GW 4869 10mg 10mg | Purity Not Available
Adooq Bioscience
W4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageW4869 is a cell permeable, selective inhibitor of N-SMase (neutral sphingomyelinase).
More Information Supplier PageNecrostatin-1 is an ATP-competitive, allosteric inhibitor of receptor-interacting protein kinase 1 (RIPK1) (EC50 = 182 nM).
More Information Supplier PageNecrostatin-1 is an ATP-competitive, allosteric inhibitor of receptor-interacting protein kinase 1 (RIPK1) (EC50 = 182 nM).
More Information Supplier PageNecrostatin-1 is an ATP-competitive, allosteric inhibitor of receptor-interacting protein kinase 1 (RIPK1) (EC50 = 182 nM).
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 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.
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