(S)-Methyl 2-((S)-2-((S)-2-amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoate 2,2,2-trifluoroacetate

• CAT Number: R031047
• CAS Number: 868539-99-5
• Molecular Formula: C28H36F3N3O6
• Molecular Weight: 567.60
• Purity: ≥95%
• Synonyms: methyl (2S)-2-[[(2S)-2-[[(2S)-2-amino-4-phenylbutanoyl]amino]-4-methylpentanoyl]amino]-3-phenylpropanoate;2,2,2-trifluoroacetic acid
• InChI: InChI=1S/C26H35N3O4.C2HF3O2/c1-18(2)16-22(28-24(30)21(27)15-14-19-10-6-4-7-11-19)25(31)29-23(26(32)33-3)17-20-12-8-5-9-13-20;3-2(4,5)1(6)7/h4-13,18,21-23H,14-17,27H2,1-3H3,(H,28,30)(H,29,31);(H,6,7)/t21-,22-,23-;/m0./s1
• InChIKey: LAPJYAIMBWUZSL-RGRVRPFLSA-N
• SMILES: CC(C)C[C@@H](C(=O)N[C@@H](CC1=CC=CC=C1)C(=O)OC)NC(=O)[C@H](CCC2=CC=CC=C2)N.C(=O)(C(F)(F)F)O

(S)-Methyl 2-((S)-2-((S)-2-amino-4-phenylbutanamido)-4-methylpentanamido)-3-phenylpropanoate 2,2,2-trifluoroacetate（Cat No.:R031047）is a specialized peptide derivative used in advanced peptide synthesis and pharmaceutical research. It incorporates several stereochemically defined (S)-configurations, ensuring high specificity in biological interactions. The trifluoroacetate salt form enhances the compound’s solubility and stability in aqueous solutions, facilitating its use in various chemical and biological applications. The presence of functional groups like amino and phenylbutanamido allows for potential targeting of specific protein interactions. This compound is valuable for studying bioactive peptides, drug design, and understanding peptide-mediated biological processes.