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63 articles for thisTarget

The following articles (labelled with PubMed ID or TBD) are for your review
PMIDDataArticle TitleOrganization
27888721 14 Discovery of resveratrol derivatives as novel LSD1 inhibitors: Design, synthesis and their biological evaluation.EBI Xinxiang Medical University
28435523 9 Discovery of [1,2,3]Triazolo[4,5-EBI Key Laboratory of Technology of Drug Preparation (Zhengzhou University)
28065500 8 Activation of lysine-specific demethylase 1 inhibitor peptide by redox-controlled cleavage of a traceless linker.EBI Nagoya City University
27046190 10 Impact of Binding Site Comparisons on Medicinal Chemistry and Rational Molecular Design.EBI TU Dortmund University
27105028 1 Efficient synthesis of new antiproliferative steroidal hybrids using the molecular hybridization approach.EBI Zhengzhou University
26710088 248 Recent Progress in Histone Demethylase Inhibitors.EBI University of Oxford
26819657 8 Cyclopropanamine Compounds and Use Thereof.EBI Temple University
26700437 32 Identification of SNAIL1 Peptide-Based Irreversible Lysine-Specific Demethylase 1-Selective Inactivators.EBI Kyoto Prefectural University of Medicine
26794039 12 Evaluation of phenylcyclopropylamine compounds by enzymatic assay of lysine-specific demethylase 2 in the presence of NPAC peptide.EBI Waseda University
26652247 60 3-(Piperidin-4-ylmethoxy)pyridine Containing Compounds Are Potent Inhibitors of Lysine Specific Demethylase 1.EBI Baylor College of Medicine
26086931 38 Strategies for the Discovery of Target-Specific or Isoform-Selective Modulators.EBI Shandong University
25699146 13 Pure Diastereomers of a Tranylcypromine-Based LSD1 Inhibitor: Enzyme Selectivity and In-Cell Studies.EBI Sapienza University of Roma
25768700 30 Pure enantiomers of benzoylamino-tranylcypromine: LSD1 inhibition, gene modulation in human leukemia cells and effects on clonogenic potential of murine promyelocytic blasts.EBI Sapienza University of Roma
25610955 53 Design, synthesis, and structure-activity relationship of novel LSD1 inhibitors based on pyrimidine-thiourea hybrids as potent, orally active antitumor agents.EBI Zhengzhou University
25827526 33 Histone H3 peptide based LSD1-selective inhibitors.EBI Waseda University
25725609 18 Structure-activity study for (bis)ureidopropyl- and (bis)thioureidopropyldiamine LSD1 inhibitors with 3-5-3 and 3-6-3 carbon backbone architectures.EBI John Hopkins University
25173853 50 Synthesis, biological activity and mechanistic insights of 1-substituted cyclopropylamine derivatives: a novel class of irreversible inhibitors of histone demethylase KDM1A.EBI European Institute of Oncology
24883177 10 Synthesis and evaluation of novel cyclic Peptide inhibitors of lysine-specific demethylase 1.EBI Medical University of South Carolina
24237195 46 High-throughput virtual screening identifies novel N'-(1-phenylethylidene)-benzohydrazides as potent, specific, and reversible LSD1 inhibitors.EBI University of Utah
24131029 90 Triazole-dithiocarbamate based selective lysine specific demethylase 1 (LSD1) inactivators inhibit gastric cancer cell growth, invasion, and migration.EBI Zhengzhou University
24007511 10 Nonpeptidic propargylamines as inhibitors of lysine specific demethylase 1 (LSD1) with cellular activity.EBI University of Freiburg
22876979 2 Low molecular weight amidoximes that act as potent inhibitors of lysine-specific demethylase 1.EBI Wayne State University
22975593 62 Oncoepigenomics: making histone lysine methylation count.EBI TBA
20568780 2 (Bis)urea and (bis)thiourea inhibitors of lysine-specific demethylase 1 as epigenetic modulators.EBI Wayne State University
21955276 60 Lysine demethylases inhibitors.EBI Kyoto Prefectural University of Medicine
21596573 46 Inhibitors of histone demethylases.EBI University of Copenhagen
21382717 19 Enantioselective synthesis of tranylcypromine analogues as lysine demethylase (LSD1) inhibitors.EBI University of Southampton
21227703 3 Synthesis and biological activity of optically active NCL-1, a lysine-specific demethylase 1 selective inhibitor.EBI Nagoya City University
28336409 14 Development and crystallographic evaluation of histone H3 peptide with N-terminal serine substitution as a potent inhibitor of lysine-specific demethylase 1.EBI Nagoya City University
28460360 13 Design, synthesis and biological activity of 3-oxoamino-benzenesulfonamides as selective and reversible LSD1 inhibitors.BDB China Pharmaceutical University
25346381 6 Identification of Novel Selective Lysine-Specific Demethylase 1 (LSD1) Inhibitors Using a Pharmacophore-Based Virtual Screening Combined with Docking.BDB China Pharmaceutical University
24707965 33 A Selective Phenelzine Analogue Inhibitor of Histone Demethylase LSD1.BDB Johns Hopkins University School of Medicine , Baltimore, Maryland 21205, United States
20568732 14 Structurally designed trans-2-phenylcyclopropylamine derivatives potently inhibit histone demethylase LSD1/KDM1 .BDB RIKEN Systems and Structural Biology Center