trans-Cinnamoyl-Phe-OH contains a phenylalanine-derived backbone bearing a trans-cinnamoyl acyl substituent on the amino acid framework, classifying it as an amino acid derivative rather than a free amino acid. The molecule features a carboxylic acid group (-COOH) and an acylated amide linkage to the cinnamoyl moiety, with the cinnamoyl double bond specified as trans and the aromatic side chain of phenylalanine retained for hydrophobic and π-interaction behavior. trans-Cinnamoyl-Phe-OH is used in peptide chemistry and chemical biology as a substrate-like or building-block derivative for preparing more complex acylated amino acid and peptide analogues, as well as for analytical method development and structure-property studies involving arylacylated phenylalanine motifs.
CAT No: CP27149
CAS No:4950-65-6
Synonyms/Alias:TRANS-CINNAMOYL-PHE-OH;4950-65-6;AC1O5JEV;CHEMBL3276007;N-(trans-Cinnamoyl)-L-Phe-OH;SCHEMBL10725101;ZINC25156;7807AH;N-(3-Phenylacryloyl)-L-phenylalanine;K-9218;(2S)-3-phenyl-2-[[(E)-3-phenylprop-2-enoyl]amino]propanoicacid
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