ACS Medicinal Chemistry Letters

Papers
(The H4-Index of ACS Medicinal Chemistry Letters is 30. 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 2022-08-01 to 2026-08-01.)
ArticleCitations
Psychiatric Treatments with Short-Duration Psychedelics and AI-Driven Behavioral Monitoring163
Discovery of Tumor-Targeted 6-Methyl Substituted Pemetrexed and Related Antifolates with Selective Loss of RFC Transport139
Issue Editorial Masthead92
Issue Publication Information74
Cancer-Cell-Selective Targeting by Arylcyclopropylamine–Vorinostat Conjugates62
Clozapine as an E3 Ligand for PROTAC Technology56
Tryptamines and Mental Health: Activating the 5-HT Receptor for Therapeutic Potential53
Polybromo-1 Bromodomain Inhibitor Selectivity Is Mediated by a Unique Ligand-Binding Pocket51
Novel PSMA-Targeting Radionuclide Peptidomimetics for Treating Prostate Cancer48
Design and Synthesis of a Structurally Stabilized B-Chain Antagonist Targeting Relaxin Family Peptide Receptor 3 (RXFP3)48
Novel Heterocyclic Pyrimidine Derivatives as GSK3α Inhibitors46
Novel Tetrahydrobenzo[b]pyrazolo[3,4-e][1,4]diazepine Compounds as Oxytocin Receptor Agonists for Treating Autism Spectrum Disorders44
In This Issue, Volume 14, Issue 543
Call for Papers: Fungal Pathogens – Life Cycle, Infection, Host Immunity and Drug Discovery41
Novel Phosphorylpurinone Compounds for Treating Cancer40
Methyl and Fluorine Effects in Novel Orally Bioavailable Keap1–Nrf2 PPI Inhibitor39
Design and Characterization of 1,3-Dihydro-2H-benzo[d]azepin-2-ones as Rule-of-5 Compliant Bivalent BET Inhibitors39
Emerging Techniques in Cancer Therapy: Precision Targeting for Improved Outcomes38
Discovery of Pyridopyrazine Inverse Agonists Targeting G Protein-Coupled Receptor 637
Modulation of Cancer Networks through Protein Degradation, DNA Repair Inhibition, and Quantitative Interactomics36
Discovery of Niclosamide Analogs with Potent Mitochondrial Uncoupling Activity and Reduced Mitochondrial Inhibition–Associated Toxicity36
Multimodal Control of STAT6 Signaling through Small-Molecule Modulation and Targeted Degradation33
Discovery of Orally Bioavailable FGFR2/FGFR3 Dual Inhibitors via Structure-Guided Scaffold Repurposing Approach33
Structure–Activity Relationship and In Silico Evaluation of cis- and trans-PCPA-Derived Inhibitors of LSD1 and LSD233
Introducing the Potential Binding Interface between the TRAIL-Mimicking Peptide and DR5 via Alanine Scan32
Application of Deuterated N,N-Dimethyltryptamine in the Potential Treatment of Psychiatric and Neurological Disorders31
Discovery of Quinazolinone Derivatives as Potent PARP1 Inhibitors31
Identification and Optimization of Small Molecule Pyrazolopyrimidine TLR7 Agonists for Applications in Immuno-oncology31
Conformationally Restricted Analogues of α-Galactosylceramide as Adjuvant in COVID-19 Subunit Vaccine30
Targeting the “Undruggable” Driver Protein, KRASG12D, as Potential Therapy in Prostate Cancer30
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