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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

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

中文名稱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
中文同義詞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;BAY 61-3606游離;BAY 61-3606 游離堿;2-((7-(3,4-二甲氧基苯基)咪唑并[1,2-C]嘧啶-5-基)氨基)吡啶-3-甲酰胺;化合物BAY 61-3606,10 MM DMSO 溶液
英文名稱BAY 61-3606
英文同義詞Syk Inhibitor IV, BAY 61-3606: sc-202351 hydrochloride;Syk Inhibitor IV, BAY 61-3606 HCl;BAY 61-3606;BAY 61-3606 hydrate hydrochloride;2-[[7-(3,4-Dimethoxyphenyl)imidazo[1,2-c]pyrimidin-5-yl]amino]-3-pyridinecarboxamide;BAY-61-360;Syk Inhibitor IV, BAY 61-3606;BAY 61-3606 free base
CAS號732983-37-8
分子式C20H18N6O3
分子量390.4
EINECS號
相關(guān)類別
Mol文件732983-37-8.mol
結(jié)構(gòu)式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 結(jié)構(gòu)式

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 性質(zhì)

密度1.41
儲存條件2-8°C
溶解度可溶于水中
形態(tài)固體
顏色粘黃色

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 用途與合成方法

BAY 61-3606 是一種有效的,具有口服活性的,ATP 競爭性的,可逆的選擇性 Syk 抑制劑,Ki 為 7.5 nM,IC50 為 10 nM。BAY 61-3606 降低神經(jīng)母細(xì)胞瘤細(xì)胞中的 ERK1/2 和 Akt 磷酸化。BAY 61-3606 降低 K-rn 細(xì)胞裂解物中 Syk 磷酸化。Bay 61-3606 作用于乳腺癌細(xì)胞,通過下調(diào) Mcl-1 促進(jìn) TRAIL 誘導(dǎo)的細(xì)胞凋亡。

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

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.

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.

安全信息

WGK Germany3

MSDS信息

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 上下游產(chǎn)品信息

"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"相關(guān)產(chǎn)品信息
苯甲醇 2-甲氧基苯乙酸 對羥基苯乙酮 苯甲酸鈉
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