aspartic acid has been researched along with imatinib mesylate in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (20.00) | 18.2507 |
2000's | 2 (40.00) | 29.6817 |
2010's | 2 (40.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Dan, S; Kizaki, A; Mashima, T; Naito, M; Seimiya, H; Tsuruo, T | 1 |
Dougan, DR; Kraus, ML; Mol, CD; Sang, BC; Scheibe, DN; Schneider, TR; Skene, RJ; Snell, GP; Wilson, KP; Zou, H | 1 |
Brownlow, N; Dibb, NJ; Domin, J; Taylor, JR | 1 |
Berner, JM; Bruland, ØS; Holm, R; Joensuu, H; Kristian, A; Malinen, E; Revheim, ME; Seierstad, T | 1 |
Bardaweel, SK; El-Abadelah, MM; Habashneh, AY; Taha, MO | 1 |
5 other study(ies) available for aspartic acid and imatinib mesylate
Article | Year |
---|---|
Activation of c-Abl tyrosine kinase requires caspase activation and is not involved in JNK/SAPK activation during apoptosis of human monocytic leukemia U937 cells.
Topics: Apoptosis; Aspartic Acid; Benzamides; Calcium-Calmodulin-Dependent Protein Kinases; Caspase Inhibitors; Caspases; Enzyme Activation; Humans; Imatinib Mesylate; JNK Mitogen-Activated Protein Kinases; Leukemia, Myeloid; Mitogen-Activated Protein Kinases; Piperazines; Proto-Oncogene Proteins c-abl; Pyrimidines; U937 Cells | 1999 |
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase.
Topics: Amino Acid Motifs; Amino Acid Sequence; Aspartic Acid; Benzamides; Catalytic Domain; Conserved Sequence; Crystallography, X-Ray; Enzyme Activation; Enzyme Inhibitors; Humans; Imatinib Mesylate; In Vitro Techniques; Models, Molecular; Molecular Sequence Data; Mutagenesis, Site-Directed; Piperazines; Protein Conformation; Proto-Oncogene Proteins c-kit; Pyrimidines; Receptor Protein-Tyrosine Kinases; Recombinant Proteins; Sequence Homology, Amino Acid; Static Electricity | 2004 |
FMS receptor for M-CSF (CSF-1) is sensitive to the kinase inhibitor imatinib and mutation of Asp-802 to Val confers resistance.
Topics: Animals; Antineoplastic Agents; Aspartic Acid; Benzamides; Disease Progression; Dose-Response Relationship, Drug; Down-Regulation; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Inflammation; Inhibitory Concentration 50; Macrophage Colony-Stimulating Factor; Mice; Mutation; Neoplasms; Oncogene Protein v-cbl; Phosphorylation; Piperazines; Protein Structure, Tertiary; Proto-Oncogene Proteins c-crk; Proto-Oncogene Proteins c-kit; Pyrimidines; Rats; Receptor Protein-Tyrosine Kinases; Receptor, Macrophage Colony-Stimulating Factor; Signal Transduction; Time Factors; Valine | 2006 |
Intermittent and continuous imatinib in a human GIST xenograft model carrying KIT exon 17 resistance mutation D816H.
Topics: Amino Acid Substitution; Animals; Antineoplastic Agents; Aspartic Acid; Benzamides; Drug Administration Schedule; Drug Resistance, Neoplasm; Gastrointestinal Neoplasms; Gastrointestinal Stromal Tumors; Histidine; Humans; Imatinib Mesylate; Mice; Mice, Nude; Mutation, Missense; Piperazines; Proto-Oncogene Proteins c-kit; Pyrimidines; Xenograft Model Antitumor Assays | 2013 |
Synthesis and Structure-Activity Relationship; Exploration of some Potent Anti-Cancer Phenyl Amidrazone Derivatives.
Topics: Antineoplastic Agents; Aspartic Acid; Cell Line, Tumor; Drug Screening Assays, Antitumor; Fusion Proteins, bcr-abl; Humans; Hydrazones; Hydrogen Bonding; Imatinib Mesylate; Ligands; Molecular Docking Simulation; Piperazines; Protein Binding; Structure-Activity Relationship; Threonine | 2018 |