Search Results - "GHAZAL, Nabil B"

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  1. 1

    Asymmetric Synthesis of Cis-Fused Bicyclic Pyrrolidines and Pyrrolidinones via Chiral Polycyclic Lactams by Ennis, Michael D, Hoffman, Robert L, Ghazal, Nabil B, Old, David W, Mooney, Pamela A

    Published in Journal of organic chemistry (23-08-1996)
    “…Condensation of racemic keto-ester 2 and 1.1 equiv of (R)-(−)-phenylglycinol in toluene with azeotropic removal of water and methanol gave rise to a…”
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    5-HT1D Receptor Agonist Properties of Novel 2-[5-[[(Trifluoromethyl)sulfonyl]oxy]indolyl]ethylamines and Their Use as Synthetic Intermediates by Barf, Tjeerd A, de Boer, Peter, Wikström, Håkan, Peroutka, Stephen J, Svensson, Kjell, Ennis, Michael D, Ghazal, Nabil B, McGuire, James C, Smith, Martin W

    Published in Journal of medicinal chemistry (22-11-1996)
    “…2-[5-[[(Trifluoromethyl)sulfonyl]oxy]-1H-indol-3-yl]ethylamine (18), its N,N-di-n-propyl (12), N,N-diethyl (13), and N,N-dimethyl (14) derivatives, and…”
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    Differential pharmacology between the guinea‐pig and the gorilla 5‐HT 1D receptor as probed with isochromans (5‐HT 1D ‐selective ligands) by Pregenzer, Jeffrey F, Alberts, Glen L, Im, Wha Bin, Slightom, Jerry L, Ennis, Michael D, Hoffman, Robert L, Ghazal, Nabil B, TenBrink, Ruth E

    Published in British journal of pharmacology (29-01-2009)
    “…Both the 5‐HT 1D and 5‐HT 1B receptors are implicated in migraine pathophysiology. Recently isochromans have been discovered to bind primate 5‐HT 1D receptors…”
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    Differential pharmacology between the guinea‐pig and the gorilla 5‐HT1D receptor as probed with isochromans (5‐HT1D‐selective ligands) by Pregenzer, Jeffrey F, Alberts, Glen L, Im, Wha Bin, Slightom, Jerry L, Ennis, Michael D, Hoffman, Robert L, Ghazal, Nabil B, TenBrink, Ruth E

    Published in British journal of pharmacology (01-05-1999)
    “…Both the 5‐HT1D and 5‐HT1B receptors are implicated in migraine pathophysiology. Recently isochromans have been discovered to bind primate 5‐HT1D receptors…”
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    Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 2. Effect of 8-amino nitrogen substitution on serotonin receptor binding and pharmacology by Ennis, MD, Stjernloef, P, Hoffman, R L, Ghazal, N B, Smith, M W, Svensson, K, Wikstroem, H, Haadsma-Svensson, SR, Lin, Chiu-Hong

    Published in Journal of medicinal chemistry (09-06-1995)
    “…A series of analogs of the potent and selective 5-HT sub(1A) agonist 8-(di-n-propylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1-carbald ehyde (2b) (OSU191) was…”
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  16. 16

    Synthesis of ( r )‐ and ( s )‐1‐formyl‐6,7,8,9‐tetrahydro‐ N,N ‐(dipropyl)‐3 H ‐benz[ e ]indol‐8‐amines: Potent and orally active 5‐ht 1a receptor agonists by Lin, Chiu‐Hong, Ennis, Michael D., Hoffman, Robert L., Phillips, Gillian, Haadsma‐Svensson, Susanne R., Ghazal, Nabil B., Chidester, Connie G.

    Published in Journal of heterocyclic chemistry (01-01-1994)
    “…Abstract An efficient synthesis of the potent and orally active 5‐HT 1A agonists, ( R )‐(+)‐ and ( S )‐(‐)‐1‐formyl‐6,7,8,9‐tetrahydro‐ N,N ‐dipropyl‐3 H…”
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  17. 17

    Synthesis of (r)- and (s)-1-formyl-6,7,8,9-tetrahydro- N,N-(dipropyl)-3H-benz[e]indol-8-amines: Potent and orally active 5-ht1a receptor agonists by Lin, Chiu-Hong, Ennis, Michael D., Hoffman, Robert L., Phillips, Gillian, Haadsma-Svensson, Susanne R., Ghazal, Nabil B., Chidester, Connie G.

    Published in Journal of heterocyclic chemistry (01-01-1994)
    “…An efficient synthesis of the potent and orally active 5‐HT1A agonists, (R)‐(+)‐ and (S)‐(‐)‐1‐formyl‐6,7,8,9‐tetrahydro‐N,N‐dipropyl‐3H‐benz[e]indol‐8‐amines…”
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