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N-(L-2-aminopentanoyl)-L-phenylalanine dihydrate, a hydrophobic dipeptide with a nonproteinogenic residue.

Carl Henrik GörbitzVitthal N Yadav
Published in: Acta crystallographica. Section C, Crystal structure communications (2013)
The title dipeptide, better known as L-norvalyl-L-phenylalanine {systematic name: (S)-2-[(S)-2-aminopentanamido]-3-phenylpropanoic acid dihydrate}, C14H20N2O3·2H2O, has a nonproteinogenic N-terminal residue. In the solid state, it takes on a molecular conformation typical for one of the three classes of nanoporous dipeptides, but like two related compounds with a hydrophobic N-terminal residue and a C-terminal L-phenylalanine, it fails to form channels or pores. Instead, the crystal structure is divided into distinct hydrophobic and hydrophilic layers, the latter encompassing cocrystallized water molecules connecting the charged N- and C-terminal groups.
Keyphrases
  • crystal structure
  • solid state
  • ionic liquid
  • aqueous solution
  • amino acid
  • liquid chromatography
  • molecular dynamics simulations
  • metal organic framework
  • tandem mass spectrometry