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Showing 1 to 8 of 8 entries
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Fauna europaea: Diptera - brachycera.

Biodiversity data journal

Pape T, Beuk P, Pont AC, Shatalkin AI, Ozerov AL, Woźnica AJ, Merz B, Bystrowski C, Raper C, Bergström C, Kehlmaier C, Clements DK, Greathead D, Kameneva EP, Nartshuk E, Petersen FT, Weber G, Bächli G, Geller-Grimm F, Van de Weyer G, Tschorsnig HP, de Jong H, van Zuijlen JW, Vaňhara J, Roháček J, Ziegler J, Majer J, Hůrka K, Holston K, Rognes K, Greve-Jensen L, Munari L, de Meyer M, Pollet M, Speight MC, Ebejer MJ, Martinez M, Carles-Tolrá M, Földvári M, Chvála M, Barták M, Evenhuis NL, Chandler PJ, Cerretti P, Meier R, Rozkosny R, Prescher S, Gaimari SD, Zatwarnicki T, Zeegers T, Dikow T, Korneyev VA, Richter VA, Michelsen V, Tanasijtshuk VN, Mathis WN, Hubenov Z, de Jong Y.
PMID: 25733962
Biodivers Data J. 2015 Feb 20;(3):e4187. doi: 10.3897/BDJ.3.e4187. eCollection 2015.

Fauna Europaea provides a public web-service with an index of scientific names (including important synonyms) of all extant multicellular European terrestrial and freshwater animals and their geographical distribution at the level of countries and major islands (east of the...

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Pape T, Beuk P, Pont AC, et al. Fauna europaea: Diptera - brachycera. Biodivers Data J. 2015;(3):e4187doi: 10.3897/BDJ.3.e4187.
Pape, T., Beuk, P., Pont, A. C., Shatalkin, A. I., Ozerov, A. L., Woźnica, A. J., Merz, B., Bystrowski, C., Raper, C., Bergström, C., Kehlmaier, C., Clements, D. K., Greathead, D., Kameneva, E. P., Nartshuk, E., Petersen, F. T., Weber, G., Bächli, G., Geller-Grimm, F., Van de Weyer, G., Tschorsnig, H. P., de Jong, H., van Zuijlen, J. W., Vaňhara, J., Roháček, J., Ziegler, J., Majer, J., Hůrka, K., Holston, K., Rognes, K., Greve-Jensen, L., Munari, L., de Meyer, M., Pollet, M., Speight, M. C., Ebejer, M. J., Martinez, M., Carles-Tolrá, M., Földvári, M., Chvála, M., Barták, M., Evenhuis, N. L., Chandler, P. J., Cerretti, P., Meier, R., Rozkosny, R., Prescher, S., Gaimari, S. D., Zatwarnicki, T., Zeegers, T., Dikow, T., Korneyev, V. A., Richter, V. A., Michelsen, V., Tanasijtshuk, V. N., Mathis, W. N., Hubenov, Z., & de Jong, Y. (2015). Fauna europaea: Diptera - brachycera. Biodiversity data journal, (3), e4187. https://doi.org/10.3897/BDJ.3.e4187
Pape, Thomas, et al. "Fauna europaea: Diptera - brachycera." Biodiversity data journal vol. ,3 (2015): e4187. doi: https://doi.org/10.3897/BDJ.3.e4187
Pape T, Beuk P, Pont AC, Shatalkin AI, Ozerov AL, Woźnica AJ, Merz B, Bystrowski C, Raper C, Bergström C, Kehlmaier C, Clements DK, Greathead D, Kameneva EP, Nartshuk E, Petersen FT, Weber G, Bächli G, Geller-Grimm F, Van de Weyer G, Tschorsnig HP, de Jong H, van Zuijlen JW, Vaňhara J, Roháček J, Ziegler J, Majer J, Hůrka K, Holston K, Rognes K, Greve-Jensen L, Munari L, de Meyer M, Pollet M, Speight MC, Ebejer MJ, Martinez M, Carles-Tolrá M, Földvári M, Chvála M, Barták M, Evenhuis NL, Chandler PJ, Cerretti P, Meier R, Rozkosny R, Prescher S, Gaimari SD, Zatwarnicki T, Zeegers T, Dikow T, Korneyev VA, Richter VA, Michelsen V, Tanasijtshuk VN, Mathis WN, Hubenov Z, de Jong Y. Fauna europaea: Diptera - brachycera. Biodivers Data J. 2015 Feb 20;(3):e4187. doi: 10.3897/BDJ.3.e4187. eCollection 2015. PMID: 25733962; PMCID: PMC4339814.
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Accommodation of a dimer in an Ar-like lattice: exploring the generic structural motifs.

Physical chemistry chemical physics : PCCP

Ozerov GK, Bezrukov DS, Buchachenko AA.
PMID: 31313774
Phys Chem Chem Phys. 2019 Aug 14;21(30):16549-16563. doi: 10.1039/c9cp02119a. Epub 2019 Jul 17.

A global optimization strategy is applied to Lennard-Jones models describing the stable trapping sites of a dimer in the face-centered cubic Ar-like lattice. Effective volumes of the trapping sites, quantified as the number of host atoms dislodged from the...

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Ozerov GK, Bezrukov DS, Buchachenko AA. Accommodation of a dimer in an Ar-like lattice: exploring the generic structural motifs. Phys Chem Chem Phys. 2019;21(30):16549-16563doi: 10.1039/c9cp02119a.
Ozerov, G. K., Bezrukov, D. S., & Buchachenko, A. A. (2019). Accommodation of a dimer in an Ar-like lattice: exploring the generic structural motifs. Physical chemistry chemical physics : PCCP, 21(30), 16549-16563. https://doi.org/10.1039/c9cp02119a
Ozerov, Georgiy K, et al. "Accommodation of a dimer in an Ar-like lattice: exploring the generic structural motifs." Physical chemistry chemical physics : PCCP vol. 21,30 (2019): 16549-16563. doi: https://doi.org/10.1039/c9cp02119a
Ozerov GK, Bezrukov DS, Buchachenko AA. Accommodation of a dimer in an Ar-like lattice: exploring the generic structural motifs. Phys Chem Chem Phys. 2019 Aug 14;21(30):16549-16563. doi: 10.1039/c9cp02119a. Epub 2019 Jul 17. PMID: 31313774.
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Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors.

Scientific reports

Spasov A, Ozerov A, Vassiliev P, Kosolapov V, Gurova N, Kucheryavenko A, Naumenko L, Babkov D, Sirotenko V, Taran A, Litvinov R, Borisov A, Klochkov V, Merezhkina D, Miroshnikov M, Uskov G, Ovsyankina N.
PMID: 34934125
Sci Rep. 2021 Dec 21;11(1):24380. doi: 10.1038/s41598-021-03722-w.

The Na

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Spasov A, Ozerov A, Vassiliev P, et al. Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Sci Rep. 2021;11(1):24380doi: 10.1038/s41598-021-03722-w.
Spasov, A., Ozerov, A., Vassiliev, P., Kosolapov, V., Gurova, N., Kucheryavenko, A., Naumenko, L., Babkov, D., Sirotenko, V., Taran, A., Litvinov, R., Borisov, A., Klochkov, V., Merezhkina, D., Miroshnikov, M., Uskov, G., & Ovsyankina, N. (2021). Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Scientific reports, 11(1), 24380. https://doi.org/10.1038/s41598-021-03722-w
Spasov, Alexander, et al. "Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors." Scientific reports vol. 11,1 (2021): 24380. doi: https://doi.org/10.1038/s41598-021-03722-w
Spasov A, Ozerov A, Vassiliev P, Kosolapov V, Gurova N, Kucheryavenko A, Naumenko L, Babkov D, Sirotenko V, Taran A, Litvinov R, Borisov A, Klochkov V, Merezhkina D, Miroshnikov M, Uskov G, Ovsyankina N. Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Sci Rep. 2021 Dec 21;11(1):24380. doi: 10.1038/s41598-021-03722-w. PMID: 34934125.
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Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors.

Scientific reports

Spasov A, Ozerov A, Vassiliev P, Kosolapov V, Gurova N, Kucheryavenko A, Naumenko L, Babkov D, Sirotenko V, Taran A, Litvinov R, Borisov A, Klochkov V, Merezhkina D, Miroshnikov M, Uskov G, Ovsyankina N.
PMID: 34934125
Sci Rep. 2021 Dec 21;11(1):24380. doi: 10.1038/s41598-021-03722-w.

The Na

Cite
Spasov A, Ozerov A, Vassiliev P, et al. Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Sci Rep. 2021;11(1):24380doi: 10.1038/s41598-021-03722-w.
Spasov, A., Ozerov, A., Vassiliev, P., Kosolapov, V., Gurova, N., Kucheryavenko, A., Naumenko, L., Babkov, D., Sirotenko, V., Taran, A., Litvinov, R., Borisov, A., Klochkov, V., Merezhkina, D., Miroshnikov, M., Uskov, G., & Ovsyankina, N. (2021). Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Scientific reports, 11(1), 24380. https://doi.org/10.1038/s41598-021-03722-w
Spasov, Alexander, et al. "Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors." Scientific reports vol. 11,1 (2021): 24380. doi: https://doi.org/10.1038/s41598-021-03722-w
Spasov A, Ozerov A, Vassiliev P, Kosolapov V, Gurova N, Kucheryavenko A, Naumenko L, Babkov D, Sirotenko V, Taran A, Litvinov R, Borisov A, Klochkov V, Merezhkina D, Miroshnikov M, Uskov G, Ovsyankina N. Synthesis and multifaceted pharmacological activity of novel quinazoline NHE-1 inhibitors. Sci Rep. 2021 Dec 21;11(1):24380. doi: 10.1038/s41598-021-03722-w. PMID: 34934125; PMCID: PMC8692498.
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Corrigendum: Exploration of acetanilide derivatives of 1-(ω-phenoxyalkyl)uracils as novel inhibitors of Hepatitis C Virus replication.

Scientific reports

Magri A, Ozerov AA, Tunitskaya VL, Valuev-Elliston VT, Wahid A, Pirisi M, Simmonds P, Ivanov AV, Novikov MS, Patel AH.
PMID: 27558078
Sci Rep. 2016 Aug 25;6:31529. doi: 10.1038/srep31529.

No abstract available.

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Magri A, Ozerov AA, Tunitskaya VL, et al. Corrigendum: Exploration of acetanilide derivatives of 1-(ω-phenoxyalkyl)uracils as novel inhibitors of Hepatitis C Virus replication. Sci Rep. 2016;6:31529doi: 10.1038/srep31529.
Magri, A., Ozerov, A. A., Tunitskaya, V. L., Valuev-Elliston, V. T., Wahid, A., Pirisi, M., Simmonds, P., Ivanov, A. V., Novikov, M. S., & Patel, A. H. (2016). Corrigendum: Exploration of acetanilide derivatives of 1-(ω-phenoxyalkyl)uracils as novel inhibitors of Hepatitis C Virus replication. Scientific reports, 631529. https://doi.org/10.1038/srep31529
Magri, Andrea, et al. "Corrigendum: Exploration of acetanilide derivatives of 1-(ω-phenoxyalkyl)uracils as novel inhibitors of Hepatitis C Virus replication." Scientific reports vol. 6 (2016): 31529. doi: https://doi.org/10.1038/srep31529
Magri A, Ozerov AA, Tunitskaya VL, Valuev-Elliston VT, Wahid A, Pirisi M, Simmonds P, Ivanov AV, Novikov MS, Patel AH. Corrigendum: Exploration of acetanilide derivatives of 1-(ω-phenoxyalkyl)uracils as novel inhibitors of Hepatitis C Virus replication. Sci Rep. 2016 Aug 25;6:31529. doi: 10.1038/srep31529. PMID: 27558078; PMCID: PMC4997718.
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1-(4-Phenoxybenzyl) 5-Aminouracil Derivatives and Their Analogues - Novel Inhibitors of Human Adenovirus Replication.

Acta naturae

Nikitenko NA, Gureeva ES, Ozerov AA, Tukhvatulin AI, Izhaeva FM, Prassolov VS, Deryabin PG, Novikov MS, Logunov DY.
PMID: 30116616
Acta Naturae. 2018 Apr-Jun;10(2):58-64.

Adenovirus infections are characterized by widespread distribution. The lack of causal therapy, which is effective in treating this group of diseases, explains the need for new therapeutic drugs. Notably, anti-adenoviral activity of [4-(phenoxy)benzyl]-5-(phenylamino)-6-azauracil, 1-[4-(phenoxy)benzyl]-5-(morpholino) uracil, 1-[4-(4-chlorophenoxy)benzyl]-5-(morpholino) uracil, and 1-[4-(4-fluorophenoxy)-benzyl]-5-(morpholino)...

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Nikitenko NA, Gureeva ES, Ozerov AA, et al. 1-(4-Phenoxybenzyl) 5-Aminouracil Derivatives and Their Analogues - Novel Inhibitors of Human Adenovirus Replication. Acta Naturae. 2018;10(2):58-64
Nikitenko, N. A., Gureeva, E. S., Ozerov, A. A., Tukhvatulin, A. I., Izhaeva, F. M., Prassolov, V. S., Deryabin, P. G., Novikov, M. S., & Logunov, D. Y. (2018). 1-(4-Phenoxybenzyl) 5-Aminouracil Derivatives and Their Analogues - Novel Inhibitors of Human Adenovirus Replication. Acta naturae, 10(2), 58-64.
Nikitenko, N A, et al. "1-(4-Phenoxybenzyl) 5-Aminouracil Derivatives and Their Analogues - Novel Inhibitors of Human Adenovirus Replication." Acta naturae vol. 10,2 (2018): 58-64.
Nikitenko NA, Gureeva ES, Ozerov AA, Tukhvatulin AI, Izhaeva FM, Prassolov VS, Deryabin PG, Novikov MS, Logunov DY. 1-(4-Phenoxybenzyl) 5-Aminouracil Derivatives and Their Analogues - Novel Inhibitors of Human Adenovirus Replication. Acta Naturae. 2018 Apr-Jun;10(2):58-64. PMID: 30116616; PMCID: PMC6087815.
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Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives.

Acta naturae

Paramonova MP, Khandazhinskaya AL, Ozerov AA, Kochetkov SN, Snoeck R, Andrei G, Novikov MS.
PMID: 33173603
Acta Naturae. 2020 Jul-Sep;12(3):134-139. doi: 10.32607/actanaturae.10983.

A series of uracil derivatives containing a 4-oxoquinazoline fragment bound to the nitrogen atom N3 of the pyrimidine ring by a short methylene bridge was synthesized to search for new antiviral agents. Some compounds in this series are shown...

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Paramonova MP, Khandazhinskaya AL, Ozerov AA, et al. Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives. Acta Naturae. 2020;12(3):134-139doi: 10.32607/actanaturae.10983.
Paramonova, M. P., Khandazhinskaya, A. L., Ozerov, A. A., Kochetkov, S. N., Snoeck, R., Andrei, G., & Novikov, M. S. (2020). Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives. Acta naturae, 12(3), 134-139. https://doi.org/10.32607/actanaturae.10983
Paramonova, M P, et al. "Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives." Acta naturae vol. 12,3 (2020): 134-139. doi: https://doi.org/10.32607/actanaturae.10983
Paramonova MP, Khandazhinskaya AL, Ozerov AA, Kochetkov SN, Snoeck R, Andrei G, Novikov MS. Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives. Acta Naturae. 2020 Jul-Sep;12(3):134-139. doi: 10.32607/actanaturae.10983. PMID: 33173603; PMCID: PMC7604896.
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2-(2,4-Dioxy-1,2,3,4-Tetrahydropyrimidin-1-yl)-N-(4-Phenoxyphenyl)-Acetamides as a Novel Class of Cytomegalovirus Replication Inhibitors.

Acta naturae

Babkov DA, Paramonova MP, Ozerov AA, Khandazhinskaya AL, Snoeck R, Andrei G, Novikov MS.
PMID: 26798502
Acta Naturae. 2015 Oct-Dec;7(4):142-5.

A series of novel uracil derivatives, bearing N-(4-phenoxyphenyl)acetamide moiety at N3 of a pyrimidine ring, has been synthesized. Their antiviral activity has been evaluated. It has been found that the novel compounds possess high inhibitory activity against replication of...

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Babkov DA, Paramonova MP, Ozerov AA, et al. 2-(2,4-Dioxy-1,2,3,4-Tetrahydropyrimidin-1-yl)-N-(4-Phenoxyphenyl)-Acetamides as a Novel Class of Cytomegalovirus Replication Inhibitors. Acta Naturae. 2015;7(4):142-5
Babkov, D. A., Paramonova, M. P., Ozerov, A. A., Khandazhinskaya, A. L., Snoeck, R., Andrei, G., & Novikov, M. S. (2015). 2-(2,4-Dioxy-1,2,3,4-Tetrahydropyrimidin-1-yl)-N-(4-Phenoxyphenyl)-Acetamides as a Novel Class of Cytomegalovirus Replication Inhibitors. Acta naturae, 7(4), 142-5.
Babkov, D A, et al. "2-(2,4-Dioxy-1,2,3,4-Tetrahydropyrimidin-1-yl)-N-(4-Phenoxyphenyl)-Acetamides as a Novel Class of Cytomegalovirus Replication Inhibitors." Acta naturae vol. 7,4 (2015): 142-5.
Babkov DA, Paramonova MP, Ozerov AA, Khandazhinskaya AL, Snoeck R, Andrei G, Novikov MS. 2-(2,4-Dioxy-1,2,3,4-Tetrahydropyrimidin-1-yl)-N-(4-Phenoxyphenyl)-Acetamides as a Novel Class of Cytomegalovirus Replication Inhibitors. Acta Naturae. 2015 Oct-Dec;7(4):142-5. PMID: 26798502; PMCID: PMC4717260.
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Showing 1 to 8 of 8 entries