104465-44-3Relevant academic research and scientific papers
Synthesis of substituted pyrimidine hydrazine acids (PHA) and their use in peptide recognition
Miltschitzky, Stefan,Michlova, Veronika,Stadlbauer, Stefan,Koenig, Burkhard
, p. 135 - 160 (2007/10/03)
Substituted pyrimidine-hydrazine-acids (PHA) were prepared from orotic acid in five synthetic steps and high yields. Their geometry of hydrogen bond acceptor and donor sites make them suitable for the molecular recognition of peptide β-sheets. In non-protic solvents the PHA unit emits at around 420 nm after irradiation at 281 nm. The emission intensity decreases upon peptide binding and signals the binding event. Peptides consisting of PHAs and natural amino acids or a turn structure motif were prepared. The investigation of the intramolecular binding pattern by NMR spectroscopy revealed the expected interaction of the PHA and peptide β-sheet.
Inhibition of Cathepsin D by Substrate Analogues Containing Statine and by Analogues of Pepstatin
Agarwal, Nirankar S.,Rich, Daniel H.
, p. 2519 - 2524 (2007/10/02)
Five new cathepsin D inhibitors were synthesized and tested as inhibitors of bovine cathepsin D.The compounds were derived by replacing a Phe-Phe dipeptidyl unit of a good cathepsin D substrate, Boc-Phe-Leu-Ala-Phe-Phe-Val-Leu-OR, with statine ((3S,4S)-4-
