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Nordazepam a unique benzo? GABA-A partial agonism vs positive allosteric modulation

Memantine

Bluelighter
Joined
May 16, 2015
Messages
304
What is the difference in effect and dependence potential of nordazepam vs other benzo's?
 
How, in terms of binding, could the loss of the methyl group have a significant effect on the intrinsic activity of the compound? All I can think of is that due to a new H-bond donor in the molecule, that could facilitate a binding mode which only results in partial agonism.
 
How, in terms of binding, could the loss of the methyl group have a significant effect on the intrinsic activity of the compound? All I can think of is that due to a new H-bond donor in the molecule, that could facilitate a binding mode which only results in partial agonism.

In the existing benzodiazepine pharmacophore, that part of the molecule is believed to interact with a H-bond donor in the binding site (even the partial agonists). But the efficacy difference could be something as simple as a change in the H-bond angle, a change in the angle/stregnth of a pi stacking interaction, or a difference in the number of water molecules excluded from the site.
 
#1, The dependence potential may be lower, but I could be wrong about that.
 
I think my textbook said something about how partial agonists possibly may not produce the same sort of long term benzo receptor changes that are seen with full agonists. I could be remembering wrong.
 
#6,

I seem to remember having read something like that. But does anyone have a source ?
 
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