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19 articles for thisTarget


The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
27658368 54 Design and synthesis of selective, dual fatty acid binding protein 4 and 5 inhibitors.EBI F. Hoffmann-La Roche
27460668 18 The discovery of novel and selective fatty acid binding protein 4 inhibitors by virtual screening and biological evaluation.EBI Chinese Academy of Sciences
25461324 18 Novel fatty acid binding protein 4 (FABP4) inhibitors: virtual screening, synthesis and crystal structure determination.EBI Chinese Academy of Sciences
24581547 11 Interaction kinetics of liposome-incorporated unsaturated fatty acids with fatty acid-binding protein 3 by surface plasmon resonance.EBI Osaka University
23395658 49 Structure-guided design, synthesis and in vitro evaluation of a series of pyrazole-based fatty acid binding protein (FABP) 3 ligands.EBI Okayama University 1-1-1
21481589 14 New aromatic substituted pyrazoles as selective inhibitors of human adipocyte fatty acid-binding protein.EBI Chinese Academy of Sciences
20471252 22 Discovery of highly selective inhibitors of human fatty acid binding protein 4 (FABP4) by virtual screening.EBI Chinese Academy of Sciences
19754198 5 Identification and characterization of a small molecule inhibitor of Fatty Acid binding proteins.EBI University of Minnesota
19217286 45 N-Benzyl-indolo carboxylic acids: Design and synthesis of potent and selective adipocyte fatty-acid binding protein (A-FABP) inhibitors.EBI Biovitrum
17502136 66 Potent and selective biphenyl azole inhibitors of adipocyte fatty acid binding protein (aFABP).EBI Bristol-Myers Squibb Pharmaceutical Research Institute
15357970 26 Substituted benzylamino-6-(trifluoromethyl)pyrimidin-4(1H)-ones: a novel class of selective human A-FABP inhibitors.EBI Biovitrum
15357969 45 Discovery of inhibitors of human adipocyte fatty acid-binding protein, a potential type 2 diabetes target.EBI Biovitrum
32202425 47 Exploration of Fragment Binding Poses Leading to Efficient Discovery of Highly Potent and Orally Effective Inhibitors of FABP4 for Anti-inflammation.EBI Chinese Academy of Sciences
31420256 52 Identification of new dual FABP4/5 inhibitors based on a naphthalene-1-sulfonamide FABP4 inhibitor.EBI Fudan University
29803996 141 SAR studies on truxillic acid mono esters as a new class of antinociceptive agents targeting fatty acid binding proteins.EBI Stony Brook University
29775936 51 From hit to lead: Structure-based discovery of naphthalene-1-sulfonamide derivatives as potent and selective inhibitors of fatty acid binding protein 4.EBI Fudan University