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Merck
CN

SML0330

Sigma-Aldrich

S3I-201

≥97% (HPLC)

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别名:
2-羟基-4-[[[[(4-甲基苯基)磺酰基]氧基]乙酰基]氨基]-苯甲酸, NSC 74859
经验公式(希尔记法):
C16H15NO7S
分子量:
365.36
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77

质量水平

检测方案

≥97% (HPLC)

形式

powder

颜色

white to beige

溶解性

DMSO: >10 mg/mL

储存温度

−20°C

SMILES字符串

Cc1ccc(cc1)S(=O)(=O)OCC(=O)Nc2ccc(C(O)=O)c(O)c2

InChI

1S/C16H15NO7S/c1-10-2-5-12(6-3-10)25(22,23)24-9-15(19)17-11-4-7-13(16(20)21)14(18)8-11/h2-8,18H,9H2,1H3,(H,17,19)(H,20,21)

InChI key

HWNUSGNZBAISFM-UHFFFAOYSA-N

相关类别

应用

S3I-201 已作为信号转导和转录激活剂 3 (STAT3) 的抑制剂,被用于:
  • 确认 STAT3 磷酸化在肺上皮细胞中白细胞介素 (IL)-33 的产生 和在经分选的3类先天淋巴细胞 (ILC3s) 中 IL-22 mRNA 表达中的作用
  • 研究在各种细胞系中由β-六氯环己烷 (β-HCH) 触发的STAT3细胞反应
  • 检测响应血管紧张素 II (ang II) 所产生的STAT3对肾上皮细胞纤维化蛋白诱导的影响

生化/生理作用

S3I-201 是细胞可渗透的 Stat3 抑制剂,它结合 Stat3-SH2 结构域,阻止 Stat3 磷酸化/活化、二聚化,以及与 DNA 结合。
通过S3I-201抑制信号转导和转录激活因子 3 (STAT3) 的活性,可能是治疗高血压肾病的一种潜在治疗策略。

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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