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repaglinid har høj bindingsaffinitet til plasmaproteiner i mennesker (over 98%).
repaglinide is highly bound to plasma proteins in humans (greater than 98%).

aripiprazol viser også moderat bindingsaffinitet for serotonin-reuptake site og ingen væsentlig affinitet for muscarine receptorer.
aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for muscarinic receptors.

aripiprazol har også udvist moderat bindingsaffinitet til serotonin reuptake-sitet og ingen målbar affinitet til kolinerge muskarine receptorer.
aripiprazole also exhibited moderate binding affinity for the serotonin reuptake site and no appreciable affinity for cholinergic muscarinic receptors.

dialyse virker måske ikke med hensyn til at fjerne tolvaptan på grund af dets høje bindingsaffinitet for human plasmaprotein (>98 %).
dialysis may not be effective in removing tolvaptan because of its high binding affinity for human plasma protein (>98%).

den lange virkningsvarighed af zoledronsyre kan tilskrives høj bindingsaffinitet til det aktive site i farnesylpyrofosfatsyntase (fpp) og dets stærke bindingsaffinitet til knoglemineral.
the long duration of action of zoledronic acid is attributable to its high binding affinity for the active site of farnesyl pyrophosphate (fpp) synthase and its strong binding affinity to bone mineral.

zoledronsyres relativt lange virkningsperiode skyldes dens høje bindingsaffinitet for det aktive sted for farnesyl pyrofosfatsyntase (fpp) og dens stærke bindingsaffinitet for knoglemineral.
the relatively long duration of action of zoledronic acid is attributable to its high binding affinity for the active site of farnesyl pyrophosphate (fpp) synthase and its strong binding affinity to bone mineral.

palonosetron er en 5-ht3-receptorantagonist med en kraftig bindingsaffinitet for denne receptor, og en lille eller ingen affinitet for andre receptorer.
palonosetron is a 5-ht3 receptor antagonist with a strong binding affinity for this receptor and little or no affinity for other receptors.

aripiprazol har høj bindingsaffinitet in vitro for dopamin d2 - og d3 -, serotonin 5- ht1a - og 5- ht2a -
aripiprazole exhibited high binding affinity in vitro for dopamine d2 and d3, serotonin 5ht1a and 5ht2a receptors and moderate affinity for dopamine d4, serotonin 5ht2c and 5ht7, alpha-1 adrenergic and histamine h1 receptors.

det er et humaniseret monoklonalt antistoffragment (fab), som binder til dabigatran med meget høj affinitet, cirka 300 gange stærkere end dabigatrans bindingsaffinitet til trombin.
it is a humanized monoclonal antibody fragment (fab) that binds to dabigatran with very high affinity, approximately 300-fold more potent than the binding affinity of dabigatran for thrombin.

aripiprazol har høj bindingsaffinitet in vitro for dopamin d2- og d3-, serotonin 5-ht1a- og 5-ht2a- receptorer og moderat affinitet for dopamin d4-, serotonin 5-ht2c- og 5-ht7-, alfa 1-adrenerge og histamin h1- receptorer.
aripiprazole exhibited high binding affinity in vitro for dopamine d2 and d3, serotonin 5-ht1a and 5-ht2a receptors and moderate affinity for dopamine d4, serotonin 5-ht2c and 5-ht7, alpha-1 adrenergic and histamine h1 receptors.