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Yamaguchi, Y., Takatsuka, Y., & Kamio, Y

And that's the weird world that we find ourselves in with people defending that because their ideology opposes the opposite

It's part of the problem

Novel covalent inhibitors such as ML210, which uses nitroisoxazole as a prodrug form and covalently binds GPx4 after intracellular conversion to an electrophilic moiety, have selectivity and pharmacokinetic properties superior to that of chloroacetamide inhibitors, and BCP-T.A, a thiazole analog containing an alkyne-based electrophilic moiety, has been found to have inhibitory activity on specific cells up to the low-nanomolar level with high selectivity

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