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Results 1 - 10 of 666 > >>
EC Number BRENDA No. Title Journal Volume Pages Year Organism PubMed ID
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1761673 Development of potent inhibitors of receptor tyrosine kinases by ligand-based drug design and target-biased phenotypic screening J. Med. Chem. 61 2104-2110 2018 Homo sapiens 29466002
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1760677 Discovery and rational design of 2-aminopyrimidine-based derivatives targeting Janus kinase 2 (JAK2) and FMS-like tyrosine kinase 3 (FLT3) Bioorg. Chem. 104 104361 2020 Homo sapiens 33142418
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1760669 High levels of receptor tyrosine kinases in ccm3-deficient cells increase their susceptibility to tyrosine kinase inhibition Biomedicines 8 1-16 2020 Homo sapiens 33348877
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1761659 Mechanism of Mer receptor tyrosine kinase inhibition of glomerular endothelial cell inflammation J. Leukoc. Biol. 103 709-717 2018 Mus musculus 29350876
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1760845 Monitoring activities of receptor tyrosine kinases using a universal adapter in genetically encoded split TEV assays Cell. Mol. Life Sci. 76 1185-1199 2019 Homo sapiens 30623207
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1761882 Receptor tyrosine kinase signaling networks define sensitivity to ERBB inhibition and stratify KRAS-mutant lung cancers Mol. Cancer Ther. 18 1863-1874 2019 Homo sapiens 31320402
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1760838 RET functions as a dual-specificity kinase that requires allosteric inputs from juxtamembrane elements Cell Rep. 17 3319-3332 2016 Homo sapiens 28009299
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1762104 Synthesis and in vitro cytotoxicity of the 4-(halogenoanilino)-6-bromoquinazolines and their 6-(4-fluorophenyl) substituted derivatives as potential inhibitors of epidermal growth factor receptor tyrosine kinase Pharmaceuticals 10 87 2017 Homo sapiens 29156606
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1737831 4-Aminoindazolyl-dihydrofuro[3,4-d]pyrimidines as non-covalent inhibitors of mutant epidermal growth factor receptor tyrosine kinase Bioorg. Med. Chem. Lett. 26 534-539 2016 Homo sapiens 26639762
Display the word mapDisplay the reaction diagram Show all sequences 2.7.10.1737820 4-Substituted quinazoline derivatives as novel EphA2 receptor tyrosine kinase inhibitors Bioorg. Med. Chem. Lett. 24 4080-4083 2014 Homo sapiens 25124116
Results 1 - 10 of 666 > >>