Compounds > imipramine

imipramine and cp 101,606

imipramine has been researched along with cp 101,606 in 4 studies

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (50.00)29.6817
2010's2 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Lombardo, F; Obach, RS; Waters, NJ1
Chupka, J; El-Kattan, A; Feng, B; Miller, HR; Obach, RS; Troutman, MD; Varma, MV1
Alhambra, C; Brown, DG; Campbell, JB; Chen, T; Ciaccio, PJ; Cumberledge, J; Elmore, CS; Gupta, A; Hirata, LT; Hoerter, TN; Hu, T; Jiang, J; Johansson, MJ; Krumrine, JR; Lasota, CC; Liu, F; Maciag, CM; Maier, DL; Mathisen, D; McCarthy, DJ; Menhaji-Klotz, E; Peng, Z; Roberts, J; Scott, CW; Sutton, EJ; Sylvester, MA; Trivedi, S; Wang, J; Wang, X; Wen, X; Wilkins, DE; Wood, MW; Xia, J1
Oniszczuk, A; Poleszak, E; Serefko, A; Stasiuk, W; Świąder, K; Szopa, A; Wlaź, P; Wośko, S; Wyska, E1

Other Studies

4 other study(ies) available for imipramine and cp 101,606

ArticleYear
Trend analysis of a database of intravenous pharmacokinetic parameters in humans for 670 drug compounds.
    Drug metabolism and disposition: the biological fate of chemicals, 2008, Volume: 36, Issue:7

    Topics: Blood Proteins; Half-Life; Humans; Hydrogen Bonding; Infusions, Intravenous; Pharmacokinetics; Protein Binding

2008
Physicochemical determinants of human renal clearance.
    Journal of medicinal chemistry, 2009, Aug-13, Volume: 52, Issue:15

    Topics: Humans; Hydrogen Bonding; Hydrogen-Ion Concentration; Hydrophobic and Hydrophilic Interactions; Kidney; Metabolic Clearance Rate; Molecular Weight

2009
2,6-Disubstituted pyrazines and related analogs as NR2B site antagonists of the NMDA receptor with anti-depressant activity.
    Bioorganic & medicinal chemistry letters, 2011, Jun-01, Volume: 21, Issue:11

    Topics: Animals; Antidepressive Agents; Binding Sites; Binding, Competitive; Dose-Response Relationship, Drug; Inhibitory Concentration 50; Mice; Molecular Structure; Motor Activity; Protein Binding; Pyrazines; Receptors, N-Methyl-D-Aspartate

2011
Traxoprodil, a selective antagonist of the NR2B subunit of the NMDA receptor, potentiates the antidepressant-like effects of certain antidepressant drugs in the forced swim test in mice.
    Metabolic brain disease, 2016, Volume: 31, Issue:4

    Topics: Animals; Antidepressive Agents; Behavior, Animal; Citalopram; Depression; Disease Models, Animal; Excitatory Amino Acid Antagonists; Fluoxetine; Imipramine; Mice; Motor Activity; Piperidines; Receptors, N-Methyl-D-Aspartate; Swimming; Treatment Outcome

2016