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F. Ivy Carroll

Researcher at Research Triangle Park

Publications -  301
Citations -  11139

F. Ivy Carroll is an academic researcher from Research Triangle Park. The author has contributed to research in topics: Nicotinic agonist & Dopamine transporter. The author has an hindex of 52, co-authored 301 publications receiving 10411 citations. Previous affiliations of F. Ivy Carroll include RTI International & St. Joseph's Hospital and Medical Center.

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Synthesis and stereoselective reduction of (±)-, (+)- and (–)-6-substituted-6-azabicyclo[3.2.1]octan-3-one

TL;DR: In this paper, a three-step general synthetic route to both racemic and optically active 6-substituted 6-azabicyclo[321]octan-3-ones has been developed.
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Design, Synthesis, and Biological Evaluation of Structurally Rigid Analogues of 4-(3-Hydroxyphenyl)piperidine Opioid Receptor Antagonists.

TL;DR: Evaluation of the conformationally constrained series showed that structural rigid compounds having the 3-hydroxyphenyl group locked in the piperidine equatorial orientation had potencies equal to or better than similar compounds having more flexible structures similar to 1.1.0.
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Studies of the biogenic amine transporters. 10. Characterization of a novel cocaine binding site in brain membranes prepared from dopamine transporter knockout mice.

TL;DR: The relatively high density of site “X” in brain membranes and the fact that the Ki values of cocaine and cocaethylene for site ‘X�’ are in the range achieved in the brain following cocaine administration suggests that site ’X’ could contribute to the pharmacological or toxicological effects of cocaine.
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Synthesis, structural identification, and ligand binding of tropane ring analogs of paroxetine and an unexpected aza-bicyclo[3.2.2]nonane rearrangement product.

TL;DR: The structural requirements for high affinity at the serotonin transporter (5-HTT) have been investigated through the preparation of rigid paroxetine analogs and nucleophilic addition to the intermediate 2beta-methanesulfonyloxymethyl-3beta-(4-fluorophenyl)tropane unexpectedly provided the aza-bicyclo[3.2.2]nonane derivative 10a.
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The κ-opioid receptor antagonist JDTic decreases ethanol intake in alcohol-preferring AA rats.

TL;DR: It is suggested that κ-opioid receptor antagonists may be a valuable adjunct in the pharmacotherapy of ethanol use disorders and that accumbal λ-opIOid receptors participate in the modulation of the reinforcing effects of ethanol.