1380237-22-8Relevant academic research and scientific papers
Molecular design of histone deacetylase inhibitors by aromatic ring shifting in chlamydocin framework
Shivashimpi, Gururaj M.,Amagai, Satoshi,Kato, Tamaki,Nishino, Norikazu,Maeda, Satoko,Nishino, Tomonori G.,Yoshida, Minoru
, p. 7830 - 7839 (2008/09/16)
Chlamydocin, a cyclic tetrapeptide containing aminoisobutyric acid (Aib), l-phenylalanine (l-Phe), d-proline (d-Pro), and a unique amino acid l-2-amino-8-oxo-9,10-epoxydecanoic acid, inhibits the histone deacetylases (HDACs), a class of enzymes, which pla
