F
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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3α-(4-Substituted phenyl)nortropane-2β-carboxylic acid methyl esters show selective binding at the norepinephrine transporter
TL;DR: 3α-(4-Methylphenyl)nortropane-2β-carboxylic acid methyl ester (4c) was found to be selective and highly potent for the norepinephrine transporter (NET) relative to the dopamine and serotonin transporters.
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Potent cocaine analogs inhibit [3H]dopamine uptake in rat mesencephalic cells in primary cultures: pharmacological selectivity of embryonic cocaine sites
Aline Brouard,Didier Pélaprat,John W. Boja,F. Ivy Carroll,M. Vial,Michael J. Kuhar,William Rostène +6 more
TL;DR: The order of potencies found for the three cocaine analogs on mesencephalic cultures was similar to that previously obtained in [3H] WIN 35,428 binding experiments, suggesting that the pharmacological selectivity of cocaine sites functionally related to the DA transporter in cultured embryonic neurons does not differ from that obtained in adult rat brain.
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p-Hydroxymethadone: synthesis, crystal structure and CD properties
George A. Brine,Karl G. Boldt,D. Prakash,Dennis J. Kotchmar,Virginia C. Bondeson,David J. Bradley,Pankaj Singh,F. Ivy Carroll +7 more
TL;DR: Alkylation of 2-chloro-N,N-dimethylpropylamine with the lithium salt derived from 2-(p-methoxyphenyl)-2-phenylacetonitrile 1 afforded a mixture of p-methyloxymethadone nitrile 3 and pmethoxyisomethadone nitrizone 4 The nitriles were separated chromatographically and the amino nitrizle 3 was converted subsequently into the diastereoisomeric p-hydroxymethaddone 8 hydrochlorides Careful rec
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Synthesis of a radiotracer for studying σ receptors in vivo using PET: (+)‐N‐[11C]‐benzyl‐N‐normetazocine (1S, 5S,9S‐(+)‐cis‐2‐[11C]‐2′‐hydroxy‐5,9‐dimethyl‐6,7‐benzomorphan)
TL;DR: In this article, a radiotracer was prepared by N-benzylation of (+)-cis-N-normetazocine with [α-11C]-benzmanyl iodide in ethanol using sodium hydrogen carbonate as the proton acceptor.
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A new synthesis of the ORL-1 antagonist 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay
Emilie D. Smith,N. Ariane Vinson,Desong Zhong,Bertold D. Berrang,Jennifer L. Catanzaro,James B. Thomas,Hernán A. Navarro,Brian P. Gilmour,Jeffrey R. Deschamps,F. Ivy Carroll +9 more
TL;DR: A new chiral synthesis of the ORL-1 antagonist 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (2, J-113397) was developed.