2-(Aminomethyl)-3-(4-methoxyphenyl)propanoic acid, also known by its CAS number 682803-14-1, is an organic compound characterized by its amino acid structure. It features a propanoic acid backbone with an amino group and a methoxy-substituted phenyl group, which contributes to its unique properties. This compound is typically a white to off-white solid and is soluble in polar solvents, reflecting its polar functional groups. It exhibits both acidic and basic characteristics due to the presence of the carboxylic acid and amino groups, making it a zwitterionic species in solution. The methoxy group enhances its lipophilicity, potentially influencing its biological activity and interactions. This compound may be of interest in pharmaceutical research, particularly in the development of drugs targeting specific biological pathways. Its structural features suggest potential applications in medicinal chemistry, where modifications can lead to derivatives with enhanced efficacy or selectivity. As with many amino acid derivatives, it may also play a role in biochemical processes or serve as a building block for more complex molecules.

2-(aminomethyl)-3-(4-methoxyphenyl)propanoic acid

682803-14-1: 3-Amino-2-(4-methoxybenzyl)propanoic acid, Benzenepropanoic acid, α-(aminomethyl)-4-methoxy-

2-Aminomethyl-3-(4-methoxyphenyl)propionic acid (2AMMPP) is an amide derivative of the β-amino acid, phenylalanine. It has been used in the treatment of rheumatoid arthritis and other disorders because it inhibits the formation of amyloid fibrils. 2AMMPP binds to the n-terminal region of a protein and prevents its aggregation into amyloid fibrils by binding to two adjacent hydrophobic residues on one side of the β-amino acid residue. Crystallographic studies have shown that 2AMMPP binds to a specific site on the protein. The binding site is located near a salt bridge between two amino acids and is stabilized by hydrogen bonding interactions with three water molecules.
2AMMPP also exhibits x-ray crystallography, birefringence, morphology, and staining properties as well as therapeutic effects for rhe

CAS 682803-14-1: 2-(aminomethyl)-3-(4-methoxyphenyl)propanoic acid

2-Aminomethyl-3-(4-methoxyphenyl)propionic acid

Ref: 3D-HCB80314

3-Amino-2-(4-methoxybenzyl)propanoic acid

Ref: 54-OR97868

2-Aminomethyl-3-(4-methoxyphenyl)propionic acid

Ref: 10-F036723

2-AMINOMETHYL-3-(4-METHOXY-PHENYL)-PROPIONIC ACID

Ref: IN-DA00FAJO