Self-Association and Nitroaromatic-Induced Deaggregation of Pyrene Substituted Pyridine Amides | Journal of the American Chemical Society
Crystallography and QM/MM Simulations Identify Preferential Binding of Hydrolyzed Carbapenem and Penem Antibiotics to the L1 Metallo-β-Lactamase in the Imine Form | Journal of Chemical Information and Modeling
Multiscale Workflow for Modeling Ligand Complexes of Zinc Metalloproteins | Journal of Chemical Information and Modeling
![Self-Association and Nitroaromatic-Induced Deaggregation of Pyrene Substituted Pyridine Amides | Journal of the American Chemical Society Self-Association and Nitroaromatic-Induced Deaggregation of Pyrene Substituted Pyridine Amides | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja411672f/asset/images/medium/ja-2013-11672f_0015.gif)
Self-Association and Nitroaromatic-Induced Deaggregation of Pyrene Substituted Pyridine Amides | Journal of the American Chemical Society
Trimesic acid–Theophylline and Isopthalic acid–Caffeine Cocrystals: Synthesis, Characterization, Solubility, Molecular Docking, and Antimicrobial Activity | Crystal Growth & Design
Cocrystals of Oxymatrine: Reducing Hygroscopicity and Affecting the Dissolution Rate | Crystal Growth & Design
![Crystals | Free Full-Text | Isolation, Identification, Spectral Studies and X-ray Crystal Structures of Two Compounds from Bixa orellana, DFT Calculations and DNA Binding Studies Crystals | Free Full-Text | Isolation, Identification, Spectral Studies and X-ray Crystal Structures of Two Compounds from Bixa orellana, DFT Calculations and DNA Binding Studies](https://www.mdpi.com/crystals/crystals-12-00380/article_deploy/html/images/crystals-12-00380-g001.png)
Crystals | Free Full-Text | Isolation, Identification, Spectral Studies and X-ray Crystal Structures of Two Compounds from Bixa orellana, DFT Calculations and DNA Binding Studies
![Co-Crystals of Sulfamethazine with Some Carboxylic Acids and Amides: Co-Former Assisted Tautomerism in an Active Pharmaceutical Ingredient and Hydrogen Bond Competition Study | Crystal Growth & Design Co-Crystals of Sulfamethazine with Some Carboxylic Acids and Amides: Co-Former Assisted Tautomerism in an Active Pharmaceutical Ingredient and Hydrogen Bond Competition Study | Crystal Growth & Design](https://pubs.acs.org/cms/10.1021/cg200334m/asset/images/medium/cg-2011-00334m_0011.gif)