H-ASP-PHE-OH

• CAT Number: M059321
• CAS Number: 13433-09-5
• Molecular Formula: C13H16N2O5
• Molecular Weight: 280.28
• Purity: ≥95%
• Storage: Store at -20°C
• IUPAC Name: (3S)-3-amino-4-[[(1S)-1-carboxy-2-phenylethyl]amino]-4-oxobutanoic acid
• InChI: InChI=1S/C13H16N2O5/c14-9(7-11(16)17)12(18)15-10(13(19)20)6-8-4-2-1-3-5-8/h1-5,9-10H,6-7,14H2,(H,15,18)(H,16,17)(H,19,20)/t9-,10-/m0/s1
• InChIKey: YZQCXOFQZKCETR-UWVGGRQHSA-N
• SMILES: C1=CC=C(C=C1)C[C@@H](C(=O)O)NC(=O)[C@H](CC(=O)O)N

H-Asp-Phe-OH（Cat No.:M059321）is a dipeptide composed of L-aspartic acid (Asp) and L-phenylalanine (Phe), with a free N-terminal hydrogen (H-) and a free C-terminal carboxylic acid (-OH). This peptide sequence combines the acidic, polar side chain of aspartic acid with the bulky, hydrophobic aromatic ring of phenylalanine, offering a balance of solubility and structural diversity. H-Asp-Phe-OH is used in peptide synthesis, structure–activity relationship (SAR) studies, and as a model for protein folding, receptor binding, or enzyme-substrate interactions. It may also serve as a precursor in pharmaceutical or biochemical research applications.