LDN193189 is a highly potent small molecule BMP inhibitor that inhibits BMP type I receptors ALK2 (IC50: 5 nM), ALK3 (IC50: 30 nM) and ALK6 (TGF??1/BMP signaling) and subsequent SMAD phosphorylation.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PageGW3965 HCl is a selective and orally active liver X receptor (LXR) full agonist.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PageA 922500 is a diacylglycerol acyltransferase 1 (DGAT-1) inhibitor (IC50 values are 7 and 24 nM at human and mouse DGAT-1 respectively).
More Information Supplier PageA 922500 is a diacylglycerol acyltransferase 1 (DGAT-1) inhibitor (IC50 values are 7 and 24 nM at human and mouse DGAT-1 respectively).
More Information Supplier PageD-106669 is a highly potent and selective PI3K inhibitor, (PI3Kα IC50 <10 nM, >3 log selectivity against tyrosine or serine/threonine kinases, except ERK1 and 2).
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