化学
选择性
酶
酶抑制剂
立体化学
微粒体
前列腺素E2
前列腺素
生物化学
医学
内科学
催化作用
作者
Jane Wang,David C. Limburg,Jeff Carter,Gabriel Mbalaviele,James K. Gierse,Michael L. Vazquez
标识
DOI:10.1016/j.bmcl.2010.01.060
摘要
Here we describe the SAR of a series of potent and selective mPGES-1 inhibitors based on an oxicam template. Compound 13j demonstrated low nanomolar mPGES-1 inhibition in an enzyme assay. In addition, it displayed PGE(2) inhibition in a cell-based assay (0.42microM) and had over 238-fold selectivity for mPGES-1 over COX-2 and over 200-fold selectivity for mPGES-1 over 6-keto PGF(1alpha).
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