常用名:(S,R,S)-AHPC-PEG3-N3
产品描述:
(S, R, S)-AHPC-PEG3-N3 (VHL Ligand-Linker Conjugates 8) is a synthesized E3 ligase ligand-linker conjugate. (S, R, S)-AHPC-PEG3-N3 incorporates the (S, R, S)-AHPC based VHL ligand and 3-unit PEG linker used in PROTAC technology.
体外活性 (S,R,S)-AHPC-PEG3-N3 is extracted from patent WO/2016/146985A1, figure 11. PROTAC has been developed with an A-L-B structure that can tether a bromodomain inhibitor via a moiety which binds to a protein within the bromo- and Extra-terminal (BET) family of proteins to a small molecule E3 ubiquintin ligase protein binding ligand compound via a suitable linker[1][2].
别名 VHL Ligand-Linker Conjugates 8, VH032-PEG3-N3, E3 ligase Ligand-Linker Conjugates 12
分子量 645.77
分子式 C30H43N7O7S
CAS No. 1797406-80-4
存储
store at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year
溶解度
DMSO: 50 mg/mL (77.43 mM), Sonication is recommended.
PROteolysis TArgeting Chimeras (PROTACs) 通过将靶蛋白和 E3 连接酶结合起来,从而“劫持”细胞的泛素-蛋白酶体系统(UPS)来实现蛋白质的降解。由于 PROTACs 只需具有高选择性地结合其靶标(而不是抑制靶蛋白的酶活性),目前有许多努力将先前无效的抑制剂分子改造为 PROTACs,用作下一代药物。
产地:西安
用途:科研!
厂家:西安齐岳生物科技有限公司
温馨提示:仅用于科研,不能用于人体实验!
相关产品:
Thalidomide-O-amido-C2-NH2 hydrochloride
Thalidomide-O-amido-C4-NH2 hydrochloride
Thalidomide-O-amido-C6-NH2 hydrochloride
Thalidomide-O-amido-C8-NH2 hydrochloride
Thalidomide-O-amido-C3-PEG3-C1-NH2