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SLV-2436

CAS No. : 2095704-43-9

MCE 站：SLV-2436

产品活性：SLV-2436 是一种高效且 ATP 竞争性的 MNK1 和 MNK2 抑制剂，IC₅₀ 分别为 10.8 nM 和 5.4 nM。

研究领域：MAPK/ERK Pathway

作用靶点：MNK

In Vitro: To confirm the kinome selectivity of SLV-2436 (SEL201), the broad KINOMEscan competitive binding assay is performed at 1 μM, which includes 450 distinct kinases. The observed binding profile for SLV-2436 is significantly concentrated in the CAMK family of kinases that comprises MNK1 ａnd MNK2. SLV-2436-treated KIT-mutant melanoma cells have lower oncogenicity ａnd reduced metastatic ability.

In Vivo: To investigate the pharmacodynamic properties of SLV-2436 (SEL201), 5 consecutive oral doses of 10, 25, ａnd 50 mg/kg are administered to mice every 12 hours (twice-daily schedule). At the 10 mg/kg twice-daily dosage, 4 hours after the fifth administration, a low plasma concentration of 125 ng/mL SLV-2436 is determined. However, dosing at 25 ａnd 50 mg/kg twice daily, equivalent to 50 ａnd 100 mg/kg/d of SLV-2436, yields substantially increased dose-dependent plasma exposure, reaching an average level of 1,299 ng/mL ａnd 2,075 ng/mL, respectively. At the 24-hour time point, SLV-2436 is still detectable in the plasma, with dose-dependent concentrations of 9, 73, ａnd 124 ng/mL in the 10, 25, ａnd 50 mg/kg twice-daily treatment groups. Oral (p.o.) administration of SLV-2436 at the dosage of 50 mg/kg twice daily, that is, 100 mg/kg/d, for 37 days is well tolerated in mice.

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