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Timapiprant 5 mg | 99.89%
TargetMol
OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
More Information Supplier PageTimapiprant 50 mg | 99.89%
TargetMol
OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
More Information Supplier PageTimapiprant 25 mg | 99.89%
TargetMol
OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
More Information Supplier PageTimapiprant 10 mg | 99.89%
TargetMol
OC000459 is a potent and selective D prostanoid receptor 2 (DP2) antagonist (IC50: 13 nM).
More Information Supplier PageGSK2801 10 mg | 99.88%
TargetMol
GSK2801 is an effective, specific and cell active acetyl-lysine competitive inhibitor of BAZ2A(Kd: 136 nM) and BAZ2B(Kd: 257 nM) bromodomains.
More Information Supplier PageGSK2801 5 mg | 99.88%
TargetMol
GSK2801 is an effective, specific and cell active acetyl-lysine competitive inhibitor of BAZ2A(Kd: 136 nM) and BAZ2B(Kd: 257 nM) bromodomains.
More Information Supplier PageIC261 10 mg | 99.86%
TargetMol
IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50 of IC261 for CK1 was 16 μM and for Cdk5 is 4.5 mM.
More Information Supplier PageIC261 50 mg | 99.86%
TargetMol
IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50 of IC261 for CK1 was 16 μM and for Cdk5 is 4.5 mM.
More Information Supplier PageIC261 5 mg | 99.86%
TargetMol
IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50 of IC261 for CK1 was 16 μM and for Cdk5 is 4.5 mM.
More Information Supplier Page
