Search

Your search keyword '"Decicco, C. P."' showing total 83 results

Search Constraints

Start Over You searched for: Author "Decicco, C. P." Remove constraint Author: "Decicco, C. P."
83 results on '"Decicco, C. P."'

Search Results

1. Purification and Cloning of Aggrecanase-1: A Member of the ADAMTS Family of Proteins

2. Biology of TACE inhibition

13. Discovery of CC Chemokine Receptor-3 (CCR3) Antagonists with Picomolar Potency

14. Design, Synthesis, and Evaluation of Benzothiadiazepine Hydroxamates as Selective Tumor Necrosis Factor-α Converting Enzyme Inhibitors

15. Discovery of γ-Lactam Hydroxamic Acids as Selective Inhibitors of Tumor Necrosis Factor α Converting Enzyme:  Design, Synthesis, and Structure−Activity Relationships

16. Discovery and Structure−Activity Relationship of N-(Ureidoalkyl)-Benzyl-Piperidines As Potent Small Molecule CC Chemokine Receptor-3 (CCR3) Antagonists

18. Design and Synthesis of a Series of (2R)-N<SUP>4</SUP>-Hydroxy-2-(3-hydroxybenzyl)-N<SUP>1</SUP>- [(1S,2R)-2-hydroxy-2,3-dihydro-1H-inden- 1-yl]butanediamide Derivatives as Potent, Selective, and Orally Bioavailable Aggrecanase Inhibitors

19. Discovery of Macrocyclic Hydroxamic Acids Containing Biphenylmethyl Derivatives at P1‘, a Series of Selective TNF-α Converting Enzyme Inhibitors with Potent Cellular Activity in the Inhibition of TNF-α Release

20. Design, Synthesis, and Structure−Activity Relationships of Macrocyclic Hydroxamic Acids That Inhibit Tumor Necrosis Factor α Release in Vitro and in Vivo

21. Intramolecular O-Arylation of Phenols with Phenylboronic Acids:  Application to the Synthesis of Macrocyclic Metalloproteinase Inhibitors

24. Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family.

25. Generation and characterization of aggrecanase. A soluble, cartilage-derived aggrecan-degrading activity.

27. Cleavage of native cartilage aggrecan by neutrophil collagenase (MMP-8) is distinct from endogenous cleavage by aggrecanase.

33. Sultam Hydroxamates as Novel Matrix Metalloproteinase Inhibitors

34. A Concise Synthesis of Silanediol-Based Transition-State Isostere Inhibitors of Proteases

35. 1-Aminocyclopropaneboronic Acid:  Synthesis and Incorporation into an Inhibitor of Hepatitis C Virus NS3 Protease

44. Discovery of macrocyclic hydroxamic acids containing biphenylmethyl derivatives at P1', a series of selective TNF-alpha converting enzyme inhibitors with potent cellular activity in the inhibition of TNF-alpha release.

45. Photochemically enhanced binding of small molecules to the tumor necrosis factor receptor-1 inhibits the binding of TNF-alpha.

46. Design, synthesis, and structure-activity relationships of macrocyclic hydroxamic acids that inhibit tumor necrosis factor alpha release in vitro and in vivo.

47. Alpha-ketoamides, alpha-ketoesters and alpha-diketones as HCV NS3 protease inhibitors.

48. Therapeutic potential and strategies for inhibiting tumor necrosis factor-alpha.

49. Aggrecanase. A target for the design of inhibitors of cartilage degradation.

50. P1, P2'-linked macrocyclic amine derivatives as matrix metalloproteinase inhibitors.

Catalog

Books, media, physical & digital resources