Discovery of 5-Nitro-6-thiocyanatopyrimidines as Inhibitors of Cryptococcus neoformans and Cryptococcus gattii | ACS Medicinal Chemistry Letters
ACS Medicinal Chemistry Letters | Vol 11, No 11
LogD Contributions of Substituents Commonly Used in Medicinal Chemistry | ACS Medicinal Chemistry Letters
Metabolically Stable tert-Butyl Replacement | ACS Medicinal Chemistry Letters
Supramolecular Self-Assembly To Control Structural and Biological Properties of Multicomponent Hydrogels | Chemistry of Materials
Discovery of Novel Cyanamide-Based Inhibitors of Cathepsin C | ACS Medicinal Chemistry Letters
Myeloid Differentiation Primary Response Protein 88 (MyD88): The Central Hub of TLR/IL-1R Signaling | Journal of Medicinal Chemistry
Publications - The Frantz Lab
Class 1 PI3K Clinical Candidates and Recent Inhibitor Design Strategies: A Medicinal Chemistry Perspective | Journal of Medicinal Chemistry
Discovery of a Selective Phosphoinositide-3-Kinase (PI3K)-γ Inhibitor (IPI-549) as an Immuno-Oncology Clinical Candidate | ACS Medicinal Chemistry Letters
Discovery of APD371: Identification of a Highly Potent and Selective CB2 Agonist for the Treatment of Chronic Pain | ACS Medicinal Chemistry Letters
Robust and Tunable Hybrid Hydrogels from Photo-Cross-Linked Soy Protein Isolate and Regenerated Silk Fibroin | ACS Sustainable Chemistry & Engineering
Structure–Activity Relationships of (+)-Naltrexone-Inspired Toll-like Receptor 4 (TLR4) Antagonists | Journal of Medicinal Chemistry
a-Factor Analogues Containing Alkyne- and Azide-Functionalized Isoprenoids Are Efficiently Enzymatically Processed and Retain Wild-Type Bioactivity | Bioconjugate Chemistry
Metabolically Stable tert-Butyl Replacement | ACS Medicinal Chemistry Letters
Sortase A Inhibitors: Recent Advances and Future Perspectives | Journal of Medicinal Chemistry
Applications of Deuterium in Medicinal Chemistry | Journal of Medicinal Chemistry
Metabolically Stable tert-Butyl Replacement | ACS Medicinal Chemistry Letters
Minor Structural Change to Tertiary Sulfonamide RORc Ligands Led to Opposite Mechanisms of Action | ACS Medicinal Chemistry Letters
Discovery of a Novel Series of 7-Azaindole Scaffold Derivatives as PI3K Inhibitors with Potent Activity | ACS Medicinal Chemistry Letters
Discovery of Highly Isoform Selective Thiazolopiperidine Inhibitors of Phosphoinositide 3-Kinase γ | Journal of Medicinal Chemistry
Publications - The Frantz Lab
Dehydrozingerone Inspired Styryl Hydrazine Thiazole Hybrids as Promising Class of Antimycobacterial Agents | ACS Medicinal Chemistry Letters
