| Literature DB >> 16913725 |
Lin Zhang1, Junhua Fan, Khang Vu, Kevin Hong, Jean-Yves Le Brazidec, Jiandong Shi, Marco Biamonte, David J Busch, Rachel E Lough, Roy Grecko, Yingqing Ran, John L Sensintaffar, Adeela Kamal, Karen Lundgren, Francis J Burrows, Robert Mansfield, Gregg A Timony, Edgar H Ulm, Srinivas R Kasibhatla, Marcus F Boehm.
Abstract
We report on the discovery of benzo- and pyridino- thiazolothiopurines as potent heat shock protein 90 inhibitors. The benzothiazole moiety is exceptionally sensitive to substitutions on the aromatic ring with a 7'-substituent essential for activity. Some of these compounds exhibit low nanomolar inhibition activity in a Her-2 degradation assay (28-150 nM), good aqueous solubility, and oral bioavailability profiles in mice. In vivo efficacy experiments demonstrate that compounds of this class inhibit tumor growth in an N87 human colon cancer xenograft model via oral administration as shown with compound 37 (8-(7-chlorobenzothiazol-2-ylsulfanyl)-9-(2-cyclopropylamino-ethyl)-9H- purin-6-ylamine).Entities:
Mesh:
Substances:
Year: 2006 PMID: 16913725 DOI: 10.1021/jm051146h
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446