Search Results - "Houlihan, William J."
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γ-Secretase Partitioning into Lipid Bilayers Remodels Membrane Microdomains after Direct Insertion
Published in Langmuir (16-06-2020)“…γ-Secretase is a multisubunit complex that catalyzes intramembranous cleavage of transmembrane proteins. The lipid environment forms membrane microdomains that…”
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Antitumor Activity of 5-Aryl-2,3-dihydroimidazo[2,1-a]isoquinolines
Published in Journal of medicinal chemistry (01-01-1995)“…A series of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinolines previously reported to be platelet activating factor (PAF) receptor antagonists were evaluated for…”
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Structural modification of 5-aryl-2,3-dihydroimidazo[2,1-a]isoquinoline platelet activating factor receptor antagonists
Published in Journal of medicinal chemistry (01-10-1993)“…In an effort to determine the effect of modification of the imidazo[2,1-a]isoquinoline portion of the PAF-receptor antagonist SDZ 64-412 (1), several new…”
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Three-Dimensional Quantitative Structure−Activity Relationships of Mazindol Analogues at the Dopamine Transporter
Published in Journal of medicinal chemistry (12-09-2002)“…A three-dimensional quantitative structure−activity relationship (3D-QSAR) study was performed on a series of mazindol analogues using the comparative…”
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Mazindol Analogues as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter
Published in Journal of medicinal chemistry (12-09-2002)“…A series of mazindol (2) and homomazindol (3) analogues with a variety of electron-donating and electron-withdrawing groups in the pendant aryl group and the…”
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Assessment of mazindane, a pro-drug form of mazindol, in assays used to define cocaine treatment agents
Published in European journal of pharmacology (05-01-2003)“…The current studies compared mazindane (5-(4-chlorophenyl)-2,3-dihydro-5H-imidazo [2,1a] isoindole) hydrogen sulfate, a water soluble pro-drug of mazindol…”
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Benzo- and Cyclohexanomazindol Analogues as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter
Published in Journal of medicinal chemistry (12-09-2002)“…A series of mazindol (1), homomazindol (2), and bishomomazindol (3) derivatives with a benzo or cyclohexano ring fused at various sites were prepared as part…”
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Novel cycloaddition products formed by the modified Madelung indole synthesis
Published in Journal of organic chemistry (01-10-1981)Get full text
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Halogenated Mazindol Analogs as Potential Inhibitors of the Cocaine Binding Site at the Dopamine Transporter
Published in Journal of medicinal chemistry (06-12-1996)“…A series of halogenated (F, Cl, Br, I), pyrimido and diazepino homologs of mazindol were prepared and evaluated for their ability to displace [3H]WIN 35,428…”
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Modification of Lipid Microenvironments on Solid Support Structures for Use in Transmembrane Protein Assays
Published 01-01-2019“…Gamma-Secretase (γ-secretase) is a transmembrane protease of increasing interest, which has been shown to have significant connections to both cancer and…”
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Dissertation -
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High Affinity Recognition of Serotonin Transporter Antagonists Defined by Species-scanning Mutagenesis
Published in The Journal of biological chemistry (31-07-1998)“…Human and Drosophila melanogasterserotonin (5-HT) transporters (SERTs) exhibit similar 5-HT transport kinetics and can be distinguished pharmacologically by…”
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Synthesis and biological evaluation of substituted 2,2'-oxybis(propionic acid) derivatives and related compounds
Published in Journal of medicinal chemistry (01-05-1976)Get full text
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Antitumor Activity of the R- and S-Enantiomers of RS-2-[[Hydroxy[[2-[(octadecyloxy)methyl]tetrahydrofuran-2-yl]methoxy]phosphinyl]oxy]-N,N,N-trimethylethylaminium Hydroxide Inner Salt
Published in Journal of medicinal chemistry (19-01-1996)“…The R- and S-enantiomers of 2-[[hydroxy[[2-[(octadecyloxy)methyl]tetrahydrofuran-2-yl]methoxy]phosphinyl]oxy]-N,N,N-trimethylethylaminium hydroxide salt (SRI…”
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Lithiation of N-(2-alkylphenyl)alkanamides and related compounds. A modified Madelung indole synthesis
Published in Journal of organic chemistry (01-10-1981)Get full text
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Directed lithiation of 2-phenyl- and 2-(o-methylphenyl)imidazoline
Published in Journal of organic chemistry (01-12-1982)Get full text
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High affinity recognition of serotonin transporter antagonists defined by species-scanning mutagenesis. An aromatic residue in transmembrane domain I dictates species-selective recognition of citalopram and mazindol
Published in The Journal of biological chemistry (31-07-1998)“…Human and Drosophila melanogaster serotonin (5-HT) transporters (SERTs) exhibit similar 5-HT transport kinetics and can be distinguished pharmacologically by…”
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The Addition of Methyl Grignard to 4-t-Butylcyclohexanone
Published in Journal of organic chemistry (01-11-1962)Get full text
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Hofmann elimination of heterocycles containing bridgehead hydrazines. I. 2,6-Benzodiazonine and dibenzo[c,h][1,6]diazecine derivatives
Published in Journal of organic chemistry (01-09-1969)Get full text
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Sleep-inducing N-alkyl-5-[m-(trifluoromethyl)phenyl]-5-hydroxy-2-pyrrolidinones and N-alkyl-3-(trifluoromethyl)cinnamamides
Published in Journal of medicinal chemistry (01-01-1985)“…A series of N-alkyl-3-[m-(trifluoromethyl)phenyl]-5-hydroxy-2-pyrrolidinones and N-alkyl-3-(trifluoromethyl)-cinnamamides were prepared and screened in a…”
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Journal Article