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2. The Augustinian Values Institute: Preserving a Legacy of Augustinian Education

11. A Novel Inhaled Dry-Powder Formulation of Ribavirin Allows for Efficient Lung Delivery in Healthy Participants and Those with Chronic Obstructive Pulmonary Disease in a Phase 1 Study

15. 10-Formyl-5,10-dideaza-acyclic-5,6,7,8-tetrahydrofolic acid (10-Formyl-DDACTHF): A potent cytotoxic agent acting by selective inhibition of human GAR Tfase and the de novo purine biosynthetic pathway

18. Synthesis and antiviral activity of novel HCV NS3 protease inhibitors with P4 capping groups

22. Synthesis and SAR of acyclic HCV NS3 protease inhibitors with novel P4-benzoxaborole moieties

23. Synthesis and evaluation of novel α-amino cyclic boronates as inhibitors of HCV NS3 protease

27. Novel macrocyclic HCV NS3 protease inhibitors derived from α-amino cyclic boronates

29. Synthesis and biological evaluations of P4-benzoxaborole-substituted macrocyclic inhibitors of HCV NS3 protease

30. Synthesis of new acylsulfamoyl benzoxaboroles as potent inhibitors of HCV NS3 protease

32. Discovery of a Novel Class of Boron-Based Antibacterials with Activity against Gram-Negative Bacteria

33. Discovery of Novel Urea-Based Hepatitis C Protease Inhibitors with High Potency against Protease-Inhibitor-Resistant Mutants

37. ChemInform Abstract: Discovery and Structure—Activity Study of a Novel Benzoxaborole Antiinflammatory Agent (AN2728) for the Potential Topical Treatment of Psoriasis and Atopic Dermatitis.

38. Synthesis of isotopically labelled [3‐14C]‐ and [3,3‐2H2]‐5‐fluoro‐1,3‐dihydro‐1‐hydroxy‐2,1‐benzoxaborole (AN2690), a new antifungal agent for the potential treatment of onychomycosis

41. Identification of a novel boron-containing antibacterial agent (AN0128) with anti-inflammatory activity, for the potential treatment of cutaneous diseases

42. Discovery of a New Boron-Containing Antifungal Agent, 5-Fluoro-1,3-dihydro-1-hydroxy-2,1- benzoxaborole (AN2690), for the Potential Treatment of Onychomycosis

43. Identification of Borinic Esters as Inhibitors of Bacterial Cell Growth and Bacterial Methyltransferases, CcrM and MenH

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