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Delphinidin-3-O-glucoside chloride inhibits EGFR with an IC50 of 2
InChi: InChI=1S/C15H12N2O3/c1-2-20-15(19)11-8-17-13-10(14(11)18)6-5-9-4-3-7-16-12(9)13/h3-8H
CFM-2 is a potent and selective non-competitive AMPAR antagonist
GW806742X (1 μM) retards MLKL translocation to the membrane
51)/b13-11+
Lenalidomide-PEG3-iodine 3683 Delphinidin-3-O-glucoside chloride inhibits EGFR withLenalidomide PEG3 iodine is a synthesized E3 ligase ligand linker conjugate that incorporates the Lenalidomide based cereblon ligand and a 3 unit PEG linker. Lenalidomide PEG3 iodine can be used in the synthesis of a series of PROTACs, such as SJF620 (HY 133137). SJF620 is a potent PROTAC BTK degrader with a DC50 of 7. 9 nM. Product information Molecular Weight: 502. 30 Formula: C19H23IN2O6 Chemical Name: 3 [6 [2 [2 (2 iodoethoxy)ethoxy]ethoxy] 3 oxo