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Molecular Diversity|October 31, 2012

The synthesis of low molecular weight pyrrolo[2,3-c]pyridine-7-one scaffoldMaxim A Nechayev, Nikolay Yu Gorobets, Alexander V Borisov, et al.

Drug Discovery Today|February 13, 2022

Drug repurposing against SARS-CoV-2 using computational approachesSumit Kumar, Svitlana Kovalenko, Shakshi Bhardwaj, et al.

Acta Crystallographica. Section E, Crystallographic Communications|December 20, 2021

The first coordination complex of (5R,6R,7S)-5-(furan-2-yl)-7-phenyl-4,5,6,7-tetra-hydro-[1,2,4]triazolo[1,5-a]pyrimidin-6-amine with zinc(II) acetate-chlorideMariia O Shyshkina, Svitlana V Shishkina, Konstantin S Ostras, et al.

Journal of Combinatorial Chemistry|April 24, 2009

Diversification of a thieno[2,3-d]pyrimidin-4-one scaffold via regioselective alkylation reactionsSergey G Dzhavakhishvili, Nikolay Yu Gorobets, Svetlana V Shishkina, et al.

ACS Combinatorial Science|August 30, 2014

Three-component reaction of a 2-aminoazine, a 2-oxoaldehyde, and a cyclic 1,3-dicarbonyl compound for the synthesis of imidazo[1,2-a]azine derivativesVsevolod A Peshkov, Anatoly A Peshkov, Olga P Pereshivko, et al.

Molecular Diversity|May 31, 2018

Dihydrobenzo[4,5]imidazo[1,2-a]pyrimidine-4-ones as a new class of CK2 inhibitorsMykola V Protopopov, Olga V Ostrynska, Sergiy A Starosyla, et al.

Journal of Biomolecular Structure & Dynamics|June 21, 2021

Computational study of novel inhibitory molecule, 1-(4-((2S,3S)-3-amino-2-hydroxy-4-phenylbutyl)piperazin-1-yl)-3-phenylurea, with high potential to competitively block ATP binding to the RNA dependent RNA polymerase of SARS-CoV-2 virusPrem Prakash Sharma, Sumit Kumar, Sukrit Srivastava, et al.

Beilstein Journal of Organic Chemistry|June 6, 2019

Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compoundsVictoria V Lipson, Tetiana L Pavlovska, Nataliya V Svetlichnaya, et al.

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Showing results (11-20 of 18) with videos related to

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You have reached the last page of results.This site can display upto 18 results.

Molecular Diversity|October 31, 2012

The synthesis of low molecular weight pyrrolo[2,3-c]pyridine-7-one scaffoldMaxim A Nechayev, Nikolay Yu Gorobets, Alexander V Borisov, et al.

Drug Discovery Today|February 13, 2022

Drug repurposing against SARS-CoV-2 using computational approachesSumit Kumar, Svitlana Kovalenko, Shakshi Bhardwaj, et al.

Acta Crystallographica. Section E, Crystallographic Communications|December 20, 2021

The first coordination complex of (5R,6R,7S)-5-(furan-2-yl)-7-phenyl-4,5,6,7-tetra-hydro-[1,2,4]triazolo[1,5-a]pyrimidin-6-amine with zinc(II) acetate-chlorideMariia O Shyshkina, Svitlana V Shishkina, Konstantin S Ostras, et al.

Journal of Combinatorial Chemistry|April 24, 2009

Diversification of a thieno[2,3-d]pyrimidin-4-one scaffold via regioselective alkylation reactionsSergey G Dzhavakhishvili, Nikolay Yu Gorobets, Svetlana V Shishkina, et al.

ACS Combinatorial Science|August 30, 2014

Three-component reaction of a 2-aminoazine, a 2-oxoaldehyde, and a cyclic 1,3-dicarbonyl compound for the synthesis of imidazo[1,2-a]azine derivativesVsevolod A Peshkov, Anatoly A Peshkov, Olga P Pereshivko, et al.

Molecular Diversity|May 31, 2018

Dihydrobenzo[4,5]imidazo[1,2-a]pyrimidine-4-ones as a new class of CK2 inhibitorsMykola V Protopopov, Olga V Ostrynska, Sergiy A Starosyla, et al.

Journal of Biomolecular Structure & Dynamics|June 21, 2021

Computational study of novel inhibitory molecule, 1-(4-((2S,3S)-3-amino-2-hydroxy-4-phenylbutyl)piperazin-1-yl)-3-phenylurea, with high potential to competitively block ATP binding to the RNA dependent RNA polymerase of SARS-CoV-2 virusPrem Prakash Sharma, Sumit Kumar, Sukrit Srivastava, et al.

Beilstein Journal of Organic Chemistry|June 6, 2019

Novel (2-amino-4-arylimidazolyl)propanoic acids and pyrrolo[1,2-c]imidazoles via the domino reactions of 2-amino-4-arylimidazoles with carbonyl and methylene active compoundsVictoria V Lipson, Tetiana L Pavlovska, Nataliya V Svetlichnaya, et al.

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