M. B. Nawrozkij

发表

One-class approach: models for virtual screening of non-nucleoside HIV-1 reverse transcriptase inhibitors based on the concept of continuous molecular fields

N. Zefirov, I. Baskin, I. Novakov, 2011 .

Effect of α-Methoxy Substitution on the Anti-HIV Activity of Dihydropyrimidin-4(3 H)-ones.

A. Mai, I. A. Kirillov, E. Crespan, 2018, Journal of medicinal chemistry.

Structural insight into the optimization of ethyl 5-hydroxybenzo[g]indol-3-carboxylates and their bioisosteric analogues as 5-LO/m-PGES-1 dual inhibitors able to suppress inflammation.

A. Olğaç, O. Werz, M. de Rosa, 2018, European journal of medicinal chemistry.

Experimental and quantum chemical study of the reactions of 2-methyloxirane with 5-alkyl-6-(2,6-dihalobenzyl)-2-thioxo1,2-dihydropyrimidine-4(3H)-one derivatives

V. Minkin, I. Novakov, D. Steglenko, 2015, Russian Chemical Bulletin.

6-(Arylmethyl)pyrimidin-4(3H)-ones: anthology and prospects of highly efficient anti-HIV agents

A. Mai, M. Artico, D. Rotili, 2012, Russian Chemical Bulletin.

Diarylpyrimidine-dihydrobenzyloxopyrimidine hybrids: new, wide-spectrum anti-HIV-1 agents active at (sub)-nanomolar level.

B. Clotet, A. Mai, G. Maga, 2011, Journal of medicinal chemistry.

The specific character of the reaction of derivatives of 2-thioxo-2,3-dihydropyrimidin-4(1H)-one with iodomethane and alkyl chloromethyl sulfides

A. Mai, E. Gordeeva, J. Esté, 2010 .

Arbidol: a quarter-century after. Past, present and future of the original Russian antiviral

K. Balakin, S. Lavrenov, R. Filosa, 2018, Russian Chemical Reviews.

5-Alkyl-6-benzyl-2-(2-oxo-2-phenylethylsulfanyl)pyrimidin-4(3H)-ones, a series of anti-HIV-1 agents of the dihydro-alkoxy-benzyl-oxopyrimidine family with peculiar structure-activity relationship profile.

A. Mai, S. Zanoli, G. Maga, 2008, Journal of medicinal chemistry.

The synthesis of new acyclic analogs of 3-phenacyluridine and comparative evaluation of their in vivo biological activity

I. A. Kirillov, I. Novakov, T. Tolstikova, 2020, Chemistry of Heterocyclic Compounds.

3-phenacyluridine-derived hypnotics: Anthology, structure-activity relationships and synthesis of several acyclonucleoside analogues

I. A. Kirillov, I. Novakov, M. B. Nawrozkij, 2020 .

Structure-Based Design, Synthesis, and Biological Evaluation of the Cage–Amide Derived Orthopox Virus Replication Inhibitors

S. Arkhipov, N. Salakhutdinov, R. Maksyutov, 2022, Viruses.

Efficient solid-phase synthesis of isocytosine derivatives

E. N. Gerasimov, E. Gordeeva, I. Novakov, 2009 .

Synthesis and biological properties of novel 2-aminopyrimidin-4(3H)-ones highly potent against HIV-1 mutant strains.

A. Mai, G. Maga, M. Artico, 2007, Journal of medicinal chemistry.

Synthesis of novel N2-adamantyl derivatives of 2-amino-6-methyl-4(3H)-pyrimidinone as potential activators of tumor necrosis factor (TNF) release

I. Novakov, B. S. Orlinson, G. Novikova, 2006 .

2-(Alkyl/aryl)amino-6-benzylpyrimidin-4(3H)-ones as inhibitors of wild-type and mutant HIV-1: enantioselectivity studies.

Ira Musmuca, Rino Ragno, Flavio Ballante, 2012, Journal of medicinal chemistry.

Design, Synthesis, and Biological Evaluation of (+)‐Camphor‐ and (−)‐Fenchone‐Based Derivatives as Potent Orthopoxvirus Inhibitors

N. Salakhutdinov, O. Yarovaya, A. Sokolova, 2022, ChemMedChem.

Pyrimidine thioethers: A novel class of antidepressant agents, endowed with anxiolytic, performance enhancing and nootropic activity.

I. A. Kirillov, R. Ragno, D. Rotili, 2022, European journal of medicinal chemistry.

Exploring the role of 2-chloro-6-fluoro substitution in 2-alkylthio-6-benzyl-5-alkylpyrimidin-4(3H)-ones: effects in HIV-1-infected cells and in HIV-1 reverse transcriptase enzymes.

Rino Ragno, Flavio Ballante, Roberto Cirilli, 2014, Journal of medicinal chemistry.

The Specific Character of the Reaction of Derivatives of 2-Thioxo-2,3-dihydropyrimidin-4(1H)-one with Iodomethane and Alkyl Chloromethyl Sulfides.

A. Mai, M. Artico, E. Gordeeva, 2010 .