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Results for "

asparagine residue

" in MedChemExpress (MCE) Product Catalog:
Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-118161
    1-Adamantylaspartate

    beta-1-Adamantylaspartic acid

    		 Biochemical Assay Reagents Others
    1-Adamantylaspartate is a newly developed β-β-1-imidopropionic acid used to synthesize the C-terminal octapeptide of the β subunit of human chorionic gonadotropin (hCG) and the hexadecapeptide of the α subunit of the insulin receptor (30-55) by conventional solution methods and solid phase methods, aiming to inhibit the formation of asparagine during the synthesis of asparagyl peptides. Studies have shown that β-β-1-imidopropionic acid is an effective protector of the β-carboxyl function of aspartic acid residues.
    1-Adamantylaspartate
  • HY-E70997
    Glycopeptidase A, Almonds

    		Biochemical Assay Reagents Metabolic Disease
    Glycopeptidase A, Almonds (EC 3.5.1.52) is an enzyme that catalyzes a chemical reaction that cleaves a N4-(acetyl-beta-D-glucosaminyl)asparagine residue in which the glucosamine residue may be further glycosylated, to yield a (substituted) N-acetyl-beta-D-glucosaminylamine and a peptide containing an aspartate residue. Glycopeptidase A, Almonds (EC 3.5.1.52) belongs to the family of hydrolases, specifically those acting on carbon-nitrogen bonds other than peptide bonds in linear amides.
    Glycopeptidase A, Almonds
  • HY-182987
    SMARCA2/SMARCA4 ligand-1

    		Ligands for Target Protein for PROTAC SWI/SNF Complex Cancer
    SMARCA2/SMARCA4 ligand-1 is a SMARCA2/SMARCA4 ligand with KD values of 1.2 and 10.3 nM. SMARCA2/SMARCA4 ligand-1 binds SMARCA2/4 bromodomain via hydrogen bonds with asparagine and tyrosine residues, and a salt bridge with a glutamate residue. SMARCA2/SMARCA4 ligand-1 shows antiproliferative activity against cancer cells. SMARCA2/SMARCA4 ligand-1 can be used for the research of cancer, such as smarca4 mutant nonsmall cell lung cancer .
    SMARCA2/SMARCA4 ligand-1
  • HY-120340
    nNOS-IN-7

    		NO Synthase Neurological Disease
    nNOS-IN-7 is a selective nNOS inhibitor with a Ki value of 0.049 μM against rat nNOS. nNOS-IN-7 is applicable to the research of neurodegenerative diseases .
    nNOS-IN-7

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