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Identification of a Selective Inhibitor of Human Monocarboxylate Transporter 4
Biochemical and Biophysical Research Communications
Biochemistry
Cell Biology
Molecular Biology
Biophysics
Imidazole-Dioxolane Compounds as Isozyme-Selective Heme Oxygenase Inhibitors
N-Substituted Arylsulfonamides as Alternative Building Blocks in Peptoid and Peptide Synthesis
Safety of 4-Factor Prothrombin Complex Concentrate (4f-Pcc) for Emergent Reversal of Factor Xa Inhibitors
Journal of Intensive Care
Critical Care
Intensive Care Medicine
Directed Ortho Metalation-Cross Coupling Strategies. N-Cumyl Arylsulfonamides. Facile Deprotection and Expedient Route to 4- And 4, 7-Substituted Saccharins
Directed Ortho Metalation-Cross Coupling Strategies. N-Cumyl Arylsulfonamides. Facile Deprotection and Expedient Route to 4- And 4, 7-Substituted Saccharins
Benzimidazole Derivatives Bearing Substituted Biphenyls as Hepatitis C Virus NS5B RNA-Dependent RNA Polymerase Inhibitors: Structure-Activity Relationship Studies and Identification of a Potent and Highly Selective Inhibitor JTK-109
The Prosegments of Furin and PC7 as Potent Inhibitors of Proprotein Convertases
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Synthesis and Biological Evaluation of Cyclopropyl Analogues of Fosmidomycin as PotentPlasmodiumfalciparumGrowth Inhibitors
Journal of Medicinal Chemistry
Drug Discovery
Molecular Medicine
Drug Repositioning of Mevalonate Pathway Inhibitors as Antitumor Agents for Ovarian Cancer
Oncotarget
Oncology
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