38 results on '"Kutchukian, Peter S."'
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2. Molecular Profiling Reveals a Common Metabolic Signature of Tissue Fibrosis
3. Enhancing the Small-Scale Screenable Biological Space beyond Known Chemogenomics Libraries with Gray Chemical Matter─Compounds with Novel Mechanisms from High-Throughput Screening Profiles
4. CHEMGENIE: integration of chemogenomics data for applications in chemical biology
5. Pocket Crafter: A 3D Generative Modeling Based Workflow for the Rapid Generation of Hit Molecules in Drug Discovery
6. Prospective Assessment of Virtual Screening Heuristics Derived Using a Novel Fusion Score
7. New insights from old data - Hunting for compounds with novel mechanisms using cellular high-throughput screening profiles with Grey Chemical Matter
8. Large Scale Meta-Analysis of Fragment-Based Screening Campaigns: Privileged Fragments and Complementary Technologies
9. Enforced Presentation of an Extrahelical Guanine to the Lesion Recognition Pocket of Human 8-Oxoguanine Glycosylase, hOGG1
10. Mapping Targetable Sites on Human Telomerase RNA Pseudoknot/Template Domain Using 2′-OMe RNA-interacting Polynucleotide (RIPtide) Microarrays
11. Fragment Library Design: Using Cheminformatics and Expert Chemists to Fill Gaps in Existing Fragment Libraries
12. CHEMOMETRIC APPLICATIONS OF NAÏVE BAYESIAN MODELS IN DRUG DISCOVERY
13. In SilicoFragment-Based Generation of Drug-Like Compounds
14. Discovery of an Anion-Dependent Farnesyltransferase Inhibitor from a Phenotypic Screen
15. Chemistry informer libraries: a chemoinformatics enabled approach to evaluate and advance synthetic methods† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c5sc04751j Click here for additional data file
16. Reaction of Superoxide and Nitric Oxide with Peroxynitrite: IMPLICATIONS FOR PEROXYNITRITE-MEDIATED OXIDATION REACTIONSIN VIVO
17. Discovery of an Anion-Dependent Farnesyltransferase Inhibitor from a Phenotypic Screen.
18. All-atom model for stabilization of [alpha]-helical structure in peptides by hydrocarbon staples
19. Molecular Profiling Reveals a Common Metabolic Signature of Tissue Fibrosis
20. Linking High-Throughput Screens to Identify MoAs and Novel Inhibitors of Mycobacterium tuberculosis Dihydrofolate Reductase
21. Representing high throughput expression profiles via perturbation barcodes reveals compound targets
22. Iterative Focused Screening with Biological Fingerprints Identifies Selective Asc-1 Inhibitors Distinct from Traditional High Throughput Screening
23. Synthesis of Complex Druglike Molecules by the Use of Highly Functionalized Bench-Stable Organozinc Reagents
24. Linking High-Throughput Screens to Identify MoAs and Novel Inhibitors of Mycobacterium tuberculosisDihydrofolate Reductase
25. Correction to “Stitched α-Helical Peptides via Bis Ring-Closing Metathesis”
26. Stitched α-Helical Peptides via Bis Ring-Closing Metathesis
27. Efficient Search of Chemical Space: Navigating from Fragments to Structurally Diverse Chemotypes
28. Construction of Drug‐Like Compounds by Markov Chains
29. Inside the Mind of a Medicinal Chemist: The Role of Human Bias in Compound Prioritization during Drug Discovery
30. Structure of the Stapled p53 Peptide Bound to Mdm2
31. De novodesign: balancing novelty and confined chemical space
32. Introduction of All-Hydrocarbon i,i+3 Staples into α-Helices via Ring-Closing Olefin Metathesis
33. FOG: Fragment Optimized Growth Algorithm for the de Novo Generation of Molecules Occupying Druglike Chemical Space
34. All-Atom Model for Stabilization of α-Helical Structure in Peptides by Hydrocarbon Staples
35. Efficient Search of ChemicalSpace: Navigating fromFragments to Structurally Diverse Chemotypes.
36. Structure of the Stapled p53 Peptide Bound to Mdm2.
37. Fragment library design: using cheminformatics and expert chemists to fill gaps in existing fragment libraries.
38. De novo design: balancing novelty and confined chemical space.
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