A. Khandazhinskaya

发表

New derivatives of alkyl-and aminocarbonylphosphonic acids containing 3′-azido-3′-deoxythymidine

O. Plyasunova, M. Jasko, A. V. Shipitsyn, 2006, Russian Journal of Bioorganic Chemistry.

5′-Aminocarbonyl Phosphonates as New Zidovudine Depot Forms: Antiviral Properties, Intracellular Transformations, and Pharmacokinetic Parameters

M. Kukhanova, S. Shram, M. Jasko, 2009, Drug Metabolism and Disposition.

HIV-1 non-nucleoside reverse transcriptase inhibitors: incorporation of benzylphosphonate moiety for solubility improvement

V. Valuev-Elliston, A. Chizhov, E. Matyugina, 2016 .

Uracil-Containing Heterodimers of a New Type: Synthesis and Study of Their Anti-Viral Properties

S. Kochetkov, G. Andrei, R. Snoeck, 2020, Molecules.

Hydrophobic-core PEGylated graft copolymer-stabilized nanoparticles composed of insoluble non-nucleoside reverse transcriptase inhibitors exhibit strong anti-HIV activity.

A. Bogdanov, M. Gottikh, S. Kochetkov, 2016, Nanomedicine : nanotechnology, biology, and medicine.

1,6-Bis[(benzyloxy)methyl]uracil derivatives-Novel antivirals with activity against HIV-1 and influenza H1N1 virus.

C. Pannecouque, L. Naesens, S. Kochetkov, 2016, Bioorganic & medicinal chemistry.

Synthesis and anti-HCMV activity of 1-[ω-(phenoxy)alkyl]uracil derivatives and analogues thereof

J. Balzarini, G. Andrei, R. Snoeck, 2013, Bioorganic & Medicinal Chemistry.

Analogues of Pyrimidine Nucleosides as Mycobacteria Growth Inhibitors

S. Kochetkov, D. A. Makarov, L. Alexandrova, 2022, Microorganisms.

5′-Norcarbocyclic nucleoside analogs

E. Matyugina, A. Khandazhinskaya, 2014, Russian Chemical Bulletin.

Scaffold hopping: exploration of acetanilide-containing uracil analogues as potential NNRTIs.

A. V. Ivanov, C. Pannecouque, J. Balzarini, 2015, Bioorganic & medicinal chemistry.

Structure-activity evaluation of new uracil-based non-nucleoside inhibitors of HIV reverse transcriptase

S. Kochetkov, V. Valuev-Elliston, A. Chizhov, 2013 .

Novel 1-[5-(4-bromophenoxy)pentyl]-3-(2-arylamino- 2-oxoethyl)uracils and their antiviral properties

M. Novikov, A. Khandazhinskaya, K. Seley‐Radtke, 2017, Mendeleev Communications.

N1,N3-disubstituted uracils as nonnucleoside inhibitors of HIV-1 reverse transcriptase

A. V. Ivanov, C. Pannecouque, J. Balzarini, 2013, Bioorganic & Medicinal Chemistry.

Evaluation of the antiprotozoan properties of 5'-norcarbocyclic pyrimidine nucleosides.

Khalid J. Alzahrani, E. Matyugina, A. Khandazhinskaya, 2017, Bioorganic & medicinal chemistry letters.

Methods for the synthesis of aza(deaza)xanthines as a basis of biologically active compounds

M. Novikov, A. Khandazhinskaya, D. Babkov, 2016 .

Novel 5′-Norcarbocyclic Derivatives of Bicyclic Pyrrolo- and Furano[2,3-d]Pyrimidine Nucleosides

M. Zenkova, S. Kochetkov, P. N. Solyev, 2018, Molecules.

5′-Norcarbocyclic analogues of furano[2,3-d]pyrimidine nucleosides

M. Zenkova, S. Kochetkov, E. Logashenko, 2015 .

New Derivatives of 5-Substituted Uracils: Potential Agents with a Wide Spectrum of Biological Activity

G. Andrei, R. Snoeck, A. Chizhov, 2022, Molecules.

Novel 5′-Norcarbocyclic Pyrimidine Derivatives as Antibacterial Agents

S. Kochetkov, P. N. Solyev, V. Popenko, 2018, Molecules.

5‐Arylaminouracil Derivatives: New Inhibitors of Mycobacterium tuberculosis

S. Lutz, A. Chizhov, I. Karpenko, 2015, Chemical biology & drug design.

Synthesis of 3-hetarylpyrroles by Suzuki–Miyaura cross-coupling

S. Kochetkov, E. Matyugina, A. Khandazhinskaya, 2020, Mendeleev Communications.

Synthesis of uracil–coumarin conjugates as potential inhibitors of virus replication

G. Andrei, R. Snoeck, A. Chizhov, 2019, Mendeleev Communications.

Toward the discovery of dual HCMV–VZV inhibitors: Synthesis, structure activity relationship analysis, and cytotoxicity studies of long chained 2-uracil-3-yl-N-(4-phenoxyphenyl)acetamides

G. Andrei, R. Snoeck, A. Chizhov, 2015, Bioorganic & Medicinal Chemistry.

A highly facile approach to the synthesis of novel 2-(3-benzyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-1-yl)-N-phenylacetamides

A. Chizhov, M. Novikov, A. Khandazhinskaya, 2012, Tetrahedron Letters.

Carbocyclic Analogues of Inosine-5’-Monophosphate: Synthesis and Biological Activity

T. Smirnova, E. Matyugina, A. Khandazhinskaya, 2012, Acta naturae.

ANTI-HIV ACTIVITY OF NOVEL PHOSPHONATE DERIVATIVES OF AZT, d4T, AND ddA

A. Krayevsky, I. Karpenko, A. Pokrovsky, 2001, Nucleosides, nucleotides & nucleic acids.

Investigation of 5’-Norcarbocyclic Nucleoside Analogues as Antiprotozoal and Antibacterial Agents

Khalid J. Alzahrani, Manal J. Natto, H. D. de Koning, 2019, Molecules.

1-Benzyl derivatives of 5-(arylamino)uracils as anti-HIV-1 and anti-EBV agents.

R. Buckheit, M. Novikov, A. Khandazhinskaya, 2010, Bioorganic & medicinal chemistry.

5′‐Phosphonate Derivatives of 2′,3′‐Dideoxy‐3′‐Thiacytidine as New Anti‐HIV Prodrugs

N. A. Golubeva, M. Kukhanova, P. N. Solyev, 2011, Chemical biology & drug design.

Aminocarbonyl phosphonates as new AZT depot forms : antiviral properties , intracellular transformations and pharmacokinetic parameters

S. Shram, M. Jasko, Engelhardt, 2008 .

5′-Nor carbocyclic nucleosides: unusual nonnucleoside inhibitors of HIV-1 reverse transcriptase

J. Balzarini, S. Kochetkov, V. Valuev-Elliston, 2013 .

Dual‐targeted anti‐TB/anti‐HIV heterodimers

L. Margolis, C. Vanpouille, S. Zicari, 2017, Antiviral research.

P-(Alkyl)-Nucleoside 5′-Hydrogenphosphonates as Depot Forms of Antiviral Nucleotide Analogues

A. Krayevsky, N. Zakirova, I. Karpenko, 2000, Nucleosides, nucleotides & nucleic acids.

Interaction Of 5-Substituted Pyrimidine Nucleoside Analogues And M.Tuberculosis: A View Through An Electron Microscope.

S. Kochetkov, V. Popenko, L. Alexandrova, 2020, Biochimie.

New Nonnucleoside Substrates for Terminal Deoxynucleotidyl Transferase: Synthesis and Dependence of Substrate Properties on Structure

M. Kukhanova, M. Jasko, A. Khandazhinskaya, 2005, Russian journal of bioorganic chemistry.

Aryl-Containing Esters Of Triphosphoric Acid As Substrates Of Terminal Deoxynucleotidyl Transferase

M. Kukhanova, M. Jasko, L. Alexandrova, 2007, Nucleosides, nucleotides & nucleic acids.

1,2,4-Triazoloazine derivatives as a new type of herpes simplex virus inhibitors.

M. Kukhanova, O. Chupakhin, V. Rusinov, 2010, Bioorganic chemistry.

Synthesis and Antiviral Properties of 1-Substituted 3-[ω-(4-Oxoquinazolin-4(3H)-yl)alkyl]uracil Derivatives

S. Kochetkov, G. Andrei, R. Snoeck, 2020, Acta Naturae.

Synthesis of 1-[ω-(Bromophenoxy)alkyl]-3-naphthalenylmethyl Derivatives of Uracil and Their Analogues As Probable Inhibitors of Human Cytomegalovirus Replication

S. Kochetkov, R. Snoeck, G. Andrei, 2023, Doklady Biochemistry and Biophysics.

Hydrophobic-core PEGylated graft copolymer-stabilized nanoparticles composed of insoluble non-nucleoside reverse transcriptase inhibitors exhibit strong anti-HIV activity.

A. Bogdanov, M. Gottikh, S. Kochetkov, 2016, Nanomedicine : nanotechnology, biology, and medicine.

A new antiviral: chimeric 3TC-AZT phosphonate efficiently inhibits HIV-1 in human tissues ex vivo.

L. Margolis, S. Kochetkov, C. Vanpouille, 2014, Antiviral research.

New acetamide derivatives containing (ω-p-bromophenoxyalkyl)uracil moiety and their anticytomegalovirus activity

G. Andrei, R. Snoeck, M. Novikov, 2020 .