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. Author manuscript; available in PMC: 2010 Dec 1.
Published in final edited form as: J Biomed Inform. 2009 Jun 16;42(6):990–1003. doi: 10.1016/j.jbi.2009.05.010

Table 7.

While LOEs were designed separately for each assertion type, many of the resulting LOEs were alike. As a result, only 15 LOEs were defined for the 22 assertion types in the DIKB’s rule-based theory of metabolic drug-drug interactions. This table enumerates the assertion types that share the same LOEs.

LOE ID Applies to
A bioavailability
maximum-concentration
B first-pass-effect
fraction-absorbed
C primary-total-clearance-mechanism
D controls-formation-of
substrate-of
is-not-substrate-of
E primary-total-clearance-enzyme
F primary-metabolic-clearance-enzyme
G has-metabolite
H inhibition-constant
I inhibits
J does-not-inhibit
K does-not-permanently-deactivate-catalytic-function
permanently-deactivates-catalytic-function
in-vitro-probe-substrate-of-enzyme
L in-vitro-selective-inhibitor-of-enzyme
M in-viVo-selective-inhibitor-of-enzyme
sole-PK-effect-alter-metabolic-clearance
N pceut-entity-of-concern
O polymorphic-enzyme