pyrimidine has been researched along with quinoline in 8 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (25.00) | 18.2507 |
| 2000's | 2 (25.00) | 29.6817 |
| 2010's | 3 (37.50) | 24.3611 |
| 2020's | 1 (12.50) | 2.80 |
| Authors | Studies |
|---|---|
| Barclay, LR; Crowe, E; Edwards, CD | 1 |
| Fetzner, S | 1 |
| Kaur, P; Kaur, S; Kumar, S; Luxami, V; Singh, P | 1 |
| Chen, CH; Hsu, MH; Huang, LJ; Hung, CY; Hwang, CS; Kuo, SC; Lee, O; Wu, CY | 1 |
| Cheng, M; Du, X; Gong, P; Li, P; Li, R; Lin, H; Tang, Q; Zhang, G; Zhao, Y; Zhu, W | 1 |
| Desai, NC; Kotadiya, GM; Trivedi, AR | 1 |
| Ahmed, N; Hassan, MI; Idrees, D; Khan, P; Parveen, I | 1 |
| Ademola, IK; Gordon, M; Karpoormath, R; Kayamba, F; Kushwaha, ND; Mahlalela, M; Malimabe, T; Mudau, PT; Nyamori, VO; Pooe, OJ; Shonhai, A; van Zyl, RL; Zininga, T | 1 |
8 other study(ies) available for pyrimidine and quinoline
| Article | Year |
|---|---|
Photo-initiated peroxidation of lipids in micelles by azaaromatics.
Topics: Antioxidants; Chromans; Free Radicals; Kinetics; Linoleic Acid; Linoleic Acids; Lipid Peroxidation; Micelles; Models, Chemical; Nicotinic Acids; Photochemistry; Purines; Pyridines; Pyrimidines; Quinolines | 1997 |
Bioconversion of pyrimidine by resting cells of quinoline-degrading bacteria.
Topics: Biodegradation, Environmental; Catalysis; Gram-Negative Aerobic Rods and Cocci; Hydroxylation; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Pseudomonas; Pyrimidines; Quinolines; Rhodococcus; Substrate Specificity; Uracil | 1999 |
Syntheses and anti-cancer activities of 2-[1-(indol-3-yl-/pyrimidin-5-yl-/pyridine-2-yl-/quinolin-2-yl)-but-3-enylamino]-2-phenyl-ethanols.
Topics: Antineoplastic Agents; Cell Proliferation; Drug Screening Assays, Antitumor; Humans; Indoles; Molecular Structure; Neoplasms; Pyridines; Pyrimidines; Quinolines; Structure-Activity Relationship; Tumor Cells, Cultured | 2007 |
Synthesis of 1-substituted 3-pyridinylmethylidenylindolin-2-ones and 1-substituted 3-quinolinylmethylidenylindolin-2-ones as the enhancers of ATRA-induced differentiation in HL-60 cells.
Topics: Cell Differentiation; Cell Proliferation; Cell Shape; HL-60 Cells; Humans; Magnetic Resonance Spectroscopy; Methylation; Molecular Structure; Pyrimidines; Quinolines; Structure-Activity Relationship; Tretinoin | 2008 |
Discovery of novel 6,7-disubstituted-4-phenoxyquinoline derivatives bearing 5-(aminomethylene)pyrimidine-2,4,6-trione moiety as c-Met kinase inhibitors.
Topics: Antineoplastic Agents; Binding Sites; Cell Line, Tumor; Cell Survival; Drug Evaluation, Preclinical; Enzyme Activation; HT29 Cells; Humans; Molecular Docking Simulation; Protein Kinase Inhibitors; Protein Structure, Tertiary; Proto-Oncogene Proteins c-met; Pyrimidines; Quinolines; Structure-Activity Relationship | 2014 |
Studies on molecular properties prediction, antitubercular and antimicrobial activities of novel quinoline based pyrimidine motifs.
Topics: Anti-Bacterial Agents; Antitubercular Agents; Bacteria; Cell Proliferation; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; HeLa Cells; Humans; Microbial Sensitivity Tests; Molecular Structure; Pyrimidines; Quinolines; Structure-Activity Relationship | 2014 |
Synthesis, estrogen receptor binding affinity and molecular docking of pyrimidine-piperazine-chromene and -quinoline conjugates.
Topics: Antineoplastic Agents; Benzopyrans; Binding Sites; Cell Proliferation; Cell Survival; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; HEK293 Cells; Humans; MCF-7 Cells; Molecular Docking Simulation; Molecular Structure; Piperazine; Piperazines; Proto-Oncogene Proteins c-bcl-2; Pyrimidines; Quinolines; Structure-Activity Relationship | 2017 |
Design and synthesis of quinoline-pyrimidine inspired hybrids as potential plasmodial inhibitors.
Topics: Antimalarials; Cell Survival; Dose-Response Relationship, Drug; Drug Design; HEK293 Cells; Humans; Models, Molecular; Molecular Structure; Parasitic Sensitivity Tests; Plasmodium falciparum; Pyrimidines; Quinolines; Structure-Activity Relationship; Thermodynamics | 2021 |