Epinephrine/zinc phenolsulfonate

product description：A cell-permeable, orally bioavailable, non-toxic thiazolyl-quinolinone derived compound that acts as a potent, selective and reversible inhibitor of CD38 (IC50 = 7.3 &amp: 1.9 nM for human &amp: mouse CD38, respectively: Ki = 0.3

A selective inhibitor of MNK1 in vitro (IC₅₀ = 2.2 &muM), with no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases blocks the phosphorylation of eIF4E in response to TNF-&alpha, arsenite, anisomycin, PMA, or

A selective inhibitor of MNK1 in vitro (IC₅₀ = 2.2 &muM), with no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases blocks the phosphorylation of eIF4E in response to TNF-&alpha, arsenite, anisomycin, PMA, or

A selective inhibitor of MNK1 in vitro (IC₅₀ = 2.2 &muM), with no inhibitory activity against p38, JNK1, ERK1/2, PKC, or Src-like kinases blocks the phosphorylation of eIF4E in response to TNF-&alpha, arsenite, anisomycin, PMA, or

Coproporphyrin III (Zincphyrin) is a naturally occurring porphyrin derivative that is mainly found in urine.IC50和靶点：Human Endogenous MetaboliteIn Vitro：Coproporphyrin III methyl ester is repeatedly isolated in considerable amount from both feces and

Coproporphyrin III (Zincphyrin) is a naturally occurring porphyrin derivative that is mainly found in urine.IC50和靶点：Human Endogenous MetaboliteIn Vitro：Coproporphyrin III methyl ester is repeatedly isolated in considerable amount from both feces and

Coproporphyrin III (Zincphyrin) is a naturally occurring porphyrin derivative that is mainly found in urine.IC50和靶点：Human Endogenous MetaboliteIn Vitro：Coproporphyrin III methyl ester is repeatedly isolated in considerable amount from both feces and

Coproporphyrin III (Zincphyrin) is a naturally occurring porphyrin derivative that is mainly found in urine.IC50和靶点：Human Endogenous MetaboliteIn Vitro：Coproporphyrin III methyl ester is repeatedly isolated in considerable amount from both feces and

CWP232228, a highly potent selective Wnt/β-catenin signaling inhibitor, antagonizes binding of β-catenin to T-cell factor (TCF) in the nucleus. CWP232228 suppresses tumor formation and metastasis without toxicity through the inhibition of the growth

CWP232228, a highly potent selective Wnt/β-catenin signaling inhibitor, antagonizes binding of β-catenin to T-cell factor (TCF) in the nucleus. CWP232228 suppresses tumor formation and metastasis without toxicity through the inhibition of the growth

CWP232228, a highly potent selective Wnt/β-catenin signaling inhibitor, antagonizes binding of β-catenin to T-cell factor (TCF) in the nucleus. CWP232228 suppresses tumor formation and metastasis without toxicity through the inhibition of the growth

Biochem/physiol Actions CYM-5442 is a highly-selective S1P1 (Spingosine 1-Phosphate Receptor 1) agonist that activates S1P1-dependent pathways in vitro and to levels of full efficacy in vivo through a hydrophobic pocket, separable from the