Search Results - "Ismaiel, Abd M."

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    Ketanserin Analogs: The Effect of Structural Modification on 5-HT2 Serotonin Receptor Binding by Ismaiel, Abd M, Arruda, Kim, Teitler, Milt, Glennon, Richard A

    Published in Journal of medicinal chemistry (01-03-1995)
    “…Ketanserin (1) is a fairly selective 5-HT2 antagonist that binds both at 5-HT2A and 5-HT2C receptors. A previous structure-affinity relationship study revealed…”
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    5-HT1 and 5-HT2 binding profiles of the serotonergic agents .alpha.-methylserotonin and 2-methylserotonin by Ismaiel, Abd M, Titeler, Milt, Miller, Keith J, Smith, Thomas S, Glennon, Richard A

    Published in Journal of medicinal chemistry (01-02-1990)
    “…alpha-Methyl-5-hydroxytryptamine (alpha-Me-5-HT; 2) and 2-methyl-5-hydroxytryptamine (2-Me-5-HT; 3) are considered to be 5-HT2-selective and 5-HT3-selective…”
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    Ketanserin and spiperone as templates for novel serotonin 5-HT(2A) antagonists by Glennon, Richard A, Metwally, Kamel, Dukat, Malgorzata, Ismaiel, Abd M, De los Angeles, Joseph, Herndon, Jeffery, Teitler, Milt, Khorana, Nantaka

    Published in Current topics in medicinal chemistry (01-06-2002)
    “…The structures of ketanserin (1) and spiperone (2) were examined in detail to determine the role of various substituent groups on 5-HT(2A) receptor affinity…”
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    Structure−Activity Relationships for the Binding of Arylpiperazines and Arylbiguanides at 5-HT3 Serotonin Receptors by Dukat, Małgorzata, Abdel-Rahman, Ashraf A, Ismaiel, Abd M, Ingher, Stacy, Teitler, Milt, Gyermek, Laszlo, Glennon, Richard A

    Published in Journal of medicinal chemistry (27-09-1996)
    “…Arylpiperazines are nonselective agents that bind at 5-HT3 serotonin receptors with moderate to high affinity, whereas 1-phenylbiguanide is a low-affinity but…”
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    Antagonism of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane stimulus with a newly identified 5-HT2- versus 5-HT1C-selective antagonist by Ismaiel, Abd M, De Los Angeles, Joseph, Teitler, Milt, Ingher, Stacy, Glennon, Richard A

    Published in Journal of medicinal chemistry (01-08-1993)
    “…DOM [i.e., 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane] is a 5-HT1C/2 serotonin agonist that exerts stimulus control of behavior in animals. In order to…”
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    2-(1-Naphthyloxy)ethylamines with Enhanced Affinity for Human 5-HT1D β (h5-HT1B) Serotonin Receptors by Ismaiel, Abd M, Dukat, Malgorzata, Law, Ho, Kamboj, Rajender, Fan, Ermi, Lee, David K. H, Mazzocco, Lucia, Buekschkens, Donna, Teitler, Milt, Pierson, Myles E, Glennon, Richard A

    Published in Journal of medicinal chemistry (19-12-1997)
    “…Although the β-adrenergic antagonist propranolol (1) binds at rodent 5-HT1B serotonin receptors, it displays low affinity (K i > 10 000 nM) for its species…”
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    Novel 1-phenylpiperazine and 4-phenylpiperidine derivatives as high-affinity .sigma. ligands by Glennon, Richard A, Yousif, Mamoun Y, Ismaiel, Abd M, El-Ashmawy, Mahmoud B, Herndon, J. L, Fischer, James B, Server, Alfred C, Howie, Kathleen J. Burke

    Published in Journal of medicinal chemistry (01-12-1991)
    “…sigma receptors may represent an exciting new approach for the development of novel psychotherapeutic agents. Unfortunately, many of the commonly used sigma…”
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    N-(phthalimidoalkyl) derivatives of serotonergic agents: a common interaction at 5-HT1A serotonin binding sites? by Glennon, Richard A, Naiman, Noreen A, Pierson, M. Edward, Smith, J. Doyle, Ismaiel, Abd M, Titeler, Milt, Lyon, Robert A

    Published in Journal of medicinal chemistry (01-08-1989)
    “…Several classes of agents are known to bind at central 5-HT1A serotonin sites In order to challenge the hypothesis that these agents bind in a relatively…”
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    Identification and exploitation of the .sigma.-opiate pharmacophore by Glennon, Richard A, Smith, J. Doyle, Ismaiel, Abd M, El-Ashmawy, Mahmoud, Battaglia, George, Fischer, James B

    Published in Journal of medicinal chemistry (01-03-1991)
    “…Certain benzomorphan "sigma-opiates" such as N-allylnormetazocine (NANM) bind at sigma receptors with modest affinity and with little selectivity (i.e., they…”
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    Binding of substituted and conformationally restricted derivatives of N-(3-phenyl-n-propyl)-1-phenyl-2-aminopropane at .sigma.-receptors by Glennon, Richard A, Ismaiel, Abd M, Smith, J. Doyle, Yousif, Mamoun, El-Ashmawy, Mahmoud, Herndon, J. L, Fischer, James B, Howie, Kathleen J. Burke, Server, Alfred C

    Published in Journal of medicinal chemistry (01-06-1991)
    “…Certain benzomorphans, such as N-allylnormetazocine, are classical "sigma-opiates" that bind both at sigma and phencyclidine (PCP) binding sites with modest…”
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    Thioxanthene-derived analogs as sigma(1) receptor ligands by Glennon, Richard A, Ismaiel, Abd M, Ablordeppey, Seth, El-Ashmawy, Mahmoud, Fisher, James B

    Published in Bioorganic & medicinal chemistry letters (03-05-2004)
    “…An investigation of the structure-affinity relationships for the binding of thioxanthene-related structures indicates that an intact thioxanthene ring is not…”
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    Binding of arylpiperazines to 5-HT3 serotonin receptors: results of a structure-affinity study by Glennon, R A, Ismaiel, A E, McCarthy, B G, Peroutka, S J

    Published in European journal of pharmacology (22-09-1989)
    “…The binding affinities of a series of arylpiperazine derivatives at [3H]quipazine-labeled central 5-HT3 sites were investigated. Features determined to be…”
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    The binding of propranolol at 5-hydroxytryptamine1D beta T355N mutant receptors may involve formation of two hydrogen bonds to asparagine by Glennon, R A, Dukat, M, Westkaemper, R B, Ismaiel, A M, Izzarelli, D G, Parker, E M

    Published in Molecular pharmacology (01-01-1996)
    “…Although the beta-adrenergic receptor antagonist (-)-propranolol binds with relatively low affinity at human 5-hydroxytryptamine1D beta receptors (Ki = 10,200…”
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    NAN-190: agonist and antagonist interactions with brain 5-HT1A receptors by Rydelek-Fitzgerald, L, Teitler, M, Fletcher, P W, Ismaiel, A M, Glennon, R A

    Published in Brain research (05-11-1990)
    “…NAN-190 has been reported to be a 5-HT1A antagonist in drug discrimination studies. In order to determine if the effect of NAN-190 was directly due to…”
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