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glycosidic linkage

" in MedChemExpress (MCE) Product Catalog:

29

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1

Biochemical Assay Reagents

5

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Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-131166
    Curdlan
    2 Publications Verification

    Bacterial Toll-like Receptor (TLR) NO Synthase C-type Lectin-like Receptors (CTLRs) Reactive Oxygen Species (ROS) Inflammation/Immunology
    Curdlan is a polysaccharide found in bacteria, consisting of a glucose homopolymer with β-1,3-glycosidic linkages . Curdlan can be recognized by Dectin-1 (a C-type lectin receptor), inducing immune responses in tissue mast cells and enhancing dendritic cell effects in tumor immunity. Curdlan holds potential for research in cancer and immune-inflammatory diseases .
    Curdlan
  • HY-B2193
    α-Amylase
    2 Publications Verification

    Environmental Pollutants Amylases Others
    α-Amylase is a hydrolase enzyme that catalyses the hydrolysis of internal α-1, 4-glycosidic linkages in starch to yield products like glucose and maltose.
    α-Amylase
  • HY-P2857

    Amyloglucosidase, Aspergillus niger

    Endogenous Metabolite Metabolic Disease
    Amyloglucosidase, Aspergillus niger (Amyloglucosidase, Aspergillus niger) is a starch-hydrolyzing enzyme with high catalytic efficiency towards soluble starch and raw starch. Amyloglucosidase, Aspergillus niger hydrolyzes α-1,4 and α-1,6 glycosidic linkages in starch and similar substrates, and primarily releases β-glucose molecules from the non-reducing ends. Amyloglucosidase, Aspergillus niger participates in glycogen metabolism and is associated with type II glycogen storage disease. Amyloglucosidase, Aspergillus niger converts starch into glucose, and is applicable to the industrial production of high-fructose syrup, ethanol and other fermented products .
    Glucoamylase, Aspergillus niger
  • HY-P2968

    Amylases Others
    Bacterial α-Amylase catalyses the hydrolysis of internal α-1,4-glycosidic linkages in starch in low molecular weight products, such glucose, maltose and maltotriose units. Bacterial α-Amylase is often used in biochemical studies .
    Bacterial α-Amylase
  • HY-E70038

    Endogenous Metabolite Metabolic Disease
    Endoglycoceramidase II (EGCase II) is an endo-β-glucosidase that releases intact glycans from ceramides in glycosphingolipids. Endoglycoceramidase II catalyzes the hydrolysis of β-glycosidic linkages between oligosaccharides and ceramides in various glycosphingolipids .
    Endoglycoceramidase II (EGCase II)
  • HY-N7948

    Endogenous Metabolite Others
    Isomaltotetraose is an orally active branched isomaltooligosaccharide with α-(1,6) glycosidic linkages. Isomaltotetraose is a prebiotic oligosaccharide present in honey and also a component of isomaltooligosaccharide mixtures. Isomaltotetraose maintains the growth of Prevotella or sustains the *Prevotella* enterotype in both in vitro systems and mouse models .
    Isomaltotetraose
  • HY-P3173

    R-enzyme

    Biochemical Assay Reagents Others
    Pullulanase (R-enzyme) is a key starch debranching enzyme that specifically hydrolyzes α-1,6-glycosidic linkages in polysaccharides such as amylopectin and pullulan, facilitating the efficient degradation of starch into fermentable sugars .
    Pullulanase
  • HY-107824

    Endogenous Metabolite Others
    D-Melibiose is a disaccharide which is composed of one galactose and one glucose moiety in an alpha (1-6) glycosidic linkage.
    D-Melibiose
  • HY-B2193A

    1,4-alpha-D-Glucan-glucanohydrolase, ptyalin

    Biochemical Assay Reagents Metabolic Disease Inflammation/Immunology
    α-Amylase, Human Saliva (1,4-alpha-D-Glucan-glucanohydrolase) is a hydrolase enzyme that can be isolated from human saliva. α-Amylase, Human Saliva catalyses the hydrolysis of internal α-1, 4-glycosidic linkages in starch to yield products like glucose and maltose. α-Amylase, Human Saliva can be used in life science research .
    α-Amylase, Human Saliva
  • HY-B2193C

    1,4-alpha-D-Glucan-glucanohydrolase, amy2, PPA, PA

    Biochemical Assay Reagents Others
    α-Amylase, Porcine Pancreatic (1,4-alpha-D-Glucan-glucanohydrolase) is a hydrolase enzyme that can be isolated from porcine pancreatic. α-Amylase, Porcine Pancreatic catalyses the hydrolysis of internal α-1, 4-glycosidic linkages in starch to yield products like glucose and maltose. α-Amylase, Porcine Pancreatic can be used in life science research .
    α-Amylase, Porcine Pancreatic
  • HY-E70116

    Glycogen α-1,6-glucanohydrolase

    Glycosidase Others
    Isoamylase (Glycogen α-1,6-glucanohydrolase) catalyzes the hydrolysis of α-1,6-glycosidic linkages in glycogen, amylopectin and α/β-limit dextrins .
    Isoamylase
  • HY-B2193B

    Amylase, a-Amylase, 1,4-a-D-glucan glucanohydrolase, glycogenase

    Biochemical Assay Reagents Others
    α-Amylase, Human Pancreas (Amylase) is a hydrolase enzyme that can be isolated from human pancreas. α-Amylase, Human Pancreas catalyses the hydrolysis of internal α-1, 4-glycosidic linkages in starch to yield products like glucose and maltose. α-Amylase, Human Pancreas can be used in life science research .
    α-Amylase, Human Pancreas
  • HY-P2857A

    Amyloglucosidase, Rhizopus sp.

    Endogenous Metabolite Metabolic Disease
    Glucoamylase, Rhizopus sp. (Amyloglucosidase, Rhizopus sp.) is a starch-hydrolyzing enzyme with high catalytic efficiency towards soluble starch and raw starch. Glucoamylase, Rhizopus sp. hydrolyzes α-1,4 and α-1,6 glycosidic linkages in starch and similar substrates, and primarily releases β-glucose molecules from the non-reducing ends. Glucoamylase, Rhizopus sp. participates in glycogen metabolism and is associated with type II glycogen storage disease. Glucoamylase, Rhizopus sp. converts starch into glucose, and is applicable to the industrial production of high-fructose syrup, ethanol and other fermented products .
    Glucoamylase, Rhizopus sp.
  • HY-E70879

    EndoM N175Q

    Glycosidase Others
    Endoglycosidase M (N175Q mutant) (EndoM N175Q) can transfer natural N-glycans or oxazoline N-glycans to any peptide or protein with a GlcNAc residue to form a β1-4-glycosidic linkage. Endoglycosidase M (N175Q mutant) is a useful tool in the synthesis of homogeneous glycopeptides and glycoproteins .
    Endoglycosidase M (N175Q mutant)
  • HY-E70039

    Others Others
    alpha-2-3,6,8-Sialidosidase (SpNanA) catalyses hydrolysis of alpha-(2->3)-, alpha-(2->6)-, alpha-(2->8)- glycosidic linkages of terminal sialic acid residues in oligosaccharides, glycoproteins, glycolipids, colominic acid and synthetic substrates .
    alpha-2-3,6,8-Sialidosidase (SpNanA)
  • HY-B2220B

    Endogenous Metabolite Others
    Thermostable cellulase recombinant is a cellulose hydrolase present in hyperthermophiles, which catalyzes the hydrolysis of β-1,4 glycosidic bonds in cellulose. Thermostable cellulase recombinant targets carboxymethyl cellulose (CMC) as its primary substrate, and retains high residual activity even after incubation at high temperatures. The activity of Thermostable cellulase recombinant is inhibited by ionic and non-ionic detergents, and can be enhanced by cobalt ions. Thermostable cellulase recombinant can be applied in the paper industry .
    Thermostable cellulase (recombinant)
  • HY-E70046A

    Bovine B4GALT1

    Glycosyltransferase Others
    Bovine beta-1,4-Galactosyltransferase (Bovine B4GALT1) is a one member of the glycosyltransferase family of enzymes. Bovine beta-1,4-Galactosyltransferase transfers galactose from UDP-galactose to N-acetylglucosamine (GlcNAc) to produce N-acetyllactosamine with a β-1,4-glycosidic linkage .
    Bovine beta-1,4-Galactosyltransferase
  • HY-N8279

    Endo-β-1,3-1,4-glucanase

    Glycosidase Metabolic Disease
    β-1,3-1,4-glucanase (Endo-β-1,3-1,4-glucanase) is a glycoside hydrolase family 16 enzyme (some members belong to subfamily 25). β-1,3-1,4-glucanase shows high substrate specificity toward mixed‑linked β‑glucans and cleaves β‑1,4 glycosidic bonds adjacent to β‑1,3 linkages in an endo‑type pattern. β-1,3-1,4-glucanase can be used in industrial enzyme applications and monogastric animal feed supplementation .
    β-1,3-1,4-Glucanase
  • HY-E70156

    EC:2.4.1.-; FUT7

    Biochemical Assay Reagents Others
    Fucosyltransferase 7 (FUT7) is a golgi stack membrane protein. Fucosyltransferase 7catalyzes the final fucosylation step in the synthesis of Lewis antigens and generates a unique glycosylated product sialyl Lewis X (sLeX). Fucosyltransferase 7 catalyzes alpha-1,3 glycosidic linkages involved in the expression of sialyl Lewis X antigens .
    Fucosyltransferase 7
  • HY-D1510

    Biochemical Assay Reagents Others
    4-Nitrophenyl 2-O-(β-L-Fucopyranosyl)-β-D-Galactopyranoside is a synthetic chromogenic substrate and can be used in the assay of α-fucosidases which hydrolyze the glycosidic linkage Fuc α1-2Gal. The assay is based on the sequential action of α-fucosidase and an exogenously added exo-β-d-galactosidase to release the easily measurable p-nitrophenol moiety .
    4-Nitrophenyl 2-O-(β-L-Fucopyranosyl)-β-D-Galactopyranoside
  • HY-107824R

    Endogenous Metabolite Reference Standards Inflammation/Immunology
    D-Melibiose (Standard) is the analytical standard of D-Melibiose. This product is intended for research and analytical applications. D-Melibiose is a disaccharide which is composed of one galactose and one glucose moiety in an alpha (1-6) glycosidic linkage.
    D-Melibiose (Standard)
  • HY-E70281

    rEGCase II

    Biochemical Assay Reagents Metabolic Disease
    Recombinant endoglycoceramidase II (rEGCase II) is an endo-β-glucosidase releasing the complete glycan from ceramide in glycosphingolipids. Recombinant endoglycoceramidase II catalyzes the hydrolysis of the β-glycosidic linkage between oligosaccharides and ceramides in various glycosphingolipids .
    Recombinant endoglycoceramidase II
  • HY-E70280

    rEGCase I

    Biochemical Assay Reagents Metabolic Disease
    Recombinant endoglycoceramidase I (rEGCase I) is a glycosidase that catalyzes the hydrolysis of the β-glycosidic linkage between oligosaccharides and ceramides. Recombinant endoglycoceramidase I catalyzes a transglycosylation reaction, which transfers the sugar moiety of glycosphingolipids (GSLs) to the primary hydroxyl group of several 1-alkanols .
    Recombinant endoglycoceramidase I
  • HY-P2988H

    Influenza Virus Infection
    Neuraminidase,Vibrio cholerae (EC 3.2.1.18) is a glycoside hydrolase enzyme that cleave the glycosidic linkages of neuraminic acids.
    Neuraminidase,Vibrio cholerae
  • HY-E71012

    Endogenous Metabolite Metabolic Disease
    Neuraminidase Agarose, Clostridium perfringens (C. welchii) (EC 3.2.1.18) cleave the glycosidic linkages of neuraminic acids.
    Neuraminidase Agarose, Clostridium perfringens (C. welchii)
  • HY-E70895

    Endogenous Metabolite Metabolic Disease
    α2-3 Neuraminidase S, Streptococcus pneumoniae is a glycoside hydrolase enzyme that cleave the glycosidic linkages of neuraminic acids.
    α2-3 Neuraminidase S, Streptococcus pneumoniae
  • HY-P2988E

    Endogenous Metabolite Metabolic Disease
    α2-3 Neuraminidase, Salmonella typhimurium LT2 is a glycoside hydrolase enzyme that cleave the glycosidic linkages of neuraminic acids.
    α2-3 Neuraminidase, Salmonella typhimurium LT2
  • HY-P2988D

    Endogenous Metabolite Metabolic Disease
    α2-3,6,8 Neuraminidase, Clostridium perfringens is a glycoside hydrolase enzyme that cleave the glycosidic linkages of neuraminic acids.
    α2-3,6,8 Neuraminidase, Clostridium perfringens
  • HY-B2220D

    Endogenous Metabolite Others
    Cellulase, Cellvibrio mixtus (EC 3.2.1.4) catalyzes cellulolysis, the decomposition of cellulose and of some related polysaccharides; specifically, the hydrolysis of the 1,4-beta-D-glycosidic linkages in cellulose, hemicellulose, lichenin, and cereal beta-D-glucans.
    Cellulase, Cellvibrio mixtus

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