PIT-1结构式
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常用名 | PIT-1 | 英文名 | PIT-1 |
|---|---|---|---|---|
| CAS号 | 53501-41-0 | 分子量 | 351.765 | |
| 密度 | 1.6±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C14H10ClN3O4S | 熔点 | N/A | |
| MSDS | 美版 | 闪点 | N/A | |
| 符号 |
GHS07, GHS09 |
信号词 | Warning |
PIT-1用途PIT-1是一种选择性PIP3(磷脂酰肌醇3,4,5-三磷酸)拮抗剂。PIT-1通过抑制PIP3依赖的PI3K/Akt信号传导抑制癌细胞存活并诱导凋亡。PIT-1在体内具有抗肿瘤活性[1]。 |
| 英文名 | N-[(3-chloro-2-hydroxy-5-nitrophenyl)carbamothioyl]benzamide |
|---|---|
| 英文别名 | 更多 |
| 描述 | PIT-1是一种选择性PIP3(磷脂酰肌醇3,4,5-三磷酸)拮抗剂。PIT-1通过抑制PIP3依赖的PI3K/Akt信号传导抑制癌细胞存活并诱导凋亡。PIT-1在体内具有抗肿瘤活性[1]。 |
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| 相关类别 | |
| 参考文献 |
| 密度 | 1.6±0.1 g/cm3 |
|---|---|
| 分子式 | C14H10ClN3O4S |
| 分子量 | 351.765 |
| 精确质量 | 351.008057 |
| PSA | 139.27000 |
| LogP | 4.28 |
| InChIKey | RIGXBXPAOGDDIG-UHFFFAOYSA-N |
| SMILES | O=C(NC(=S)Nc1cc([N+](=O)[O-])cc(Cl)c1O)c1ccccc1 |
| 折射率 | 1.747 |
| 储存条件 | -20°C,密闭,干燥 |
| 符号 |
GHS07, GHS09 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H302-H400 |
| 警示性声明 | P273 |
| 危险品运输编码 | UN 3077 9 / PGIII |
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Small molecule inhibition of phosphatidylinositol-3,4,5-triphosphate (PIP3) binding to pleckstrin homology domains.
Proc. Natl. Acad. Sci. U. S. A. 107(46) , 20126-31, (2010) The PI3-kinase (PI3K) pathway regulates many cellular processes, especially cell metabolism, cell survival, and apoptosis. Phosphatidylinositol-3,4,5-trisphosphate (PIP3), the product of PI3K activity... |
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Inhibition of cell migration by PITENINs: the role of ARF6.
Oncogene 31(39) , 4317-32, (2012) We have reported previously the development of small-molecule phosphatidylinositol-3,4,5-trisphosphate (PIP3) antagonists (PITs) that block pleckstrin homology (PH) domain interaction, including activ... |
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实验名称:Fluorescence-based counterscreen assay for HCV NS3 helicase inhibitors of a ChemBridg...
来源:1102
靶标:N/A
External Id:20130627FPNS3INTERFERECB
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实验名称:Fluorescence polarization based primary biochemical high throughput screening assay o...
来源:1102
靶标:NS3 [Hepatitis C virus]
External Id:20130624FPNS3DACB
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实验名称:Inhibition of Akt PH domain (unknown origin) binding to PI(3,4)P2 at 100 uM by lipid ...
来源:ChEMBL
靶标:RAC-alpha serine/threonine-protein kinase
External Id:CHEMBL3599554
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实验名称:Fluorescence Polarization Assay from US Patent US8628961: "Small molecule antagonists...
来源:BindingDB
靶标:N/A
External Id:BindingDB_6166_1
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| N-[[(3-Chloro-2-hydroxy-5-nitrophenyl)amino]thioxomethyl]-benzamide |
| PIT-1 |
| Impentamine dihydrobromide |
| N-[(3-Chloro-2-hydroxy-5-nitrophenyl)carbamothioyl]benzamide |