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48 results on '"Centrella, Paolo A."'

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1. Rational Design of Macrocyclic Noncovalent Inhibitors of SARS-CoV‑2 Mpro from a DNA-Encoded Chemical Library Screening Hit That Demonstrate Potent Inhibition against Pan-Coronavirus Homologues and Nirmatrelvir-Resistant Variants.

2. Novel irreversible covalent BTK inhibitors discovered using DNA-encoded chemistry

4. Rational Design of Macrocyclic Noncovalent Inhibitors of SARS-CoV-2 Mprofrom a DNA-Encoded Chemical Library Screening Hit That Demonstrate Potent Inhibition against Pan-Coronavirus Homologues and Nirmatrelvir-Resistant Variants

5. A resource to enable chemical biology and drug discovery of WDR Proteins

6. Development of Potent Mcl-1 Inhibitors: Structural Investigations on Macrocycles Originating from a DNA-Encoded Chemical Library Screen

7. Discovery of a First-in-Class Small-Molecule Ligand for WDR91 Using DNA-Encoded Chemical Library Selection Followed by Machine Learning

8. Agonists and Antagonists of Protease-Activated Receptor 2 Discovered within a DNA-Encoded Chemical Library Using Mutational Stabilization of the Target

10. Discovery of Small Molecule Interleukin 17A Inhibitors with Novel Binding Mode and Stoichiometry: Optimization of DNA-Encoded Chemical Library Hits to In Vivo Active Compounds

12. Correction: Author Correction: Prioritizing multiple therapeutic targets in parallel using automated DNA-encoded library screening

13. Discovery of Novel UDP-N-Acetylglucosamine Acyltransferase (LpxA) Inhibitors with Activity against Pseudomonas aeruginosa

14. Design, synthesis and selection of DNA-encoded small-molecule libraries

15. Discovery of Novel, Potent Inhibitors of Hydroxy Acid Oxidase 1 (HAO1) Using DNA-Encoded Chemical Library Screening

18. Corrigendum: Discovery of a Potent BTK Inhibitor with a Novel Binding Mode by Using Parallel Selections with a DNAEncoded Chemical Library

19. Isoform-Selective ATAD2 Chemical Probe with Novel Chemical Structure and Unusual Mode of Action

20. Correction to “Structure Based Design of Non-Natural Peptidic Macrocyclic Mcl-1 Inhibitors”

21. Prioritizing multiple therapeutic targets in parallel using automated DNA-encoded library screening

22. Abstract 5084: Potent and isoform-selective ATAD2 bromodomain inhibitor with unprecedented chemical structure and mode of action

23. Inside Cover: Discovery of a Potent BTK Inhibitor with a Novel Binding Mode by Using Parallel Selections with a DNA-Encoded Chemical Library (ChemBioChem 9/2017)

24. Discovery of a Potent BTK Inhibitor with a Novel Binding Mode by Using Parallel Selections with a DNA-Encoded Chemical Library

25. Structure Based Design of Non-Natural Peptidic Macrocyclic Mcl-1 Inhibitors

26. Design and Synthesis of Biaryl DNA-Encoded Libraries

28. A Target Class Ligandability Evaluation of WD40 Repeat-Containing Proteins

29. Cell-Based Selection Expands the Utility of DNA-Encoded Small-Molecule Library Technology to Cell Surface Drug Targets: Identification of Novel Antagonists of the NK3 Tachykinin Receptor

30. Discovery, SAR, and X-ray Binding Mode Study of BCATm Inhibitors from a Novel DNA-Encoded Library

31. Encoded Library Synthesis Using Chemical Ligation and the Discovery of sEH Inhibitors from a 334-Million Member Library

32. Discovery of a Potent Class of PI3Kα Inhibitors with Unique Binding Mode via Encoded Library Technology (ELT)

33. Encoded Library Technology as a Source of Hits for the Discovery and Lead Optimization of a Potent and Selective Class of Bactericidal Direct Inhibitors of Mycobacterium tuberculosis InhA

34. Antiparasitic activities of novel, orally available fumagillin analogs

35. Orally Active Fumagillin Analogues: Transformations of a Reactive Warhead in the Gastric Environment

37. Metabolites of PPI-2458, a Selective, Irreversible Inhibitor of Methionine Aminopeptidase-2: Structure Determination and In Vivo Activity

38. Discovery of Highly Potent and Selective Small Molecule ADAMTS-5 Inhibitors That Inhibit Human Cartilage Degradation via Encoded Library Technology (ELT)

39. Carbamate Analogues of Fumagillin as Potent, Targeted Inhibitors of Methionine Aminopeptidase-2

40. Erratum: Design, synthesis and selection of DNA-encoded small-molecule libraries

41. Cell-Based Selection Expands the Utility of DNA-Encoded Small-Molecule Library Technology to Cell Surface Drug Targets: Identification of Novel Antagonists of the NK3 Tachykinin Receptor.

42. Encoded Library Technologyas a Source of Hits forthe Discovery and Lead Optimization of a Potent and Selective Classof Bactericidal Direct Inhibitors of Mycobacterium tuberculosisInhA.

43. Discovery of Highly Potentand Selective Small MoleculeADAMTS-5 Inhibitors That Inhibit Human Cartilage Degradationvia Encoded Library Technology (ELT).

44. Author Correction: Prioritizing multiple therapeutic targets in parallel using automated DNA-encoded library screening.

45. Rational Design of Macrocyclic Noncovalent Inhibitors of SARS-CoV-2 M pro from a DNA-Encoded Chemical Library Screening Hit That Demonstrate Potent Inhibition against Pan-Coronavirus Homologues and Nirmatrelvir-Resistant Variants.

46. Identification and Evaluation of Reversible Covalent Binders to Cys55 of Bfl-1 from a DNA-Encoded Chemical Library Screen.

47. Inhibitors of the Thioesterase Activity of Mycobacterium tuberculosis Pks13 Discovered Using DNA-Encoded Chemical Library Screening.

48. Structure Based Design of Non-Natural Peptidic Macrocyclic Mcl-1 Inhibitors.

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