Variable domain mutational analysis to probe the molecular mechanisms of high viscosity of an IgG1 antibodyMABSIF7.32024-01-257OAAI
Discovery of Selective Tertiary Amide Inhibitors of Cyclin-Dependent Kinase 2 (CDK2)ACS MEDICINAL CHEMISTRY LETTERSIF42023-08-244OA
Assessment of KRAS G12C Target Engagement by a Covalent Inhibitor in Tumor Biopsies Using an Ultra-Sensitive Immunoaffinity 2D-LC-MS/MS ApproachANALYTICAL CHEMISTRYIF6.72022-09-0910PRE
Increased ER Stress After Experimental Ischemic Optic Neuropathy and Improved RGC and Oligodendrocyte Survival After Treatment With Chemical ChaperonINVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCEIF4.72019-05-0619OAAI
Disrupting Gram-Negative Bacterial Outer Membrane Biosynthesis through Inhibition of the Lipopolysaccharide Transporter MsbA通过抑制脂多糖转运蛋白MsbA破坏革兰氏阴性细菌外膜生物合成ANTIMICROBIAL AGENTS AND CHEMOTHERAPYIF4.52018-11-0153OAAI
Chemically Diverse Group I p21-Activated Kinase (PAK) Inhibitors Impart Acute Cardiovascular Toxicity with a Narrow Therapeutic WindowJOURNAL OF MEDICINAL CHEMISTRYIF6.82016-05-2455PREAI
Design of Selective PAK1 Inhibitor G-5555: Improving Properties by Employing an Unorthodox Low-pKa Polar MoietyACS MEDICINAL CHEMISTRY LETTERSIF42015-11-0372OAAI
Back Pocket Flexibility Provides Group II p21-Activated Kinase (PAK) Selectivity for Type I 1/2 Kinase InhibitorsJOURNAL OF MEDICINAL CHEMISTRYIF6.82014-02-0465PREAI
Novel Staphylococcal Glycosyltransferases SdgA and SdgB Mediate Immunogenicity and Protection of Virulence-Associated Cell Wall ProteinsPLOS PATHOGENSIF4.92013-10-1070OAAI
Structure-Based Discovery of Novel Amide-Containing Nicotinamide Phosphoribosyltransferase (Nampt) InhibitorsJOURNAL OF MEDICINAL CHEMISTRYIF6.82013-07-3184PREAI
Structure-Based Identification of Ureas as Novel Nicotinamide Phosphoribosyltransferase (Nampt) InhibitorsJOURNAL OF MEDICINAL CHEMISTRYIF6.82013-06-1369PREAI
Drugging the undruggable: Small molecule inhibition of the Ras oncoproteinCANCER RESEARCHIF16.62012-04-010PRE
Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity小分子配体与Ras中不同的口袋结合并抑制SOS介导的核苷酸交换活性PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICAIF9.12012-03-19612OAAI