Synthesis, Identification, and Structure–Activity Relationship Analysis of GATA4 and NKX2-5 Protein–Protein Interaction Modulators | Journal of Medicinal Chemistry
Identification of a Potent and Selective 5-HT1A Receptor Agonist with In Vitro and In Vivo Antinociceptive Activity | ACS Chemical Neuroscience
Culture-independent method for identification of microbial enzyme-encoding genes by activity-based single-cell sequencing using a water-in-oil microdroplet platform | Scientific Reports
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Discovery of re-purposed drugs that slow SARS-CoV-2 replication in human cells | PLOS Pathogens
Color-Multiplexing-Based Fluorescent Test Paper: Dosage-Sensitive Visualization of Arsenic(III) with Discernable Scale as Low as 5 ppb | Analytical Chemistry
Frontiers | Environmental DNA (eDNA) for monitoring marine mammals: Challenges and opportunities
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Methyl Scanning: Total Synthesis of Demethylasterriquinone B1 and Derivatives for Identification of Sites of Interaction with and Isolation of Its Receptor(s) | Journal of the American Chemical Society
Cysteine and iron accelerate the formation of ribose-5-phosphate, providing insights into the evolutionary origins of the metabolic network structure | PLOS Biology
Chemoproteomic identification of CO2-dependent lysine carboxylation in proteins | Nature Chemical Biology
Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood | Nature Communications
Small molecule photocatalysis enables drug target identification via energy transfer | PNAS
Identification of N-(4-((1R,3S,5S)-3-Amino-5 -methylcyclohexyl)pyridin-3-yl)-6-(2,6-difluorophenyl)-5-fluoropicolinamide (PIM447), a Potent and Selective Proviral Insertion Site of Moloney Murine Leukemia (PIM) 1, 2, and 3 Kinase Inhibitor in Clinical ...
Heavy iron in large gem diamonds traces deep subduction of serpentinized ocean floor | Science Advances
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Identification of durable and non-durable FeNx sites in Fe–N–C materials for proton exchange membrane fuel cells | Nature Catalysis
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Mechanism of Action of Mycobacterium tuberculosis Gyrase Inhibitors: A Novel Class of Gyrase Poisons | ACS Infectious Diseases
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Structure–Activity Relationship (SAR) Optimization of 6-(Indol-2-yl)pyridine-3-sulfonamides: Identification of Potent, Selective, and Orally Bioavailable Small Molecules Targeting Hepatitis C (HCV) NS4B | Journal of Medicinal Chemistry
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