Potent, selective, orally bioavailable inhibitors of tumor necrosis factor-alpha converting enzyme (TACE): discovery of indole, benzofuran, imidazopyridine and pyrazolopyridine P1' substituents.

Citation: Lu Z, Ott GR, Anand R, Liu RQ, Covington MB, Vaddi K, Qian M, Newton RC, Christ DD, Trzaskos J, Duan JJ.: Potent, selective, orally bioavailable inhibitors of tumor necrosis factor-alpha converting enzyme (TACE): discovery of indole, benzofuran, imidazopyridine and pyrazolopyridine P1' substituents. Bioorg Med Chem Lett, Volume 18 (6), 2008
Authors: Anand R, Christ DD, Covington MB, Duan JJ., Liu RQ, Lu Z, Newton RC, Ott GR, Qian M, Trzaskos J, Vaddi K
Journal: Bioorg Med Chem Lett
Year: 2008
DOI: 10.1016/j.bmcl.2008.01.120
PubMed: 18282708
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