CDC37 and acute kidney injury: Furthermore, Ser50, which formed three C–H bonds with luteolin in the conformation corresponding to the lowest free energy in our study, together with Glu47, constitutes the previously reported Cdc37 binding site, while the inhibitor C‐316‐1 that binds to this site had been shown to exert a protective effect in cisplatin‐induced acute kidney injury (Liu, Liu, et al. 2022).