ACS Chemical Biology

Papers
(The H4-Index of ACS Chemical Biology is 34. 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 2021-08-01 to 2025-08-01.)
ArticleCitations
Simple Enzymatic Incorporation of 2′OMeU Nucleotide at the End of the Poly-A Tail for Enhancement of the mRNA Stability and Protein Expression228
Introducing Our Authors106
Introducing Our Authors104
A Robust α-l-Fucosidase from Prevotella nigrescens for Glycoengineering Therapeutic Antibodies94
Molecular Targeted Engagement of DPP9 in Rat Tissue Using CETSA, SP3 Processing, and Absolute Quantitation Mass Spectrometry83
Visualization of Ectopic Serine Protease Activity by Förster Resonance Energy Transfer-Based Reporters68
Antimicrobial Lasso Peptide Cloacaenodin Utilizes a Unique TonB-Dependent Transporter to Access Susceptible Bacteria64
Correction to “Characterization of the Iron–Sulfur Cluster in the NCOA4 Fragment (383–522) and Its Interaction with Ferritin”62
Spatiotemporal Proximity Labeling Tools to Track GlcNAc Sugar-Modified Functional Protein Hubs during Cellular Signaling58
Multi-TACs: Targeting Solid Tumors with Multiple Immune Cell Co-engagers57
Discovery of Small-Molecule Inhibitors of the PTK7/β-Catenin Interaction Targeting the Wnt Signaling Pathway in Colorectal Cancer54
Ferroptosis Inhibitors Suppress Prostaglandin Synthesis in Lipopolysaccharide-Stimulated Macrophages54
Targeting IRAK3 for Degradation to Enhance IL-12 Pro-inflammatory Cytokine Production52
Structural and Biochemical Insights into Lignin-Oxidizing Activity of Bacterial Peroxidases against Soluble Substrates and Kraft Lignin49
Target-Responsive DNA Hydrogels with Encapsulation and Release Properties Using Programmable CRISPR-Cas12a49
In Situ Labeling of Pathogenic Tau Using Photo-Affinity Chemical Probes47
Dynamic Regulation of 5-Formylcytidine on tRNA45
Robust Chemoenzymatic Synthesis of Keratinimicin Aglycone Analogues Facilitated by the Structure and Selectivity of OxyB45
Reengineering of Circularly Permuted Caspase-2 to Enhance Enzyme Stability and Enable Crystallographic Studies44
Repurposing of the RIPK1-Selective Benzo[1,4]oxazepin-4-one Scaffold for the Development of a Type III LIMK1/2 Inhibitor43
Dichlorophenylpyridine-Based Molecules Inhibit Furin through an Induced-Fit Mechanism42
Chemical Synthetic Lethality Screens Identify Selective Drug Combinations against Pseudomonas aeruginosa42
Biosynthesis of Physcion and Identification of an O-Methyltransferase with C6–OH Selectivity in Aspergillus chevalieri BYST0141
Spontaneous Cleavage at Glu and Gln Residues in Long-Lived Proteins40
Deposition Bias of Chromatin Proteins Inverts under DNA Replication Stress Conditions40
Structure and Function of the β-Asp-Arg Polymerase Cyanophycin Synthetase 240
A Nonfunctional Halogenase Masquerades as an Aromatizing Dehydratase in Biosynthesis of Pyrrolic Polyketides by Type I Polyketide Synthases39
Enzymatic Macrolactamization of mRNA Display Libraries for Inhibitor Selection39
HiBiT-SpyTag: A Minimal Tag for Covalent Protein Capture and Degrader Development39
An Inherent Difference between Serine and Threonine Phosphorylation: Phosphothreonine Strongly Prefers a Highly Ordered, Compact, Cyclic Conformation38
Issue Publication Information37
Enzymatic Pathway for Kupyaphore Degradation in Mycobacterium tuberculosis: Mechanism of Metal Homeostasis and Turnover36
Discovery and Validation of a Novel Class of Necroptosis Inhibitors Targeting RIPK135
Issue Editorial Masthead35
Analysis of the Valgamicin Biosynthetic Pathway Reveals a General Mechanism for Cyclopropanol Formation across Diverse Natural Product Scaffolds34
Mechanistic Studies on Dehydration in Class V Lanthipeptides34
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