| Absorption, distribution, metabolism and excretion | ADME |
| Area under the curve AUC ratio |
AUC AUCR |
| Clinical Pharmacogenetics Implementation Consortium | CPIC |
| Cytochrome P450 | CYP450 |
| Drug–drug interaction | DDI |
| Fold error | FE |
| High-performance liquid chromatography | HPLC |
| Human-liver microsome 50% inhibitory concentration |
HLM IC50 |
| Reversible inhibition constant | Ki |
| Observed inactivation rate of the affected enzyme | kobs |
| Maximum inactivation rate constant | kinact |
| Inhibitor concentration causing half-maximal inactivation | KI |
| Mass spectrometry | MS |
| Nicotinamide adenine dinucleotide phosphate | NADPH |
| Physiologically based pharmacokinetic | PBPK |
| Area under the curve ratio | AUCR |
| Reversible inhibition | RI |
| Schisandrin A | SIA |
| Schisantherin A | STA |
| Schizandrol A | SZA |
| Schizandrol B | SZB |
| Tacrolimus | FK-506 |
| Time-dependent inhibition | TDI |
| Traditional Chinese medicine | TCM |
| Wuzhi capsule | WZC |