产品说明
应用
Used for chemical probe synthesis, this trifunctional building block contains a light-activated benzophenone, alkyne tag, and bromine synthetic handle. When appended to a ligand or pharmacophore through its brominated linker, this building block allows for UV light-induced covalent modification of a biological target with potential for downstream applications via the alkyne tag. Use alone or in parallel with other multi-functional building blocks to discover the optimal probe for your chemical biology experiments.
包装
100 mg in glass bottle
其他说明
Technology Spotlight: Trifuctional Probe Building Blocks
Development of Sulfonamide Photoaffinity Inhibitors for Probing Cellular γ-Secretase
A library approach to rapidly discover photoaffinity probes of the mRNA decapping scavenger enzyme DcpS
基本信息
| 经验(实验)分子式 | C17H13BrO2 |
| 分子量 | 329.19 |
| MDL编号 | MFCD30737994 |
产品性质
| 质量水平 | 100 |
| 测定 | ≥95% |
| 形式 | solid |
| reaction suitability | reaction type: click chemistry |
| 储存温度 | −20℃ |
| SMILES string | O=C(C1=CC=C(OCC#C)C=C1)C2=CC=C(CBr)C=C2 |
安全信息
| 储存分类代码 | 13 - Non Combustible Solids |
| WGK | WGK 3 |
| 闪点(F) | Not applicable |
| 闪点(C) | Not applicable |
