1132667-24-3Relevant articles and documents
Synthesis and histone deacetylase inhibitory activity of largazole analogs: Alteration of the zinc-binding domain and macrocyclic scaffold
Bowers, Albert A.,West, Nathan,Newkirk, Tenaya L.,Troutman-Youngman, Annie E.,Schreiber, Stuart L.,Wiest, Olaf,Bradner, James E.,Williams, Robert M.
, p. 1301 - 1304 (2009)
Fourteen analogs of the marine natural product largazole have been prepared and assayed against histone deacetylases (HDACs) 1, 2, 3, and 6. Olefin cross-metathesis was used to efficiently access six variants of the side-chain zinc-binding domain, while adaptation of our previously reported modular synthesis allowed probing of the macrocyclic cap group.