urea has been researched along with imatinib mesylate in 17 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (11.76) | 29.6817 |
2010's | 8 (47.06) | 24.3611 |
2020's | 7 (41.18) | 2.80 |
Authors | Studies |
---|---|
Barnes, JC; Bradley, P; Day, NC; Fourches, D; Reed, JZ; Tropsha, A | 1 |
Breitenstein, W; Brüggen, J; Cowan-Jacob, SW; Furet, P; Manley, PW; Mestan, J; Meyer, T | 1 |
Akizawa, T; Iyoda, M; Kawaguchi, M; Shibata, T; Yamaoka, T | 1 |
Ashihara, E; Kimura, S; Lyons, JF; Maekawa, T; Nagao, R; Ottmann, OG; Reule, M; Smyth, T; Squires, MS; Takeuchi, M; Tanaka, R; Thompson, NT; Yamauchi, T; Yao, H; Yokota, A | 1 |
Brdar, I; Deng, X; Faessler, R; Mani, NS; Roessler, A; Sales, ZS; Wu, J | 1 |
Gallipoli, P; Holyoake, T; Jørgensen, H; Lyons, J; Shah, M | 1 |
Fang, Z; Hong, S; Hong, SS; Jung, KH; Kim, J; Kim, SJ; Lee, H; Shin, S; Son, MK; Yan, HH; Yun, SM | 1 |
Fang, Z; Hong, S; Hong, SS; Jung, KH; Kim, J; Kim, SJ; Lee, H; Lee, S; Lim, JH; Ryu, YL; Son, MK; Suh, JK; Yan, HH | 1 |
Jin, J; Lei, H; Li, X; Liu, M; Luo, H; Wu, Y; Xu, H; Yang, L | 1 |
Chang, JY; Chen, CT; Chen, LT; Hsu, T; Hsueh, CC; Jiaang, WT; Kung, FC; Lee, LC; Lin, HY; Lin, WH; Lu, CT; Peng, YH; Shiao, HY; Song, JS; Su, YC; Tsai, HJ; Tu, CH; Wang, PC; Wu, SY; Wu, TS; Yeh, TK | 1 |
Achour, H; Bauer, S; Blay, JY; Choucair, K; Gelderblom, H; George, S; Heinrich, MC; Mehren, MV; Nemunaitis, J; Ruiz-Soto, R; Schöffski, P; Zalcberg, J | 1 |
George, S; Serrano, C | 1 |
Dong, Z; Li, J | 1 |
Li, X; Meade, J; Ruiz-Soto, R; Shelton, MJ; Wang, J | 1 |
Cai, S; Cao, H; Deng, Y; Dong, J; Huang, Z; Li, J; Shen, L; Wu, X; Zhang, J; Zhou, Y | 1 |
Goggin, C; Huang, P; Jones, RL; Mahalingam, P; Napolitano, A; Smith, MJ; Stansfeld, A; Thway, K | 1 |
Charlab, R; Doros, L; Fashoyin-Aje, LA; Kumar, V; Lemery, SJ; Mushti, SL; Pazdur, R; Spehalski, EI; Tang, S; Theoret, MR; Thompson, M; Thompson, MD; Zhao, H | 1 |
2 review(s) available for urea and imatinib mesylate
Article | Year |
---|---|
Gastrointestinal Stromal Tumor: Challenges and Opportunities for a New Decade.
Topics: Apoptosis; Drug Resistance, Neoplasm; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Molecular Targeted Therapy; Naphthyridines; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-kit; Pyrazoles; Pyrroles; Receptor, Platelet-Derived Growth Factor alpha; Triazines; Urea | 2020 |
Ripretinib in advanced gastrointestinal stromal tumors: an overview of current evidence and drug approval.
Topics: Antineoplastic Agents; Drug Approval; Drug Resistance, Neoplasm; Gastrointestinal Neoplasms; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Mutation; Naphthyridines; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-kit; Urea | 2022 |
3 trial(s) available for urea and imatinib mesylate
Article | Year |
---|---|
Intrigue: Phase III study of ripretinib versus sunitinib in advanced gastrointestinal stromal tumor after imatinib.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Drug Resistance, Neoplasm; Female; Follow-Up Studies; Gastrointestinal Neoplasms; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Male; Middle Aged; Mutation; Naphthyridines; Prognosis; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-kit; Receptor, Platelet-Derived Growth Factor alpha; Research Design; Sunitinib; Survival Rate; Urea; Young Adult | 2020 |
Efficacy and Safety of Ripretinib in Chinese Patients with Advanced Gastrointestinal Stromal Tumors as a Fourth- or Later-Line Therapy: A Multicenter, Single-Arm, Open-Label Phase II Study.
Topics: China; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Naphthyridines; Sunitinib; Urea | 2022 |
FDA Approval Summary: Ripretinib for Advanced Gastrointestinal Stromal Tumor.
Topics: Adult; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Naphthyridines; Urea | 2023 |
12 other study(ies) available for urea and imatinib mesylate
Article | Year |
---|---|
Cheminformatics analysis of assertions mined from literature that describe drug-induced liver injury in different species.
Topics: Animals; Chemical and Drug Induced Liver Injury; Cluster Analysis; Databases, Factual; Humans; MEDLINE; Mice; Models, Chemical; Molecular Conformation; Quantitative Structure-Activity Relationship | 2010 |
Urea derivatives of STI571 as inhibitors of Bcr-Abl and PDGFR kinases.
Topics: Animals; Benzamides; Cell Line, Tumor; Genes, abl; Humans; Imatinib Mesylate; Mice; Piperazines; Protein Binding; Protein Kinase Inhibitors; Pyrimidines; Receptors, Platelet-Derived Growth Factor; Urea | 2004 |
Preventive and therapeutic effects of imatinib in Wistar-Kyoto rats with anti-glomerular basement membrane glomerulonephritis.
Topics: Animals; Basement Membrane; Benzamides; Creatinine; Glomerulonephritis; Imatinib Mesylate; Kidney Glomerulus; Macrophages; Piperazines; Protective Agents; Proteinuria; Pyrimidines; Rats; Rats, Wistar; Treatment Outcome; Urea | 2009 |
Activity of the multitargeted kinase inhibitor, AT9283, in imatinib-resistant BCR-ABL-positive leukemic cells.
Topics: Animals; Antineoplastic Agents; Benzamides; Benzimidazoles; Cell Proliferation; Drug Delivery Systems; Drug Resistance, Neoplasm; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Mice; Neoplasm Transplantation; Neoplasms, Experimental; Piperazines; Protein Kinase Inhibitors; Pyrimidines; Urea | 2010 |
Direct, metal-free amination of heterocyclic amides/ureas with NH-heterocycles and N-substituted anilines in POCl3.
Topics: Amides; Amination; Aniline Compounds; Anticholesteremic Agents; Azabicyclo Compounds; Benzamides; Catalysis; Chemistry, Pharmaceutical; Erlotinib Hydrochloride; Eszopiclone; Fluorobenzenes; Heterocyclic Compounds; Humans; Hydrogen-Ion Concentration; Hypnotics and Sedatives; Hypoglycemic Agents; Imatinib Mesylate; Molecular Structure; Phosphorus Compounds; Piperazines; Prescription Drugs; Protein Kinase Inhibitors; Pyrimidines; Quinazolines; Rosiglitazone; Rosuvastatin Calcium; Sulfonamides; Thiazolidinediones; Urea | 2011 |
Effects of the novel aurora kinase/JAK inhibitor, AT9283 and imatinib on Philadelphia positive cells in vitro.
Topics: Antineoplastic Agents; Aurora Kinases; Benzamides; Benzimidazoles; Cell Line, Tumor; Cell Survival; Cells, Cultured; Humans; Imatinib Mesylate; Janus Kinases; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Piperazines; Protein Kinase Inhibitors; Protein Serine-Threonine Kinases; Pyrimidines; Urea | 2012 |
HS-438, a new inhibitor of imatinib-resistant BCR-ABL T315I mutation in chronic myeloid leukemia.
Topics: Animals; Antineoplastic Agents; Apoptosis; Benzamides; Benzothiazoles; Binding Sites; Cell Cycle Checkpoints; Cell Line, Tumor; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Membrane Potential, Mitochondrial; Mice; Mice, Nude; Models, Molecular; Mutation; Piperazines; Protein Kinase Inhibitors; Pyrimidines; Time Factors; Tumor Burden; Urea | 2014 |
HS-543 induces apoptosis of Imatinib-resistant chronic myelogenous leukemia with T315I mutation.
Topics: Animals; Antineoplastic Agents; Apoptosis; Cell Line, Tumor; Cell Proliferation; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Male; Mice; Mice, Inbred BALB C; Mice, Nude; Models, Molecular; Mutation; Piperazines; Random Allocation; Signal Transduction; Urea; Xenograft Model Antitumor Assays | 2015 |
Chk1 inhibitors overcome imatinib resistance in chronic myeloid leukemia cells.
Topics: Animals; Apoptosis; Cell Line, Tumor; Cell Proliferation; Checkpoint Kinase 1; Drug Resistance, Neoplasm; Fusion Proteins, bcr-abl; Humans; Imatinib Mesylate; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Mice; Mice, Inbred BALB C; Pyrazoles; Pyrimidines; Thiophenes; Urea; Xenograft Model Antitumor Assays | 2018 |
Discovery of Conformational Control Inhibitors Switching off the Activated c-KIT and Targeting a Broad Range of Clinically Relevant c-KIT Mutants.
Topics: Animals; Binding Sites; Cell Line, Tumor; Cell Proliferation; Crystallography, X-Ray; Drug Evaluation, Preclinical; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Mice; Mice, Inbred ICR; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-kit; Pyrimidines; Structure-Activity Relationship; Urea; Xenograft Model Antitumor Assays | 2019 |
[Current status and progress in novel drug research for gastrointestinal stromal tumors].
Topics: Antineoplastic Agents; Drug Resistance, Neoplasm; Gastrointestinal Stromal Tumors; Humans; Imatinib Mesylate; Naphthyridines; Protein Kinase Inhibitors; Pyrazoles; Pyrroles; Triazines; Urea | 2020 |
Effects of CYP3A Inhibition, CYP3A Induction, and Gastric Acid Reduction on the Pharmacokinetics of Ripretinib, a Switch Control KIT Tyrosine Kinase Inhibitor.
Topics: Adult; Cytochrome P-450 CYP3A Inducers; Cytochrome P-450 CYP3A Inhibitors; Drug Therapy, Combination; Gastric Acid; Humans; Imatinib Mesylate; Itraconazole; Naphthyridines; Pantoprazole; Protein Kinase Inhibitors; Proton Pump Inhibitors; Rifampin; Urea | 2022 |