Page last updated: 2024-08-21

quinazolines and 4-methylquinazoline

quinazolines has been researched along with 4-methylquinazoline in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's6 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ruther, J; Steiner, S; Thal, K1
Buellesbach, J; Gadau, J; Gibson, JD; Hanner, C; Judson, AK; Mutti, NS; Niehuis, O; Pothmann, D; Ruther, J; Schmitt, T1
Li, JX; Shen, Q; Wang, Y; Zhao, D; Zhu, MX1
Dinkel, V; Gloor, SL; Grina, J; Hansen, JD; Hastings, G; Laird, ER; Mathieu, S; Moreno, D; Rana, S; Rasor, K; Ren, L; Rudolph, J; Sturgis, HL; Vigers, G; Voegtli, WC; Wenglowsky, S; Willis, B1
Chen, J; Chen, X; Dong, Y; Ji, M; Jin, J; Li, Y; Lin, S; Lv, Y; Sheng, L; Wang, C; Wu, D; Xu, H; Zhang, J; Zhang, K1
Chen, X; Du, T; Fu, R; Ji, M; Jin, J; Li, Y; Lin, S; Liu, Y; Sheng, L; Tian, H; Wang, M; Wu, D; Xu, H; Zhang, J; Zhang, K; Zhang, Y1

Other Studies

6 other study(ies) available for quinazolines and 4-methylquinazoline

ArticleYear
Pheromone communication in Nasonia vitripennis: abdominal sex attractant mediates site fidelity of releasing males.
    Journal of chemical ecology, 2011, Volume: 37, Issue:2

    Topics: Abdomen; Animal Communication; Animals; Biological Assay; Female; Hymenoptera; Male; Quinazolines; Sex Attractants; Sexual Behavior, Animal

2011
Behavioural and genetic analyses of Nasonia shed light on the evolution of sex pheromones.
    Nature, 2013, Feb-21, Volume: 494, Issue:7437

    Topics: Animals; Biological Evolution; Female; Gene Knockdown Techniques; Genetic Speciation; Lactones; Male; Mating Preference, Animal; Molecular Sequence Data; Phylogeny; Quinazolines; Selection, Genetic; Sex Attractants; Species Specificity; Wasps

2013
Pd(0)-catalyzed benzylic arylation-oxidation of 4-methylquinazolines via sp3 C-H activation under air conditions.
    Organic & biomolecular chemistry, 2013, Oct-07, Volume: 11, Issue:37

    Topics: Air; Benzene; Catalysis; Molecular Structure; Oxidation-Reduction; Oxygen; Palladium; Quinazolines

2013
Highly potent and selective 3-N-methylquinazoline-4(3H)-one based inhibitors of B-Raf(V600E) kinase.
    Bioorganic & medicinal chemistry letters, 2014, Apr-15, Volume: 24, Issue:8

    Topics: Animals; Antineoplastic Agents; Crystallography, X-Ray; Drug Design; Enzyme Activation; Humans; Inhibitory Concentration 50; Molecular Structure; Protein Kinase Inhibitors; Proto-Oncogene Proteins B-raf; Quinazolines; Tumor Burden; Xenograft Model Antitumor Assays

2014
Discovery and Optimization of 2-Amino-4-methylquinazoline Derivatives as Highly Potent Phosphatidylinositol 3-Kinase Inhibitors for Cancer Treatment.
    Journal of medicinal chemistry, 2018, Jul-26, Volume: 61, Issue:14

    Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Drug Design; Enzyme Inhibitors; Humans; Molecular Docking Simulation; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Protein Conformation; Quinazolines; Signal Transduction; Structure-Activity Relationship

2018
Discovery of 4-Methylquinazoline Based PI3K Inhibitors for the Potential Treatment of Idiopathic Pulmonary Fibrosis.
    Journal of medicinal chemistry, 2019, 10-10, Volume: 62, Issue:19

    Topics: Animals; Bleomycin; Cell Line; Cell Proliferation; Crystallography, X-Ray; Drug Evaluation, Preclinical; Half-Life; Humans; Idiopathic Pulmonary Fibrosis; Isoenzymes; Lung; Mice; Mice, Inbred ICR; Molecular Conformation; Phosphatidylinositol 3-Kinases; Phosphoinositide-3 Kinase Inhibitors; Phosphorylation; Quinazolines; Signal Transduction; Structure-Activity Relationship

2019