Cell Chemical Biology

Papers
(The H4-Index of Cell Chemical Biology is 42. 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 2020-05-01 to 2024-05-01.)
ArticleCitations
PROTACs: An Emerging Therapeutic Modality in Precision Medicine249
Targeted protein degradation: A promise for undruggable proteins120
The Chemical Biology of Ferroptosis in the Central Nervous System109
MGST1 is a redox-sensitive repressor of ferroptosis in pancreatic cancer cells101
Targeted degradation of transcription factors by TRAFTACs: TRAnscription Factor TArgeting Chimeras96
Chemoproteomics-enabled discovery of covalent RNF114-based degraders that mimic natural product function93
Targeted degradation of the enhancer lysine acetyltransferases CBP and p30086
Haven't got a glue: Protein surface variation for the design of molecular glue degraders81
The Chemical Biology of Reversible Lysine Post-translational Modifications80
Recent advances in identifying protein targets in drug discovery74
Discovery of a Functional Covalent Ligand Targeting an Intrinsically Disordered Cysteine within MYC69
Development of potent and selective inhibitors targeting the papain-like protease of SARS-CoV-267
Chemical Tools for Endogenous Protein Labeling and Profiling65
Introduction to Thiopeptides: Biological Activity, Biosynthesis, and Strategies for Functional Reprogramming64
Development of a potent and selective chemical probe for the pleiotropic kinase CK264
Expanding the arsenal of E3 ubiquitin ligases for proximity-induced protein degradation63
Seeing (and Using) the Light: Recent Developments in Bioluminescence Technology63
Illuminating RNA Biology: Tools for Imaging RNA in Live Mammalian Cells62
Targeted Degradation of SLC Transporters Reveals Amenability of Multi-Pass Transmembrane Proteins to Ligand-Induced Proteolysis61
Structure-Aided Development of Small-Molecule Inhibitors of ENPP1, the Extracellular Phosphodiesterase of the Immunotransmitter cGAMP59
Using the Oxytosis/Ferroptosis Pathway to Understand and Treat Age-Associated Neurodegenerative Diseases58
An E3 ligase guide to the galaxy of small-molecule-induced protein degradation57
Eradicating Bacterial Persisters with Combinations of Strongly and Weakly Metabolism-Dependent Antibiotics56
Inhibition of Resistance-Refractory P. falciparum Kinase PKG Delivers Prophylactic, Blood Stage, and Transmission-Blocking Antiplasmodial Activity55
The role of reversible and irreversible covalent chemistry in targeted protein degradation54
FADS2-dependent fatty acid desaturation dictates cellular sensitivity to ferroptosis and permissiveness for hepatitis C virus replication53
A Cell-Based Target Engagement Assay for the Identification of Cereblon E3 Ubiquitin Ligase Ligands and Their Application in HDAC6 Degraders52
Development of Potent, Selective Surrogate WNT Molecules and Their Application in Defining Frizzled Requirements52
An automatic pipeline for the design of irreversible derivatives identifies a potent SARS-CoV-2 Mpro inhibitor48
How to untie G-quadruplex knots and why?48
A biaryl-linked tripeptide from Planomonospora reveals a widespread class of minimal RiPP gene clusters47
Specific Knockdown of α-Synuclein by Peptide-Directed Proteasome Degradation Rescued Its Associated Neurotoxicity45
A Robust, GFP-Orthogonal Photoswitchable Inhibitor Scaffold Extends Optical Control over the Microtubule Cytoskeleton45
Modulating Androgen Receptor-Driven Transcription in Prostate Cancer with Selective CDK9 Inhibitors45
Context-dependent regulation of ferroptosis sensitivity44
HSP90 Inhibition Enhances Cancer Immunotherapy by Modulating the Surface Expression of Multiple Immune Checkpoint Proteins44
Chemo-proteomics exploration of HDAC degradability by small molecule degraders44
Chemogenomics identifies acetyl-coenzyme A synthetase as a target for malaria treatment and prevention44
Lanthanide-Based Optical Probes of Biological Systems44
Strategies for Tuning the Selectivity of Chemical Probes that Target Serine Hydrolases43
CRISPR-Mediated Protein Tagging with Nanoluciferase to Investigate Native Chemokine Receptor Function and Conformational Changes42
Targeting Endogenous K-RAS for Degradation through the Affinity-Directed Protein Missile System42
Inducible Degradation of Target Proteins through a Tractable Affinity-Directed Protein Missile System42
0.051255941390991