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- 详细信息
- 文献和实验
- 技术资料
- 库存:
173
- 英文名:
RAF265
- CAS号:
927880-90-8
- 保质期:
2年
- 供应商:
北京百奥莱博科技有限公司
- 保存条件:
-20℃,有效期2年,溶入溶剂后-20℃
- 规格:
1mL(10mM)|5mg|10mg|50mg
特别提示:包括C-Raf/B-Raf/B-Raf V600E抑制剂(RAF265)在内,本公司的所有产品仅可用于科研实验,严禁用于临床医疗及其他非科研用途!
产品名称:C-Raf/B-Raf/B-Raf V600E抑制剂(RAF265)
英文名称:RAF265
产品货号:M02842
产品规格:1mL(10mM)|5mg|10mg|50mg
RAF265(CHIR-265)对C-Raf/B-Raf/B-Raf V600E有抑制性,IC50为3-60nM,对VEGFR2磷酸化的EC50为30nM。
注:本品仅可用于科研实验,严禁用于临床医疗及其他用途!
CAS号:927880-90-8
别名:CHIR-265
纯度:99.40%
分子式:C₂₄H₁₆F₆N₆O
分子量:518.41
结构式:
储存条件:-20℃,有效期2年,溶入溶剂后-20℃请尽量在一个月内使用。
除了C-Raf/B-Raf/B-Raf V600E抑制剂(RAF265),CHIR-265,我公司还供应以下相关产品:
| 货号 | 名称 | 规格 |
| M00126 | PERK抑制剂(GSK2606414) | 1mL(10mM)|2mg|5mg|10mg|50mg|100mg|200mg |
| M00504 | PKCβ抑制剂(Enzastaurin) | 1mL(10mM)|5mg|10mg|50mg|100mg|200mg |
| M00694 | 芳香酶抑制剂(Anastrozole) | 1mL(10mM)|10mg|50mg|100mg|200mg|500mg |
| M00950 | CDK8andWnt抑制剂(Wogonin) | 1mL(10mM)|5mg|10mg|50mg |
| M01055 | Btk抑制剂(ONO-4059 analog) | 1mL(10mM)|5mg|10mg|25mg|50mg|100mg |
| M01092 | 凋亡信号调节激酶1(ASK1)抑制剂(NQDI-1) | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M01130 | MEK5/ERK5抑制剂(BIX02189) | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M01180 | GSK-3β抑制剂(Indirubin-3-monoxime) | 1mL(10mM)|5mg|10mg|50mg |
| M01239 | Arp2/3复合物抑制剂(CK-636) | 1mL(10mM)|10mg|50mg|100mg |
| M01620 | Notch抑制剂(BMS-983970) | 1mL(10mM)|2mg|5mg|10mg|50mg|100mg |
| M01648 | 微管抑制剂(Cevipabulin) | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M01744 | RMG1和RMG2抑制剂(Lurbinectedin) | 1mL(10mM)|1mg|2mg |
| M01947 | IDH1-R132H抑制剂(alpha-Mangostin) | 1mL(10mM)|10mg|25mg|50mg|100mg |
| M02192 | Raf激酶抑制剂(L-779450) | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M03373 | H+/K+,ATPase抑制剂(TAK-438 free base) | 1mL(10mM)|50mg|100mg |
| M03817 | 外排泵抑制剂(PAβN dihydrochloride) | 1mL(10mM)|5mg|10mg|25mg|50mg|100mg|250mg |
| M04436 | β2AR激动剂(Salmeterol xinafoate) | 1mL(10mM)|10mg|50mg|100mg|200mg |
| M04708 | Lck激酶抑制剂(AMG-47a) | 1mL(10mM)|2mg|5mg|10mg|25mg|50mg |
| M06139 | NK受体抑制剂(SB-222200) | 1mL(10mM)|10mg|50mg |
| M06793 | 乙酰胆碱酯酶(AChE)和丁酰胆碱酯酶(BChE)抑制剂 | 1mL(10mM)|100mg |
| M06974 | c-Fos/activator protein(AP)-1抑制剂 | 1mL(10mM)|5mg|10mg|50mg|100mg |
| M08062 | HCV RNA复制抑制剂(Sofosbuvir impurity E) | 1mL(10mM)|1mg|5mg |
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文献和实验Monitoring Oncogenic B-RAF-Induced Senescence in Melanocytes
The B-RAF kinase is a downstream effector of the RAS family of proto-oncogenes and is constitutively activated in the majority of human melanomas. The common oncogenic B-RAFV600E mutant cooperates with additional genetic lesions to transform
Deciphering Signaling Pathways In Vivo: The Ras/Raf/Mek/Erk Cascade
are still incompletely known. Here, we describe immunohistochemical and immunofluorescence methods that can be used to define the essential function(s) and the relevant downstream targets of Raf-1, B-Raf, and Mek-1 in in vivo models of organ development, remodeling
Raf/MEK/MAPK Signaling Stimulates the Nuclear Translocation and Transactivating Activity of FOXM1
, but not FOXM1b, on the cyclin B1 promoter in transient reporter assays. Here, we describe in detail the methods involved in generating these findings, which support the notion that FOXM1 is an effector of Raf/MEK/MAPK signaling in G2/M regulation.
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