Experiment 610509
Worktypes
Compounds isolated
Details
| Property | Value |
|---|---|
| Pharmacology | |
| Administration route | INTRAGASTRIC |
| Organism | Empty organism |
| Citation | TSAI,TH: CHOU,CJ: LEE,TF: WANG,LC: CHEM,CF:. (1996). PHARMACOKINETIC AND PHARMACODYNAMIC STUDIES OF MAGNOLOL AFTER ORAL ADMINISTRATION IN RATS.. 2(4) |
| Amount utilized | |
| Compound isolated | |
| Disease | THE ABSORPTION HALF-LIFE, THE ELIMINATION HALF-LIFE, THE TIME OF MAXIMUM CONCENTRATION AND MAXIMUM CONCENTRATION WERE 0.63 H, 2.33 H, 1.12 H, AND 0.16 MCG PER ML. ORAL BIOAVAIABILITY WAS 4.9%. |
| Dose amount | 20.0 MG |
| Number | 1 |
| Qualitative result | ACTIVE |
| Animal | RAT |
| Per unit | KG |
| Dose expression | DOSE |