Title : A Mechanism-Based Pharmacokinetic Enzyme Turnover Model for Dichloroacetic Acid Autoinhibition in Rats.

Pub. Date : 2017 May

PMID : 28163135






4 Functional Relationships(s)
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1 DCA was found to inhibit its own metabolism by irreversibly inactivating glutathione transferase zeta 1 (GSTZ1-1), resulting in nonlinear kinetics and abnormally high accumulation ratio after repeated dosing. Dichloroacetic Acid glutathione S-transferase zeta 1 Rattus norvegicus
2 DCA was found to inhibit its own metabolism by irreversibly inactivating glutathione transferase zeta 1 (GSTZ1-1), resulting in nonlinear kinetics and abnormally high accumulation ratio after repeated dosing. Dichloroacetic Acid glutathione S-transferase zeta 1 Rattus norvegicus
3 The maximum rate constant for DCA-induced GSTZ1-1 inactivation is estimated to be 0.96/h, which is 110 times that of the rate constant for GSTZ1-1 natural degradation (0.00875/h). Dichloroacetic Acid glutathione S-transferase zeta 1 Rattus norvegicus
4 The maximum rate constant for DCA-induced GSTZ1-1 inactivation is estimated to be 0.96/h, which is 110 times that of the rate constant for GSTZ1-1 natural degradation (0.00875/h). Dichloroacetic Acid glutathione S-transferase zeta 1 Rattus norvegicus