benzimidazole has been researched along with pyrimidine in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 2 (33.33) | 29.6817 |
2010's | 4 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brugel, TA; De, B; Easwaran, V; Evdokimov, A; Golebiowski, A; Hsieh, LC; Janusz, MJ; Laufersweiler, MJ; Maier, J; Mekel, MJ; Sabat, M; VanRens, JC; Walter, RL | 1 |
El-Gendy, Bel-D; Ghiviriga, I; Katritzky, AR; Steel, PJ | 1 |
Abdel-Mohsen, HT; El Diwani, HI; Ragab, FA; Ramla, MM | 1 |
Dhamanage, A; Kulkarni, S; Singh, A; Singh, RK; Yadav, D; Yadav, M | 1 |
Attia, YM; El Abd, YS; El Diwani, HI; El-Rashedy, AA; El-Shenawy, R; Galal, SA; Kandil, OM; Khattab, M; Ramadan, R; Shouman, SA; Tabll, A | 1 |
Abdelgawad, MA; Ahmad, W; Al-Sanea, MM; Bakr, RB; Elshemy, HAH | 1 |
6 other study(ies) available for benzimidazole and pyrimidine
Article | Year |
---|---|
The development of 2-benzimidazole substituted pyrimidine based inhibitors of lymphocyte specific kinase (Lck).
Topics: Benzimidazoles; Hydrogen Bonding; Inhibitory Concentration 50; Interleukin-2; Lymphocyte Specific Protein Tyrosine Kinase p56(lck); Molecular Structure; Protein Kinase Inhibitors; Proto-Oncogene Proteins c-hck; Pyrimidines; Structure-Activity Relationship | 2006 |
Tautomerism of guanidines studied by (15)N NMR: 2-hydrazono-3-phenylquinazolin-4(3H)-ones and related compounds.
Topics: Analgesics; Anti-Inflammatory Agents; Benzimidazoles; Crystallography, X-Ray; Drug Discovery; Guanine; Hydrazines; Isomerism; Magnetic Resonance Spectroscopy; Pyrimidines; Quinazolinones | 2009 |
Novel benzimidazole-pyrimidine conjugates as potent antitumor agents.
Topics: Antineoplastic Agents; Benzimidazoles; Cell Line, Tumor; Cell Proliferation; Humans; Lethal Dose 50; Pyrimidines | 2010 |
Molecular modeling, synthesis and biological evaluation of N-heteroaryl compounds as reverse transcriptase inhibitors against HIV-1.
Topics: Benzimidazoles; Binding Sites; Catalytic Domain; Cell Line; Cell Survival; Drug Design; Genotype; HIV Reverse Transcriptase; HIV-1; Humans; Hydrogen Bonding; Hydrophobic and Hydrophilic Interactions; Molecular Docking Simulation; Pyrimidines; Reverse Transcriptase Inhibitors; Structure-Activity Relationship; Virus Replication | 2015 |
Part III: Novel checkpoint kinase 2 (Chk2) inhibitors; design, synthesis and biological evaluation of pyrimidine-benzimidazole conjugates.
Topics: Benzimidazoles; Cell Cycle; Cell Proliferation; Checkpoint Kinase 2; Dose-Response Relationship, Drug; Drug Design; Humans; MCF-7 Cells; Models, Molecular; Molecular Structure; Protein Kinase Inhibitors; Pyrimidines; Structure-Activity Relationship | 2018 |
New pyrimidine-benzoxazole/benzimidazole hybrids: Synthesis, antioxidant, cytotoxic activity, in vitro cyclooxygenase and phospholipase A2-V inhibition.
Topics: Antineoplastic Agents; Antioxidants; Benzimidazoles; Benzoxazoles; Biphenyl Compounds; Cell Line, Tumor; Cell Proliferation; Cyclooxygenase 1; Cyclooxygenase 2; Cyclooxygenase Inhibitors; Dose-Response Relationship, Drug; Drug Screening Assays, Antitumor; Group V Phospholipases A2; Humans; Molecular Docking Simulation; Molecular Structure; Phospholipase A2 Inhibitors; Picrates; Pyrimidines; Structure-Activity Relationship | 2019 |