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- 文献和实验
- 技术资料
- 库存：
100
- 供应商：
上海羽朵
- 英文名：
Mutant EGFR inhibitor
- 规格：
1g
| 中文名称: | N-[5-[[5-氯-4-(1H-吲哚-3-基)-2-嘧啶基]氨基]-2-[[2-(二甲基氨基)乙基]甲基氨基]-4-甲氧基-苯基]-2-丙烯-酰胺 |
| 中文同义词: | N-[5-[[5-氯-4-(1H-吲哚-3-基)-2-嘧啶基]氨基]-2-[[2-(二甲基氨基)乙基]甲基氨基]-4-甲氧基-苯基]-2-丙烯-酰胺;MDK3627 |
| 英文名称: | Mutant EGFR inhibitor |
| 英文同义词: | Mutant EGFR inhibitor;N-[5-[[5-Chloro-4-(1H-indol-3-yl)-2-pyrimidinyl]amino]-2-[[2-(dimethylamino)ethyl]methylamino]-4-methoxyphenyl]-2-propenamide |
| CAS号: | 1421373-62-7 |
| 分子式: | C27H30ClN7O2 |
| 分子量: | 520.0258 |
| EINECS号: | |
| 相关类别: | 小分子抑制剂;小分子抑制剂，天然产物;Inhibitors |
| Mol文件: | 1421373-62-7.mol |
![N-[5-[[5-氯-4-(1H-吲哚-3-基)-2-嘧啶基]氨基]-2-[[2-(二甲基氨基)乙基]甲基氨基]-4-甲氧基苯基]-2-丙烯酰胺](https://img1.dxycdn.com/p/s14/2024/0422/078/0251106178096632871.gif) |
|
| PF-3274167 | 900510-03-4 |
| 2-氨基-N-[3-[N-[3-[(2-氯-5-甲氧基-苯基)氨基]喹喔啉-2-基]氨基磺酰基]苯基]-2-甲基丙酰胺 | 934526-89-3 |
| N/A | 873786-09-5 |
| PRT-060318 | 1194961-19-7 |
| N/A | 1454619-14-7 |
| N/A | 1417162-36-7 |
| SANT1 | 304909-07-7 |
| 反式-1-(4-羟基环己基)-4-(4-氟-苯基)-5-(2-甲氧基嘧啶-4-基)咪唑 | 193551-21-2 |
| 司马西特 | 425386-60-3 |
| SNG--1153 | |
| SU 6656 | 330161-87-0 |
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文献和实验EGFR and Tumor Suppressor Function in Brain Cancer Development
interventions. Using cutting edge Cre/Lox technologies, we created compound conditional transgenic strains based on a Cre-induced expression of mutant EGFRvIII with the concomitant loss of the Cdkn2a and PTEN tumor suppressor genes. The introduction
Methods for Studying the Interaction of Barnase with Its Inhibitor Barstar
inside the cell. The three-dimentional structures of barnase and barstar are known both from X-ray crystallography and NMR spectroscopy (1 –4 ). The crystal structure of the complex of barnase with the barstar (C40A/C82A) double mutant has been solved by Guillet
antibody and progression in tumor therapy【abstract】EGFR is encoded by the c-erb-B1 proto-oncngene. it is reported that the over-expressed and mutant EGFR have good relationship with tumor.Now it has become a new field in tumor therapy.This text
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