NGI-1结构式
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常用名 | NGI-1 | 英文名 | NGI 1 |
|---|---|---|---|---|
| CAS号 | 790702-57-7 | 分子量 | 394.512 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | N/A | |
| 分子式 | C17H22N4O3S2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
NGI-1用途NGI-1 是一种细胞渗透性抑制剂。 |
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NGI-1作用体外活性:如所评估的,NGI-1阻断肺腺癌细胞中的EGFR N-连接糖基化。 在对照中,EGFR是生物素化的,与其质膜表达一致,但在NGI-1处理的细胞中,EGFR主要存在于非生物素化的细胞内部分中,表明细胞定位发生了变化。 |
| 中文名 | NGI-1 |
|---|---|
| 英文名 | NGI-1 |
| 英文别名 | 更多 |
| 描述 | NGI-1 是一种细胞渗透性抑制剂。 |
|---|---|
| 相关类别 | |
| 体外研究 | 如所评估的,NGI-1阻断肺腺癌细胞中的EGFR N-连接糖基化。在对照中,EGFR是生物素化的,与其质膜表达一致,但在NGI-1处理的细胞中,EGFR主要存在于非生物素化的细胞内部分中,表明细胞定位发生了变化[1]。 |
| 参考文献 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 分子式 | C17H22N4O3S2 |
| 分子量 | 394.512 |
| 精确质量 | 394.113342 |
| LogP | 2.75 |
| InChIKey | QPKGRLIYJGBKJL-UHFFFAOYSA-N |
| SMILES | Cc1cnc(NC(=O)c2cc(S(=O)(=O)N(C)C)ccc2N2CCCC2)s1 |
| 外观性状 | 粉末 |
| 折射率 | 1.634 |
| 储存条件 | -20℃ |
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实验名称:Cell Viability qHTS for small molecule stabilizers of the endoplasmic reticulum resid...
来源:NCGC
靶标:N/A
External Id:SERCaMPGluc-f3-cellviability-42h
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实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
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实验名称:Confirmatory qHTS for small molecule stabilizers of the endoplasmic reticulum residen...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-f1_f3-antagonist
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实验名称:Counterscreen qHTS for small molecule stabilizers of the endoplasmic reticulum reside...
来源:NCGC
靶标:N/A
External Id:SERCaMPGLuc-f3-counterscreen-19h
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
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实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
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实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
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实验名称:Single concentration confirmation of small molecule activators of the apoptotic arm o...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A406-UPR-CHOP-CP-Agonist-Assay
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实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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| MFCD06358908 |
| 5-(Dimethylsulfamoyl)-N-(5-methyl-1,3-thiazol-2-yl)-2-(1-pyrrolidinyl)benzamide |