Metamfetamine or methamphetamine

Biochem/physiol Actions GZ-11608 is a potent and selective inhibitor of vesicular monoamine transporter-2 (VMAT2) that diminished hERG interaction. GZ-11608 reduces behavioral effects of methamphetamine such as locomotor activity,

Biochem/physiol Actions GZ-11608 is a potent and selective inhibitor of vesicular monoamine transporter-2 (VMAT2) that diminished hERG interaction. GZ-11608 reduces behavioral effects of methamphetamine such as locomotor activity,

Biochem/physiol Actions GZ-793A is a selective inhibitor of vesicular monoamine transporter 2 (VMAT2), which transports the monoamine neurotransmitters from cellular cytosol into synaptic vesicles. GZ-793A is 50-fold selective for VMAT over the

Immunotag™ Human Metabotropic glutamate receptor 5 ELISA Kit

Immunotag™ Rat Metabotropic glutamate receptor 5 ELISA Kit

General description A monohydroxy analog of JWH-210, a synthetic cannabinoid found in blends of the herbal mixture Spice or K2. A major urinary metabolite of JWH-210, this biomarker is also referred to as the omega-1 hydroxy metabolite of JWH-210.

A selective Group III metabotropic glutamate receptor agonist that functions presynaptically to suppress glutamate release (IC₅₀= 2.5 &muM) depresses synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb,

A selective Group III metabotropic glutamate receptor agonist that functions presynaptically to suppress glutamate release (IC₅₀= 2.5 &muM) depresses synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb,

A selective Group III metabotropic glutamate receptor agonist that functions presynaptically to suppress glutamate release (IC₅₀= 2.5 &muM) depresses synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb,

A selective Group III metabotropic glutamate receptor agonist that functions presynaptically to suppress glutamate release (IC₅₀= 2.5 &muM) depresses synaptic transmission in glutamatergic pathways in the hippocampus, olfactory bulb,

A potent and selective antagonist of the group II metabotropic glutamate receptors mGluR2 and mGluR3 (IC₅₀s = 21 and 14 nM, respectively) less effectively blocks mGluR8 and mGluR7 (IC₅₀s = 173 and 990 nM, respectively) can be

A potent and selective antagonist of the group II metabotropic glutamate receptors mGluR2 and mGluR3 (IC₅₀s = 21 and 14 nM, respectively) less effectively blocks mGluR8 and mGluR7 (IC₅₀s = 173 and 990 nM, respectively) can be