Pimelic Diphenylamide 106 nogin 4-d]pyrimidin-1-yl}ethyl)-5-chloro-2-ethoxy-6-fluorophenyl]pyrrolidin-2-one

4-d]pyrimidin-1-yl}ethyl)-5-chloro-2-ethoxy-6-fluorophenyl]pyrrolidin-2-one

and genistein

This conversion is practically complete

8-dihydroquinoline-5-sulfonic acid

has IC50s of 7

Pimelic Diphenylamide 106 nogin 4-d]pyrimidin-1-yl}ethyl)-5-chloro-2-ethoxy-6-fluorophenyl]pyrrolidin-2-onePimelic Diphenylamide 106 is a slow, tight binding inhibitor of class I HDAC (HDAC 1, 2, and 3, with IC50 values of 150 nM , 760nM, and 370 nM, respectively), demonstrating no activity against class II HDACs. IC50 value: 150 nM (HDAC1), 370 nM (HDAC3), 760nM(HDAC2)Target: HDAC in vitro: Pimelic Diphenylamide 106 has preference toward HDAC3 with Ki of 14 nM, 15 times lower than the Ki for HDAC1. Pimelic Diphenylamide 106 exhibits weaker inhibitory