Compounds > 1-aminoisoquinoline
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1-aminoisoquinoline and alpha-aminopyridine

1-aminoisoquinoline has been researched along with alpha-aminopyridine in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Jones, M; Milliner, KJ; Rana, KK; Ward, JG; Young, RC1
Caldwell, CG; Chabin, RM; Chen, P; Durette, PL; Esser, CK; Fletcher, D; Grant, SK; Green, BG; Guthikonda, R; Hagmann, WK; Humes, JL; Kelly, TM; Kopka, IE; Lanza, TJ; Luell, S; MacCoss, M; Meurer, R; Moore, V; Pacholok, SG; Pavia, T; Shah, SK; Williams, HR; Wong, KK1
Booker, GW; Branson, KM; Cawthray, JF; Fritz, D; Inglis, SR; Pyke, SM; Stojkoski, C; Wiadrowski, E1
Ackermann, B; Erdel, V; Ferner, J; Göbel, MW; Kalden, E; Scheffer, U; Schwalbe, H; Shoja-Bazargani, F; Stark, S; Zeiger, M1
Bach, A; Bucciarelli, S; Gotfredsen, CH; Høj, LJ; Langkilde, AE; Meier, S; Narayanan, D; Sattler, M; Softley, C; Solbak, SMØ; Zang, J1

Other Studies

5 other study(ies) available for 1-aminoisoquinoline and alpha-aminopyridine

ArticleYear
Purine derivatives as competitive inhibitors of human erythrocyte membrane phosphatidylinositol 4-kinase.
    Journal of medicinal chemistry, 1990, Volume: 33, Issue:8

    Topics: 1-Phosphatidylinositol 4-Kinase; Adenine; Adenosine; Adenosine Triphosphate; Binding, Competitive; Chemical Phenomena; Chemistry; Erythrocyte Membrane; Humans; Molecular Structure; Phosphotransferases; Purines; Structure-Activity Relationship

1990
Substituted 2-aminopyridines as inhibitors of nitric oxide synthases.
    Bioorganic & medicinal chemistry letters, 2000, Sep-04, Volume: 10, Issue:17

    Topics: Aminopyridines; Enzyme Inhibitors; Humans; Nitric Oxide Synthase; Structure-Activity Relationship

2000
Identification and specificity studies of small-molecule ligands for SH3 protein domains.
    Journal of medicinal chemistry, 2004, Oct-21, Volume: 47, Issue:22

    Topics: Amino Acid Sequence; Aminoquinolines; Animals; Binding Sites; Binding, Competitive; Fluorescence Polarization; Ligands; Magnetic Resonance Spectroscopy; Mice; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Proline; Protein-Tyrosine Kinases; Quinazolines; Sequence Alignment; src Homology Domains; Structure-Activity Relationship

2004
Fragment based search for small molecule inhibitors of HIV-1 Tat-TAR.
    Bioorganic & medicinal chemistry letters, 2014, Dec-15, Volume: 24, Issue:24

    Topics: Amino Acid Sequence; Base Sequence; Binding Sites; HIV Long Terminal Repeat; HIV-1; Humans; Ligands; Magnetic Resonance Spectroscopy; Nucleic Acid Conformation; RNA, Viral; Small Molecule Libraries; tat Gene Products, Human Immunodeficiency Virus

2014
Developing Inhibitors of the p47phox-p22phox Protein-Protein Interaction by Fragment-Based Drug Discovery.
    Journal of medicinal chemistry, 2020, 02-13, Volume: 63, Issue:3

    Topics: Azoles; Drug Discovery; Humans; Indoles; Isoindoles; Molecular Structure; NADPH Oxidase 2; NADPH Oxidases; Organoselenium Compounds; Protein Binding; Structure-Activity Relationship

2020