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8-Glucosidase

Hydrolases. Enzymes catalysing the hydrolytic cleavage ofC —O, C —N and C —C bonds. The systematic name always includes hydrolase but the recommended name is often formed by the addition of ase to the substrate. Examples are esterases, glucosidases, peptidases, proteinases, phospholipases. Other bonds may be cleaved besides those cited, e.g. during the action of sulphatases and phosphatases. [Pg.159]

Acarbose is a nonabsorbable a-glucosidase inhibitor which blocks the digestion of starch, sucrose, and maltose. The digestion of complex carbohydrates is delayed and occurs throughout the small intestine rather than in the upper part of the jejunum. Absorption of glucose and other monosaccharides is not affected. Acarbose is adrninistered orally three times a day and chewed with the first mouthful of food. [Pg.342]

An example of a direct spectrophotometrical assay is the use of synthetic peptide -nitroanilide substrates to determine protease activity. The /)-nitroani1ine group Hberated from the substrates by the protease can be determined spectrophotometricaHy at 410 nm. An example of an indirect (coupled) spectrophotometric assay is the determination of a-amylase using -nitrophenyLmaltoheptaoside. Initially, the substrate is cleaved by the a-amylase and subsequentiy one of the reaction products, -nitrophenyLmaltotrioside, is cleaved by a-glucosidase, hberating -nitrophenyl, a chromophore... [Pg.288]

Deoxy-2-fluoroglucosides ( ) are mechanism-based glucosidase inhibitors Fluorine at C-2 slows the rate of the acetal C-OR (R = 2,4-dinitrophenyl) bond cleavage in S by destabilizing the proposed oxocarbonium lon-like transition state for glucosidase-catalyzed hydrolyses [28]... [Pg.1014]

Amygdalin Glucosidase Glucose, Benzaldehyde, CN- NaH2P04 pH 6.4 Cyanide 10 2 10"5 M... [Pg.255]

The first member of this class, acarbose, was introduced in the early 1990s. a-Glucosidase inhibitors slow the intestinal process of carbohydrate digestion by competitive inhibition of the activity of a-glucosidase enzymes located in the brush border of the enterocytes... [Pg.120]

When a-glucosidase activity is inhibited, carbohydrate digestion is prolonged and takes place further along the intestinal tract. This in turn delays and spreads the period of glucose absorption, which reduces the extent of the postprandial rise in blood glucose concentrations. The effectiveness of a-glucosidase inhibitors is dq en-dent on the consumption of a meal rich in complex carbohydrate. [Pg.121]

Acarbose and Miglitol These agents are specific inhibitors of intestinal glucosidases and reduce the conversion of sucrose and starch to glucose. Their main effect is a delay, not a complete inhibition, of the absorption of carbohydrates. Postprandial blood sugar excursions are effectively reduced. Because a small portion of the carbohydrates enters the colon, their microbial degradation frequently causes flatulence or... [Pg.425]


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0-D-Glucosidase

0-Glucosidase synthesis

0-Glucosidase, cofactors

8-Glucosidases electrophoresis

8-Glucosidases enzyme affinity

8-Glucosidases kinetic parameters

8-Glucosidases localization

8-Glucosidases properties

8-Glucosidases purification

8-Glucosidases thermostability

A-D-Glucosidase

A-Glucosidase inhibition

A-Glucosidase inhibitory activity

A-Glucosidase maltase

A-Glucosidase/albumin

A-glucosidase inhibitors

A-glucosidases

A-l.6-Glucosidase

A-o-Glucosidase

Acarbose as a-glucosidase inhibitors

Acid P-glucosidase

Acid alpha-glucosidase deficiency

Almond 3-D-glucosidase

Alpha 1,4 glucosidase deficiency

Alpha glucosidase inhibitors pharmacokinetics

Alpha-glucosidase inhibitors

Alpha-glucosidase inhibitors Antidiabetics

Alpha-glucosidase inhibitors Insulin

Alpha-glucosidase inhibitors Sulfonylureas

Alpha-glucosidase inhibitors drugs

Amylo-1, 6-glucosidase, deficiency

Amylo-1,6-D-glucosidases

Amylo-1,6-glucosidase storage disease

Amylo-1—»6-glucosidase

Amylo-l,6-D-glucosidases

Amylo-l,6-glucosidase

Amylo-l,6-glucosidase/4-aglucanotransferase

Amylo-l,6-glucosidases

Amylopectin-1,6-glucosidase

Anthocyanins and a-Glucosidase Activity

Aryl-0-glucosidase

Aryl-0-glucosidase activity

B-D-Glucosidases

B-glucosidase

Bacterial P-glucosidase

Best Glucosidase

Beta glucosidase

Beta-glucosidase Kinetics

Carbaoxirose/carbaoxetoses as glucosidase inhibitor

Castanospermine P-glucosidases inhibition

Castanospermine a-glucosidase inhibition

Castanospermine glucosidase inhibition

Castanospermine glucosidase inhibitor

Castanospermine glucosidases

Castanospermine inhibitor of a,p,-glucosidases

Cellobiose glucosidase

Cellobiose inducer, 8-glucosidase

Cellulases P-glucosidase

Chimeric -glucosidases with increased

Chimeric -glucosidases with increased heat stability

Coniferin glucosidase

Ct-Glucosidase

Cyanogenic glucosidases

Cytosolic /?-glucosidase

D-Glucosidases

Direct glucosidase-catalyzed

Emulsin, glucosidase

Enzymatic glucosidases

Enzymes glucosidase

Enzymes glucosidase reaction

Enzymology glucosidase

Exo-l,4-a-D-glucosidase

Fi Glucosidase

Gaucher Glucosidase

Glucosaminidase Glucosidase

Glucose Glucosidase

Glucose Glucosidase inhibitors

Glucose isomerase 3-glucosidases

Glucose oxidase 1-Glucosidase

Glucosidase 2-acetamido-2-deoxy

Glucosidase II

Glucosidase a and

Glucosidase almond emulsin

Glucosidase alpha

Glucosidase assay

Glucosidase australine

Glucosidase castanospermine

Glucosidase cleaves

Glucosidase cloning

Glucosidase deoxynojirimycin

Glucosidase inhibition

Glucosidase inhibitor valiolamines

Glucosidase inhibitors

Glucosidase isolation

Glucosidase mannosidase

Glucosidase mutants

Glucosidase properties

Glucosidase purification

Glucosidase specificity

Glucosidase substrate analog inhibitor

Glucosidase substrate specificity

Glucosidase-catalysed hydrolysis

Glucosidase-transferase

Glucosidase-transferase assay

Glucosidases

Glucosidases

Glucosidases 2-acetamido-2-deoxy

Glucosidases almond emulsin

Glucosidases amyloglucosidase

Glucosidases glycosides

Glucosidases inhibition

Glucosidases molecular weight

Glucosidases myrosinases

Glucosidases nojirimycin inhibition

Glucosidases p-glucosidase

Glucosidases regulation

Glucosidases specificities

Glucosidases substrate specificity

Glycogen 1,6-glucosidase

Human Retaining P-Glucosidase Active Site Residues

Immobilized (3-glucosidase

Inhibition of a-glucosidase

Inhibition of glucosidase

Inhibitors of /3-glucosidases

J8-glucosidases

Lysosomal a-glucosidase

Lysosomal glucosidase

Mutated (3-glucosidase

N-Glucosidase

Nojirimycin P-glucosidase inhibitors

Nojirimycin a-glucosidase inhibitors

Nojirimycin, glucosidase inhibition

Oc-glucosidase

Occurrence and Specificity of Other -Glucosidases

Of P-glucosidase

Of p-glucosidases

Oligo-1,6-D-Glucosidases

Oligo-1,6-glucosidase

Oligo-l,6-glucosidase

Oligosaccharides glucosidase

P-D-Glucosidase

P-D-Glucosidases

P-D-glucosidase activity

P-Glucosidase

P-Glucosidase DMDP inhibition with

P-Glucosidase australine inhibition with

P-Glucosidase inhibition by acarbose

P-Glucosidase inhibition by validamycin

P-glucosidase inhibitors

P-glucosidases

PNPG glucosidase

Raucaffricine glucosidase

Snail 0-glucosidase

Soybean, -glucosidase

Strictosidine Glucosidase (SG)

Strictosidine P-D-glucosidase

Strictosidine glucosidase

Strictosidine glucosidase, biosynthesis

Substrate Glucosidase

Sweet almond, -glucosidase

Terpenoid indole alkaloids strictosidine glucosidase

Transfer reactions 3-glucosidases

Transferases glucosidase transferase

Trichoderma glucosidase

Trichoderma reesei 8-glucosidase

Turbo connutus mixed glucosidase from

Validamycin as a-glucosidase inhibitors

Valienamine yeast a-glucosidase inhibitor

Valiolamine yeast a-glucosidase inhibitor

Valiolamines as glucosidase inhibitor

Yeast a-glucosidase

Yeast a-glucosidase inhibitor

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