Clesacostat (PF-05221304; PF05221304) is a potent, oral and selective ACC inhibitor (hACC1 IC50 = 13nM; hACC@ IC50 = 9 nM). PF-0522130 selectively inhibits liver DNL in animals, while demonstrating considerable safety margins against platelet reduction in a nonhuman primate model. PF-05221304 directly improves a variety of non-alcoholic fatty liver (NAFL) and non-alcoholic steatohepatitis (NASH) pathogenic […]
Lometrexol hydrate is a novel and potent antipurine antifolate
LtaS-IN-1 is a novel and potent inhibitor of Lipoteichoic acid (LTA)
Ac4GlcNAlk is a novel and potent PROTAC linker
Eriosematin is a novel and potent bioactive compound
AU-15330 (AU15330) is a PROTAC degrader of the SWI/SNF ATPase subunits, SMARCA2 and SMARCA4 with anticancer activity.
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Neohesperidose is a naturally occurring disaccharide isolated from species of typha.
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