SLAS Discovery

Papers
(The TQCC of SLAS Discovery is 8. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
E3 Ligase Ligands for PROTACs: How They Were Found and How to Discover New Ones188
RNA-Dependent RNA Polymerase as a Target for COVID-19 Drug Discovery123
Probing the SAM Binding Site of SARS-CoV-2 Nsp14 In Vitro Using SAM Competitive Inhibitors Guides Developing Selective Bisubstrate Inhibitors59
High-Throughput Screening for Drugs That Inhibit Papain-Like Protease in SARS-CoV-244
Cryo-EM: The Resolution Revolution and Drug Discovery39
High-Throughput Imaging Assay for Drug Screening of 3D Prostate Cancer Organoids37
Recommended Guidelines for Developing, Qualifying, and Implementing Complex In Vitro Models (CIVMs) for Drug Discovery37
High-Throughput Mass Spectrometry for Hit Identification: Current Landscape and Future Perspectives35
Acoustic Ejection Mass Spectrometry: A Fully Automatable Technology for High-Throughput Screening in Drug Discovery34
Discovery of Drug-Like Ligands for the Mac1 Domain of SARS-CoV-2 Nsp332
In Vitro three-dimensional (3D) cell culture tools for spheroid and organoid models30
Development of a High-Throughput Screening Assay to Identify Inhibitors of the SARS-CoV-2 Guanine-N7-Methyltransferase Using RapidFire Mass Spectrometry30
Identification of Compounds for Butyrylcholinesterase Inhibition29
Using chemical and biological data to predict drug toxicity29
Selecting Approaches for Hit Identification and Increasing Options by Building the Efficient Discovery of Actionable Chemical Matter from DNA-Encoded Libraries28
Changing the HTS Paradigm: AI-Driven Iterative Screening for Hit Finding28
CDK Family PROTAC Profiling Reveals Distinct Kinetic Responses and Cell Cycle–Dependent Degradation of CDK227
Discovery of SARS-CoV-2 main protease covalent inhibitors from a DNA-encoded library selection26
Target Validation Using PROTACs: Applying the Four Pillars Framework26
Identification of potent small molecule inhibitors of SARS-CoV-2 entry25
A High-Throughput RNA Displacement Assay for Screening SARS-CoV-2 nsp10-nsp16 Complex toward Developing Therapeutics for COVID-1924
A Review of the Preclinical and Clinical Efficacy of Remdesivir, Hydroxychloroquine, and Lopinavir-Ritonavir Treatments against COVID-1924
A Tale of Two Tails: Efficient Profiling of Protein Degraders by Specific Functional and Target Engagement Readouts22
High-Throughput Quantitative Assay Technologies for Accelerating the Discovery and Optimization of Targeted Protein Degradation Therapeutics22
Comparison of Approaches for Determining Bioactivity Hits from High-Dimensional Profiling Data22
A High-Throughput Radioactivity-Based Assay for Screening SARS-CoV-2 nsp10-nsp16 Complex22
Validating ADME QSAR Models Using Marketed Drugs22
Public-Private Partnerships: Compound and Data Sharing in Drug Discovery and Development21
Comparative Analysis of Multiple Immunoassays for Cytokine Profiling in Drug Discovery21
Small-Molecule Degraders beyond PROTACs—Challenges and Opportunities21
Repurposing Nimesulide, a Potent Inhibitor of the B0AT1 Subunit of the SARS-CoV-2 Receptor, as a Therapeutic Adjuvant of COVID-1920
ASCT1 and ASCT2: Brother and Sister?19
Lead identification using 3D models of pancreatic cancer19
Label-Free Screening of SARS-CoV-2 NSP14 Exonuclease Activity Using SAMDI Mass Spectrometry18
The Problems of Applying Classical Pharmacology Analysis to Modern In Vitro Drug Discovery Assays: Slow Binding Kinetics and High Target Concentration18
Development of High-Throughput Assays for Evaluation of Hematopoietic Progenitor Kinase 1 Inhibitors18
A high throughput screening assay for inhibitors of SARS-CoV-2 pseudotyped particle entry18
Efficiency Improvements and Discovery of New Substrates for a SARS-CoV-2 Main Protease FRET Assay17
MALDI-TOF-Based Affinity Selection Mass Spectrometry for Automated Screening of Protein–Ligand Interactions at High Throughput17
Evaluating Very Deep Convolutional Neural Networks for Nucleus Segmentation from Brightfield Cell Microscopy Images17
Brief Guide: Experimental Strategies for High-Quality Hit Selection from Small-Molecule Screening Campaigns16
Discovery of the SMYD3 Inhibitor BAY-6035 Using Thermal Shift Assay (TSA)-Based High-Throughput Screening16
Detection and impact of hypoxic regions in multicellular tumor spheroid cultures formed by head and neck squamous cell carcinoma cells lines16
A Method for Determining the Kinetics of Small-Molecule-Induced Ubiquitination15
COMPARE Analysis, a Bioinformatic Approach to Accelerate Drug Repurposing against Covid-19 and Other Emerging Epidemics15
waveRAPID—A Robust Assay for High-Throughput Kinetic Screens with the Creoptix WAVEsystem15
A Scalable Approach Reveals Functional Responses of iPSC Cardiomyocyte 3D Spheroids15
The Vital Role of Proteomics in Characterizing Novel Protein Degraders14
Development of a Homogeneous Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) Assay for the Inhibition of Keap1–Nrf2 Protein–Protein Interaction13
CETSA MS Profiling for a Comparative Assessment of FDA-Approved Antivirals Repurposed for COVID-19 Therapy Identifies TRIP13 as a Remdesivir Off-Target13
Characterizations of the Urate Transporter, GLUT9, and Its Potent Inhibitors by Patch-Clamp Technique12
Luminescence Energy Transfer–Based Screening and Target Engagement Approaches for Chemical Biology and Drug Discovery12
Activity-Based Screening Assay for Mono-ADP-Ribosylhydrolases12
Optimization of a Colorimetric Assay to Determine Lactate Dehydrogenase B Activity Using Design of Experiments12
A Perspective on Synthetic Biology in Drug Discovery and Development—Current Impact and Future Opportunities12
Evolution and impact of high content imaging11
Operationalizing the Use of Biofabricated Tissue Models as Preclinical Screening Platforms for Drug Discovery and Development11
Development of high-throughput lacrimal gland organoid platforms for drug discovery in dry eye disease11
deepOrganoid: A brightfield cell viability model for screening matrix-embedded organoids11
Epithelial Barrier Integrity Profiling: Combined Approach Using Cellular Junctional Complex Imaging and Transepithelial Electrical Resistance11
Development of a Novel Label-Free and High-Throughput Arginase-1 Assay Using Self-Assembled Monolayer Desorption Ionization Mass Spectrometry11
Identification of Small-Molecule Inhibitors of Neutral Ceramidase (nCDase) via Target-Based High-Throughput Screening11
The Extensive and Expensive Impacts of HEp-2 [HeLa], Intestine 407 [HeLa], and Other False Cell Lines in Journal Publications11
Automation of Organoid Cultures: Current Protocols and Applications11
A multiparametric calcium signal screening platform using iPSC-derived cortical neural spheroids.10
Development of a high-throughput TR-FRET screening assay for LAG-3/FGL1 interaction10
Fragment-based screening: A new paradigm for ligand and target discovery10
Saporin, a Polynucleotide–Adenosine Nucleosidase, May Be an Efficacious Therapeutic Agent for SARS-CoV-2 Infection10
Hit Discovery for Public Target Programs in the European Lead Factory: Experiences and Output from Assay Development and Ultra-High-Throughput Screening10
High throughput screening of 0.5 million compounds against CRAF using Alpha CETSAⓇ9
Mass spectrometry-based proteomics of 3D cell culture: A useful tool to validate culture of spheroids and organoids9
Point-of-use, automated fabrication of a 3D human liver model supplemented with human adipose microvessels9
Multifunctional profiling of triple-negative breast cancer patient-derived tumoroids for disease modeling9
Development of a Testing Funnel for Identification of Small-Molecule Modulators Targeting Secretin Receptors8
Based on Principles and Insights of COVID-19 Epidemiology, Genome Sequencing, and Pathogenesis: Retrospective Analysis of Sinigrin and ProlixinRX (Fluphenazine) Provides Off-Label Drug Candidates8
Epithelial 3D-spheroids as a tool to study air pollutant-induced lung pathology8
High-Throughput Affinity Selection Mass Spectrometry Using SAMDI-MS to Identify Small-Molecule Binders of the Human Rhinovirus 3C Protease8
Regenerable Biosensors for Small-Molecule Kinetic Characterization Using SPR8
0.035609006881714