Activin and Inhibin

JTP10-△-R9 TFA is a selective JNK2 peptide inhibitor, with an IC 50 of 89 nM, exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.Appearance:SolidIC50&amp: Target:JNK2 89 nM (IC 50 ) JNK1 1.1 μM (IC 50 ) JNK3 1.2 μM (IC 50 )In

JTP10-△-TATi TFA is a selective JNK2 peptide inhibitor, with an IC 50 of 92 nM, exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.Appearance:SolidIC50&amp: Target:JNK2 92 nM (IC 50 ) JNK1 1.16 μM (IC 50 ) JNK3 1.2 μM (IC 50 )In

JTP10-△-TATi TFA is a selective JNK2 peptide inhibitor, with an IC 50 of 92 nM, exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.Appearance:SolidIC50&amp: Target:JNK2 92 nM (IC 50 ) JNK1 1.16 μM (IC 50 ) JNK3 1.2 μM (IC 50 )In

JTP10-△-TATi TFA is a selective JNK2 peptide inhibitor, with an IC 50 of 92 nM, exhibiting 10-fold selectivity for JNK2 over JNK1 and JNK3.Appearance:SolidIC50&amp: Target:JNK2 92 nM (IC 50 ) JNK1 1.16 μM (IC 50 ) JNK3 1.2 μM (IC 50 )In

JTT 551 is selective a protein tyrosine phosphatase 1B ( PTP1B ) inhibitor, with K i s of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively: JTT 551 can be used in the research of type 2 diabetes mellitus.In

JTT 551 is selective a protein tyrosine phosphatase 1B ( PTP1B ) inhibitor, with K i s of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively: JTT 551 can be used in the research of type 2 diabetes mellitus.In

JTT 551 is selective a protein tyrosine phosphatase 1B ( PTP1B ) inhibitor, with K i s of 0.22 μM and 9.3 μM for PTP1B and TCPTP (T-cell protein tyrosine phosphatase), respectively: JTT 551 can be used in the research of type 2 diabetes mellitus.In

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 ( ACAT-1 ) inhibitor with an IC 50 of 0.45±0.06 μM.In VitroThe potency and selectivity of K-604 for human ACAT-1 and ACAT-2 is examined. The IC 50 value of K-604

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 ( ACAT-1 ) inhibitor with an IC 50 of 0.45±0.06 μM.In VitroThe potency and selectivity of K-604 for human ACAT-1 and ACAT-2 is examined. The IC 50 value of K-604

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 ( ACAT-1 ) inhibitor with an IC 50 of 0.45±0.06 μM.In VitroThe potency and selectivity of K-604 for human ACAT-1 and ACAT-2 is examined. The IC 50 value of K-604

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 ( ACAT-1 ) inhibitor with an IC 50 of 0.45±0.06 μM.In VitroThe potency and selectivity of K-604 for human ACAT-1 and ACAT-2 is examined. The IC 50 value of K-604

K-604 dihydrochloride is a potent and selective acyl-CoA:cholesterol acyltransferase 1 ( ACAT-1 ) inhibitor with an IC 50 of 0.45±0.06 μM.In VitroThe potency and selectivity of K-604 for human ACAT-1 and ACAT-2 is examined. The IC 50 value of K-604