Compounds > cisapride

cisapride and l 706000

cisapride has been researched along with l 706000 in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (60.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Bianucci, AM; Calderone, V; Coi, A; Massarelli, I; Testai, L1
Finley, MR; Freeman, LC; Ganta, S; Gilmour, RF; Hua, F; Li, Y; Lillich, J; Mitchell, KE1
Fernandez, D; Ghanta, A; Kauffman, GW; Sanguinetti, MC1
Aqvist, J; Boukharta, L; de Groot, BL; Karimi-Nejad, Y; Stary, A; Vriend, G; Wacker, SJ; Zachariae, U1
Gardner, A; Sanguinetti, MC; Wu, W1

Other Studies

5 other study(ies) available for cisapride and l 706000

ArticleYear
Identification of "toxicophoric" features for predicting drug-induced QT interval prolongation.
    European journal of medicinal chemistry, 2008, Volume: 43, Issue:11

    Topics: Amino Acid Sequence; Heart; Humans; Models, Molecular; Molecular Sequence Data; Molecular Structure; Protein Subunits; Sequence Alignment; Structure-Activity Relationship; Trans-Activators; Transcriptional Regulator ERG

2008
Expression and coassociation of ERG1, KCNQ1, and KCNE1 potassium channel proteins in horse heart.
    American journal of physiology. Heart and circulatory physiology, 2002, Volume: 283, Issue:1

    Topics: Action Potentials; Animals; Anti-Arrhythmia Agents; Benzopyrans; Cell Line; Cisapride; Cricetinae; ERG1 Potassium Channel; Ether-A-Go-Go Potassium Channels; Horses; Humans; Immunoblotting; Immunohistochemistry; In Vitro Techniques; KCNQ Potassium Channels; KCNQ1 Potassium Channel; Long QT Syndrome; Myocardium; Patch-Clamp Techniques; Piperidines; Potassium; Potassium Channel Blockers; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Binding; RNA, Messenger; Swine

2002
Physicochemical features of the HERG channel drug binding site.
    The Journal of biological chemistry, 2004, Mar-12, Volume: 279, Issue:11

    Topics: Amino Acid Motifs; Amino Acid Sequence; Animals; Benzopyrans; Binding Sites; Biophysical Phenomena; Biophysics; Cation Transport Proteins; Cisapride; Ether-A-Go-Go Potassium Channels; Histamine H1 Antagonists; Inhibitory Concentration 50; Kinetics; Models, Molecular; Molecular Sequence Data; Mutation; Oocytes; Phenylalanine; Piperidines; Point Mutation; Potassium Channels; Potassium Channels, Voltage-Gated; Protein Binding; Protein Structure, Tertiary; RNA, Complementary; Sequence Homology, Amino Acid; Serotonin Receptor Agonists; Temperature; Terfenadine; Tyrosine; Xenopus

2004
Toward a consensus model of the HERG potassium channel.
    ChemMedChem, 2010, Mar-01, Volume: 5, Issue:3

    Topics: Amino Acid Sequence; Benzopyrans; Cisapride; Crystallography, X-Ray; Ether-A-Go-Go Potassium Channels; Humans; Molecular Dynamics Simulation; Molecular Sequence Data; Piperidines; Protein Binding; Protein Conformation; Protein Structure, Tertiary; Sequence Alignment; Terfenadine

2010
The Link between Inactivation and High-Affinity Block of hERG1 Channels.
    Molecular pharmacology, 2015, Volume: 87, Issue:6

    Topics: Animals; Benzopyrans; Cisapride; Ether-A-Go-Go Potassium Channels; Female; Humans; Ion Channel Gating; Oocytes; Patch-Clamp Techniques; Phenethylamines; Piperidines; Point Mutation; Potassium Channel Blockers; Protein Multimerization; Protein Subunits; Sulfonamides; Xenopus laevis

2015