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Publications in Math-Net.Ru
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New abiraterone analogue with atypical position of N-heterocyclic substituent: synthesis, crystal structure and CYP17A1/CYP3A4 binding affinity
Mendeleev Commun., 36:2 (2026), 138–141
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Substituted 3-aryl-4-nitroisoxazoles as potential blockers of the transport protein GLUT5: molecular design, synthesis and primary biotesting
Mendeleev Commun., 36:1 (2026), 12–14
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New adamantane-containing compounds targeting rimantadine-resistant influenza virus A/PR/8/34: molecular design, synthesis and SAR study
Mendeleev Commun., 35:1 (2025), 50–53
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The homodimer approach to the design of a new long-acting depot prodrug of abiraterone
Mendeleev Commun., 34:4 (2024), 502–504
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Annulated bicyclic isothioureas: identification of active and selective butyrylcholinesterase inhibitors
Mendeleev Commun., 33:1 (2023), 77–79
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Bicyclic isothioureas for conjugation with tubulin targeted anticancer agents
Mendeleev Commun., 32:6 (2022), 766–768
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Podophyllotoxin esters with alicyclic residues: an insight into the origin of microtubule-curling effect in cancer cells
Mendeleev Commun., 32:2 (2022), 173–175
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N-(4-Methoxyphenyl)-substituted bicyclic isothioureas: effect on morphology of cancer cells
Mendeleev Commun., 31:3 (2021), 288–290
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Molecular design and synthesis of new heterobivalent compounds based on chlorambucil and colchicine
Mendeleev Commun., 30:6 (2020), 706–708
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Tubulin targeted antimitotic agents based on adamantane lead compound: synthesis, SAR and molecular modeling
Mendeleev Commun., 30:4 (2020), 421–423
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New compounds with 4-azatricyclo[4.3.1.13,8]undecane framework
Mendeleev Commun., 30:2 (2020), 145–146
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Tubuloclustin analogues with ether moiety: synthesis and evaluation of tubulin clustering and antimitotic activity in cancer cells
Mendeleev Commun., 30:1 (2020), 106–108
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Synthesis and biotesting of new carrier prodrugs of 2-methoxyestradiol
Mendeleev Commun., 30:1 (2020), 7–9
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Bicyclic bridged isothioureas: synthesis and evaluation of activity in a model of lipopolysaccharide-induced septic shock
Mendeleev Commun., 29:1 (2019), 14–16
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Novel bridged and caged C4-podophyllotoxin derivatives as microtubule disruptors: synthesis, cytotoxic evaluation and structure–activity relationship
Mendeleev Commun., 28:5 (2018), 475–478
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Synthesis and antihypotensive properties of 2-amino-2-thiazoline analogues with enhanced lipophilicity
Mendeleev Commun., 28:4 (2018), 390–392
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Homologous series of novel adamantane–colchicine conjugates: synthesis and cytotoxic effect on human cancer cells
Mendeleev Commun., 28:3 (2018), 308–310
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Synthesis of non-steroidal 2-methoxyestradiol mimetics based on the bicyclo[3.3.1]nonane structural motif
Mendeleev Commun., 27:3 (2017), 240–242
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Synthesis and antimitotic activity of novel 5-aminoisoxazoles bearing alkoxyaryl moieties
Mendeleev Commun., 27:3 (2017), 228–230
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Synthesis of 5-hydroxy-4-methoxytricyclo[7.3.1.02,7]trideca-2,4,6-trien- 8-one – precursor of putative bioisosteric colchicine analogues
Mendeleev Commun., 24:6 (2014), 370–371
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Synthesis of 2-thia-4-azabicyclo[3.3.1]non-3-en-3-amine – bridged nitric oxide synthase inhibitor with enhanced lipophilicity
Mendeleev Commun., 23:2 (2013), 76–77
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Synthesis and biological testing of conformationally restricted serotonin analogues with bridgehead moieties
Mendeleev Commun., 22:2 (2012), 75–77
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Molecular and crystal structures of hetero-analogues of bicyclo[3.3.1]nonane with nitrogen and sulfur atoms
Mendeleev Commun., 21:5 (2011), 247–249
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Phosphates of bridgehead alcohols as putative inositol monophosphatase inhibitors: molecular design and synthetic approach
Mendeleev Commun., 21:5 (2011), 242–244
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Design, synthesis and biotest of a bicyclo[3.3.1]nonane analogue of 2-amino-5,6-dihydro-4H-1,3-thiazine
Mendeleev Commun., 20:6 (2010), 323–325
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Synthesis of indole derivatives fused with bicyclo[3.2.1]octane framework
Mendeleev Commun., 19:1 (2009), 10–11
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Design, synthesis and bioactivity of simplified taxol analogues on the basis of bicyclo[3.3.1]nonane derivatives
Mendeleev Commun., 18:4 (2008), 183–185
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Crystal structure of the tritylated product of 3-hydroxymethylbicyclo[3.3.1]nonan-2-on-7-ol ethylene acetal cyclization
Mendeleev Commun., 17:6 (2007), 332–334
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Physiologically active compounds interacting with serotonin (5-hydroxytryptamine) receptors
Usp. Khim., 70:4 (2001), 382–407
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The crystal- and molecular structure of $3{,}7$-dimethyl-$1{,}5$-diphenylbispidone-$9$-copper $(\mathrm{II})$ chloride $1:1$ complex
Dokl. Akad. Nauk SSSR, 289:4 (1986), 876–879
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