Search Results - "GHAZAL, Nabil B"
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Asymmetric Synthesis of Cis-Fused Bicyclic Pyrrolidines and Pyrrolidinones via Chiral Polycyclic Lactams
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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2,3,4,5-tetrahydro- and 2,3,4,5,11,11a-hexahydro-1H-[1,4]diazepino[1,7-a]indoles: New templates for 5-HT2C agonists
Published in Bioorganic & medicinal chemistry letters (21-07-2003)Get full text
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5-HT1D Receptor Agonist Properties of Novel 2-[5-[[(Trifluoromethyl)sulfonyl]oxy]indolyl]ethylamines and Their Use as Synthetic Intermediates
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)
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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1,4-Dihydronaphthoquinones, hydroindoloquinones, benzofurans, and benzothiophenes as inhibitors of 5-lipoxygenase. Synthesis and structure-activity studies
Published in Journal of medicinal chemistry (01-02-1990)“…A series of substituted 1,4-dihydronaphthoquinones, hydroindoloquinones, benzofuran-4,7-dihydroquinones, and benzothiophene-4,7-dihydroquinones were…”
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Differential pharmacology between the guinea‐pig and the gorilla 5‐HT1D receptor as probed with isochromans (5‐HT1D‐selective ligands)
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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2,3,4,5-tetrahydro- and 2,3,4,5,11,11a-hexahydro-1H-[1,4]diazepino[1,7-a]indoles: new templates for 5-HT(2C) agonists
Published in Bioorganic & medicinal chemistry letters (21-07-2003)“…The design and synthesis of the novel 2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,7-a]indole 5 is described. This azepinoindole has excellent affinity for 5-HT(2C)…”
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2,3,4,5-Tetrahydro- and 2,3,4,5,11,11a-hexahydro-1H-[1,4]diazepino[1,7- a]indoles: new templates for 5-HT 2C agonists
Published in Bioorganic & medicinal chemistry letters (2003)“…The design and synthesis of the novel 2,3,4,5-tetrahydro-1H-[1,4]diazepino[1,7- a]indole 5 is described. This azepinoindole has excellent affinity for 5-HT 2C…”
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Structure-activity relationships in the 8-amino-6,7,8,9-tetrahydro-3H-benz[e]indole ring system. 1. Effects of substituents in the aromatic system on serotonin and dopamine receptor subtypes
Published in Journal of medicinal chemistry (09-06-1995)“…A series of 1-, 3-, and 4-substituted analogs to the potent 5-HT1A against 8-(dipropylamino)-6,7,8,9-tetrahydro-3H-benz[e]indole-1-carbaldehyde (5) were…”
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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
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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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
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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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
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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