Liliya F. Saifina

A.E. Arbuzov Institute of Organic and Physical Chemistry — Russia

Materials Science · Physical Sciences

13h-index399citations63works0.82yr avg
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Research Topics

Crystallization and Solubility Studies(16), X-ray Diffraction in Crystallography(16), Synthesis and Characterization of Heterocyclic Compounds(15), Click Chemistry and Applications(14), Synthesis and biological activity(11)

Publications63 total

Antimicrobial and Cytotoxic Agents in 6-methyluracil Molecules of Amphiphilic Nature with Nonsaturated Substituents at Uracil Ring
Recent Advances in Anti-Infective Drug Discovery·2026
Nucleoterpenoids on the basis of diterpenoid isosteviol, nucleobases and nucleoside analogues. Synthesis and cytotoxicity of a series of conjugates of isosteviol and uracil. Part 2
Nucleosides Nucleotides & Nucleic Acids·2025
Antimicrobial activity of triphenylphosphonium (TPP) conjugates of alkynyl−substituted nucleic bases and their analogues
The Journal of Antibiotics·2025· 2 cited
In vitro cytotoxicity evaluation of triphenylphosphonium (TPP) conjugates of some acetylenated nucleic bases and their analogues
Medicinal Chemistry Research·2025
Ionic and Non-Ionic Counterparts Based on Bis(Uracilyl)Alkane Moiety with Highest Selectivity Towards Acetylcholinesterase for Protection Against Organophosphate Poisoning and Treating Alzheimer’s Disease
International Journal of Molecular Sciences·2025Open Access
Triphenylphosphonium (TPP) conjugates of 1,2,3-triazolyl nucleoside analogues. Synthesis, cytotoxicity and antimicrobial activity
Medicinal Chemistry Research·2024· 1 cited
Synthesis and Cytotoxicity Against M-HeLa, HuTu 80, and MCF-7 Human Cancer Cells of the First Nucleoterpenoids of the Isosteviol Diterpenoid Platform
Chemistry of Natural Compounds·2024· 3 cited
Synthesis and antiviral activity of homodimers of 1,2,3-triazolyl nucleoside analogs
Russian Chemical Bulletin·2024· 1 citedOpen Access
Synthesis and Antiviral Activity of Homodimers of 1,2,3-Triazolyl Nucleoside Analogues Based on Quinazoline-2,4-dione
Russian Journal of General Chemistry·2024· 1 cited
Synthesis and Antiviral Activity of New Dimeric 1,2,3-Triazolyl Pyrimidine Nucleoside Analogues
Russian Journal of Organic Chemistry·2024
Acetylenyl substituted nucleic bases and their triphenylphosphonium (TPP) conjugates. Unexpected surge in cytotoxicity
Bioorganic Chemistry·2023· 3 cited
Conjugates of nucleobases with triazole-hydroxamic acids for the reactivation of acetylcholinesterase and treatment of delayed neurodegeneration induced by organophosphate poisoning
Bioorganic Chemistry·2023· 3 cited
CCDC 2259862: Experimental Crystal Structure Determination
The Cambridge Structural Database·2023Open Access
Applicability of transferable multipole pseudo-atoms for restoring inner-crystal electronic force density fields. Chemical bonding and binding features in the crystal and dimer of 1,3-bis(2-hydroxyethyl)-6-methyluracil
IUCrJ·2023· 17 citedOpen Access
Synthesis, antiviral evaluation, molecular docking study and cytotoxicity of 5′-phosphorylated 1,2,3-triazolyl nucleoside analogues with thymine and 6-methyl uracil moieties
Medicinal Chemistry Research·2023· 2 cited
Synthesis and antiviral activity of 1,2,3-triazolyl nucleoside analogues with <i>N</i>-acetyl-<scp>d</scp>-glucosamine residue
Nucleosides Nucleotides & Nucleic Acids·2023· 4 cited
First Macrocyclic 1,2,3-Triazolyl Uridine Analogues
Macroheterocycles·2023Open Access
Novel slow-binding reversible acetylcholinesterase inhibitors based on uracil moieties for possible treatment of myasthenia gravis and protection from organophosphate poisoning
European Journal of Medicinal Chemistry·2022· 2 citedOpen Access
The First 5′-Phosphorylated 1,2,3-Triazolyl Nucleoside Analogues with Uracil and Quinazoline-2,4-Dione Moieties: A Synthesis and Antiviral Evaluation
Molecules·2022· 14 citedOpen Access
Novel Slow-Binding Reversible Acetylcholinesterase Inhibitors Based on Uracil Moieties for Possible Treatment of Myasthenia Gravis and Protection from Organophosphate Poisoning
SSRN Electronic Journal·2022Open Access
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Frequent Co-authors

Vyacheslav E. Semenov(40), В. Е. Катаев(19), О. В. Андреева(17), M. M. Shulaeva(16), Mayya G. Belenok(15), B. F. Garifullin(13), Alexandra D. Voloshina(13), В. С. Резник(11), Anna P. Lyubina(10), I. Yu. Strobykina(9), Alina F. Saifina(9), Владимир В. Зарубаев(8), Alexander V. Slita(8), Robert R. Fayzullin(8), Irina V. Zueva(7), K. A. PETROV(7), L. Ya. Zakharova(6), Sergey A. Shteingolts(6), С. Г. Фаттахов(6), I.А. Litvinov(6)