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Rational Design of Sulfonamide Inhibitor Specific for Human Carbonic Anhydrase I Isozyme
Acta Crystallographica Section A Foundations of Crystallography
Engineered Single Human CD4 Domains as Potent HIV-1 Inhibitors and Components of Vaccine Immunogens
Journal of Virology
Insect Science
Immunology
Microbiology
Virology
Enantioselective Ring-Opening Polymerization of Rac-Lactide Dictated by Densely Substituted Amino Acids
Structure–activity Relationships of Natural and Non-Natural Amino Acid-Based Amide and 2-Oxoamide Inhibitors of Human Phospholipase A2 Enzymes
Bioorganic and Medicinal Chemistry
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Expanding Dynamic Kinetic Protocols: Transaminase-Catalyzed Synthesis of Α-Substituted Β-Amino Ester Derivatives
Chemical Communications
Surfaces
Alloys
Materials Chemistry
Coatings
Metals
Optical
Magnetic Materials
Films
Catalysis
Chemistry
Electronic
Composites
Ceramics
Pd-Catalyzed Allylation of Imines to Access a -CF3-substituted a -Amino Acid Derivatives
European Journal of Organic Chemistry
Organic Chemistry
Theoretical Chemistry
Physical
Discovery of Benzylidenebenzofuran-3(2h)-One (Aurones) as Inhibitors of Tyrosinase Derived From Human Melanocytes
New 4-Amino-1,2,3-Triazole Inhibitors of Indoleamine 2,3-Dioxygenase Form a Long-Lived Complex With the Enzyme and Display Exquisite Cellular Potency
ChemBioChem
Organic Chemistry
Biochemistry
Molecular Medicine
Molecular Biology
Structural Comparison of Protiated, H/D-Exchanged and Deuterated Human Carbonic Anhydrase IX
Acta Crystallographica Section D: Structural Biology
Structural Biology
Identification of Human Epididymis Protein-4 as a Fibroblast-Derived Mediator of Fibrosis
Nature Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
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