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Merck

SML1415

Sigma-Aldrich

VE-821

≥98% (HPLC)

别名:

3-氨基-6-(4-(甲磺酰基)苯基)-N-苯基吡嗪-2-甲酰胺, 3-氨基-6-[4-(甲磺酰基)苯基]-N-苯基-2-吡嗪甲酰胺, VE821

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About This Item

经验公式(希尔记法):
C18H16N4O3S
分子量:
368.41
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77

品質等級

化驗

≥98% (HPLC)

形狀

powder

顏色

white to beige

溶解度

DMSO: ≥10 mg/mL, clear

儲存溫度

−20°C

SMILES 字串

CS(C(C=C1)=CC=C1C2=NC(C(NC3=CC=CC=C3)=O)=C(N)N=C2)(=O)=O

InChI

1S/C18H16N4O3S/c1-26(24,25)14-9-7-12(8-10-14)15-11-20-17(19)16(22-15)18(23)21-13-5-3-2-4-6-13/h2-11H,1H3,(H2,19,20)(H,21,23)

InChI 密鑰

DUIHHZKTCSNTGM-UHFFFAOYSA-N

應用

VE-821 已用作人癌细胞中 ATM 和 Rad3 相关(ATR)蛋白的抑制剂。

生化/生理作用

VE-821 是一种有效的 ATP 竞争性抑制剂,可抑制 DNA 损伤应答(DDR)激酶共济失调毛细血管扩张突变(ATM)以及与 ATM 和 Rad3 相关(ATR),Ki 值为 13 nM。VE-821 对相关 PIKKs ATM、DNA 依赖性蛋白激酶(DNA-PK)、mTOR 和 PI3-激酶-γ 的交叉反应极小(Ki 值分别为 16 μM、2.2 μM、>1 μM 和 3.9 μM),并针对大量无关的蛋白激酶。在大部分癌细胞中单独使用 VE-821 会导致细胞死亡,并且还显示出与遗传毒性剂的强大协同作用。VE-821 增加了细胞对放射线的敏感性,并使癌细胞对多种化学治疗剂敏感。

其他說明

VE-821 已由化学探针门户网站进行了专家审查和推荐。有关更多信息,请访问化学探针门户网站上的 VE-821 探针摘要

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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