Fmoc-Met-Gly-OH, also known as Fmoc-Methionine-Glycine-OH, is a protected amino acid derivative commonly used in peptide synthesis. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis process. This compound features methionine and glycine as its constituent amino acids, contributing to its unique properties. It is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. The presence of the methionine side chain, which contains a sulfur atom, imparts specific biochemical characteristics, including potential roles in redox reactions and protein structure stabilization. Fmoc-Met-Gly-OH is widely utilized in the field of biochemistry and molecular biology for the synthesis of peptides, facilitating the study of protein interactions and functions. Proper handling and storage conditions are essential to maintain its stability and reactivity.

Fmoc-Met-Gly-OH

77275-43-5: Fmoc-Met-Gly-OH, also known as Fmoc-Methionine-Glycine-OH, is a protected amino acid derivative commonly used in peptide synthesis. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective moiety for the amino group, allowing for selective reactions during the synthesis process. This compound features methionine and glycine as its constituent amino acids, contributing to its unique properties. It is typically a white to off-white solid and is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. The presence of the methionine side chain, which contains a sulfur atom, imparts specific biochemical characteristics, including potential roles in redox reactions and protein structure stabilization. Fmoc-Met-Gly-OH is widely utilized in the field of biochemistry and molecular biology for the synthesis of peptides, facilitating the study of protein interactions and functions. Proper handling and storage conditions are essential to maintain its stability and reactivity.

CAS 77275-43-5

Fmoc-Met-Gly-OH

N-α-(9-Fluorenylmethyloxycarbonyl)-L-methionyl-glycine

Ref: IN-DA00VQNV

Fmoc-Met-Gly-OH

Ref: 54-OR36500

N-α-(9-Fluorenylmethyloxycarbonyl)-L-methionyl-glycine

Ref: 10-F864033