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 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
Bispecific Antibodies Produced via Chemical Site-Specific Conjugation Technology: AJICAP Second-Generation29
Discovery of Selective Inhibitors of NaV1.7 Templated on Saxitoxin as Therapeutics for Pain27
Macrocyclic Oxindole Peptide Epoxyketones─A Comparative Study of Macrocyclic Inhibitors of the 20S Proteasome26
Synthesis of Monofluorinated 7-Hydroxycoumarin-3-Carboxamides as Cell-Permeable Fluorescent Molecular Probes26
Novel Compounds as 5-HT2A Agonists for Treating Mental Illness or CNS Disorders25
Structure–Activity Relationship Analysis of Macrocyclic Peptide RAS Inhibitors: Spotlight on the Solvent-Exposed Region25
Design and Synthesis of Phosphonoproline-Proline Bioisosteric Mimetics of Proline Dimers: Pseudopeptide Constructs as Potential Inhibitors of the Zn-Metalloprotease PPEP-1 Associated with 24
From Virtual Screens to Cellular Target Engagement: New Small Molecule Ligands for the Immune Checkpoint LAG-324
Virtual Screening-Guided Discovery of Small-Molecule CHI3L1 Inhibitors with Functional Activity in Glioblastoma Spheroids23
Novel Triazines as NLRP3 Inhibitors for Treating Multiple Diseases22
Novel Papain-Like Protease Inhibitors for Treating Viral Infections, in Particular Coronavirus Infections22
Discovery of a Novel sp3-Rich M1 Positive Allosteric Modulators (PAMs) Chemotype via Scaffold Hopping22
Tricyclic and Novel Chemotypes as Selective WRN Helicase Inhibitors for MSI-H Cancer Therapy22
Targeting Cancer: A New Era in Cancer Therapy through Immune Fitness Modulation and KRAS Degradation22
Announcing the Early Career Board of ACS Medicinal Chemistry Letters22
Novel Indazole Compounds as PKMYT1 Kinase Inhibitors for Treating Cancer21
Enantioselective Bioreduction of Medicinally Relevant Nitrogen-Heteroaromatic Ketones21
Evaluating the Diversity and Target Addressability of DELs using Scaffold Analysis and Machine Learning21
N -Myristoyltransferase Inhibitors as a Potential Starting Point for the Development of Antischistosomal Agents21
ACS Medicinal Chemistry Letters Patent Highlights: A Look Back21
Fused Bicyclic Heteroaryl Compounds as NLRP3 Inhibitors for Treating Asthma or COPD21
Synthesis and Evaluation of Halogenated Pralidoximes in Reactivation of Organophosphate-Inhibited Cholinesterases21
Novel 3-Cycloaminoindole Compounds as Serotonergic Psychedelic Agents for Treating Psychosis, Mental Illness, and CNS Disorders21
Issue Editorial Masthead21
(−)-Epigallocatechin Gallate is a Noncompetitive Inhibitor of NAD Kinase20
Discovery of Sovleplenib, a Selective Inhibitor of Syk in Clinical Development for Autoimmune Diseases and Cancers20
N-Arylsulfonylated C-Homoaporphines as a New Class of Antiplatelet and Antimicrobial Agents20
Pyrazole Ureas as Low Dose, CNS Penetrant Glucosylceramide Synthase Inhibitors for the Treatment of Parkinson’s Disease20
SAR Study of 4,8-Disubstituted Pyrimido[5,4-d]pyrimidines Exhibiting Antitrypanosomal and Antileishmanial Activity20
Targeting Oncogenic Pathways: Advances in KRAS, CDK, EGFR, and PROTAC-Based Therapies20
Novel Compounds as 5-HT2A Receptor Modulators for Treating Psychiatric and Neurological Disorders19
The Synergistic Effects of 5-HT2A and TRP Agonism/Antagonism in Reducing Inflammation for Enhanced Mental and Physical Health19
Novel Piperidinylpyridinylcarbonitrile Derivatives as QPCT and QPCTL Inhibitors for Treating Cancer19
Novel Isoindolinone-Containing PARP Inhibitors: Synthesis and Therapeutic Applications in CNS Cancer Treatment19
Identification and Exploration of a Series of SARS-Cov-2 MPro Cyano-Based Inhibitors Revealing Ortho-Substitution Effects within the P3 Biphenyl Group19
Charting the Chemical Space of Acrylamide-Based Inhibitors of zDHHC2018
Design, Synthesis, and Protective Activity against Doxorubicin-Induced Cardiotoxicity of Novel Water-Soluble Small-Molecule GPx Mimics18
Discovery of Novel MTA-Cooperative PRMT5 Inhibitors with a 2,3-Dihydro-1H-imidazo[1,2-b]pyrazole Scaffold18
N -Alkyl and N -Aryl Aminopyrazole Spirocarbamates: A Two-Pronged Lead Optimization Strategy to Identify Orally Bioavailable P18
Discovery and Characterization of a Chemical Probe for Cyclin-Dependent Kinase-Like 218
Discovery and Optimization of Potent and Subtype-Selective Urea-Derived Na V 1.8 Inhibitors18
Discovery of a Potent and Selective Naphthyridine-Based Chemical Probe for Casein Kinase 218
Synthesis and In Vitro/In Silico α-Glucosidase Inhibitory Study of Novel Ethanones Containing Naphthalene-Linked 1,2,4-Triazole17
Neuropharmacological Advances: Harnessing 5-HT2A Receptor Modulators and Psychoplastogens17
Synthesis and Preclinical Evaluation of Novel 68Ga-DOTA-RBB as Potential PET Radiotracer for Imaging CDK4/6 in Tumors17
Mechanistic Insights from Differences in the Aggregate Morphologies of Amphotericin B and Its Less Toxic Variant Am-2-19 (Turletricin)17
Novel Compounds as Glucagon Receptor Agonists for Treating Type 2 Diabetes Mellitus and Obesity17
Issue Publication Information17
A Novel Peptide-Based PD-L1 PET Tracer: Design, Synthesis, and Preclinical Imaging Validation17
Synthesis and Biochemical Characterization of Investigational Pyrazolopyrimidine-Based Allosteric KRAS Modulators17
Fragment-Based Dynamic Combinatorial Chemistry for Identification of Selective α-Glucosidase Inhibitors16
Optimized Parenteral and Intranasal Formulations of Tryptamine Psychedelics for Rapid-Acting Antidepressant Therapy16
Discovery of Pyrazole-Containing 4-Arylindolines as Potent Small-Molecule Inhibitors of the Programmed Cell Death-1/Programmed Cell Death-Ligand 1 Interaction16
Constructive On-DNA Abramov Reaction and Pudovik Reaction for DEL Synthesis16
Heparan Sulfate-Mimicking Glycopolymers Bind SARS-CoV-2 Spike Protein in a Length- and Sulfation Pattern-Dependent Manner16
Discovery of a Potent and Highly Selective Inhibitor of Aurora A Kinase16
Novel Indolinyl Compounds as Helicase Primase Inhibitors for Treating Viral Infections, in particular, Herpesvirus Infections15
3AcFNP-59 for Positron Emission Tomography Imaging of Cholesterol Trafficking and Utilization15
Machine Learning ADME Models in Practice: Four Guidelines from a Successful Lead Optimization Case Study15
6,7-Dihalo-Benzothiadiazines as Potent and Selective AMPA Receptor Modulators for Cognitive Enhancement and Neuroprotection15
Fragment Ligands of the m6A-RNA Reader YTHDF215
An Estrogen Receptor β Agonist with AR Antagonist Activity from a Modern Asymmetric De Novo Steroid Synthesis15
Discovery of N-(4-(Aminomethyl)phenyl)-5-methylpyrimidin-2-amine Derivatives as Potent and Selective JAK2 Inhibitors15
Exploiting Solvent Exposed Salt-Bridge Interactions for the Discovery of Potent Inhibitors of SOS1 Using Free-Energy Perturbation Simulations15
Issue Publication Information14
Issue Editorial Masthead14
Quantum Mechanics-Based Ranking of Predicted Proteolysis Targeting Chimeras-Mediated Ternary Complexes14
Synthesis and Biological Evaluation of 3,5-Diaryl-Substituted 1,2,4-Oxadiazole Sulfamates as Potent Steroid Sulfatase Inhibitors14
Discovery of VU6052959/BI’7927: A Selective mGlu 3 Positive Allosteric Modulator (PAM) from an Orthogonal Benzoxazine Chemotype14
Advancing New Chemical Modalities into Clinical Studies14
Issue Editorial Masthead14
An Automated Purification Workflow Coupled with Material-Sparing High-Throughput 1H NMR for Parallel Medicinal Chemistry14
NADPH-Oxidase 4 (NOX4) Inhibitors as a Treatment for Idiopathic Pulmonary Disease, Fibrotic Diseases, Inflammatory Diseases, and Cancer14
Homogeneous Dual-Payload Antibody-Drug Conjugates Produced by Combined Distinct Conjugation Strategies14
Identification of an Allene Warhead That Selectively Targets a Histidine Residue in the Escherichia coli Oxidoreductase Enzyme DsbA14
In-Silico Screening-Based Discovery of New Natural eEF2K Inhibitors with Neuritogenic Activity14
Issue Publication Information14
Advancing Next-Generation Psychedelic Therapeutics through Selective 5-HT2A Activation, Precision Aerosol Delivery, and Optimized 5-MeO-DMT Treatment Paradigms14
First-in-Class Potent, Dual HDAC6/Proteasome Inhibitors Lacking a Hydroxamic Acid Motif: Discovery of Novel Anti-Multiple Myeloma Agents14
In Retrospect: Root-Cause Analysis of Structure–Activity Relationships in IRAK4 Inhibitor Zimlovisertib (PF-06650833)14
Novel Indole Derivatives as Serotonergic Psychedelic Agents for Treating Psychosis, Mental Illness, and CNS Disorders13
Targeting the Glucokinase–Glucokinase Regulatory Protein Axis: Pharmacophore-Based Identification of Novel Antidiabetic Small Molecules13
Chemical Design and Pharmacokinetics Enable Precision Psychedelic Therapeutics13
Novel Furopyridine and Furopyrimidine Compounds as PI4K Inhibitors for Treating Malaria and Viral Infection13
In the Quest for Potent and Selective Malic Enzyme 3 Inhibitors for the Treatment of Pancreatic Ductal Adenocarcinoma13
Issue Editorial Masthead13
Discovery of Biased Dual-Agonists of Glucagon-Like Peptide 1 and Glucagon Receptors through Mutation of a Conserved Aspartate13
Exploring the Therapeutic Potential of Entheogens in Postoperative Cognitive Decline and Psychological Resilience13
Identification and Preliminary Characterization of a Novel Tasquinimod Analog that Unexpectedly Induces Mitotic Arrest by Alteration of Microtubule Dynamics13
From Solid-State Control to Predictive Precision: Building a Deployable Ecosystem for Psychedelic Therapeutics13
Structure–Activity Relationships for the N-Me- Versus N-H-Amide Modification to Macrocyclic ent-Verticilide Antiarrhythmics12
Discovery of Small-Molecule GLP-1 Receptor Agonists with Improved Oral Pharmacokinetics Based on Orforglipron12
Call for Papers: Allosteric Modulators in Drug Discovery12
Novel Benzofuran Derivatives as SARM1 Inhibitors for Treating Axonal Degeneration12
Novel Compounds for Treating Huntington’s Disease12
Novel Imidazotriazine Derivatives as IL-17 Modulators for Treating Inflammatory and Autoimmune Disorders12
Discovery of Potent and Oral Bioavailable MAT2A Inhibitors for the Treatment of MTAP-Deleted Tumors12
Proline Homologation in Melanostatin Neuropeptide: Discovery of Potent Modulators of the Dopamine D 2 Receptors12
Discovery of First-in-Class BAZ2A/B and BAZ2B-Selective Degraders12
DNA-Encoded Library (DEL) Selection Identifies a Distinct DDB1 Ligand Binding Site12
Introducing Conformational Restraints on 25CN-NBOH: A Selective 5-HT2A Receptor Agonist12
Hybrids of Membrane-Translocating Antimicrobial Peptides Show Enhanced Activity through Membrane Permeabilization12
Pharmacophore-Based Structure Optimization of S-Trityl-l-Cysteine Derivatives for Cytotoxic Payload Applications12
Lead Optimization of Small Molecule ENL YEATS Inhibitors to Enable In Vivo Studies: Discovery of TDI-1105512
2-Aminoimidazole-benzimidazole Conjugates Potentiate the Gram-Positive Selective Antibiotic Clarithromycin against Acinetobacter baumannii12
Small Molecules Blocking the Assembly of TCAB1 and Telomerase Complexes: Lead Discovery and Biological Activity12
Targeted Degradation of Androgen Receptor for the Potential Treatment of Prostate Cancer12
Targeted Degradation of EGFR and PKC Isoforms: Emerging Bifunctional and Peptidic Modalities in Oncology and Immune Regulation11
In this Issue, Volume 16, Issue 511
Lipase-Catalyzed Synthesis and Biological Evaluation of N-Picolineamides as Trypanosoma cruzi Antiproliferative Agents11
Structure-Guided Temporin L Analogs Development to Inhibit the Main Protease of SARS-CoV-211
Novel N-Substituted Indole Derivatives as Serotonergic Psychedelic Agents for Treating Psychosis, Mental Illness, and CNS Disorders11
Novel Compounds as 5-HT2A Agonists for Treating Mental Illness or CNS Disorders11
Novel 2 H -Pyrazolo[3,4- d ]thiazole Compounds Targeting NLRP3 for the Treatment of Neurodegenerative Dise11
The Value of Academic and Industrial Collaborations in Drug Discovery11
Inhibitors of the Cyclic GMP-AMP Synthase (cGAS) as Potential Treatment for Autoimmune and Inflammatory Diseases11
Novel Fused Heterocycles as 5-HT2A Receptor Agonists for Treating Neurological Diseases, Namely, Depression, Anxiety, Substance Abuse, and Headaches11
Structure-Guided Virtual Screening of Small Peptide Inhibitors Targeting PD-L1 for Cancer Immunotherapy11
Novel Pyrimidinyl Sulfonamide Derivatives as GPR17 Modulators11
Issue Publication Information11
Novel Nonpeptide as Oxytocin Receptor Agonist11
Discovery of CVN636 : A Highly Potent, Selective, and CNS Penetrant mGluR 7 Allosteric Agonist11
Issue Editorial Masthead11
Tambjamines as Promising Leads for the Development of Next-Generation Antifungals against Candida auris11
Discovery of 5,7-Dihydro-6H-pyrrolo[2,3-d]pyrimidin-6-ones as Highly Selective CDK2 Inhibitors11
Novel Substituted Pyrazoles as 5-HT1A Agonists for Treating Neuropsychiatric Diseases11
Amino-cyclohexane Carboxylic Acid Inhibitors of Arginase11
Re-evaluation of Cyclic Peptide Binding to Neurotensin Receptor 1 by Shifting the Peptide Register during Synthesis11
Synthesis and Evaluation of Novel meso-Tetraphenyltetrabenzoporphyrins for Photodynamic Therapy11
Issue Editorial Masthead11
Novel Compounds as MALT1 Inhibitors for Treating Cancer11
Synthesis and Evaluation of Benzylamine Inhibitors of Neuropathogenic Naegleria fowleri “Brain-Eating” Amoeba11
Novel Substituted Aryl Sulfonamides and Sulfuric Diamides As Transglutaminase 2 Inhibitors11
Reducing Self-Assembly by Increasing Net Charge: Effect on Biological Activity of Mastoparan C10
Novel Compounds for Treating Hemoglobinopathies, Namely, Anemia, Sickle Cell Disease, or Thalassemia10
Broad-Spectrum Antimicrobial Efficacy of Cyclic Antimicrobial Peptide Against Multidrug-Resistant Staphylococcus aureus Infections10
Glycine Betaine-Functionalized Ionic Liquids: Design of Versatile Bioplatform for Incorporating Biologically Active Moieties into Cations10
Beyond 20 in the 21st Century: Prospects and Challenges of Non-canonical Amino Acids in Peptide Drug Discovery10
Fentanyl-Rewired: A 2-Azaspiro[3.3]heptane Core Preserves μ-Opioid Function10
Discovery of Small-Molecule Ligands for the E3 Ligase STUB1/CHIP from a DNA-Encoded Library Screen10
Next-Generation GLUT Inhibitors: Lactone to Lactam Conversion in Rapaglutin A Confers Resistance to Plasma Esterases10
5-Nitrofuran-Semicarbazone Hybrids as Antitrypanosomal Agents: Structure–Activity Relationship and Nitroreductase Activation10
N-Biphenyl Pyrrolinones and Dibenzofurans as RNA-Binding Protein LIN28 Inhibitors Disrupting the LIN28–Let-7 Interaction10
Fragment-Based Discovery of Drug-like LRH-1 Agonists10
Potentiometric Determination of Acid Dissociation Constants (pKa) for an Anticancer Pyrrole-Imidazole Polyamide10
Endocyclic Trisubstituted Hydroxylamine Isosteres of Basic Amines for ADME Modulation and Reduction of hERG Activity10
Peripherally Restricted Fused Heterocyclic Peptidomimetic Multifunctional Opioid Agonists as Novel, Potent Analgesics10
Design, Synthesis, and Evaluation of 8-(o-Tolyl)quinazoline Derivatives as Small-Molecule PD-1/PD-L1 Antagonists10
Synthesis and Monoamine Oxidase Inhibitory Activity of Halogenated Flavones10
Structure–Activity Relationship Study of 1H-Pyrrole-3-carbonitrile Derivatives as STING Receptor Agonists10
Accelerated Discovery of Macrocyclic CDK2 Inhibitor QR-6401 by Generative Models and Structure-Based Drug Design10
Degradation and Detection: Integrating BCL6 Targeted Protein Degradation with Biomarker-Guided BET Inhibition in Cancer10
Identification of Boc2Lys-Linked Ethacrynic Acid and Its Analogues As Efficient Glutathione S-Transferase Degraders10
Property-Based Optimization of Cereblon-Based Molecular Glue Degraders10
Innovative Psychedelic Therapies: Harnessing 5-MeO-DMT and DMT for Mental Health Treatment10
Pyrroloquinolone-Based Compounds as a Novel Antimycobacterial Chemotype10
Neutrophil Elastase-Responsive Linkers for Precision Antibody–Drug Conjugates10
Targeted Degradation of Histone Deacetylases via Bypassing E3 Ligase Targeting Chimeras (BYETACs)10
Novel Lactams as Cbl-b Inhibitors for Treating Cancer9
Correction to “Study of Chalcogen Aspirin Derivatives with Carbonic Anhydrase Inhibitory Properties for Treating Inflammatory Pain”9
Recent Developments in Mass Spectrometry to Support Next-Generation Synthesis and Screening9
Novel 2-Pyrrolidone Derivatives as Negative Allosteric Modulators of GluN2B-Containing NMDA Receptors9
Design, Construction, and Screening of Diversified Pyrimidine-Focused DNA-Encoded Libraries9
Discovery of Novel Hydroxyimine-Tethered Benzenesulfonamides as Potential Human Carbonic Anhydrase IX/XII Inhibitors9
Potent, Selective, and Orally Bioavailable Quinazoline-Based STK17A/B Dual Inhibitors9
4-Oxo-β-lactams as Covalent Inhibitors of the Mitochondrial Intramembrane Protease PARL9
Issue Publication Information9
Development of BODIPY FL SNS 032 as a Versatile Probe for Constitutive Androstane Receptor and Multiple Kinases9
Novel Compounds as NLRP3 Inhibitors for Treating Asthma or COPD9
Decarboxylative Cross-Coupling: A Radical Tool in Medicinal Chemistry9
Uncompetitive Allosteric Inhibition of PTP1B by BP-1-102 Reveals a Potential Dual-Target Strategy toward the PTP1B–STAT3 Oncogenic Axis: Biochemical and Computational Evidence9
Issue Publication Information9
Design, Synthesis, and Biological Evaluation of Tetrazol-2-yl-acetamides as Novel Antitubercular Agents9
Discovery of Non-Covalent Inhibitors for SARS-CoV-2 PLpro: Integrating Virtual Screening, Synthesis, and Experimental Validation9
Structure-Based Design of Novel TLR7/8 Agonist Payloads Enabling an Immunomodulatory Conjugate Approach9
Novel Substituted Spiro-Ureas as Monoacylglycerol Lipase Inhibitors9
Novel Pyridine Derivatives as 5-HT2A Agonists for Treating Psychiatric Disorders9
Synthesis and Determination of Anticancer Activity of Dicobalt Hexacarbonyl 2′-Deoxy-5-alkynylfuropyrimidines9
Issue Editorial Masthead9
Discovery of New Binders for DCAF1, an Emerging Ligase Target in the Targeted Protein Degradation Field9
MALT1 Inhibitors for Treating Cancer and Immunological Diseases9
The Inhibitors of Mucosa-Associated Lymphoid Tissue Lymphoma Translocation Protein 1 (MALT-1) Protease as Potential Treatment of ABC-DLBCL and Similar Diseases9
Reducing hERG Inhibition in the Design of Potent and Bioavailable Indazole cGAS Inhibitors9
Pioneering Changes in Psychiatry: Biomarkers, Psychedelics, and AI9
Engineering the Next Generation of Psychedelic Therapeutics through Serotonergic Precision and Pharmacokinetic Control9
Issue Editorial Masthead8
Discovery of Indole-Based PDE5 Inhibitors: Synthesis and Pharmacological Evaluation8
Novel Thienopyrrole Compounds for Treating Autoimmune Diseases and Inflammatory Conditions8
A Neutral Flavin–Triphenylamine Probe for Mitochondrial Bioimaging under Different Microenvironments8
Synthesis and Evaluation of Sulfobacin A and Analogues for Their Roles in Immunological Recognition8
Novel Piperidine Substituted Pyrazolopyrimidine Derivatives as SGK1 Inhibitors for Treating Cardiovascular Diseases8
Recent Discovery of PARP7 Inhibitors as Anticancer Agents8
Perspectives of Patents in Academic and Industrial Collaborations in Drug Discovery8
Recent Advances in DNA-Encoded Library: High-Throughput Identification of Chemical Inducers of Proximity from Degraders to Non-degraders8
Innovations in Precision Oncology: Biomarker-Driven Approaches for Enhanced Cancer Therapy8
Novel Macrocyclic Antagonists of the CGRP Receptor Part 2: Stereochemical Inversion Induces an Unprecedented Binding Mode8
Integrated Advancements in Neuroplasticity, Psychedelic Therapeutics, and AI-Driven Innovations for Precision Medicine8
Design, Synthesis, and Characterization of Prodrugs of Sulfonamide TLR4 Signaling Inhibitor TAK-242 (Resatorvid)8
Issue Publication Information8
9,10-Bis[(4-(2-hydroxyethyl)piperazine-1-yl)prop2-yne-1-yl]anthracene: G-Quadruplex Selectivity and Anticancer Activity8
Discovery of INCB126503 as a Potent and Selective FGFR2/3 Inhibitor8
Discovery of Selective Aldehyde Dehydrogenase Inhibitors for the Treatment of Cancer8
4-Aminoalkylquinolines as Potent Antitubercular Agents Targeting the Cytochrome bc 1 Complex8
Structural Evaluations of a Selective Human STINGA230 Agonist and Its Use in Macrophage Immunotherapies8
Synthesis of Marine-Inspired Multifaceted DNA Damaging Spirooxindoles Combating NSCLC and Associated Bacterial Infection8
Discovery of a Colon-Targeted Prodrug As an Escherichia coli Biofilm Inhibitor for Treating Inflammatory Bowel Disease8
Call for Papers: Exploring the Use of AI/ML Technologies in Medicinal Chemistry and Drug Discovery8
Integrating Neuroprotective and Anti-inflammatory Strategies in the Development of PI3K Inhibitors for Enhanced Cancer Therapy8
Issue Publication Information8
Discovery of Kinesin KIF18A Inhibitor ATX020: Tactical Application of Silicon Atom Replacement8
Identification of 5-Thiocyanatothiazol-2-amines Disrupting WDR5-MYC Protein–Protein Interactions8
Biological Effects of Modifications of the Englerin A Glycolate8
NMR-Based Fragment Screen of the von Hippel-Lindau Elongin C&B Complex8
Discovery of a Novel Photocaged PI3K Inhibitor Capable of Real-Time Reporting of Drug Release8
Selective Wee1 Inhibitors Led to Antitumor Activity In Vitro and Correlated with Myelosuppression8
Novel Ergoline Compounds as 5-HT2A Agonists for Treating Mood Disorders Such as Depressive Disorders and Bipolar Disorders8
Exploring the 1-(4-Nitrophenyl)-3-arylprop-2-en-1-one Scaffold for the Selective Inhibition of Monoamine Oxidase B8
Radiosynthesis and Preclinical Evaluation of a Carbon-11 Labeled Phosphodiesterase 7 Inhibitor for PET Neuroimaging8
Evaluation of the Indazole Analogs of 5-MeO-DMT and Related Tryptamines as Serotonin Receptor 2 Agonists8
In This Issue, Volume 15, Issue 48
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