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Статьи (16)

# Публикация
1 Meshkova Y.V. , Baev D.S. , Sorokina I.V. , Popadyuk I.I. , Salomatina O.V. , Zhukova N.A. , Tolstikova T.G. , Salakhutdinov N.F.
Experimental Evaluation of 3-meta-Pyridine-1,2,4-Oxadiazole Derivative of Deoxycholic Acid as a Prototype of 5-α-Reductase Inhibitors in In Silico and In Vivo Models
Russian Journal of Bioorganic Chemistry. 2023. V.49. N1. P.52-64. DOI: 10.1134/s1068162023010181 WOS Scopus РИНЦ OpenAlex
2 Мешкова Ю.В. , Баев Д.С. , Сорокина И.В. , Попадюк И.И. , Саломатина О.В. , Жукова Н.А. , Толстикова Т.Г. , Салахутдинов Н.Ф.
ЭКСПЕРИМЕНТАЛЬНАЯ ОЦЕНКА 3-МЕТА-ПИРИДИН-1,2,4-ОКСАДИАЗОЛЬНОГО ПРОИЗВОДНОГО ДЕЗОКСИХОЛЕВОЙ КИСЛОТЫ КАК ПРОТОТИПА ИНГИБИТОРОВ 5-α-РЕДУКТАЗЫ В МОДЕЛЯХ IN SILICO И IN VIVO
Биоорганическая химия (RUSS J BIOORG CHEM+). 2023. Т.49. №1. С.79-92. DOI: 10.31857/S0132342323010189 РИНЦ OpenAlex
3 Chernyshov V.V. , Yarovaya O.I. , Esaulkova I.L. , Sinegubova E. , Borisevich S.S. , Popadyuk I.I. , Zarubaev V.V. , Salakhutdinov N.F.
Novel O-acylated amidoximes and substituted 1,2,4-oxadiazoles synthesised from (+)-ketopinic acid possessing potent virus-inhibiting activity against phylogenetically distinct influenza A viruses
Bioorganic and Medicinal Chemistry Letters. 2022. V.55. 128465 . DOI: 10.1016/j.bmcl.2021.128465 WOS Scopus OpenAlex
4 Salomatina O.V. , Dyrkheeva N.S. , Popadyuk I.I. , Zakharenko A.L. , Ilina E.S. , Komarova N.I. , Reynisson J. , Salakhutdinov N.F. , Lavrik O.I. , Volcho K.P.
New deoxycholic acid derived tyrosyl-dna phosphodiesterase 1 inhibitors also inhibit tyrosyl-dna phosphodiesterase 2
Molecules. 2022. V.27. N1. 72 . DOI: 10.3390/molecules27010072 WOS Scopus РИНЦ OpenAlex
5 Chernyshov V.V. , Popadyuk I.I. , Yarovaya O.I. , Salakhutdinov N.F.
Nitrogen-Containing Heterocyclic Compounds Obtained from Monoterpenes or Their Derivatives: Synthesis and Properties
Topics in Current Chemistry. 2022. V.380. N5. 42 :1-64. DOI: 10.1007/s41061-022-00399-1 WOS Scopus РИНЦ OpenAlex
6 Salomatina O.V. , Popadyuk I.I. , Zakharenko A.L. , Zakharova O.D. , Chepanova A.A. , Dyrkheeva N.S. , Komarova N.I. , Reynisson J. , Anarbaev R.O. , Salakhutdinov N.F. , Lavrik O.I. , Volcho K.P.
Deoxycholic acid as a molecular scaffold for tyrosyl-DNA phosphodiesterase 1 inhibition: A synthesis, structure–activity relationship and molecular modeling study
Steroids. 2021. V.165. 108771 . DOI: 10.1016/j.steroids.2020.108771 WOS Scopus РИНЦ OpenAlex
7 Markov A.V. , Sen'kova A.V. , Popadyuk I.I. , Salomatina O.V. , Logashenko E.B. , Komarova N.I. , Ilyina A.A. , Salakhutdinov N.F. , Zenkova M.A.
Novel 3 '-Substituted-1 ',2 ',4 '-Oxadiazole Derivatives of 18 beta H-Glycyrrhetinic Acid and Their O-Acylated Amidoximes: Synthesis and Evaluation of Antitumor and Anti-Inflammatory Potential In Vitro and In Vivo
International Journal of Molecular Sciences. 2020. V.21. N10. 3511 . DOI: 10.3390/ijms21103511 WOS Scopus РИНЦ OpenAlex
8 Kokina T.E. , Salomatina O.V. , Popadyuk I.I. , Glinskaya L.A. , Korol'kov I.V. , Sheludyakova L.A. , Rakhmanova M.I. , Salakhutdinov N.F.
Complexes of Zn(II) and Cu(II) with the Amino Derivatives of Deoxycholic Acid: Syntheses, Structures, and Properties
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 2019. V.45. N7. P.505-511. DOI: 10.1134/S1070328419070030 WOS Scopus РИНЦ OpenAlex
9 Markov A.V. , Babich V.O. , Popadyuk I.I. , Salomatina O.V. , Logashenko E.B. , Salakhutdinov N.F. , Zenkova M.A.
Novel Derivatives of Deoxycholic Acid Bearing Linear Aliphatic Diamine and Aminoalcohol Moieties and their Cyclic Analogs at the C3 Position: Synthesis and Evaluation of Their In Vitro Antitumor Potential
Molecules. 2019. V.24. N14. 2644 . DOI: 10.3390/molecules24142644 WOS Scopus РИНЦ OpenAlex
10 Кокина Т.Е. , Саломатина О.В. , Попадюк И.И. , Глинская Л.А. , Корольков И.В. , Шелудякова Л.А. , Рахманова М.И. , Салахутдинов Н.Ф.
Комплексы Zn(II) и Cu(II) c аминопроизводными дезоксихолевой кислоты: синтез, структура, свойства
Координационная химия (RUSS J COORD CHEM+). 2019. Т.45. №7. С.420-426. DOI: 10.1134/S0132344X1907003X РИНЦ OpenAlex
11 Salomatina O.V. , Popadyuk I.I. , Zakharenko A.L. , Zakharova O.D. , Fadeev D.S. , Komarova N.I. , Reynisson J. , Arabshahi H.J. , Chand R. , Volcho K.P. , Salakhutdinov N.F. , Lavrik O.I.
Novel Semisynthetic Derivatives of Bile Acids as Effective Tyrosyl-DNA Phosphodiesterase 1 Inhibitors
Molecules. 2018. V.23. N3. 679 . DOI: 10.3390/molecules23030679 WOS Scopus РИНЦ OpenAlex
12 Попадюк И.И. , Саломатина О.В. , Салахутдинов Н.Ф.
Современные подходы к модификации желчных кислот с целью синтеза соединений, обладающих ценными физико-химическими и биологическими свойствами
Успехи химии/Uspekhi Khimii. 2017. Т.86. №5. С.388-443. DOI: 10.1070/RCR4683?locatt=label:RUSSIAN РИНЦ
13 Popadyuk I.I. , Markov A.V. , Morozova E.A. , Babich V.O. , Salomatina O.V. , Logashenko E.B. , Zenkova M.A. , Tolstikova T.G. , Salakhutdinov N.F.
Synthesis and evaluation of antitumor, anti-inflammatory and analgesic activity of novel deoxycholic acid derivatives bearing aryl- or hetarylsulfanyl moieties at the C-3 position
Steroids. 2017. V.127. P.1-12. DOI: 10.1016/j.steroids.2017.08.016 WOS Scopus РИНЦ OpenAlex
14 Popadyuk I.I. , Markov A.V. , Babich V.O. , Salomatina O.V. , Logashenko E.B. , Zenkova M.A. , Salakhutdinov N.F.
Novel derivatives of deoxycholic acid bearing aliphatic or cyclic diamine moieties at the C-3 position: Synthesis and evaluation of anti-proliferative activity
Bioorganic and Medicinal Chemistry Letters. 2017. V.27. N16. P.3755-3759. DOI: 10.1016/j.bmcl.2017.06.072 WOS Scopus РИНЦ OpenAlex
15 Poopadyuk I.I. , Salomatina O.V. , Salakhutdinov N.F.
Modern approaches to modification of bile acids for the synthesis of compounds possessing valuable physicochemical and biological properties
Russian Chemical Reviews. 2017. V.86. N5. P.388-443. DOI: 10.1070/RCR4683 WOS Scopus РИНЦ OpenAlex
16 Popadyuk I.I. , Markov A.V. , Salomatina O.V. , Logashenko E.B. , Shernyukov A.V. , Zenkova M.A. , Salakhutdinov N.F.
Synthesis and biological activity of novel deoxycholic acid derivatives
Bioorganic and Medicinal Chemistry. 2015. V.23. N15. P.5022-5034. DOI: 10.1016/j.bmc.2015.05.012 WOS Scopus РИНЦ OpenAlex

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