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FA-Gly-Phe-Leu-OH

FA-Gly-Phe-Leu-OH contains an aromatic residue that introduces distinct stacking interactions, making it valuable for structural and spectroscopic studies. Its FA protection supports efficient incorporation into peptide assembly protocols. Researchers employ it to explore hydrophobic packing and side-chain contributions to folding. The tripeptide is also used in designing bioactive motifs for biochemical and materials research.

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

CAT No: F0814

Synonyms/Alias:FA-Gly-Phe-Leu-OH;390766-88-8;FA-Gly-Phe-Leu;(2S)-2-[[(2S)-2-[[2-[[(E)-3-(furan-2-yl)prop-2-enoyl]amino]acetyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoic acid;MFCD00237641;HY-P5094;DA-63359;FF110891;CS-0676123;(3-(Furan-2-yl)acryloyl)glycyl-L-phenylalanyl-L-leucine;

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C24H29N3O6
M.W/Mr.
455.5
Sequence
One Letter Code:GFL
InChI
InChI=1S/C24H29N3O6/c1-16(2)13-20(24(31)32)27-23(30)19(14-17-7-4-3-5-8-17)26-22(29)15-25-21(28)11-10-18-9-6-12-33-18/h3-12,16,19-20H,13-15H2,1-2H3,(H,25,28)(H,26,29)(H,27,30)(H,31,32)/b11-10+/t19-,20-/m0/s1
InChI Key
UADPUXIEEYQMRI-FWEDTRJPSA-N

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