Description
The abstract reports that Alectinib binds C1q with high affinity, but this is mechanistically unexpected since Alectinib is designed as a kinase inhibitor while C1q is a complement protein. Understanding this binding mechanism could reveal new drug-target interaction principles and inform rational design of complement modulators.
Gap type: unexplained_observation Source paper: Complement C1q-Targeted Microglial Membrane Camouflaged Nanolipid Carriers for Synaptic Protection in Alzheimer’s Disease: A Bioinspired Alectinib Delivery Strategy. (2026, Nano letters, PMID:41114949)