Title : Pharmacokinetic/pharmacodynamic modelling of the disposition and effect of benazepril and benazeprilat in cats.

Pub. Date : 2003 Jun

PMID : 12755906






4 Functional Relationships(s)
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1 Within this space, benazeprilat was bound nonlinearly to ACE, which was mainly tissular (89.4%) rather than circulating (10.6%). benazeprilat angiotensin I converting enzyme Felis catus
2 Nevertheless, inhibition of ACE was long-lasting (t1/2 16-23 h) due to high affinity binding of benazeprilat to ACE (Kd approximately 3.5 mmol/L, IC50 approximately 4.3 mmol/L). benazeprilat angiotensin I converting enzyme Felis catus
3 Nevertheless, inhibition of ACE was long-lasting (t1/2 16-23 h) due to high affinity binding of benazeprilat to ACE (Kd approximately 3.5 mmol/L, IC50 approximately 4.3 mmol/L). benazeprilat angiotensin I converting enzyme Felis catus
4 Simulations using the model predict a lack of proportionality between dose of benazepril, plasma benazeprilat concentrations and effect due to the nonlinear binding of benazeprilat to ACE. benazeprilat angiotensin I converting enzyme Felis catus