Page last updated: 2024-08-24

tiagabine and snap 5114

tiagabine has been researched along with snap 5114 in 11 studies

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (9.09)18.2507
2000's1 (9.09)29.6817
2010's7 (63.64)24.3611
2020's2 (18.18)2.80

Authors

AuthorsStudies
Borden, LA; Branchek, TA; Dhar, TG; Gluchowski, C; Smith, KE; Tyagarajan, S; Weinshank, RL1
Höfner, G; Kragler, A; Wanner, KT1
Faust, MR; Höfner, G; Pabel, J; Wanner, KT1
Filipek, B; Guzior, N; Höfner, GC; Kowalczyk, P; Kulig, K; Sałat, K; Wanner, KT1
Höfner, G; Renukappa-Gutke, T; Steffan, T; Wanner, KT1
Borkar, N; Clausen, RP; Ecker, GF; Jurik, A; Jørgensen, L; Madsen, KK; Nielsen, B; Rosatelli, E; Schousboe, A; Vogensen, SB1
Höfner, G; Tóth, K; Wanner, KT2
Hauke, TJ; Höfner, G; Wanner, KT1
Fijałkowski, Ł; Furgała, A; Gryzło, B; Höfner, GC; Kulig, K; Malawska, B; Malawska, K; Nowaczyk, A; Podkowa, A; Rapacz, A; Sałat, K; Wanner, KT; Zaręba, P; Żmudzki, P1
Bajda, M; Filipek, B; Höfner, GC; Jóźwiak, K; Kotniewicz, K; Kulig, K; Latacz, G; Maj, M; Malawska, B; Podkowa, A; Rapacz, A; Sałat, K; Wanner, KT; Zaręba, P; Łątka, K1

Other Studies

11 other study(ies) available for tiagabine and snap 5114

ArticleYear
Design, synthesis and evaluation of substituted triarylnipecotic acid derivatives as GABA uptake inhibitors: identification of a ligand with moderate affinity and selectivity for the cloned human GABA transporter GAT-3.
    Journal of medicinal chemistry, 1994, Jul-22, Volume: 37, Issue:15

    Topics: Animals; Binding Sites; Biological Transport; Blood-Brain Barrier; Carrier Proteins; Cell Line; Cloning, Molecular; Drug Design; GABA Antagonists; GABA Plasma Membrane Transport Proteins; gamma-Aminobutyric Acid; Humans; Ligands; Membrane Proteins; Membrane Transport Proteins; Nipecotic Acids; Organic Anion Transporters; Proline; Rats

1994
Synthesis and biological evaluation of aminomethylphenol derivatives as inhibitors of the murine GABA transporters mGAT1-mGAT4.
    European journal of medicinal chemistry, 2008, Volume: 43, Issue:11

    Topics: Animals; Benzylamines; Cell Line; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; gamma-Aminobutyric Acid; Humans; Methylation; Mice; Molecular Structure; Structure-Activity Relationship

2008
Azetidine derivatives as novel gamma-aminobutyric acid uptake inhibitors: synthesis, biological evaluation, and structure-activity relationship.
    European journal of medicinal chemistry, 2010, Volume: 45, Issue:6

    Topics: Animals; Azetidines; Biological Transport; Cattle; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; gamma-Aminobutyric Acid; Inhibitory Concentration 50; Structure-Activity Relationship

2010
2-Substituted 4-hydroxybutanamides as potential inhibitors of γ-aminobutyric acid transporters mGAT1-mGAT4: synthesis and biological evaluation.
    Bioorganic & medicinal chemistry, 2013, Sep-01, Volume: 21, Issue:17

    Topics: Amides; Animals; Behavior, Animal; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; HEK293 Cells; Humans; Male; Mice; Mice, Knockout; Protein Binding; Protein Isoforms

2013
Design, synthesis and SAR studies of GABA uptake inhibitors derived from 2-substituted pyrrolidine-2-yl-acetic acids.
    Bioorganic & medicinal chemistry, 2015, Mar-15, Volume: 23, Issue:6

    Topics: Animals; Dose-Response Relationship, Drug; Drug Design; GABA Plasma Membrane Transport Proteins; HEK293 Cells; Humans; Mice; Molecular Structure; Proline; Structure-Activity Relationship

2015
Structure activity relationship of selective GABA uptake inhibitors.
    Bioorganic & medicinal chemistry, 2015, May-15, Volume: 23, Issue:10

    Topics: Amino Acids; Animals; Carrier Proteins; GABA Agonists; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; HEK293 Cells; Humans; Ligands; Mice; Molecular Docking Simulation; Molecular Structure; Nipecotic Acids; Protein Isoforms; Structure-Activity Relationship; Tiagabine

2015
Synthesis and biological evaluation of novel N-substituted nipecotic acid derivatives with an alkyne spacer as GABA uptake inhibitors.
    Bioorganic & medicinal chemistry, 2018, 07-23, Volume: 26, Issue:12

    Topics: Alkynes; Animals; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; gamma-Aminobutyric Acid; HEK293 Cells; Humans; Mice; Nipecotic Acids; Protein Isoforms; Structure-Activity Relationship

2018
Generation and screening of pseudostatic hydrazone libraries derived from 5-substituted nipecotic acid derivatives at the GABA transporter mGAT4.
    Bioorganic & medicinal chemistry, 2019, 01-01, Volume: 27, Issue:1

    Topics: Animals; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; HEK293 Cells; Humans; Hydrazones; Mice; Molecular Structure; Nipecotic Acids; Small Molecule Libraries; Structure-Activity Relationship

2019
Synthesis and biological evaluation of novel N-substituted nipecotic acid derivatives with a cis-alkene spacer as GABA uptake inhibitors.
    Bioorganic & medicinal chemistry, 2019, 03-01, Volume: 27, Issue:5

    Topics: Alkenes; Animals; Drug Design; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; HEK293 Cells; Humans; Mice; Nipecotic Acids; Stereoisomerism; Structure-Activity Relationship; Tiagabine

2019
Novel mouse GABA uptake inhibitors with enhanced inhibitory activity toward mGAT3/4 and their effect on pain threshold in mice.
    European journal of medicinal chemistry, 2020, Feb-15, Volume: 188

    Topics: Analgesics; Animals; Diabetes Mellitus, Experimental; GABA Plasma Membrane Transport Proteins; GABA Uptake Inhibitors; Hyperalgesia; Male; Mice; Molecular Docking Simulation; Molecular Structure; Neuralgia; Oxaliplatin; Pain Threshold; Protein Binding; Streptozocin; Structure-Activity Relationship

2020
Development of tricyclic N-benzyl-4-hydroxybutanamide derivatives as inhibitors of GABA transporters mGAT1-4 with anticonvulsant, antinociceptive, and antidepressant activity.
    European journal of medicinal chemistry, 2021, Oct-05, Volume: 221

    Topics: Amides; Analgesics; Anticonvulsants; Antidepressive Agents; Dose-Response Relationship, Drug; Drug Development; GABA Uptake Inhibitors; Humans; Molecular Structure; N-Acetylglucosaminyltransferases; Structure-Activity Relationship

2021