A66 10mg 10mg | Purity Not Available
Adooq Bioscience
The S-enantiomer of A66 is a potent inhibitor of the p110alpha isoform of PI 3-kinase (PIK3CA).
More Information Supplier PageThe S-enantiomer of A66 is a potent inhibitor of the p110alpha isoform of PI 3-kinase (PIK3CA).
More Information Supplier PageBMS-806, also known as BMS-378806 , is a type of medicine called an entry inhibitor. Entry inhibitors work by blocking HIV from entering human cells. BMS-378806 (BMS-806) is a small molecule that blocks the binding of host-cell CD4 with viral gp120 protein and therefore inhibits the first steps of HIV-1 infection.
More Information Supplier PageBMS-806, also known as BMS-378806 , is a type of medicine called an entry inhibitor. Entry inhibitors work by blocking HIV from entering human cells. BMS-378806 (BMS-806) is a small molecule that blocks the binding of host-cell CD4 with viral gp120 protein and therefore inhibits the first steps of HIV-1 infection.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PagePNU-120596 is a positive allosteric modulator of ??7 neuronal nicotinic acetylcholine receptors.
More Information Supplier PageLDN193189 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 PageLDN193189 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 PageLDN193189 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 Page