| Absorption | Well absorbed from the GI tract following oral administration. |
| Volume of distribution | Not Available |
| Protein binding | No known binding |
| Metabolism | 35-65% of oral dose excreted unchanged in urine (which provides the drug's therapeutic effect). |
| Route of elimination | Not Available |
| Half life | 5-10 hours in patients with normal renal function |
| Clearance | Not Available |
| Toxicity | Oral, rat: LD50 = 4.8gm/kg. Symptoms of overdose include anorexia, malaise, lethargy, diminished sense of wellbeing, tremor, anxiety, nausea, and vomiting. |
| Affected organisms |
|
| Pathways | Not Available |
Acetohydroxamic Acid
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