Ki16198 5mg 5mg | Purity Not Available
Adooq Bioscience
Ki16198 is a potent LPA receptor antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 ??M and 0.93 ??M, respectively.
More Information Supplier PageKi16198 is a potent LPA receptor antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 ??M and 0.93 ??M, respectively.
More Information Supplier PageKi16198 is a potent LPA receptor antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 ??M and 0.93 ??M, respectively.
More Information Supplier PageKi16198 is a potent LPA receptor antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 ??M and 0.93 ??M, respectively.
More Information Supplier PageKi16198 is a potent LPA receptor antagonist and inhibits LPA1- and LPA3-induced inositol phosphate production with Ki of 0.34 ??M and 0.93 ??M, respectively.
More Information Supplier PageGW 9508 is a cell-permeable aminophenylpropanoate that acts as a potent and selective agonist for the G-protein coupled receptor (GPCR) GRP40/FFA1 receptor (EC50 ?50 nM) with reduced activity towards family members GRP120 (EC50 ?3.5 ??M), GRP41/GRP43 (EC50 >50 ??M), as well as a panel of eight other free fatty acid (FFA) and prostaglandin receptors.
More Information Supplier PageGW 9508 is a cell-permeable aminophenylpropanoate that acts as a potent and selective agonist for the G-protein coupled receptor (GPCR) GRP40/FFA1 receptor (EC50 ?50 nM) with reduced activity towards family members GRP120 (EC50 ?3.5 ??M), GRP41/GRP43 (EC50 >50 ??M), as well as a panel of eight other free fatty acid (FFA) and prostaglandin receptors.
More Information Supplier PageGW 9508 is a cell-permeable aminophenylpropanoate that acts as a potent and selective agonist for the G-protein coupled receptor (GPCR) GRP40/FFA1 receptor (EC50 ?50 nM) with reduced activity towards family members GRP120 (EC50 ?3.5 ??M), GRP41/GRP43 (EC50 >50 ??M), as well as a panel of eight other free fatty acid (FFA) and prostaglandin receptors.
More Information Supplier PageGW 9508 is a cell-permeable aminophenylpropanoate that acts as a potent and selective agonist for the G-protein coupled receptor (GPCR) GRP40/FFA1 receptor (EC50 ?50 nM) with reduced activity towards family members GRP120 (EC50 ?3.5 ??M), GRP41/GRP43 (EC50 >50 ??M), as well as a panel of eight other free fatty acid (FFA) and prostaglandin receptors.
More Information Supplier PageTCS PIM-1 4a is a selective and ATP-competitive Pim kinase inhibitor (IC50 values = 24 and 100 nM for Pim-1 and Pim-2, respectively).
More Information Supplier PageTCS PIM-1 4a is a selective and ATP-competitive Pim kinase inhibitor (IC50 values = 24 and 100 nM for Pim-1 and Pim-2, respectively).
More Information Supplier Page