(S,R,S)-AHPC-PEG2-C2-azide
貨號 | 數量 | 價格 | 交貨時間 | 購買此產品 |
---|---|---|---|---|
4530-25mg | 25 mg | $189 | 現貨 | |
4530-100mg | 100 mg | $529 | 現貨 | |
4530-500mg | 500 mg | $1598 | 現貨 |
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)
含有沙利度胺的結構單元,具有羧酸官能團,通過 4-O-位將功能化氨基接頭和配體連接到沙利度胺上,從而方便地組裝 PROTAC 分子。沙利度胺-O-PEG2-羧酸 (Thalidomide-O-PEG2-carboxylic acid)
含有沙利度胺的結構單元,具有 PEG2 連接子和羧基,用於與氨基連接子和目標蛋白配體偶聯。立即在線獲取免費快遞服務
沙利度胺-O-PEG2-疊氮化物 (Thalidomide-O-PEG2-azide)
含有沙利度胺的結構單元,具有 PEG2 連接體和疊氮官能團,可通過點擊化學反應與炔基連接體和靶蛋白配體偶聯。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. |
MSDS: | 下載 |
產品規格 |