RIPK1-IN-39 (compound 2) is a potent and selective RIPK1 inhibitor ( IC 50 = 69.40 nM) exhibiting >100-fold selectivity over RIPK3 ( IC 50 = 6946 nM). RIPK1-IN-39 protects HT-22 and HT-29 cells from necroptosis by inhibiting the phosphorylation and activation of the RIPK1-RIPK3-MLKL pathway. RIPK1-IN-39 demonstrates neuroprotective effects in a rat model of middle cerebral artery occlusion (MCAO). RIPK1-IN-39 can be used for acute ischemic stroke (AIS) research.
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