| Target/assay |
Inhibition (% control) |
| concentration of OP |
| 3μM |
30μM |
| L-type Ca2+ channel (diltiazem site) |
14 |
41 |
| Na+ channel (site 2) |
11 |
38 |
| NMDA-type glutamate receptor (PCP) |
14 |
23 |
| AMPA-type glutamate receptor |
4 |
17 |
| Kainate-type glutamate receptor |
0 |
14 |
| Serotonin 5-HT2A receptor |
4 |
13 |
| Serotonin 5-HT4e receptor |
0 |
13 |
| "Extracted from reference [59]. Note that maximum concentration of OP tested was 30 μM. Hence these, especially Ca2+ channel, Na+ channel, and NMDA-type glutamate receptor, could be affected by oseltamivir; OP: oseltamivir phosphate; OT: free form of unmetabolisedoselamivir" |
