Powder: -20°C for 3 years | In solvent: -80°C for 1 year
ERK-IN-2, an ERK2 inhibitor, exhibits an IC50 value of 1.8 nM. At doses greater than 10 μM, it may induce off-target toxicity and/or activity [1].
パッケージサイズ | 在庫状況 | 単価(税別) |
---|---|---|
25 mg | 約10-14 週間 | ¥ 349,000 |
50 mg | 約10-14 週間 | ¥ 454,500 |
100 mg | 約10-14 週間 | ¥ 574,000 |
説明 | ERK-IN-2, an ERK2 inhibitor, exhibits an IC50 value of 1.8 nM. At doses greater than 10 μM, it may induce off-target toxicity and/or activity [1]. |
ターゲット&IC50 | ERK2:1.8 nM |
In vitro | The criteria of inhibitor probe: Inhibitor potency: goal is <100 nM (IC 50 ); Selectively with target family: >30-fold. We recommend ERK-IN-2 (MRK-ERKi) to be used at a concentration of 1 μM in cell-based experiments while not recommend doses >10 μM to be employed in any experiment.ERK-IN-2 (1 μM) has effects on cell proliferation in cancer cell lines. The IC 50 values are 214 nM; 305 nM; 91 nM and 201 nM for A375SM cell, SK-MEL 30 cell; Colo 205 cell and Lovo cell, respectively [1]. |
In vivo | ERK-IN-2 (1 mpk; orally administation/0.5 mpk; intravenous injection) exhibits a DMPK value: h/r/d LM CLint: <17/235/<75 (mL/min/kg); uCLp:217 mL/min/kg; uVd 5.7 L/kg; t 1/2 : 0.4 h; rat F:13% in SD rat [1]. |
分子量 | 347.8 |
分子式 | C16H18ClN5O2 |
CAS No. | 2743576-56-7 |
Powder: -20°C for 3 years | In solvent: -80°C for 1 year
You can also refer to dose conversion for different animals. 詳細
bottom
Please see Inhibitor Handling Instructions for more frequently ask questions. Topics include: how to prepare stock solutions, how to store products, and cautions on cell-based assays & animal experiments, etc.
ERK-IN-2 2743576-56-7 MAPK ERK ERKIN2 ERK IN 2 Inhibitor inhibitor inhibit