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AT1001

Chemical Structure : AT1001

CAS No.: 2108826-18-0

AT1001 (AT-1001)

Catalog No.: PC-49428Not For Human Use, Lab Use Only.

AT1001 (AT-1001) is a high affinity and selective α3β4 nAChR antagonist with Ki value of 2.4 nM, >90-fold selectivity over the other major subtypes (α4β2 and α7 nAChR).

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

    Biological Activity

    AT1001 (AT-1001) is a high affinity and selective α3β4 nAChR antagonist with Ki value of 2.4 nM, >90-fold selectivity over the other major subtypes (α4β2 and α7 nAChR).
    AT1001 potently and reversibly blocks epibatidine-induced inward currents in HEK cells transfected with α3β4 nAChR.
    AT-1001 potently and dose-dependently blocks nicotine self-administration in rats, without affecting food responding.
    AT-1001 inhibits nicotine-induced [3H]dopamine release poorly and at significantly higher concentrations compared with mecamylamine and conotoxin MII in nucleus accumbens (NAcs) synaptosomal preparation.

    Physicochemical Properties

    M.Wt 309.251
    Formula C15H21BrN2
    Appearance Solid
    CAS No.
    Storage
    Solide Powder
    -20°C 12 Months; 4°C 6 Months
    In Solvent
    -80°C 6 Months; -20°C 6 Months
    Shipping
    Solubility

    10 mM in DMSO

    Chemical Name/SMILES

    N-(2-bromophenyl)-9-methyl-9-azabicyclo[3.3.1]nonan-3-amine

    References

    1. Toll L, et al. Neuropsychopharmacology. 2012 May;37(6):1367-76.

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