A6605

AMN082

≥98% (HPLC), solid

• Synonym(s): N,N′-Dibenzhydrylethane-1,2-diamine dihydrochloride
• Empirical Formula (Hill Notation): C₂₈H₂₈N₂ · 2HCl
• CAS Number: 97075-46-2
• Molecular Weight: 465.46
• MDL number: MFCD08702723
• UNSPSC Code: 12352200
• PubChem Substance ID: 24891112

Properties

• assay: ≥98% (HPLC)
• form: solid
• storage condition: desiccated
• color: white to off-white
• solubility: DMSO: ≥5 mg/mL
• storage temp.: −20°C
• SMILES string: Cl[H].Cl[H].C(CNC(c1ccccc1)c2ccccc2)NC(c3ccccc3)c4ccccc4
• InChI: 1S/C28H28N2.2ClH/c1-5-13-23(14-6-1)27(24-15-7-2-8-16-24)29-21-22-30-28(25-17-9-3-10-18-25)26-19-11-4-12-20-26;;/h1-20,27-30H,21-22H2;2*1H
• InChI key: YRQCDCNQANSUPB-UHFFFAOYSA-N

Description

Application

AMN082 is a selective allosteric mGluR 7 receptor agonist and has been used to study the role of this glutamate receptor type in the medial prefrontal cortex in mice. AMN082 inhibits forskolin-stimulated cAMP accumulation, and stimulates not only GTPγS binding but also the release of stress hormones.

Biochem/physiol Actions

AMN082 is a selective allosteric mGluR 7 receptor agonist and first selective pharmacological tool for mGluR7. AMN082 inhibits forskolin-stimulated cAMP accumulation (EC₅₀ = 64 nM) and stimulates GTPγS binding (EC₅₀ = 290 nM) similar to L-AP₄ and greater than L-glutamate. Thus, AMN082 is a "full agonist" and acts at an allosteric site in the transmembrane domain of mGluR7. AMN082 has no effects at other mGluR′s up to 10 μM and stimulates release of stress hormones (corticosterone and ACTH) and is orally active and brain penetrable.

AMN082 is a selective allosteric mGluR 7 receptor agonist and first selective pharmacological tool for mGluR7. AMN082 stimulates the release of stress hormones (corticosterone and ACTH), orally active and brain penetrable.

Safety Information

• Storage Class: 13 - Non Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable
• ppe: dust mask type N95 (US), Eyeshields, Faceshields, Gloves