Mixed Lineage Kinase
抑制剂选择性比较
Mixed Lineage Kinase产品
| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S8032 |
PRT062607 (P505-15) HClPRT062607 (P505-15, BIIB057) HCl是一种新型的，高度选择性Syk抑制剂，无细胞试验中IC50为1 nM，作用于Syk比作用于Fgr，PAK5，Lyn，FAK，Pyk2, FLT3, MLK1 和Zap70选择性高80倍以上。 |
Dectin-1 is involved in activation of NLRP3-inflammasome by Malassezia spp. IL-1b secretion from mature human mono-DCs incubated with Syk-inhibitors (piceatannol, R406 or P505), 1 h prior to exposure to medium, MSU, b-glucan, nigericin or live M. furfur (MOI = 10) was determined after 6 h by ELISA.
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| S2805 |
LY364947LY364947 (HTS 466284)是一种有效的ATP竞争性TGFβR-I抑制剂，无细胞试验中IC50为59 nM，比作用于TGFβR-II选择性高7倍。 |
The cytoplasmic and nuclear proteins were separated and the protein expression levels were determined by performing western blotting. LY364947 (1 uM), which is a potent ATP-competitive inhibitor of TGF-βRI, was used as the positive control. GAPDH and PARP were used as cytosolic and nuclear markers, respectively. |
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| S7343 |
URMC-099URMC-099 是一种口服生物有效的，大脑渗透性mixed lineage kinase (MLK)抑制剂，对MLK1, MLK2, MLK3,和DLK的IC50分别为19 nM, 42 nM, 14 nM,以及150 nM，也能抑制LRRK2的活性，IC50为11 nM。URMC-099 也可抑制 ABL1 对应的IC50值为6.8 nM。URMC-099 可诱导自噬。 |
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| S8251 |
NecrosulfonamideNecrosulfonamide是一种特异的、有效的细胞坏死抑制剂，通过抑制MLKL发挥其作用。 |
Necroptotic death of HT-29 cells was verified using RIP1 or MLKL inhibitors necrostatine-1 and necrosulfonamide. HT-29 were pre-treated with the combinations of 10 nM birinapant, 50 μM z-VAD, 50 μM necrostatin and 20 μM necrosulfonamide as shown for 1 h, and then treated with 100 ng/ml of TST-TRAIL-wt, 4.2, 5.1 and 5.2 for 8 h.
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| S3238New |
ResibufogeninResibufogenin (Bufogenin, Recibufogenin) 是huachansu华蟾素中具有抗癌作用的成分，通过上调 receptor-interacting protein kinase 3 (RIP3) 和磷酸化 mixed lineage kinase domain-like protein 的Ser358位点来触发坏死病。Resibufogenin 可通过诱导 reactive oxygen species (ROS) 积累发挥细胞毒性作用。Resibufogenin 可诱导凋亡和 caspase-3 和 caspase-8 活性。Resibufogenin 增加 Bax/Bcl-2 表达，并抑制 cyclin D1、cyclin E、PI3K、p-AKT、p-GSK3β 和 β-catenin 的蛋白表达。 |
| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S8032 |
PRT062607 (P505-15) HClPRT062607 (P505-15, BIIB057) HCl是一种新型的，高度选择性Syk抑制剂，无细胞试验中IC50为1 nM，作用于Syk比作用于Fgr，PAK5，Lyn，FAK，Pyk2, FLT3, MLK1 和Zap70选择性高80倍以上。 |
Dectin-1 is involved in activation of NLRP3-inflammasome by Malassezia spp. IL-1b secretion from mature human mono-DCs incubated with Syk-inhibitors (piceatannol, R406 or P505), 1 h prior to exposure to medium, MSU, b-glucan, nigericin or live M. furfur (MOI = 10) was determined after 6 h by ELISA.
|
|
| S2805 |
LY364947LY364947 (HTS 466284)是一种有效的ATP竞争性TGFβR-I抑制剂，无细胞试验中IC50为59 nM，比作用于TGFβR-II选择性高7倍。 |
The cytoplasmic and nuclear proteins were separated and the protein expression levels were determined by performing western blotting. LY364947 (1 uM), which is a potent ATP-competitive inhibitor of TGF-βRI, was used as the positive control. GAPDH and PARP were used as cytosolic and nuclear markers, respectively. |
|
| S7343 |
URMC-099URMC-099 是一种口服生物有效的，大脑渗透性mixed lineage kinase (MLK)抑制剂，对MLK1, MLK2, MLK3,和DLK的IC50分别为19 nM, 42 nM, 14 nM,以及150 nM，也能抑制LRRK2的活性，IC50为11 nM。URMC-099 也可抑制 ABL1 对应的IC50值为6.8 nM。URMC-099 可诱导自噬。 |
||
| S8251 |
NecrosulfonamideNecrosulfonamide是一种特异的、有效的细胞坏死抑制剂，通过抑制MLKL发挥其作用。 |
Necroptotic death of HT-29 cells was verified using RIP1 or MLKL inhibitors necrostatine-1 and necrosulfonamide. HT-29 were pre-treated with the combinations of 10 nM birinapant, 50 μM z-VAD, 50 μM necrostatin and 20 μM necrosulfonamide as shown for 1 h, and then treated with 100 ng/ml of TST-TRAIL-wt, 4.2, 5.1 and 5.2 for 8 h.
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| 目录号 | 产品描述 | 文献引用 | 实验数据 |
|---|---|---|---|
| S3238New |
ResibufogeninResibufogenin (Bufogenin, Recibufogenin) 是huachansu华蟾素中具有抗癌作用的成分，通过上调 receptor-interacting protein kinase 3 (RIP3) 和磷酸化 mixed lineage kinase domain-like protein 的Ser358位点来触发坏死病。Resibufogenin 可通过诱导 reactive oxygen species (ROS) 积累发挥细胞毒性作用。Resibufogenin 可诱导凋亡和 caspase-3 和 caspase-8 活性。Resibufogenin 增加 Bax/Bcl-2 表达，并抑制 cyclin D1、cyclin E、PI3K、p-AKT、p-GSK3β 和 β-catenin 的蛋白表达。 |
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