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Lisa D Aimone

Showing results (1-10 of 48) with videos related to

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Current Protocols in Pharmacology|September 29, 2011
Overview of pharmacokineticsLisa D Aimone
Current Protocols in Pharmacology|September 3, 2014
Overview of pharmacokineticsLisa D Aimone, Inés A M de Lannoy
Bioorganic & Medicinal Chemistry Letters|September 13, 2011
Synthesis and structure-activity relationships of 4,5-fused pyridazinones as histamine H₃ receptor antagonistsMing Tao, Rita Raddatz, Lisa D Aimone, et al.
Chemical Biology & Drug Design|May 18, 2013
Serendipitous discovery of a prodrug of a PARP-1 inhibitorDerek Dunn, Jean Husten, Lisa D Aimone, et al.
Bioorganic & Medicinal Chemistry Letters|May 24, 2012
Synthesis of constrained benzocinnolinone analogues of CEP-26401 (irdabisant) as potent, selective histamine H3 receptor inverse agonistsKurt A Josef, Lisa D Aimone, Jacquelyn Lyons, et al.
Bioorganic & Medicinal Chemistry Letters|February 28, 2012
Synthesis and evaluation of a new series of 1'-cyclobutyl-6-(4-piperidyloxy)spiro[benzopyran-2,4'-piperidine] derivatives as high affinity and selective histamine-3 receptor (H3R) antagonistsReddeppa Reddy Dandu, Jacquelyn A Lyons, Rita Raddatz, et al.
Journal of Medicinal Chemistry|November 24, 2011
Optimization of 5-pyridazin-3-one phenoxypropylamines as potent, selective histamine H₃ receptor antagonists with potent cognition enhancing activityMing Tao, Lisa D Aimone, Zeqi Huang, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2011
Synthesis and evaluation of 4-alkoxy-[1'-cyclobutyl-spiro(3,4-dihydrobenzopyran-2,4'-piperidine)] analogues as histamine-3 receptor antagonistsNadine C Becknell, Reddeppa Reddy Dandu, Jacquelyn A Lyons, et al.
Chemical Biology & Drug Design|November 1, 2012
Aryl-heteroaryl derivatives as novel wake-promoting agentsBrigitte Lesur, Yin G Lin, Val R Marcy, et al.
Bioorganic & Medicinal Chemistry|May 15, 2012
Synthesis and evaluation of 4- and 5-pyridazin-3-one phenoxypropylamine analogues as histamine-3 receptor antagonistsNadine C Becknell, Jacquelyn A Lyons, Lisa D Aimone, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Current Protocols in Pharmacology|September 29, 2011
Overview of pharmacokineticsLisa D Aimone
Current Protocols in Pharmacology|September 3, 2014
Overview of pharmacokineticsLisa D Aimone, Inés A M de Lannoy
Bioorganic & Medicinal Chemistry Letters|September 13, 2011
Synthesis and structure-activity relationships of 4,5-fused pyridazinones as histamine H₃ receptor antagonistsMing Tao, Rita Raddatz, Lisa D Aimone, et al.
Chemical Biology & Drug Design|May 18, 2013
Serendipitous discovery of a prodrug of a PARP-1 inhibitorDerek Dunn, Jean Husten, Lisa D Aimone, et al.
Bioorganic & Medicinal Chemistry Letters|May 24, 2012
Synthesis of constrained benzocinnolinone analogues of CEP-26401 (irdabisant) as potent, selective histamine H3 receptor inverse agonistsKurt A Josef, Lisa D Aimone, Jacquelyn Lyons, et al.
Bioorganic & Medicinal Chemistry Letters|February 28, 2012
Synthesis and evaluation of a new series of 1'-cyclobutyl-6-(4-piperidyloxy)spiro[benzopyran-2,4'-piperidine] derivatives as high affinity and selective histamine-3 receptor (H3R) antagonistsReddeppa Reddy Dandu, Jacquelyn A Lyons, Rita Raddatz, et al.
Journal of Medicinal Chemistry|November 24, 2011
Optimization of 5-pyridazin-3-one phenoxypropylamines as potent, selective histamine H₃ receptor antagonists with potent cognition enhancing activityMing Tao, Lisa D Aimone, Zeqi Huang, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2011
Synthesis and evaluation of 4-alkoxy-[1'-cyclobutyl-spiro(3,4-dihydrobenzopyran-2,4'-piperidine)] analogues as histamine-3 receptor antagonistsNadine C Becknell, Reddeppa Reddy Dandu, Jacquelyn A Lyons, et al.
Chemical Biology & Drug Design|November 1, 2012
Aryl-heteroaryl derivatives as novel wake-promoting agentsBrigitte Lesur, Yin G Lin, Val R Marcy, et al.
Bioorganic & Medicinal Chemistry|May 15, 2012
Synthesis and evaluation of 4- and 5-pyridazin-3-one phenoxypropylamine analogues as histamine-3 receptor antagonistsNadine C Becknell, Jacquelyn A Lyons, Lisa D Aimone, et al.
Pageof 5