InAADR

Protein Information

Protein Name: Ornithine decarboxylase (P11926)
Gene Name: ODC1
Description: Ornithine decarboxylase (EC 4 1 1 17) (ODC)
PDB ID: 1D7K
Protein Family:
Protein Category: Enzyme

This panel provides drug-protein interaction and their ADRs along with references

Interacting Drugs Toxicity Mechanism Reference
Acetaminophen Hepatotoxicity Liver ornithine decarboxylase (ODC) activity@ which reflects the earliest phases of cell multiplication@During the next 12 hours@decreased by 60% to 70% and cellular necrosis became evident@and reached a peak at 24 to 36 hours.So organelles may play a critical role in acetaminophen hepatotoxicity. [ ADR Type 2 ] Acetaminophen liver injury: sequential changes in two biochemical indices of regeneration and their relationship to histologic alterations
Chlorpromazine Stimulated Ornithine Decarboxylase Activity Single dose of chlorpromazine stimulated ornithine decarboxylase activity 7-fold and decreased S-adenosylmethionine decarboxylase activity to 50% from the control level [ ADR Type 1 ] The inverse changes of mouse brain ornithine and S-adenosylmethionine decarboxylase activities by chlorpromazine and imipramine Dependence of ornithine decarboxylase induction
Dexamethasone Peptic Ulcers The activity of ornithine decarboxylase (ODC) INCREASED at 4 h@accelerated turnover of histamine in oxyntic mucosa may be an important factor in the pathogenesis of peptic ulcers [ ADR Type 1 ] Effects of dexamethasone on the activity of histidine decarboxylase, ornithine decarboxylase, and dopa decarboxylase in rat oxyntic mucosa
Ifosfamide Stimulated Ornithine Decarboxylase Activity Single dose of imipramine stimulated ornithine decarboxylase activity 7-fold and decreased S-adenosylmethionine decarboxylase activity to 50% from the control level [ ADR Type 1 ] The inverse changes of mouse brain ornithine and S-adenosylmethionine decarboxylase activities by chlorpromazine and imipramine Dependence of ornithine decarboxylase induction

This panel provides information on drug category

Toxicity Source

InAADR: Drug-Protein-ADRs database