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Synthesis of Phosphinic Pseudomethionyl-Glutamyl-Histidine.
- Published in:
- Russian Journal of General Chemistry, 2023, v. 93, n. 8, p. 2022, doi. 10.1134/S1070363223080108
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- Article
Synthesis of Deuterium-Labelled Salicylcarnosine.
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- Doklady Chemistry, 2023, v. 511, n. 1, p. 181, doi. 10.1134/S0012500823600542
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- Article
Synthesis of Deuterium-Labeled Ouabain – an Internal Standard in Toxicological and Pharmacological Studies.
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- Pharmaceutical Chemistry Journal, 2023, v. 56, n. 11, p. 1491, doi. 10.1007/s11094-023-02819-y
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- Article
Synthesis of Deuterium-Labeled Pyrrolylcarnosine.
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- Doklady Biochemistry & Biophysics, 2022, v. 507, n. 1, p. 374, doi. 10.1134/S1607672922340130
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- Article
Investigation of the Membranotropic Properties of Acylated Peptide Derivatives of Dopamine and Serotonin Using the Pampa Method.
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- Pharmaceutical Chemistry Journal, 2022, v. 56, n. 5, p. 602, doi. 10.1007/s11094-022-02683-2
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- Article
Metabolism by Rhizobacteria of Abscisic Acid Deuterated in the Cyclohexene Part.
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- Pharmaceutical Chemistry Journal, 2021, v. 55, n. 7, p. 745, doi. 10.1007/s11094-021-02487-w
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- Article
Synthesis of Deuterium-Labeled N-Methyl-D-Aspartate.
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- Doklady Chemistry, 2021, v. 500, n. 1, p. 177, doi. 10.1134/S0012500821090056
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- Article
Synthesis and Study of Properties of Phosphinic Pseudo-Prolylglycylproline.
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- Doklady Chemistry, 2021, v. 498, n. 1, p. 93, doi. 10.1134/S001250082102004X
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- Article
Assessment of the Cytotoxicity of Peptide Modifications of Doxorubicin on Tetrahymena pyriformis.
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- Doklady Biochemistry & Biophysics, 2021, v. 497, n. 1, p. 104, doi. 10.1134/S1607672921020125
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- Article
Comparative Study of the Abscisic Acid Metabolism Using Analogue Tritium-Labeled in the Cyclohexene or Side Moiety.
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- Doklady Chemistry, 2020, v. 491, n. 1, p. 41, doi. 10.1134/S0012500820030015
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- Article
Efficiency of Penetration of Dopamine and Serotonin Peptide Derivatives through the Artificial Membranes.
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- Doklady Biochemistry & Biophysics, 2019, v. 488, n. 1, p. 354, doi. 10.1134/S1607672919050168
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- Article
Peptide Derivatives of Some Physiologically Active Substances.
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- Doklady Chemistry, 2019, v. 487, n. 1, p. 173, doi. 10.1134/S0012500819070048
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- Article
Prospects for Intranasal Delivery of Neuropeptides to the Brain.
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- Pharmaceutical Chemistry Journal, 2019, v. 53, n. 2, p. 89, doi. 10.1007/s11094-019-01960-x
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- Article
Synthesis of Isotopically Modified Derivatives of Dopamine, Serotonin, and Doxorubicin with Boc-Pro and Boc-[<sup>2</sup>H]Pro.
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- Doklady Chemistry, 2019, v. 485, n. 1, p. 87, doi. 10.1134/S0012500819030030
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- Article
Solid-State Catalytic Isotope Exchange of Hydrogen for Deuterium in Cyclopropylglycine.
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- Doklady Physical Chemistry, 2019, v. 484, n. 1, p. 15, doi. 10.1134/S0012501619010056
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- Article
Synthesis of Tritiated Glutamic Acid and Pyroglutamate.
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- Doklady Chemistry, 2018, v. 483, n. 1, p. 261, doi. 10.1134/S0012500818110034
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- Article
Synthesis of Deuterated or Tritiated Glycine and Its Methyl Ester.
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- Doklady Chemistry, 2018, v. 483, n. 1, p. 266, doi. 10.1134/S0012500818110071
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- Article
Synthesis and Testing of Abscisic Acid with Predominant Replacement of Protium Atoms by Tritium in the Cyclohexene Moiety.
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- Doklady Chemistry, 2018, v. 483, n. 1, p. 268, doi. 10.1134/S0012500818110113
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- Article
Stability In Vitro of 5-oxo-Pro-Arg-Pro, 5-oxo-Pro-His-Pro-Gly-ProNH<sub>2</sub>, and Phe-Pro-Leu-Pro-Ala.
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- Pharmaceutical Chemistry Journal, 2018, v. 52, n. 8, p. 685, doi. 10.1007/s11094-018-1881-7
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- Article
Synthesis of Deuterium- or Tritium-Labeled Norepinephrine and Evaluation of Its Biological Activity.
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- Doklady Chemistry, 2018, v. 480, n. 2, p. 117, doi. 10.1134/S001250081806006X
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- Article
Synthesis of tritium-labeled dermorphin fragments and kinetics of radioactivity distribution in rat organs upon intramuscular injection of these peptides.
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- Radiochemistry, 2007, v. 49, n. 1, p. 102, doi. 10.1134/S1066362207010195
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- Article
Syntheses of radiolabeled ABT-578 for ADME studies.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2006, v. 49, n. 10, p. 849, doi. 10.1002/jlcr.1091
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- Article
Synthesis of tritium-labeled Semax.
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- Radiochemistry, 2006, v. 48, n. 3, p. 288, doi. 10.1134/S1066362206030155
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- Article
Synthesis of tritium-labeled Selank.
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- Radiochemistry, 2006, v. 48, n. 3, p. 296, doi. 10.1134/S1066362206030167
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- Article
Synthesis of tritium-labelled BIBN4096, an experimental h-CGRP-antagonist.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2006, v. 49, n. 5, p. 421, doi. 10.1002/jlcr.1061
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- Article
Synthesis of steroid hormones highly labeled with tritium and their use for assessing the activity of aromatase.
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- Radiochemistry, 2004, v. 46, n. 5, p. 494, doi. 10.1007/s11137-005-0018-5
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- Article
Tritium Labeling of Biologically Active Compounds Using Fibrous Carbon as Support.
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- Radiochemistry, 2004, v. 46, n. 4, p. 400, doi. 10.1023/B:RACH.0000039120.78163.2c
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- Article
Synthesis of tritiated Cyclosporin A and FK-506 by metal-catalyzed hydrogen isotope exchange.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2004, v. 47, n. 7, p. 407, doi. 10.1002/jlcr.827
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- Article
Synthesis of Tyr-Pro-Phe-Val-Glu-L-[3,4-<sup>3</sup>H]Pro-Ile, Tyr-D-Ala-Phe-Gly-Tyr-L-[3,4-<sup>3</sup>H]Pro-Ser-NH<sub>2</sub>, and Tyr-D-Ala-Phe-Gly-Tyr-D-[3,4-<sup>3</sup>H]Pro-Ser-NH<sub>2</sub>, Labeled Analogs of Human β-Casomorphin and Dermorphin
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- Radiochemistry, 2004, v. 46, n. 1, p. 67, doi. 10.1023/B:RACH.0000024640.15004.4a
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- Article
Synthesis of Labeled Compounds Using Labeled Reagents.
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- Radiochemistry, 2004, v. 46, n. 1, p. 77, doi. 10.1023/B:RACH.0000024641.49263.14
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- Article
Tritium Labeling of Derivatives of Amino Sugars and Sialic Acids.
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- Radiochemistry, 2003, v. 45, n. 2, p. 172, doi. 10.1023/A:1023841527761
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- Article
Effect of Various Additives on the Yield and Molar Radioactivity of Labeled Products in Solid-Phase Isotope Exchange.
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- Radiochemistry, 2003, v. 45, n. 1, p. 81, doi. 10.1023/A:1022333905411
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- Article
10<sup>th</sup> Conference of the Central European Division e.V. of the International Isotope Society.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 2002, v. 45, n. 13, p. 1159, doi. 10.1002/jlcr.658
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- Article
Synthesis of labelled oxylipins: leukotriene A<sub>4</sub> and 8- epi-prostaglandin F<sub>2α</sub>.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1999, v. 42, n. 7, p. 663, doi. 10.1002/(SICI)1099-1344(199907)42:7<663::AID-JLCR228>3.0.CO;2-K
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- Article
Synthesis of tritium-labelled biologically active analogues of progesterone by selective hydrogenation of 16α,17α-cyclohex-3′-en-pregna-1,4-dien-3,20-dione.
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- Journal of Labelled Compounds & Radiopharmaceuticals, 1998, v. 41, n. 10, p. 919, doi. 10.1002/(SICI)1099-1344(1998100)41:10<919::AID-JLCR150>3.0.CO;2-A
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- Article