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(S,R,S)-AHPC-PEG2-C2-azide

貨號 數量 價格 交貨時間
4530-25mg 25 mg $189 現貨
4530-100mg 100 mg $529 現貨
4530-500mg 500 mg $1598 現貨
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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-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。

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。
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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.
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