Z-D-Ala-D-Ala-OMe, also known as Z-D-alanyl-D-alanine methyl ester, is a synthetic dipeptide derivative characterized by its structural composition, which includes two alanine residues (D-alanine) flanked by a benzyloxycarbonyl (Z) protecting group and a methyl ester functional group. This compound is often utilized in biochemical research, particularly in studies related to peptide synthesis and antibiotic resistance, as it mimics the structure of the peptidoglycan precursors in bacterial cell walls. The Z group serves to protect the amino group during synthesis, while the methyl ester enhances solubility and stability. Z-D-Ala-D-Ala-OMe is typically white to off-white in appearance and is soluble in organic solvents. Its biological relevance is underscored by its role in the mechanism of action of certain antibiotics, such as vancomycin, which target the D-Ala-D-Ala motif in bacterial cell wall synthesis. Overall, Z-D-Ala-D-Ala-OMe is a valuable compound in both synthetic chemistry and pharmacological studies.

Z-D-Ala-D-Ala-OMe

19914-26-2: Z-D-Ala-D-Ala-OMe, also known as Z-D-alanyl-D-alanine methyl ester, is a synthetic dipeptide derivative characterized by its structural composition, which includes two alanine residues (D-alanine) flanked by a benzyloxycarbonyl (Z) protecting group and a methyl ester functional group. This compound is often utilized in biochemical research, particularly in studies related to peptide synthesis and antibiotic resistance, as it mimics the structure of the peptidoglycan precursors in bacterial cell walls. The Z group serves to protect the amino group during synthesis, while the methyl ester enhances solubility and stability. Z-D-Ala-D-Ala-OMe is typically white to off-white in appearance and is soluble in organic solvents. Its biological relevance is underscored by its role in the mechanism of action of certain antibiotics, such as vancomycin, which target the D-Ala-D-Ala motif in bacterial cell wall synthesis. Overall, Z-D-Ala-D-Ala-OMe is a valuable compound in both synthetic chemistry and pharmacological studies.

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CAS 19914-26-2

Z-D-Ala-D-Ala-OMe

Z-D-Ala-D-Ala-OMe

Ref: 3D-FA111556