms molecules are nonsuperimposable each other.
in space. mirror images of each other and are
Left-Handed & Right-Handed.
- an epimers that is the most - is an epimers that is synthesized - are diastereomers whose - is biochemically the most
abundant in nature and the most from glucose in the mammary molecules differ only in the important ketohexose and aka
important from a nutritional glands for use in lactose, a configuration at one chiral center. levulose and fruit sugar.
standpoint. disaccharide consisting of a glucose - used as a dietary sugar.
-aka dextrose, blood sugar and unit and galactose unit, and aka
grape sugar. brain sugar.
- is a pentose, and a component of - is the hemiacetal carbon atom - is the resulting compounds that - are cyclic monosaccharides that
ribonucleic acids (RNAs) and present in a cyclic monosaccharide comes from the result from the differ only in the positions of the
energy-rich compounds such as structure. ability of their carbonyl group to substituents on the anomeric
adenosine triphosphate (ATP). react intramolecularly with a (hemiacetal) carbon atom.
hydroxyl group.
- D-Glucitol, aka D-sorbitol, a - is the general name for - plays important roles in the - is the important building blocks of
hexahydroxy alcohol have properties monosaccharide acetals, an acetal metabolism of carbohydrates. polysaccharides found in chitin and
similar to those of the trihydroxy formed from a cyclic mono. by hyaluronic acid.
alcohol glycerol and are moisturizing replacement of the hemiacetal
and sweeterning agents. carbon –OH group w/ an –OR group.
MARKING SYSTEM FOR BLOOD GLYCOSIDIC LINKAGE (BOND) MALTOSE CELLUBIOSE
TYPES
- is the bond in a disaccharide - 2 D-glucose units, a reducing sugar, - produce as an intermediate in the
- D-galactose, N-acetyl-a-D- resulting from the reaction between that has 3 forms in aqueous solution: hydrolysis of polysaccharide
glucosamine, N-acetyl-a-D- the hemiacetal carbon atom –OH alpha-Maltose, beta-Maltose, and Open- cellulose.
galactosamine, and a-L-Frucose (a- group of the one monosaccharide chain aldehyde form.
- Malt sugar, an interesting compound
6-Deoxy-L-galactose) and an –OH group on the other
because of its use in alcohol production
monosaccharide. (fermentation).
- is made up of a beta-D-galactose - used to describe the condition - a condition in w/c people lack the - caused by the absence of one or
unit and a D-glucose unit joined by where milk-drinking ability continues enzyme lactase, w/c is needed to more of the enzymes needed for the
a beta(1:4) glycoside linkage. into adulthood. hydrolyze lactose to galactose and conversion of galactose to glucose.
-Lactose as an Excipent used as a glucose.
filler or filler-binder.
- common table sugar, is the most - an equimolar mixture of glucose - is synthesized from sucrose by - an aspartame derivative that
abundant of all disaccharides and and fructose which is the product of substitution of three chlorine atoms differs structurally from aspartame
occurs throughout the plan sucrose (digestion). for hydroxyl groups. in that a 3,3-dimenthylbutyl group
kingdom, in which is composed of attached to the terminal –NH2 group
alpha-D-glucose and beta-D- of aspartame.
fructose.
- trisaccharide, galactose, glucose, - tetrasaccharide, galactose, - a toxin found in the potato plant, - oligosaccharide molecules that are
and fructose. glucose, and fructose with additional is another example of an attached to the plasma membrane
galactos. oligosaccharide-containing of red blood cells.
“complex” molecule.
GLYCAN IMPORTANT PARAMETERS HOMOPOLYSACCHARIDE HETEROPOLYSACCHARIDE
- an alternate name of - The identity of the monosaccharide - is a polysaccharide in which only - is polysaccharide in which more
polysaccharide and are called repeating unit(s) in the polymer chain, one type of monosaccharide than one (usually two) type of
complex carbohydrates, simple the length of the polymer chain, the monomer is present. monosaccharide monomer is
carbohydrates for monosaccharides type of glycosidic linkage between present.
monomer units, and the degree of the
& disaccharides.
branching of the polymer chain.
- the 2nd most abundant naturally - is a polysaccharides w/ a - contains alternating residue of N- - small highly-sulfated polysaccharide
occurring polysaccharide; its function is disaccharides repeating unit in w/c 1 of acetyl-b-D-glucosaminne (NAG) and with only 15-90 disccharide residues per
to give rigidity to the exoskeletons of the disaccharide components is an D-Glucuranote. chain.
crabs, lobsters, shrimp, insects, and amino acids and 1 or both disaccharide - Blood anticoagulant and the source for
other arthropods; and contains componets has negative charge due to pharmaceutical heparin is intestinal or
galacturonic acid. a sulphate group or a carboxyl group lung tissue of slaughter-house animals
and are heteropolysaccharides. (pigs and cows).