Boc-Phe-D-Leu-Phe-D-Leu-Phe-OH features alternating L- and D-residues that impose unique conformational constraints. The peptide's aromatic-rich composition promotes packing analysis in structural studies. Its Boc protection enhances handling. Researchers apply it in stereochemical folding research, peptidomimetic development, and motif organization studies.
CAT No: C4902
CAS No:66556-73-8
Synonyms/Alias:66556-73-8;BOC-PHE-D-LEU-PHE-D-LEU-PHE-OH;Bplplp;{Boc}-Phe-Leu-Phe-Leu-Phe;Boc2 cpd;Butyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanine;N-t-Boc-phe-leu-phe-leu-phe;N-t-Boc-phe-dleu-phe-dleu-phe;Butyloxycarbonyl-phe-leu-phe-leu-phe;(2S)-2-[[(2R)-4-methyl-2-[[(2S)-2-[[(2R)-4-methyl-2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]pentanoyl]amino]-3-phenylpropanoyl]amino]pentanoyl]amino]-3-phenylpropanoic acid;CHEMBL3311030;DTXSID30216738;N-Tertiary-butyloxycarbonyl-phenylalanyl-leucyl-phenylalanyl-leucyl-phenylalanine;Boc-Phe-Leu-Phe-Leu-Phe-OH;L-Phenylalanine, N-(N-(N-(N-(N-((1,1-dimethylethoxy)carbonyl)-L-phenylalanyl)-D-leucyl)-L-phenylalanyl)-D-leucyl)-;SCHEMBL6897460;Boc-Phe-D-Leu-Phe-D-Leu-Phe;DTXCID60139229;HY-P2355;BDBM50051608;AKOS040758271;FB111223;L-Phenylalanine,N-[(1,1-dimethylethoxy)carbonyl]-L-phenylalanyl-D-leucyl-L-phenylalanyl-D-leucyl-;MS-31438;CS-0132590;G12219;(6S,9R,12S,15R,18S)-6,12,18-tribenzyl-9,15-diisobutyl-2,2-dimethyl-4,7,10,13,16-pentaoxo-3-oxa-5,8,11,14,17-pentaazanonadecan-19-oic acid;
4. High fat diet and GLP-1 drugs induce pancreatic injury in mice
5. Cationic cell-penetrating peptides are potent furin inhibitors
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