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  1. 1
    Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-bioavailable 5-HT1D agonists

    Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-bioavailable 5-HT1D agonists von ISAAC, Methvin, SLASSI, Malik, NAISMITH, Angela, MADDAFORD, Shawn, PAPAC, Damon, HARRISON, Shuree, HUA WANG, DRANER, Stan, TEHIM, Ashok, TAO XIN, ARORA, Jalaj, O'BRIEN, Anne, EDWARDS, Louise, MACLEAN, Neil, WILSON, Julie, DEMSCHYSHYN, Lidia, LABRIE, Phillipe


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  2. 2
    Design, synthesis and biological activity of novel dimethyl-[2-[6-substituted-indol-1-yl]-ethyl]-amine as potent, selective, and orally-bioavailable 5-HT(1D) agonists

    Design, synthesis and biological activity of novel dimethyl-[2-[6-substituted-indol-1-yl]-ethyl]-amine as potent, selective, and orally-bioavailable 5-HT(1D) agonists von Isaac, Methvin, Slassi, Malik, Xin, Tao, Arora, Jalaj, O'Brien, Anne, Edwards, Louise, MacLean, Neil, Wilson, Julie, Demschyshyn, Lidia, Labrie, Phillipe, Naismith, Angela, Maddaford, Shawn, Papac, Damon, Harrison, Shuree, Wang, Hua, Draper, Stan, Tehim, Ashok


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  3. 3
    Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-Bioavailable 5-HT 1D agonists

    Design, synthesis and biological activity of novel dimethyl-{2-[6-substituted-indol-1-yl]-ethyl}-amine as potent, selective, and orally-Bioavailable 5-HT 1D agonists von Isaac, Methvin, Slassi, Malik, Xin, Tao, Arora, Jalaj, O'Brien, Anne, Edwards, Louise, MacLean, Neil, Wilson, Julie, Demschyshyn, Lidia, Labrie, Phillipe, Naismith, Angela, Maddaford, Shawn, Papac, Damon, Harrison, Shuree, Wang, Hua, Draper, Stan, Tehim, Ashok


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