123 results on '"Bukhtiyarova, Marina"'
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2. Continuous-flow reductive etherification of furfural over CuAlOx catalyst combined with HZSM-5-Al2O3 composite
3. Organic synthesis in flow mode by selective liquid-phase hydrogenation over heterogeneous non-noble metal catalysts.
4. In situ XPS study of methanol oxidation over a copper catalyst derived from layered double hydroxides.
5. Hydroprocessing of biomass feedstock over sulfided CoMo-, NiMo-, and NiW-supported catalysts for bio-jet fuel component production: a review.
6. Flow hydrogenation of 5-acetoxymethylfurfural over Cu-based catalysts
7. Cerastecin Inhibition of the Lipooligosaccharide Transporter MsbA to Combat Acinetobacter baumannii: From Screening Impurity to In VivoEfficacy
8. Structural characterization of nonactive site, TrkA-selective kinase inhibitors
9. Comparative Study of Batch and Continuous Flow Reactors in Selective Hydrogenation of Functional Groups in Organic Compounds: What Is More Effective?
10. Fragment-based screening approach reveals non-orthosteric pockets in the search for allosteric inhibitors of tau-tubulin kinase 1
11. CuAlOx catalyst for the batch-flow tandem synthesis of amino acid-derived furfurylamines
12. In situXPS study of methanol oxidation over a copper catalyst derived from layered double hydroxides
13. Potent targeted activator of cell kill molecules eliminate cells expressing HIV-1
14. Methanol Synthesis from Industrial CO2 Sources: A Contribution to Chemical Energy Conversion
15. Selective Hydrogenation of 5-Acetoxymethylfurfural over Cu-Based Catalysts in a Flow Reactor: Effect of Cu-Al Layered Double Hydroxides Synthesis Conditions on Catalytic Properties
16. Detailed Analysis of Human Cathepsin E Prime Region Specificity
17. Comparison of The Specificity of the Aspartic Proteinases Towards Internally Consistent Sets of Oligopeptide Substrates
18. Catalytic combustion of methane on substituted strontium ferrites
19. Flow Hydrogenation of 1,3,5-Trinitrobenzenes over Cu-Based Catalysts as an Efficient Approach for the Preparation of Phloroglucinol Derivatives
20. Effect of Phosphorus Precursor, Reduction Temperature, and Support on the Catalytic Properties of Nickel Phosphide Catalysts in Continuous-Flow Reductive Amination of Ethyl Levulinate
21. Selective catalytic reduction of nitrogen oxide by ammonia on substituted strontium ferrites
22. Selective catalytic reduction of nitrogen oxide by ammonia on Mn(Fe)-substituted Sr(La) aluminates
23. Identification of potent inhibitors of the sortilin-progranulin interaction
24. Structure and acid-base properties of hexaaluminates
25. Correlation of kinetic data with crystallographic structures of Aspartic Proteinase
26. Discovery of an Anion-Dependent Farnesyltransferase Inhibitor from a Phenotypic Screen
27. Two-Step One-Pot Reductive Amination of Furanic Aldehydes Using CuAlOx Catalyst in a Flow Reactor
28. Cu‐Al mixed oxide derived from layered double hydroxide as an efficient catalyst for continuous‐flow reductive amination of aromatic aldehydes
29. Improved expression, purification, and crystallization of p38α MAP kinase
30. A Biacore biosensor method for detailed kinetic binding analysis of small molecule inhibitors of p38α mitogen-activated protein kinase
31. Analysis of the pediocin AcH gene cluster from plasmid pSMB74 and its expression in a pediocin-negative Pediococcus acidilactici strain
32. Comparison of The Specificity of the Aspartic Proteinases Towards Internally Consistent Sets of Oligopeptide Substrates
33. Detailed Analysis of Human Cathepsin E Prime Region Specificity
34. Hepatitis C Virus NS3 Protease Requires Its NS4A Cofactor Peptide for Optimal Binding of a Boronic Acid Inhibitor as Shown by NMR
35. Discovery of an Anion-Dependent Farnesyltransferase Inhibitor from a Phenotypic Screen.
36. Analysis of imatinib and sorafenib binding to p38[alpha] compared with c-Abl and b-Raf provides structural insights for understanding the selectivity of inhibitors targeting the DFG-out form of protein kinases
37. Characterization of non-active site TrkA selective kinase inhibitors and implications on obtaining kinase selectivity
38. Structural characterization of nonactive site, TrkA-selective kinase inhibitors
39. Discovery of a novel class of non-ATP site DFG-out state p38 inhibitors utilizing computationally assisted virtual fragment-based drug design (vFBDD)
40. Structural characterization of nonactive site, TrkA-selective kinase inhibitors.
41. The rational design of a novel potent analogue of the 5′-AMP-activated protein kinase inhibitor compound C with improved selectivity and cellular activity
42. Correlation of kinetic data with crystallographic structures of Aspartic Proteinase
43. Structure-based design of substituted biphenyl ethylene ethers as ligands binding in the hydrophobic pocket of gp41 and blocking the helical bundle formation
44. Steam reforming of methane over Ni-substituted Sr hexaaluminates
45. Synthesis and Pharmacological Evaluation of N-(3-(1H-Indol-4-yl)-5-(2-methoxyisonicotinoyl)phenyl)methanesulfonamide (LP-261), a Potent Antimitotic Agent
46. Discovery and SAR of a series of 4,6-diamino-1,3,5-triazin-2-ol as novel non-nucleoside reverse transcriptase inhibitors of HIV-1
47. Mutagenesis of p38α MAP Kinase Establishes Key Roles of Phe169 in Function and Structural Dynamics and Reveals a Novel DFG-OUT State
48. Two classes of p38α MAP kinase inhibitors having a common diphenylether core but exhibiting divergent binding modes
49. Inhibition of the Bovine Viral Diarrhoea Virus NS3 Serine Protease by a Boron-Modified Peptidyl Mimetic of its Natural Substrate
50. Complete nucleotide sequence of pSMB 74, a plasmid encoding the production of pediocin AcH in Pediococcus acidilactici
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