Search research articles
Contact Us
Filters
Showing results (1-10 of 22) with videos related to
Page
of 3
Sort By:
Acta Crystallographica. Section E, Crystallographic Communications
|
February 22, 2021
Crystal structure of the non-steroidal anti-inflammatory drug (NSAID) tolmetin sodium
Irina S Konovalova, Sergiy M Kovalenko, Dmitry V Kravchenko, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
September 17, 2020
(1<i>R</i>,3<i>S</i>)-3-(1<i>H</i>-Benzo[<i>d</i>]imidazol-2-yl)-1,2,2-tri-methyl-cyclo-pentane-1-carb-oxy-lic acid as a new anti-diabetic active pharmaceutical ingredient
Sergiy M Kovalenko, Irina S Konovalova, Sergiy I Merzlikin, et al.
Natural Product Research
|
June 7, 2006
Natural products as templates for bioactive compound libraries: part 2. Novel modifications of vasicine (peganine) core via efficient and regioselective generation of 3-lithiodeoxyvasicine and its stereoselective addition to aliphatic ketones section sign
Sergey V Shevyakov, Olga I Davydova, Alex S Kiselyov, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
January 11, 2020
Crystal structure, Hirshfeld analysis and a mol-ecular docking study of a new inhibitor of the Hepatitis B virus (HBV): ethyl 5-methyl-1,1-dioxo-2-{[5-(pentan-3-yl)-1,2,4-oxa-diazol-3-yl]meth-yl}-2<i>H</i>-1,2,6-thia-diazine-4-carboxyl-ate
Alexandre V Ivachtchenko, Sergiy M Kovalenko, Dmitry V Kravchenko, et al.
Natural Product Research
|
June 7, 2006
Natural products as templates for bioactive compound libraries: synthesis of biaryl derivatives of (+/-)-vasicine
Sergey V Shevyakov, Olga I Davydova, Dmitry G Pershin, et al.
Journal of Combinatorial Chemistry
|
March 15, 2005
Parallel liquid-phase synthesis of N-substituted 6-aminosulfonyl-2-oxo-1,2-dihydroquinoline-4-carboxamide and 6-aminosulfonylquinoline-4-carboxamide derivatives
Alexandre V Ivachtchenko, Vladimir V Kobak, Alexey P Ilyn, et al.
Applied Microbiology and Biotechnology
|
August 27, 2011
Highly sensitive field test lateral flow immunodiagnostics of PVX infection
Yuri F Drygin, Anatoly N Blintsov, Vitaly G Grigorenko, et al.
Molecules (Basel, Switzerland)
|
August 12, 2022
The Efficacy of Aprotinin Combinations with Selected Antiviral Drugs in Mouse Models of Influenza Pneumonia and Coronavirus Infection Caused by SARS-CoV-2
Andrey A Ivashchenko, Bogdan A Zagribelnyy, Yan A Ivanenkov, et al.
European Journal of Medicinal Chemistry
|
January 24, 2020
Synthesis, biological evaluation and in silico modeling of novel integrase strand transfer inhibitors (INSTIs)
Andrey A Ivashchenko, Yan A Ivanenkov, Angela G Koryakova, et al.
Heliyon
|
December 18, 2019
Synthesis, X-ray crystal structure, Hirshfeld surface analysis, and molecular docking study of novel inhibitor of hepatitis B: methyl 4-fluoro-3-(morpholinosulfonyl)benzo[b]thiophene-2-carboxylate
Alexandre V Ivachtchenko, Oleg D Mitkin, Dmitry V Kravchenko, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 22) with videos related to
Sort By:
Page
of 3
Acta Crystallographica. Section E, Crystallographic Communications
|
February 22, 2021
Crystal structure of the non-steroidal anti-inflammatory drug (NSAID) tolmetin sodium
Irina S Konovalova, Sergiy M Kovalenko, Dmitry V Kravchenko, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
September 17, 2020
(1<i>R</i>,3<i>S</i>)-3-(1<i>H</i>-Benzo[<i>d</i>]imidazol-2-yl)-1,2,2-tri-methyl-cyclo-pentane-1-carb-oxy-lic acid as a new anti-diabetic active pharmaceutical ingredient
Sergiy M Kovalenko, Irina S Konovalova, Sergiy I Merzlikin, et al.
Natural Product Research
|
June 7, 2006
Natural products as templates for bioactive compound libraries: part 2. Novel modifications of vasicine (peganine) core via efficient and regioselective generation of 3-lithiodeoxyvasicine and its stereoselective addition to aliphatic ketones section sign
Sergey V Shevyakov, Olga I Davydova, Alex S Kiselyov, et al.
Acta Crystallographica. Section E, Crystallographic Communications
|
January 11, 2020
Crystal structure, Hirshfeld analysis and a mol-ecular docking study of a new inhibitor of the Hepatitis B virus (HBV): ethyl 5-methyl-1,1-dioxo-2-{[5-(pentan-3-yl)-1,2,4-oxa-diazol-3-yl]meth-yl}-2<i>H</i>-1,2,6-thia-diazine-4-carboxyl-ate
Alexandre V Ivachtchenko, Sergiy M Kovalenko, Dmitry V Kravchenko, et al.
Natural Product Research
|
June 7, 2006
Natural products as templates for bioactive compound libraries: synthesis of biaryl derivatives of (+/-)-vasicine
Sergey V Shevyakov, Olga I Davydova, Dmitry G Pershin, et al.
Journal of Combinatorial Chemistry
|
March 15, 2005
Parallel liquid-phase synthesis of N-substituted 6-aminosulfonyl-2-oxo-1,2-dihydroquinoline-4-carboxamide and 6-aminosulfonylquinoline-4-carboxamide derivatives
Alexandre V Ivachtchenko, Vladimir V Kobak, Alexey P Ilyn, et al.
Applied Microbiology and Biotechnology
|
August 27, 2011
Highly sensitive field test lateral flow immunodiagnostics of PVX infection
Yuri F Drygin, Anatoly N Blintsov, Vitaly G Grigorenko, et al.
Molecules (Basel, Switzerland)
|
August 12, 2022
The Efficacy of Aprotinin Combinations with Selected Antiviral Drugs in Mouse Models of Influenza Pneumonia and Coronavirus Infection Caused by SARS-CoV-2
Andrey A Ivashchenko, Bogdan A Zagribelnyy, Yan A Ivanenkov, et al.
European Journal of Medicinal Chemistry
|
January 24, 2020
Synthesis, biological evaluation and in silico modeling of novel integrase strand transfer inhibitors (INSTIs)
Andrey A Ivashchenko, Yan A Ivanenkov, Angela G Koryakova, et al.
Heliyon
|
December 18, 2019
Synthesis, X-ray crystal structure, Hirshfeld surface analysis, and molecular docking study of novel inhibitor of hepatitis B: methyl 4-fluoro-3-(morpholinosulfonyl)benzo[b]thiophene-2-carboxylate
Alexandre V Ivachtchenko, Oleg D Mitkin, Dmitry V Kravchenko, et al.
Page
of 3