Some of the IC50 value in drug sensitivity databases is lower than 0. I am confused that how should we explain this data. For instance, IC50 of vinblastine (GDSC2:1004) on CCK81 is -5.550494585nM. (in Drug sensitivity IC50 (Sanger GDSC2))
Does it mean that this compound would enhance the cell proliferation instead of suppress the cell viability?
I would appreciate it if someone could give any reply. Thanks in advance
Yeah,I think so.The Expression Public 22Q4 GDSC2 IC50 dataset shows that the maximum is about 6.9,which corresponds to ln(1000).Being an undergraduate student,I just couldn’t understand why it’s not clearly demonstrated,so confusing.