Discovery of re-purposed drugs that slow SARS-CoV-2 replication in human cells | PLOS Pathogens
Gut bacteria-derived 5-hydroxyindole is a potent stimulant of intestinal motility via its action on L-type calcium channels | PLOS Biology
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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
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
Amino acid - Wikipedia
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 ...
![The Identification of Potent, Selective, and Orally Available Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase: The Discovery of AZD0156 (8-{6-[3-(Dimethylamino)propoxy]pyridin-3-yl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo ...](https://pubs.acs.org/cms/10.1021/acs.jmedchem.7b01896/asset/images/acs.jmedchem.7b01896.social.jpeg_v03 "The Identification of Potent, Selective, and Orally Available Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase: The Discovery of AZD0156 (8-{6-[3-(Dimethylamino)propoxy]pyridin-3-yl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo ...")
The Identification of Potent, Selective, and Orally Available Inhibitors of Ataxia Telangiectasia Mutated (ATM) Kinase: The Discovery of AZD0156 (8-{6-[3-(Dimethylamino)propoxy]pyridin-3-yl}-3-methyl-1-(tetrahydro-2H-pyran-4-yl)-1,3-dihydro-2H-imidazo ...
Chemoproteomic identification of CO2-dependent lysine carboxylation in proteins | Nature Chemical Biology
Heavy iron in large gem diamonds traces deep subduction of serpentinized ocean floor | Science Advances
Frontiers | Environmental DNA (eDNA) for monitoring marine mammals: Challenges and opportunities
Synthesis, Identification, and Structure–Activity Relationship Analysis of GATA4 and NKX2-5 Protein–Protein Interaction Modulators | Journal of Medicinal Chemistry
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
Distal and proximal cis-regulatory elements sense X chromosome dosage and developmental state at the Xist locus - ScienceDirect
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Conformational snapshots of the bacitracin sensing and resistance transporter BceAB | PNAS
Polar Compound Retention using Aqueous Normal-Phase (ANP/HILIC) Chromatography
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Identification of a diarylpentanoid-producing polyketide synthase revealing an unusual biosynthetic pathway of 2-(2-phenylethyl)chromones in agarwood | Nature Communications
A transcriptome-wide antitermination mechanism sustaining identity of embryonic stem cells | Nature Communications
Mechanism of Action of Mycobacterium tuberculosis Gyrase Inhibitors: A Novel Class of Gyrase Poisons | ACS Infectious Diseases
Small molecule photocatalysis enables drug target identification via energy transfer | PNAS
DiD' solid; DiIC<sub>18</sub>(5) solid (1,1'-Dioctadecyl-3,3,3',3
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Identification of Small Molecule Inhibitors of RNase L by Fragment-Based Drug Discovery | Journal of Medicinal Chemistry
Microorganisms | Free Full-Text | Advances in Chemical and Biological Methods to Identify Microorganisms—From Past to Present
