Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T10424 |
AZ-3
|
JAK | Angiogenesis; Chromatin/Epigenetic; JAK/STAT signaling; Stem Cells |
AZ-3 is a potent and selective JAK1 inhibitor (IC50: 34 nM). | |||
T14365 |
AZ PFKFB3 26
|
Glucokinase | Metabolism |
AZ PFKFB3 26 是一种有效的特异性 PFKFB3 抑制剂,IC50 为 23 nM。 PFKFB1 和 PFKFB2 的 IC50 分别为 2.06 和 0.384 μM。 | |||
T21659 |
AZ 11645373
3-[1-[[(3'-NITRO[1,1'-BIPHENYL]-4-YL)OXY]METHYL]-3-(4-PYRIDINYL)PROPYL]-2,4-THIAZOLIDINEDIONE |
P2X Receptor | Membrane transporter/Ion channel; Neuroscience |
AZ 11645373 (3-[1-[[(3'-NITRO[1,1'-BIPHENYL]-4-YL)OXY]METHYL]-3-(4-PYRIDINYL)PROPYL]-2,4-THIAZOLIDINEDIONE) 是一种高度选择性和有效的人 P2X7 受体拮抗剂,对小鼠/大鼠 P2X7 受体没有影响。 | |||
T14364 |
AZ-Dyrk1B-33
3-(2-Methyl-4-pyrimidinyl)-1-(phenylmethyl)-1H-pyrrolo[2,3-c]pyridine |
DYRK | Cell Cycle/Checkpoint; Tyrosine Kinase/Adaptors |
AZ-Dyrk1B-33 (3-(2-Methyl-4-pyrimidinyl)-1-(phenylmethyl)-1H-pyrrolo[2,3-c]pyridine) 是高选择性的Dyrk1B 激酶抑制剂,其IC50=7 nM。 | |||
T26730 | AZ-PFKFB3-67 | ||
AZ-PFKFB3-67 is a novel, potent and selective inhibitor of PFKFB3. |