| Literature DB >> 21341682 |
Edgardo Laborde1, Robert W Macsata, Fanying Meng, Brian T Peterson, Louise Robinson, Steve R Schow, Reyna J Simon, Hua Xu, Kunihisa Baba, Hideaki Inagaki, Yoshiro Ishiwata, Takahito Jomori, Yukiharu Matsumoto, Atsushi Miyachi, Takashi Nakamura, Masayuki Okamoto, Tracy M Handel, Claude C A Bernard.
Abstract
Through the application of TRAP (target-related affinity profiling), we identified a novel class of heteroaroylphenylureas that inhibit human CCL2-induced chemotaxis of monocytes/macrophages both in vitro and in vivo. This inhibition was concentration-dependent and selective with regard to other chemokines. The compounds, however, did not antagonize the binding of (125)I-labeled CCL2 to the CCR2 receptor nor did they block CCR2-mediated signal transduction responses such as calcium mobilization. Optimization of early leads for potency and pharmacokinetic parameters resulted in the identification of 17, a potent inhibitor of chemotaxis (IC(50) = 80 nM) with excellent oral bioavailability in rats (F = 60%). Compound 17 reduced swelling and joint destruction in two rat models of rheumatoid arthritis and delayed disease onset and produced near complete resolution of symptoms in a mouse model of multiple sclerosis.Entities:
Mesh:
Substances:
Year: 2011 PMID: 21341682 PMCID: PMC3229226 DOI: 10.1021/jm1012903
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446