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Discovery of highly potent and selective KRAS G12C degraders by VHL-recruiting PROTACs for the treatment of tumors with KRAS G12C -mutation
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These studies help determine the maximum safe dose and identify any possible side effects
Specializing in biochemistry and anti-aging science, Dr
c ) The conjugate with GSH forms rapidly in vitro and is reversible by adding the GSH scavenger NEM
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