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Based on chemical structures and different docking sites with kinases, there are three types of small-molecule c-Met kinase inhibitors, including selective, non-selective, and special structure c-Met inhibitors (Parikh and Ghate, 2018)

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smegmatis on different antibiotic targets, which in many cases resulted in increased susceptibility of the bacteria to antimicrobials, proving that regulated protein degradation can be a valuable tool in drug development (Wei et al., 2011)