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Thalidomide-NH-C6-NH2 TFA是一种合成的 E3 连接酶配体 -linker 偶联物,包含基于 Thalidomide 的 cereblon 配体和 1 个 linker。
Thalidomide-NH-C6-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a linker used in PROTAC technology[1].
[1]. Wang Z, et al. Proteolysis Targeting Chimeras for the Selective Degradation of Mcl-1/Bcl-2 Derived from Nonselective Target Binding Ligands. J Med Chem. 2019 Sep 12;62(17):8152-8163.
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