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Various organic compounds consisting of carbon, hydrogen, and oxygen atoms that are found in foods and living tissues; typically broken down to release energy; includes sugars, sugar alcohols, sugar acids and derivatives, glycosyl compounds, and more.
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2-Azidoethyl β-D-lactoside is an azide-functionalized β-D-lactoside reagent designed for click-chemistry conjugation. It reacts with alkyne-containing molecules via copper-catalyzed azide-alkyne cycloaddition (CuAAC) or strain-promoted azide-alkyne cycloaddition (SPAAC), enabling efficient bioconjugation in glycochemistry and chemical biology workflows.
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Azidoethyl-SS-PEG2-Boc is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is also a click chemistry reagent containing an Azide group, capable of undergoing copper-catalyzed azide-alkyne cycloaddition (CuAAc) reaction with molecules containing Alkyne groups. Additionally, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
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Azidoethyl-SS-PEG2-Boc is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, featuring an Azide group. This allows it to participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules containing Alkyne groups, as well as strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
Peg-based PROTAC linker
Click chemistry reagent
Contains an Azide group for CuAAc and SPAAC reactions
For research use only
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Hyaluronic acid (HA, Hyaluronan, Hyaluronate) is an anionic, nonsulfated glycosaminoglycan distributed widely throughout connective, epithelial, and neural tissues. It is widely used in skin care.
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O-Linked GlcNAc transferase substrate is a biologically active peptide that functions as a substrate for O-linked GlcNAc transferase (OGT), a eukaryotic glycosyltransferase that utilizes UDP-GlcNAc as a glycosyl donor.
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N-acetyl D-galactosamine (CAS 1811-31-0) is an endogenous amino sugar that serves as a structural component in glycoproteins and glycolipids It functions as a fundamental building block in the biosynthesis of O-linked glycoproteins participating in post-translational modification and influencing cell signaling adhesion and molecular recognition processes Due to its role in the formation of brain heteropolysaccharides N-acetyl D-galactosamine is frequently utilized in studies investigating glycosylation neural development and carbohydrate-mediated cellular interactions within biomedical research
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D(+)-Galactosamine hydrochloride is an established experimental toxin that primarily causes liver injury by generating free radicals and depleting UTP nucleotides. It also induces renal dysfunction, with renal failure often associated with the end-stage of liver damage. Lipopolysaccharide/D(+)-Galactosamine-induced acute liver injury is a known animal model of fulminant hepatic failure.
Induces apoptosis and necrosis in primary rat hepatocyte cultures.
Causes caspase-3 activation and DNA fragmentation.
Induces hepatotoxicity similar to viral hepatitis.
Suitable for research use only.
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