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11
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47749127374
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note
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50 values are human IP3 (NFAT) agonist data except in Table 6 which are mouse CCK1R IP3 data. Both CCK1 and CCK2 % activation are expressed as the % of activation relative to CCK-8. Additional assay protocols are given in Supporting Information.
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12
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27744477331
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A series of 1,2-diary imidazoles have recently been reported as CCK1R antagonists:
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A series of 1,2-diary imidazoles have recently been reported as CCK1R antagonists:. McClure K., Hack M., Huang L., Sehon C., Morton M., Li L., Barrett T.D., Shankley N., and Breitenbucher J.G. Bioorg. Med. Chem. Lett. 16 (2006) 72
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Breitenbucher, J.G.9
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13
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27744583278
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Sehon C., McClure K., Hack M., Morton M., Gomez L., Li L., Barrett T.D., Shankley N., and Breitenbucher J.G. Bioorg. Med. Chem. Lett. 16 (2006) 77
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Lange J.H.M., van Stuivenberg H.H., Coolen H.K.A.C., Adolfs T.J.P., McCreary A.C., Keizer H.G., Wals H.C., Veerman W., Borst A.J.M., de Looff W., Verveer P.C., and Kruse C.G. J. Med. Chem. 48 (2005) 1823
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18
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47749096399
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note
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CCK2R % activation and CCK2R % inhibition at 10,000 nM data for compounds 38-50 are given in Supporting Information.
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19
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47749128171
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note
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No distinguishable behavioral features were noted between treatment and vehicle control groups of the ONFI mice at both administered doses (0.3 and 3 mg/kg). Subsequent manuscripts describing the in vivo characteristics (tolerability and efficacy) are in preparation.
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20
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0032905886
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