(S)-methyl 2-((S)-4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenylbutanamido)pentanamido)-3-phenylpropanoate

• CAT Number: I043047
• CAS Number: 1140908-89-9
• Molecular Formula: C32H44N4O6
• Molecular Weight: 580.72
• Purity: ≥95%
• Synonyms: methyl (2S)-2-[[(2S)-4-methyl-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]-4-phenylbutanoyl]amino]pentanoyl]amino]-3-phenylpropanoate
• InChI: InChI=1S/C32H44N4O6/c1-23(2)20-27(31(39)35-28(32(40)41-3)21-25-12-8-5-9-13-25)34-30(38)26(15-14-24-10-6-4-7-11-24)33-29(37)22-36-16-18-42-19-17-36/h4-13,23,26-28H,14-22H2,1-3H3,(H,33,37)(H,34,38)(H,35,39)/t26-,27-,28-/m0/s1
• InChIKey: YXDNWVZKBKEJEH-KCHLEUMXSA-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)NC(=O)CN3CCOCC3

(S)-Methyl 2-((S)-4-methyl-2-((S)-2-(2-morpholinoacetamido)-4-phenylbutanamido)pentanamido)-3-phenylpropanoate（Cat No.:I043047）is a complex peptide derivative with multiple functional groups, including amino and morpholinoacetamido moieties. The structure incorporates several stereochemically defined (S)-configurations, ensuring the specificity of the compound for particular interactions. It is typically used in advanced peptide synthesis for research into bioactive peptides or drug development. The functional groups, such as the morpholinoacetamido group, enhance solubility and stability, enabling selective peptide assembly. This compound could be studied for its biological activity, including potential anti-inflammatory or therapeutic effects in specific protein interactions.