669091-40-1Relevant academic research and scientific papers
Synthesis and histone deacetylase inhibitory activity of cyclic tetrapeptides containing a retrohydroxamate as zinc ligand
Nishino, Norikazu,Yoshikawa, Daisuke,Watanabe, Louis A.,Kato, Tamaki,Jose, Binoy,Komatsu, Yasuhiko,Sumida, Yuko,Yoshida, Minoru
, p. 2427 - 2431 (2007/10/03)
Cyclic tetrapeptide retrohydroxamic acids were prepared as histone deacetylase (HDAC) inhibitors and evaluated the inhibitory activity and found that they have potential as anticancer drugs.
Synthesis of L-α-amino-ω-bromoalkanoic acid for side chain modification
Watanabe, Louis A.,Jose, Binoy,Kato, Tamaki,Nishino, Norikazu,Yoshida, Minoru
, p. 491 - 494 (2007/10/03)
L-α-Amino-ω-bromoalkanoic acids with side chain lengths varying from 4 to 10 methylene units have been conveniently synthesized as useful intermediates for the synthesis of functionalized non-natural amino acids.
