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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

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

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

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

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

26. Stitched α-Helical Peptides via Bis Ring-Closing Metathesis

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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