Sarcolysin hydrochloride

BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11 nM.Appearance:SolidIC50&amp: Target:IC50: 11 nM (FLT3)In Vitro:BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11nM. Phosphorylation of

BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11 nM.Appearance:SolidIC50&amp: Target:IC50: 11 nM (FLT3)In Vitro:BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11nM. Phosphorylation of

BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11 nM.Appearance:SolidIC50&amp: Target:IC50: 11 nM (FLT3)In Vitro:BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11nM. Phosphorylation of

BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11 nM.Appearance:SolidIC50&amp: Target:IC50: 11 nM (FLT3)In Vitro:BPR1J-097 Hydrochloride is a novel and potent FLT3 inhibitor with an IC 50 of 11nM. Phosphorylation of

CCT128930 hydrochloride is a potent and selective inhibitor of AKT ( IC 50 =6 nM). CCT128930 hydrochloride has 28-fold selectivity over the closely related PKA kinase (IC 50 =168 nM) through the targeting of Met282 of AKT (Met173 of PKA-AKT

CCT128930 hydrochloride is a potent and selective inhibitor of AKT ( IC 50 =6 nM). CCT128930 hydrochloride has 28-fold selectivity over the closely related PKA kinase (IC 50 =168 nM) through the targeting of Met282 of AKT (Met173 of PKA-AKT

CCT128930 hydrochloride is a potent and selective inhibitor of AKT ( IC 50 =6 nM). CCT128930 hydrochloride has 28-fold selectivity over the closely related PKA kinase (IC 50 =168 nM) through the targeting of Met282 of AKT (Met173 of PKA-AKT

CCT128930 hydrochloride is a potent and selective inhibitor of AKT ( IC 50 =6 nM). CCT128930 hydrochloride has 28-fold selectivity over the closely related PKA kinase (IC 50 =168 nM) through the targeting of Met282 of AKT (Met173 of PKA-AKT

CCT128930 hydrochloride is a potent and selective inhibitor of AKT ( IC 50 =6 nM). CCT128930 hydrochloride has 28-fold selectivity over the closely related PKA kinase (IC 50 =168 nM) through the targeting of Met282 of AKT (Met173 of PKA-AKT

CXCR7 antagonist-1 hydrochloride is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (also known as the CXCL12 chemokine) or I-TAC (also known as CXCL11) to the chemokine receptor CXCR7. CXCR7 antagonist-1 hydrochloride is useful

CXCR7 antagonist-1 hydrochloride is a CXCR7 antagonist that inhibits the binding of the SDF-1 chemokine (also known as the CXCL12 chemokine) or I-TAC (also known as CXCL11) to the chemokine receptor CXCR7. CXCR7 antagonist-1 hydrochloride is useful

Dalpiciclib (SHR-6390) hydrochloride is an orally active and highly selective inhibitor of CDK4 and 6 with IC 50 values of 12.4 nM and 9.9 nM, respectively. Dalpiciclib hydrochloride shows antitumor activity against breast cancer and esophageal