848001-72-9Relevant academic research and scientific papers
Discovery of a potent and orally bioavailable dual antagonist of CC chemokine receptors 2 and 5
Carter, Percy H.,Brown, Gregory D.,Cherney, Robert J.,Batt, Douglas G.,Chen, Jing,Clark, Cheryl M.,Cvijic, Mary Ellen,Duncia, John V.,Ko, Soo S.,Mandlekar, Sandhya,Mo, Ruowei,Nelson, David J.,Pang, Jian,Rose, Anne V.,Santella, Joseph B.,Tebben, Andrew J.,Traeger, Sarah C.,Xu, Songmei,Zhao, Qihong,Barrish, Joel C.
supporting information, p. 439 - 444 (2015/04/27)
We describe the hybridization of our previously reported acyclic and cyclic CC chemokine receptor 2 (CCR2) antagonists to lead to a new series of dual antagonists of CCR2 and CCR5. Installation of a γ-lactam as the spacer group and a quinazoline as a benz
Cyclic derivatives as modulators of chemokine receptor activity
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Page/Page column 64-65, (2008/06/13)
The present application describes modulators of MCP-1 of formula (I): or pharmaceutically acceptable salt forms thereof, useful for the treatment of rheumatoid arthritis, multiple sclerosis, atherosclerosis and asthma.
