Activin and Inhibin

Cysteine Protease inhibitor hydrochloride is an inhibitor of cysteine protease .IC50 &amp: Target: Cysteine ProteaseForm:Solid.

Cysteine Protease inhibitor hydrochloride is an inhibitor of cysteine protease .IC50 &amp: Target: Cysteine ProteaseForm:Solid.

Cysteine Protease inhibitor hydrochloride is an inhibitor of cysteine protease .IC50 &amp: Target: Cysteine Protease.

cyt-PTPε Inhibitor-1 is a potent cytosolic protein tyrosine phosphatase epsilon ( cyt-PTPε ) inhibitor, binds to the catalytic domain of cyt-PTPε, blocks c-Src activation (dephosphorylation of c-Src), and exhibits anti-osteoclastic activityIn

cyt-PTPε Inhibitor-1 is a potent cytosolic protein tyrosine phosphatase epsilon ( cyt-PTPε ) inhibitor, binds to the catalytic domain of cyt-PTPε, blocks c-Src activation (dephosphorylation of c-Src), and exhibits anti-osteoclastic activityIn

CZL55 is a caspase-1 inhibitor with an IC 50 value of 24 nM. CZL55 can be used for the research of febrile seizures (FS)Form:SolidIC50&amp: Target:Caspase-1 24 nM (IC 50 ).

D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity.Appearance:SolidIn Vitro:D-Cl-amidine (200-400 μM) is effective in significantly decreasing cell viability in

D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity.Appearance:SolidIn Vitro:D-Cl-amidine (200-400 μM) is effective in significantly decreasing cell viability in

D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity.Appearance:SolidIn Vitro:D-Cl-amidine (200-400 μM) is effective in significantly decreasing cell viability in

D-Cl-amidine hydrochloride is a potent and highly selective PAD1 inhibitor. D-Cl-amidine is well-torelated with no significant toxicity.Appearance:SolidIn Vitro:D-Cl-amidine (200-400 μM) is effective in significantly decreasing cell viability in

D-JNKI-1 (AM-111) is a highly potent and cell-permeable peptide inhibitor of JNK .In VitroD-JNKI-1 (AM-111: 1 μM-1 mM) treatment prevents apoptosis and loss of neomycin-exposed hair cells. MCE has not independently confirmed the accuracy of these

D-JNKI-1 (AM-111) is a highly potent and cell-permeable peptide inhibitor of JNK .In VitroD-JNKI-1 (AM-111: 1 μM-1 mM) treatment prevents apoptosis and loss of neomycin-exposed hair cells. MCE has not independently confirmed the accuracy of these