trans-Cinnamoyl-Phe-OH

Name: trans-Cinnamoyl-Phe-OH
Brand: Creative Peptides
Rating: 5 (1 reviews)

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.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

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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cGMP Peptide

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M.F/Formula

C18H17NO3

M.W/Mr.

295.34

Size

250 mg;1 g;

InChI

1S/C18H17NO3/c20-17(12-11-14-7-3-1-4-8-14)19-16(18(21)22)13-15-9-5-2-6-10-15/h1-12,16H,13H2,(H,19,20)(H,21,22)/b12-11+/t16-/m0/s1

InChI Key

YFHVCODMDZNZEA-PCUGXKRQSA-N

Canonical SMILES

C1=CC=C(C=C1)CC(C(=O)O)NC(=O)C=CC2=CC=CC=C2

1. The spatiotemporal control of signalling and trafficking of the GLP-1R

2. Peptides as Active Ingredients: A Challenge for Cosmeceutical Industry

3. TMEM16F and dynamins control expansive plasma membrane reservoirs

4. Myotropic activity and immunolocalization of selected neuropeptides of the burying beetle Nicrophorus vespilloides (Coleoptera: Silphidae)

5. Multifunctional peptide-oligonucleotide conjugate promoted sensitive electrochemical biosensing of cardiac troponin I

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