Chemical Name:N,N'-Bis(diphenylmethyl)-1,2-ethanediamine
dihydrochloride
Important Product Information
For important information regarding the useage of this product click here.
Biological Activity:
The first selective mGlu7
agonist. Potently inhibits cAMP accumulation and stimulates GTPγS
binding in recombinant cells and on membranes expressing mGlu7 (EC50
= 64-290 nM). Selective over other mGluR subtypes and selected ionotropic
glutamate receptors up to 10 μM.
Acts via a novel allosteric site and is orally active and brain penetrant.
Flor et
al (2005) AMN082, the first selective mGluR7
agonist: activation of receptor signaling via an allosteric site in the
transmembrane domain modulates stress parameters in vivo.
Neuropharmacology 49 (Suppl. 1) 244. Mitsukawaet al
(2005) A selective metabotropic glutamate receptor 7 agonist: Activation of
receptor signaling via an allosteric site modulates stress parameters in
vivo. Proc.Natl.Acad.Sci.USA 102 18712.