(S,R,S)-AHPC-PEG2-C2-azide
目录号 | 数量 | 价格 | 提前通知时间 | 购买此产品 |
---|---|---|---|---|
4530-25mg | 25 mg | $189 | 现货 | |
4530-100mg | 100 mg | $529 | 现货 | |
4530-500mg | 500 mg | $1598 | 现货 |
Proteolysis targeting chimeras (PROTACs) are cell-permeable heterobifunctional molecules that can remove specific proteins from the cell. One end of such molecule contains a ligand to bind to the target, and the second end recruits the E3 ligase complex. Close proximity results in substrate polyubiquitination and subsequent protein degradation by cellular proteasome.
(S,R,S)-AHPC-C2-azide is a protein degrader building block for the synthesis of molecules for targeted protein degradation and PROTAC technologies. This conjugate contains a von Hippel-Lindau (VHL)-recruiting ligand and a PEG2-C2 crosslinker with an azide function group, which can be conjugated to alkyne-functionalized linkers and target protein ligands through click chemistry reactions.
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沙利度胺-羧酸 (Thalidomide-carboxylic acid)
含有沙利度胺的结构单元,具有羧酸官能团,通过 4-O-位将功能化氨基接头和配体连接到沙利度胺上,从而方便地组装 PROTAC 分子。沙利度胺-O-PEG2-羧酸 (Thalidomide-O-PEG2-carboxylic acid)
含有沙利度胺的结构单元,具有 PEG2 连接子和羧基,用于与氨基连接子和目标蛋白配体偶联。并获得免费的快递服务
沙利度胺-O-PEG2-叠氮化物 (Thalidomide-O-PEG2-azide)
含有沙利度胺的结构单元,具有 PEG2 连接体和叠氮官能团,可通过点击化学反应与炔基连接体和靶蛋白配体偶联。General properties
Appearance: | yellow glassy oil |
Molecular weight: | 615.75 |
CAS number: | 2597167-22-9 |
Molecular formula: | C29H41N7O6S |
Solubility: | methanol, ethyl acetate, DCM, THF, DMF, DMSO |
Quality control: | NMR 1H and HPLC-MS (95+%) |
Storage conditions: | 24 months after receival at -20°C in the dark. Transportation: at room temperature for up to 3 weeks. Desiccate. |
安全数据表(MSDS): | 下载 |
产品规格 |