183 results on '"Myasoedov, N. F."'
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2. The Use of D2 and Deuterated Water for the Introduction of a Label into 4-Aminobutanoic Acid
3. Development of a Novel Method for Activation of Isotope Exchange
4. Production of Deuterium-Labeled β-Alanyl-L-histidine by Isotope Exchange
5. Incorporation of Hydrogen Isotopes into Biologically Active Compounds
6. Tritium-Labeled Dopamine, Serotonin, and Doxorubicine Derivatives Containing Fragments Unstable under Hydrogenation Conditions
7. Synthesis of Tritium-Labeled Proline Derivatives of Dopamine, Serotonin, and Doxorubicin, All Containing a tert-Butyloxycarbonyl Group or Lauric Acid
8. Synthesis of Tritium-Labeled Non-Natural Analogs of Purine and Pyrimidine Nucleosides
9. Synthesis of Tritium-Labeled Deoxyglucose and Its Derivative
10. Pathways for Activating Isotope Exchange of Dopamine with D2O.
11. The Use of D2 and Deuterated Water for the Introduction of a Label into 4-Aminobutanoic Acid.
12. Heterogeneous Catalytic Synthesis of Organic Compounds Labeled with Hydrogen Isotopes without Using Solvents
13. Influence of the conditions of deuterium and tritium labeling of His–Phe–Arg–Trp–Pro–Gly–Pro oligopeptide on the isotope exchange efficiency
14. Preparation of deuterium- or tritium-labeled nicotine
15. Influence of the nature of activated hydrogen isotope species on the isotope exchange efficiency, with preparation of labeled sodium 4-phenylbenzoate as example
16. Efficiency of isotope exchange between sodium 4-phenylbenzoate and activated tritium
17. Introduction of deuterium and tritium into 2-methyl-5-(p-methoxyphenyl)benzoic acid N-methylamide and N-methyl-N-(2-methyl-4-methoxy-5-trifluoromethylphenyl)-N′-methylurea
18. Synthesis of tritium- and deuterium-labeled isopentenyladenine
19. Specific features of deuterium and tritium labeling of SB258585
20. Specific features of deuterium and tritium labeling of Pro-Gly-Pro-Leu and of physiologically active amino acids
21. Tritium labeling of bioorganic compounds by isotope exchange
22. Solid-phase catalytic reactions of tritium with carbohydrates: 5. Mechanism of isomerization of epimeric disaccharides in the course of solid-phase catalytic hydrogenation with tritium
23. Solid-phase synthesis of deuterium- and tritium-labeled dopamine using carbon nanomaterials
24. Solid-phase catalytic reactions of tritium with carbohydrates: 4. Mechanism of isomerization of D-glucose in the course of solid-phase catalytic hydrogenation with tritium
25. Synthesis of Pro-Pro-Ile, a corticoliberin fragment, labeled with tritium in proline unit
26. Introduction of hydrogen isotopes into Win 55212 and CP 55940, selective agonists of cannabinoid receptors
27. Hydrogen isotope labeling of PTC124
28. Hydrogen isotope labeling of α-hederin and a mass-spectrometric study of deuterium distribution
29. A biotechnological procedure for preparing short peptides and their radioactively labeled analogs for estimating specific binding of Semax and its metabolites in various sections of rat brain
30. Use of methyl p-toluenesulfonate labeled with hydrogen isotopes as a donor of methyl group
31. Synthesis of tritium-labeled dermorphin fragments and kinetics of radioactivity distribution in rat organs upon intramuscular injection of these peptides
32. Synthesis of tritium-labeled Semax
33. Optimization of Conditions for Tritium Labeling of Organic Compounds by Isotope Exchange with Tritium Water, Based on the Concepts of Reactions on the Catalyst Surface
34. A Comparative Study of the Reactions of Thermally Activated Tritium with Sugars and Diazines and of Solid-Phase Catalytic Hydrogenation of These Compounds with Tritium
35. Synthesis of steroid hormones highly labeled with tritium and their use for assessing the activity of aromatase
36. Synthesis of Labeled Compounds Using Labeled Reagents
37. Synthesis of Tyr-Pro-Phe-Val-Glu-L-[3,4-3H]Pro-Ile, Tyr-D-Ala-Phe-Gly-Tyr-L-[3,4-3H]Pro-Ser-NH2, and Tyr-D-Ala-Phe-Gly-Tyr-D-[3,4-3H]Pro-Ser-NH2, Labeled Analogs of Human β-Casomorphin and Dermorphin
38. Tritium Labeling of Derivatives of Amino Sugars and Sialic Acids
39. Effect of Various Additives on the Yield and Molar Radioactivity of Labeled Products in Solid-Phase Isotope Exchange
40. Effect of Technetium on the Efficiency of Solid-Phase Isotope Exchange
41. Influence of the Catalyst and Support on the Efficiency of Solid-Phase Isotope Exchange between Gaseous Tritium and Phenylalanine
42. Tritium Labeling of Androst-4-ene-3,17-dione by Liquid-Phase Selective Hydrogenation and Factors Affecting the Process
43. Influence of Tritium Spillover on the Efficiency of Labeling of Organic Compounds
44. Selective Tritium Labeling by a Solid-Phase Procedure
45. Synthesis of High-Molar-Activity Tritium-Labeled Biologically Active Compounds Containing Aromatic and Heterocyclic Fragments
46. Use of Tritium-Labeled Compounds for Analysis of Steroids and Peptides in Biological Objects
47. Synthesis of [3H]Sulfobromophthalein and Related Problems of Tritium Labeling by Solid-Phase Isotope Exchange
48. Synthesis of tritium-labeled 5-fluorouracil and 5-fluorocytosine
49. Introduction of hydrogen isotopes into Maraviroc and mass-spectrometric study of deuterium distribution
50. A Biotechnological Procedure for Preparing Short Peptides and Their Radioactively Labeled Analogs for Estimating Specific Binding of Semax and Its Metabolites in Various Sections of Rat Brain
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