ACS Medicinal Chemistry Letters

Papers
(The median citation count of ACS Medicinal Chemistry Letters is 1. 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 2021-04-01 to 2025-04-01.)
ArticleCitations
Identification and Optimization of Small Molecule Pyrazolopyrimidine TLR7 Agonists for Applications in Immuno-oncology85
Novel Pyrazolopyrazine Compounds as SHP2 Inhibitors for Treating Glioblastoma84
Discovery of Selective Inhibitors of NaV1.7 Templated on Saxitoxin as Therapeutics for Pain68
When Cofactors Aren’t X Factors: Functional Groups That Are Labile in Human Liver Microsomes in the Absence of NADPH49
A Retrospective Look at the Impact of Binding Site Environment on the Optimization of TRPA1 Antagonists49
Issue Editorial Masthead48
Monoacylglycerol Lipase Modulators for Treating Autism Spectrum Disorders46
Issue Editorial Masthead44
In This Issue, Volume 14, Issue 543
1,2,4-Triazine Derivatives as NLRP3 Inhibitors for Treating Diseases39
Issue Editorial Masthead39
Pyridazine Derivatives as NLRP3 Inhibitors for Treating Asthma, COPD, Parkinson’s Disease, and Alzheimer’s Disease33
Effective Combination Therapies for the Treatment of HER2 Cancer33
Novel Tricyclic Compounds as KRAS Inhibitors for Treating Cancer33
Reducing the Toxicity of Designer Aminoglycosides as Nonsense Mutation Readthrough Agents for Therapeutic Targets33
Unraveling Psychedelic Responses: Targeted Protein Degradation and Genetic Diversity32
Issue Publication Information32
Innovative Therapeutic Strategies in TYK2-Targeted Treatments: From Cancer to Autoimmune Disorders31
Novel PARP1 Inhibitors for Treating Cancer31
Novel Phosphorylpurinone Compounds for Treating Cancer30
Targeting the “Undruggable” Driver Protein, KRASG12D, as Potential Therapy in Prostate Cancer28
Orally Active Forms of DMT, 5-MeO-DMT, and Long-Acting MDMA for the Treatment of Neuropsychiatric Disorders28
Issue Editorial Masthead27
Unveiling New KRASG12D Inhibitors: A Promising Approach for Pancreatic Cancer Therapy27
Emopamil-Binding Protein Inhibitors for Treating Multiple Sclerosis26
Molecular Biology Clues Portray SARS-CoV-2 as a Gain-of-Function Laboratory Manipulation of Bat CoV RaTG1325
Neurosteroids and Postpartum Depression: The Mechanism, Efficacy, and Approval of Brexanolone and Zurzuvae25
Discovery of the First Non-cGMP Mimetic Small Molecule Activators of cGMP-Dependent Protein Kinase 1 α (PKG1α)25
Novel Histone Acetyltransferase (HAT) Inhibitors for Treating Diseases24
Correction to “Sweet and Blind Spots in E3 Ligase Ligand Space Revealed by a Thermophoresis-Based Assay”24
Virtual Special Issue: Epigenetics 202224
Call for Papers: Fungal Pathogens – Life Cycle, Infection, Host Immunity and Drug Discovery24
Small Molecule Inhibitors of KRAS Mutant as a Therapeutic Strategy for the Treatment of Cancer23
Boron-Containing Pyrazole Compounds as JAK Inhibitors for Treating Inflammation, Autoimmune Diseases, and Cancer23
Issue Publication Information23
Resisting Clinical Translation from Bench to Bedside: The China Case of Liver Cancer Therapeutic Revolution23
Substituted 6,7-Dihydro-5H-Benzo[7]annulene Compounds as Selective Estrogen Receptor Degraders for Treating Cancer23
Fragment-Based Discovery of Novel MUS81 Inhibitors22
Novel Compounds for Treating Malaria22
Overcoming the Pregnane X Receptor Liability: Rational Design to Eliminate PXR-Mediated CYP Induction22
Potent PROTACs Targeting EGFR Mutants in Drug Discovery22
In This Issue, Volume 14, Issue 1221
Application of Deuterated N,N-Dimethyltryptamine in the Potential Treatment of Psychiatric and Neurological Disorders21
Targeting the Inhibition of B-Cell Lymphoma 2 Protein for the Treatment of Cancer21
Development of Highly Potent and Selective Pyrazolopyridine Inhibitor of CDK8/1921
Empowering Women in Organic Chemistry (EWOC) at Five Years: Giving Back and Getting Back21
Nitrogen-Containing 2,3-Dihydroquinazolinone Compounds as Nav1.8 Inhibitors for Treating Pain and Cardiovascular Diseases21
Call for Papers: The Many Faces of Medicinal Chemistry21
The Promiscuity of Disulfiram in Medicinal Research20
Novel RIPK1 Inhibitors for Treating Neurodegenerative, Autoimmune, and Inflammatory Diseases20
In This Issue, Volume 13, Issue 320
Spiro-naphthyridine Antagonists of the Melanocortin Receptor 4 for the Treatment of Cachexia Associated with Chronic Illness20
Application of Degradation of Cyclic-AMP Response Element Binding Protein for the Potential Treatment of Cancer19
Novel Spiropiperidine Allosteric Modulators of Nicotinic Acetylcholine Receptors for Treating Central Nervous System Disorders19
3-Pyrrolidine-indole Derivatives as 5-HT2-Selective Receptor Modulators for the Potential Treatment of Mental Disorders19
Issue Editorial Masthead18
Novel CD73 Inhibitors for Treating Cancer18
Expression of Concern for “Molecular Biology Clues Portray SARS-CoV-2 as a Gain-of-Function Laboratory Manipulation of Bat CoV RaTG13”18
Issue Editorial Masthead18
Issue Editorial Masthead18
Substituted 2,3-Benzodiazepines Derivatives as Bromodomain BRD4 Inhibitors17
Advancements in Predictive Medicine: NLRP3 Inflammasome Inhibitors and AI-Driven Predictive Health Analytics17
Psychedelic-Assisted Neuroplasticity for the Treatment of Mental Health Disorders16
Novel Substituted Heterocyclic Carboxamides as Adrenoreceptor ADRAC2 Inhibitors for Treating Diseases16
Potential Therapeutic Transdermal Psychoactive Drug Delivery Technology16
Call for Papers: Academic and Industrial Collaborations in Drug Discovery16
Sulfonamide Compounds as Orexin Receptor Agonists for Treating Sleep Disorders, Namely, Narcolepsy and Hypersomnia16
Novel KRAS Inhibitors for Treating Non-Small-Cell Lung Cancer16
Issue Editorial Masthead16
In This Issue, Volume 15, Issue 1016
Novel Heterocyclic Compounds as Delta-5-Desaturase Inhibitors for Treating Metabolic and Cardiovascular Diseases16
In This Issue, Volume 12, Issue 916
Mining for Ligandable Cavities in RNA16
Discovery of Novel Nonpeptidic Proteasome Inhibitors Using Covalent Virtual Screening and Biological Evaluation16
Carboxamide-Bearing Panobinostat Analogues Designed To Interact with E103-D104 at the Cavity Opening of Class I HDAC Isoforms15
Novel Cyclopentathiophene Carboxamide Derivatives as PAFR Antagonists for Treating Ocular Diseases, Allergies, and Inflammation-Related Diseases15
Issue Editorial Masthead15
Vinylpyridine as a Tunable Covalent Warhead Targeting C797 in EGFR15
Rapid Affinity and Microsomal Stability Ranking of Crude Mixture Libraries of Histone Deacetylase Inhibitors15
Novel Tricyclic KRAS Inhibitors for the Treatment of Cancer15
Clozapine as an E3 Ligand for PROTAC Technology15
Redefining Cancer Therapy: Toward BCL-XL/BCL-2 Dual Inhibitors with Diminished Platelet Toxicity15
Novel Compounds for Preventing SARS-CoV-2 Viral Replication and Treating COVID-1915
Psychiatric Treatments with Short-Duration Psychedelics and AI-Driven Behavioral Monitoring15
Novel Indoline Derivatives as Serotonergic Psychedelic Agents for Treating Psychosis, Mental Illness and CNS Disorders15
Dual Glycolate Oxidase/Lactate Dehydrogenase A Inhibitors for Primary Hyperoxaluria15
Enhancing the Stability of 211At Radiopharmaceuticals: Insights from Ortho-Substituent Strategies14
Novel Approaches in Biotechnology: Microbial Genetic Modifications and Metabolic Disease Therapies14
Novel 3-Pyrrolidineindole Derivatives as Serotonergic Psychedelic Agents for Treating Psychosis and Mental Illnesses Such as Depression and Post-Traumatic Stress Disorder14
Novel PARP7 Inhibitors for Treating Cancer14
Novel Bicyclic Heterocyclic Compounds as CD73 Inhibitors for Treating Cancer14
New ZW4864 Derivatives as Small-Molecule Inhibitors for the β-Catenin/BCL9 Protein–Protein Interaction14
Targeted Therapeutics in Oncology and Neurology: Advances in Kinase Inhibition and Biomarkers for Brain Injury14
Issue Publication Information14
In This Issue14
A Quantum Mechanics-Based Method to Predict Intramolecular Hydrogen Bond Formation Reflecting P-glycoprotein Recognition13
Discovery of Orally Bioavailable FGFR2/FGFR3 Dual Inhibitors via Structure-Guided Scaffold Repurposing Approach13
Unveiling Reality: Psychedelics, Neural Filtering, and the Future of Psychiatric Medicine13
Discovery of a Novel Series of Potent SHP2 Allosteric Inhibitors13
Emerging Techniques in Cancer Therapy: Precision Targeting for Improved Outcomes13
Synthesis and Preclinical Evaluation of a Bispecific PSMA-617/RM2 Heterodimer Targeting Prostate Cancer13
Issue Editorial Masthead13
A Brain-Penetrant and Bioavailable Pyrazolopiperazine BACE1 Inhibitor Elicits Sustained Reduction of Amyloid β In Vivo13
Imidazopyridine Compounds as ERK5 Inhibitors for Treating Cancer13
YMCC and YSN: An Opportunity for Scientific and Cultural Exchange13
Optimization of a Novel DEL Hit That Binds in the Cbl-b SH2 Domain and Blocks Substrate Binding13
Issue Publication Information13
Pyrazolopyridine and Triazolopyridine Derivatives as DGAT2 Inhibitors for Treating Multiple Diseases13
Heterocyclic Compounds as Dihydroorotate Dehydrogenase Inhibitors for Treating Acute Myelogenous Leukemia (AML)13
Optimization of mTOR Inhibitors Using Property-Based Drug Design and Free–Wilson Analysis for Improved In Vivo Efficacy13
In This Issue, Volume 15, Issue 613
Lipid Tales: Optimizing Arylomycin Membrane Anchors13
Highly Selective Novel Heme Oxygenase-1 Hits Found by DNA-Encoded Library Machine Learning beyond the DEL Chemical Space13
Design, Synthesis, and Biological Evaluation of 3-Amino-pyrazine-2-carboxamide Derivatives as Novel FGFR Inhibitors13
Novel Aminopyrazole Inhibitors of PDE11A for the Treatment of Alzheimer’s Disease and Other Types of Dementia13
Discovery of Imidazole-Based Inhibitors of Plasmodium falciparum cGMP-Dependent Protein Kinase12
Synthesis and Biological Characterization of a Series of 2-Sulfonamidebenzamides as Allosteric Modulators of MrgX112
Dodecaborate Conjugates Targeting Tumor Cell Overexpressing Translocator Protein for Boron Neutron Capture Therapy12
Fueling the Pipeline via Innovations in Organic Synthesis12
Rapid Evaluation of Small Molecule Cellular Target Engagement with a Luminescent Thermal Shift Assay12
Comprehensive Strategies to Bicyclic Prolines: Applications in the Synthesis of Potent Arginase Inhibitors12
17β-Hydroxysteroid Dehydrogenase Type 1 Inhibition: A Potential Treatment Option for Non-Small Cell Lung Cancer12
Azapodophyllotoxin Causes Lymphoma and Kidney Cancer Regression by Disrupting Tubulin and Monoglycerols12
Design and Synthesis of Tranylcypromine-Derived LSD1 Inhibitors with Improved hERG and Microsomal Stability Profiles12
Design and Evaluation of Bispidine-Based SARS-CoV-2 Main Protease Inhibitors12
RIBOTACs: Small Molecules Selectively Destroy Cancer-Associated RNA12
Discovery of Arylsulfonamide Nav1.7 Inhibitors: IVIVC, MPO Methods, and Optimization of Selectivity Profile12
Synthesis and Preclinical Evaluation of [68Ga]SP94 for Micro-PET Imaging of GRP78 Expression in Hepatocellular Carcinoma12
Design of Coibamide A Mimetics with Improved Cellular Bioactivity12
Flavonol-Based Carbon Monoxide Delivery Molecule with Endoplasmic Reticulum, Mitochondria, And Lysosome Localization12
Design, Synthesis, and Biological Evaluation of Apcin-Based CDC20 Inhibitors12
Piperazinyl Bicyclic Derivatives as Selective Ligands of the α2δ-1 Subunit of Voltage-Gated Calcium Channels12
Rational Control of Molecular Properties Is Mandatory to Exploit the Potential of PROTACs as Oral Drugs12
Design and Optimization of Novel Competitive, Non-peptidic, SARS-CoV-2 Mpro Inhibitors12
On the Selectivity of Heparan Sulfate Recognition by SARS-CoV-2 Spike Glycoprotein12
Exploring the Activity Profile of TbrPDEB1 and hPDE4 Inhibitors Using Free Energy Perturbation11
Structure–Activity Relationship and In Silico Evaluation of cis- and trans-PCPA-Derived Inhibitors of LSD1 and LSD211
Benzo[d]isoxazole Derivatives as Hypoxia-Inducible Factor (HIF)-1α Inhibitors11
2-Amino-1,3,4-thiadiazoles as Glutaminyl Cyclases Inhibitors Increase Phagocytosis through Modification of CD47-SIRPα Checkpoint11
Synthesis and Structural Characterization of Novel Trihalo-sulfone Inhibitors of WNK111
Examination of the Impact of Triazole Position within Linkers on Solubility and Lipophilicity of a CDK9 Degrader Series11
Binding versus Enzymatic Processing of ε-Trimethyllysine Dioxygenase Substrate Analogues11
Cancer-Cell-Selective Targeting by Arylcyclopropylamine–Vorinostat Conjugates11
Hydrophobic Tagging-Induced Degradation of PDEδ in Colon Cancer Cells11
Novel CA(1–7)M(2–9) Analogs: Synthesis, Characterization, and Antibacterial Evaluation11
Stereoisomers of an Aryl Pyrazole Glucocorticoid Receptor Agonist Scaffold Elicit Differing Anti-inflammatory Responses11
Inhibition of HIV-1 Protease by a Boronic Acid with High Oxidative Stability11
Discovery of MK-8768, a Potent and Selective mGluR2 Negative Allosteric Modulator11
Discovery of Insulin/GLP-1/Glucagon Triagonists for the Treatment of Diabetes and Obesity11
Using Imidazo[2,1-b][1,3,4]thiadiazol Skeleton to Design and Synthesize Novel MNK Inhibitors11
An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline11
Optimization of 1,2,4-Triazole-Based p97 Inhibitors for the Treatment of Cancer11
Development of Esterase-Resistant and Highly Active Ghrelin Analogs via Thiol–Ene Click Chemistry11
Discovery of Futibatinib: The First Covalent FGFR Kinase Inhibitor in Clinical Use11
Discovery of MK-1462: GLP-1 and Glucagon Receptor Dual Agonist for the Treatment of Obesity and Diabetes11
A Novel 7H-[1,2,4]Triazolo[3,4-b]thiadiazine-based Cystic Fibrosis Transmembrane Conductance Regulator Potentiator Directed toward Treatment of Cystic Fibrosis10
Discovery of Tumor-Targeted 6-Methyl Substituted Pemetrexed and Related Antifolates with Selective Loss of RFC Transport10
Novel 1,8-Naphthalimide Derivatives As Antitumor Agents and Potent Demethylase Inhibitors10
Design, Synthesis, and Biological Evaluation of SSE1806, a Microtubule Destabilizer That Overcomes Multidrug Resistance10
Correction to “Bespoke Drug Discovery Training for Low-Middle Income Countries”10
Design and Characterization of 1,3-Dihydro-2H-benzo[d]azepin-2-ones as Rule-of-5 Compliant Bivalent BET Inhibitors10
Fused Imidazopyrazine-Based Tubulin Polymerization Inhibitors Inhibit Neuroblastoma Cell Function10
Macrocyclic Oxindole Peptide Epoxyketones─A Comparative Study of Macrocyclic Inhibitors of the 20S Proteasome10
Fragment-Based NMR Screening of the BPTF PHD Finger Methyl Lysine Reader Leads to the First Small-Molecule Inhibitors10
Bespoke Drug Discovery Training for Low-Middle Income Countries10
Novel PSMA-Targeting Radionuclide Peptidomimetics for Treating Prostate Cancer10
PEG: The Magic Bullet for Biophysical Analysis of Highly Aggregating Small Molecules in Aqueous Solutions10
Rimonabant-Based Compounds Bearing Hydrophobic Amino Acid Derivatives as Cannabinoid Receptor Subtype 1 Ligands10
Conformationally Restricted Analogues of α-Galactosylceramide as Adjuvant in COVID-19 Subunit Vaccine10
Forgotten Natural Products: Semisynthetic Development of Blasticidin S As an Antibiotic Lead10
Nicotinamide Phosphoribosyltransferase Positive Allosteric Modulators Attenuate Neuronal Oxidative Stress10
2-Aminopyridines as Potent and Selective Nav1.8 Inhibitors Exhibiting Efficacy in a Nonhuman Primate Pain Model10
Modular One-Pot Strategy for the Synthesis of Heterobivalent Tracers10
Development of Allosteric NIK Ligands from Fragment-Based NMR Screening10
ATP Mimetic Attack on the Nucleotide-Binding Domain to Overcome ABC Transporter Mediated Chemoresistance10
Structure-Based Optimization of Selective and Brain Penetrant CK1δ Inhibitors for the Treatment of Circadian Disruptions10
Discovery of Malarial Threonyl tRNA Synthetase Inhibitors by Screening of a Focused Fragment Library10
SARS-CoV-2 Main Protease Inhibitors That Leverage Unique Interactions with the Solvent Exposed S3 Site of the Enzyme10
Selective Recognition of c-KIT 1 G-Quadruplex by Structural Tuning of Heteroaromatic Scaffolds and Side Chains10
Dose–Response Activity-Based DNA-Encoded Library Screening10
Structural Aspects of Mycobacterium tuberculosis DNA Gyrase Targeted by Novel Bacterial Topoisomerase Inhibitors9
Novel Thienopyrimidines as Acetyl-CoA Carboxylase Inhibitors for Treating Liver Diseases9
Structure–Activity Relationship for the Picolinamide Antibacterials that Selectively Target Clostridioides difficile9
Predictive Modeling and Drug Repurposing for Type-II Diabetes9
Neuroprotective Effect of 2-(Benzyloxy)arylureas Is Not Related to CypD Inhibition nor Suppression of mPTP Opening9
Synthesis of Monofluorinated 7-Hydroxycoumarin-3-Carboxamides as Cell-Permeable Fluorescent Molecular Probes9
Synthesis and in Vitro Evaluation of CAPE Derivatives as Ferroptosis Inducers in Triple Negative Breast Cancer9
Discovery of Ring-Annulated Analogues of Cannabidiol as Potential Anticancer Agents: Synthesis and Biological Evaluation9
Design, Synthesis, and Biological Evaluation of Imidazopyridines as PD-1/PD-L1 Antagonists9
A Putative Single-Photon Emission CT Imaging Tracer for Erythropoietin-Producing Hepatocellular A2 Receptor9
In Silico Targeting of the Long Noncoding RNA MALAT19
PROTAC-Mediated Degradation of Bruton’s Tyrosine Kinase as a Therapeutic Strategy for Cancer9
In This Issue, Volume 12, Issue 49
Systematical Mutational Analysis of FRATtide against Osteoclast Differentiation by Alanine Scanning9
2′-O-Alkyl-N3-Methyluridine Functionalized Passenger Strand Improves RNAi Activity by Modulating the Thermal Stability9
Synthesis and Optimization of Small Molecule Inhibitors of Prostate Specific Antigen9
ZX703: A Small-Molecule Degrader of GPX4 Inducing Ferroptosis in Human Cancer Cells9
Improving Activity of New Arylurea Agents against Multidrug-Resistant and Biofilm-Producing Staphylococcus epidermidis9
Synthesis and Biological Evaluation of 5′-Deoxy-adenosine Derivatives as A3 Adenosine Receptor Ligands9
Induction of Apoptosis in Cancer Cells by Glutathione Transferase Inhibitor Mediated Hydrophobic Tagging Molecules9
In This Issue, Volume 12, Issue 59
Radiosynthesis and Biological Evaluation of [18F]R91150, a Selective 5-HT2A Receptor Antagonist for PET-Imaging9
Expanding the Chemical Space of Reverse Fosmidomycin Analogs9
Discovery of Novel Binders to Sterol Regulatory Element-Binding Protein-1 by High-Throughput Screening9
From Virtual Screens to Cellular Target Engagement: New Small Molecule Ligands for the Immune Checkpoint LAG-39
Chemical Space Profiling of SARS-CoV-2 PLpro Using DNA-Encoded Focused Libraries9
New Lipophilic Hydroxamates as Promising Trypanocidal Agents: Design, Synthesis, SAR, and Conformational Behavior Studies9
Correction to “An Unexpected Deuterium-Induced Metabolic Switch in Doxophylline”9
Asymmetric Synthesis and Biological Evaluation of Both Enantiomers of 5- and 6-Boronotryptophan as Potential Boron Delivery Agents for Boron Neutron Capture Therapy9
Monocyclic Nitro-heteroaryl Nitrones with Dual Mechanism of Activation: Synthesis and Antileishmanial Activity9
Dual Targeting of Function–Structure for Effective Killing of Pathogenic Free-Living Amoebae9
Design, Synthesis, and Evaluation of a New Chemotype Fluorescent Ligand for the P2Y2 Receptor8
Retraction of “Synthesis and Pharmacological Evaluation of Noncatechol G Protein Biased and Unbiased Dopamine D1 Receptor Agonists”8
Development of a GC-376 Based Peptidomimetic PROTAC as a Degrader of 3-Chymotrypsin-like Protease of SARS-CoV-28
Pyrrolidines as Main Protease Inhibitors for Treating Viral Infections, in Particular, Coronavirus Infections8
Novel Substituted Thiadiazoles as Splicing Modulators for Modulating Splicing of mRNA and Uses Thereof for Treating Diseases8
Design and Implementation of Synthetic RNA Binders for the Inhibition of miR-21 Biogenesis8
Correction to “Discovery of l-Lysine Dioxalate (LH1513) as a Novel Inhibitor of Calcium Oxalate Crystallization for Hyperoxaluria”8
Discovery of 2-Phenylquinolines with Broad-Spectrum Anti-coronavirus Activity8
Rapid PROTAC Discovery Platform: Nanomole-Scale Array Synthesis and Direct Screening of Reaction Mixtures8
Discovery and Development of Cyclic Peptide Inhibitors of CIB18
Ring Size as an Independent Variable in Cyclooligomeric Depsipeptide Antiarrhythmic Activity8
Direct-to-Biology Accelerates PROTAC Synthesis and the Evaluation of Linker Effects on Permeability and Degradation8
The Inhibitors of Protein Tyrosine Phosphatase Nonreceptor Type 2 (PTPN2) as Potential Enhancers of Cancer Immunotherapy and Type 1 (PTPN1) as Treatment of Metabolic Diseases8
Novel Pyrrolidinone Urea Compounds as FPR2 Agonists for Treating Atherosclerosis and Heart Failure8
Discovery of 1,5-Dihydro-4H-imidazol-4-one Derivatives as Potent, Selective Antagonists of CXC Chemokine Receptor 28
Leveraging Open Science Drug Development for PET: Preliminary Neuroimaging of 11C-Labeled ALK2 Inhibitors8
Exploration of a 14-3-3 PPI Pocket by Covalent Fragments as Stabilizers8
Discovery of a Novel Class of ERRα Agonists8
Development of Oligomeric Mannose-6-phosphonate Conjugates for Targeted Protein Degradation8
Bispecific Antibodies Produced via Chemical Site-Specific Conjugation Technology: AJICAP Second-Generation8
Structure–Activity Relationship Study of Splicing Modulators on Hsh155/SF3B1 through Chemical Synthesis and Yeast Genetics8
In This Issue, Volume 15, Issue 128
Advanced Delivery Systems and Novel Psilocin Derivatives for Enhanced Therapeutic Applications8
Novel Fragment-Based Screening Method to Identify Small Molecules That Selectively Bind RNA8
Discovery and Characterization of a Rapidly Fungicidal and Minimally Toxic Peptoid against Cryptococcus neoformans8
Development of Ethyl-Hydrazide-Based Selective Histone Deacetylase 6 (HDAC6) PROTACs8
Linker-Determined Folding and Hydrophobic Interactions Explain a Major Difference in PROTAC Cell Permeability8
Morita–Baylis–Hillman Adduct Chemistry as a Tool for the Design of Lysine-Targeted Covalent Ligands7
Identification of Indazole- and Azaindazole-Substituted Cyclopentapyrroles as G2019S Leucine-Rich Repeat Kinase 2 Inhibitors for the Treatment of CNS Disorders7
Structure–Activity Relationship of Potent, Selective, and Orally Bioavailable Molecular Glue Degraders of CK1α7
In-Silico Screening-Based Discovery of New Natural eEF2K Inhibitors with Neuritogenic Activity7
A Hybrid Energy-Based and AI-Based Screening Approach for the Discovery of Novel Inhibitors of AXL7
ACS Medicinal Chemistry Letters Patent Highlights: A Look Back7
Quantum Mechanics-Based Ranking of Predicted Proteolysis Targeting Chimeras-Mediated Ternary Complexes7
Discovery of Novel Indole Derivatives as Fructose-1,6-bisphosphatase Inhibitors and X-ray Cocrystal Structures Analysis7
Derivatives of Aristoquinoline Accessed through a Ritter-like Reaction7
Novel Cyclic Peptides Inhibiting Tumor Necrosis Factor Receptor 1 Activity7
Exploiting Solvent Exposed Salt-Bridge Interactions for the Discovery of Potent Inhibitors of SOS1 Using Free-Energy Perturbation Simulations7
Targeting Oncogenic Pathways: Advances in KRAS, CDK, EGFR, and PROTAC-Based Therapies7
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