It exists as an active dimer 45 and targets phosphorylation of downstream targets such as CHK2, H2AX and p53 44,47,48,49
These targets may also provide greater sensitivity to subtle or chronic forms of neuroinflammation that are not reliably captured by first- or second-generation TSPO tracers
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By enabling drug release specifically in response to MMPs, these systems hold potential for circumventing the joint toxicity associated with the broad-spectrum inhibitor marimastat, which arises from the non-selective inhibition of MMPs involved in joint formation (170,171)
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