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732983-37-8

中文名称 2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺
英文名称 BAY 61-3606
CAS 732983-37-8
分子式 C20H18N6O3
分子量 390.4
MOL 文件 732983-37-8.mol
更新日期 2024/10/14 14:22:16
732983-37-8 结构式 732983-37-8 结构式

基本信息

中文别名
BAY 61-3606游离
BAY 61-3606 游离碱
2-[[7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基]氨基]-3-吡啶甲酰胺
英文别名
CS-2745
BAY-61-360
BAY 61-3606
SYK INHIBITOR IV
BAY 61-3606 free base
Syk Inhibitor IV, BAY 61-3606
Syk Inhibitor IV, BAY 61-3606 HCl
BAY 61-3606 hydrate hydrochloride
Syk Inhibitor IV, BAY 61-3606: sc-202351 hydrochloride
2-[[7-(3,4-Dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-yl]amino]-3-pyridinecarboxamide

物理化学性质

密度1.41
储存条件2-8°C
溶解度H2O: soluble
形态solid
颜色yellow

安全数据

WGK Germany3

常见问题列表

生物活性
BAY 61-3606 是一种有效的,具有口服活性的,ATP 竞争性的,可逆的选择性 Syk 抑制剂,Ki 为 7.5 nM,IC50 为 10 nM。BAY 61-3606 降低神经母细胞瘤细胞中的 ERK1/2 和 Akt 磷酸化。BAY 61-3606 降低 K-rn 细胞裂解物中 Syk 磷酸化。Bay 61-3606 作用于乳腺癌细胞,通过下调 Mcl-1 促进 TRAIL 诱导的细胞凋亡。
靶点

Ki: 7.5 nM (Syk)
IC50: 10 nM (Syk)

体外研究

BAY 61-3606 (0.01-10 μM ; 48 hours) significantly reduces the cell viability of SYK-positive SH-SY5Y and SYK-negative SK-N-BE cells in a dose-dependent matter. SH-SY5Y cells expressing high SYK levels are significantly more sensitive to BAY 61-3606 in comparison to SK-N-BEcells expressing very low or no SYK.
BAY 61-3606 (0.4 and 0.8 μM; 4 or 24 hours) inhibits SYK activity by reducing ERK1/2 and Akt phosphorylation in neuroblastoma cell SH-SY5Y.
BAY 61-3606 (2 μM; 2 hours) induces a large decrease of Syk phosphorylation in K-rn cell lysates.

Cell Viability Assay

Cell Line: SYK-positive SH-SY5Y and SYK-negative SK-N-BE cells
Concentration: 0.01, 0.1, 1, and 10 μM
Incubation Time: 48 hours
Result: Significantly reduced the cell viability of both cell lines in a dose-dependent matter.

Western Blot Analysis

Cell Line: SH-SY5Y cells
Concentration: 0.4 and 0.8 μM
Incubation Time: 4 or 24 hours
Result: Reduced the phosphorylation of ERK1/2 and Akt after a 4 or 24 h treatment.

Western Blot Analysis

Cell Line: K-rn cell lysates
Concentration: 2 μM
Incubation Time: 2 hours
Result: Induced a large decrease of Syk phosphorylation.
体内研究

Bay 61-3606 (50 mg/kg; administered twice a week for two weeks by intraperitoneal injection) alone leads to more efficacious reductions than that of TNF-related apoptosis-inducing ligand (TRAIL; 10 mg/kg) alone in MCF-7 tumor xenograft-bearing BALB/c nude mice. Bay 61-3606 administered in TRAIL combination significantly reduces the volume of the xenografted tumor.

Animal Model: Female BALB/c nude mice (5 weeks old) bearing MCF-7 tumor xenograft
Dosage: 50 mg/kg
Administration: Injected intraperitoneally twice a week with Bay 61-3606 (50 mg/kg), TRAIL (10 mg/kg) or a combination of Bay 61-3606 (50 mg/kg) and TRAIL (10 mg/kg); TRAIL was given 2 h after the injection of Bay 61-3606; for two weeks
Result: Led to efficacious reductions in tumor growth.
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