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Prenatal Exposure to Benzophenone-3 Impairs Autophagy, Disrupts RXRs/PPARγ Signaling, and Alters Epigenetic and Post-Translational Statuses in Brain Neurons

Molecular neurobiology, 2019-07, Vol.56 (7), p.4820-4837

2019

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Lactose esters: synthesis and biotechnological applications

Critical reviews in biotechnology, 2018-02, Vol.38 (2), p.245-258

2018

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In Search of Effective Anticancer Agents-Novel Sugar Esters Based on Polyhydroxyalkanoate Monomers

International journal of molecular sciences, 2021-07, Vol.22 (13), p.7238

2021

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Lessons from chlorophylls: modifications of porphyrinoids towards optimized solar energy conversion

Molecules (Basel, Switzerland), 2014-10, Vol.19 (10), p.15938-15954

2014

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Recent Progress in Chemical Modifications of Chlorophylls and Bacteriochlorophylls for the Applications in Photodynamic Therapy

Current medicinal chemistry, 2015-09, Vol.22 (26), p.3054-3074

2015

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Serotonin type 5A receptor antagonists inhibit D-lysergic acid diethylamide discriminatory cue in rats

Journal of psychopharmacology (Oxford), 2019-11, Vol.33 (11), p.1447-1455

2019

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N-Skatyltryptamines—Dual 5-HT6R/D2R Ligands with Antipsychotic and Procognitive Potential

Molecules (Basel, Switzerland), 2021-07, Vol.26 (15), p.4605

2021

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Influence of Chemical Modifications of Polyhydroxyalkanoate-Derived Fatty Acids on Their Antimicrobial Properties

Catalysts, 2019-06, Vol.9 (6), p.510

2019

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Tuning the activity of known drugs via the introduction of halogen atoms, a case study of SERT ligands – Fluoxetine and fluvoxamine

European journal of medicinal chemistry, 2021-08, Vol.220, p.113533-113533, Article 113533

2021

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Reaction mechanism of sterol hydroxylation by steroid C25 dehydrogenase – Homology model, reactivity and isoenzymatic diversity

Journal of inorganic biochemistry, 2017-08, Vol.173, p.28-43

2017

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Virtual screening-driven discovery of dual 5-HT6/5-HT2A receptor ligands with pro-cognitive properties

European journal of medicinal chemistry, 2020-01, Vol.185, p.111857-111857, Article 111857

2020

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Fluorinated indole-imidazole conjugates: Selective orally bioavailable 5-HT7 receptor low-basicity agonists, potential neuropathic painkillers

European journal of medicinal chemistry, 2019-05, Vol.170, p.261-275

2019

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Encapsulation of curcumin in polyelectrolyte nanocapsules and their neuroprotective activity

Nanotechnology, 2016-09, Vol.27 (35), p.355101-355114

2016

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Low-basicity 5-HT7 Receptor Agonists Synthesized Using the van Leusen Multicomponent Protocol

Scientific reports, 2017-05, Vol.7 (1), p.1444-1444, Article 1444

2017

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5-HT1A receptor ligands and their therapeutic applications: review of new patents

Expert opinion on therapeutic patents, 2018-09, Vol.28 (9), p.679-689

2018

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Pyrano[2,3,4-cd]indole as a Scaffold for Selective Nonbasic 5‑HT6R Ligands

ACS medicinal chemistry letters, 2017-04, Vol.8 (4), p.390-394

2017

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2-Aminoimidazole-based antagonists of the 5-HT6 receptor – A new concept in aminergic GPCR ligand design

European journal of medicinal chemistry, 2019-10, Vol.179, p.1-15

2019

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Rationally designed N-phenylsulfonylindoles as a tool for the analysis of the non-basic 5-HT6R ligands binding mode

European journal of medicinal chemistry, 2021-01, Vol.209, p.112916-112916, Article 112916

2021

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The effect of the intramolecular C–H⋯O interactions on the conformational preferences of bis-arylsulfones – 5-HT6 receptor antagonists and beyond

RSC advances, 2018-01, Vol.8 (33), p.18672-18681

2018

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Bioisosteric Matrices for Ligands of Serotonin Receptors

ChemMedChem, 2015-04, Vol.10 (4), p.601-605

2015

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Chemo-biotechnological synthesis of precursors for biocatalytic acylation of sugars

New biotechnology, 2016-07, Vol.33, p.S106-S106

2016

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The effect of the intramolecular C-H⋯O interactions on the conformational preferences of bis-arylsulfones - 5-HT 6 receptor antagonists and beyond

RSC advances, 2018-05, Vol.8 (33), p.18672-18681

2018

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Halogen bonding enhances activity in a series of dual 5-HT 6 /D 2 ligands designed in a hybrid bioisostere generation/virtual screening protocol

RSC advances, 2016, Vol.6 (60), p.54918-54925

2016

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Pyrano[2,3,4- cd ]indole as a Scaffold for Selective Nonbasic 5-HT 6 R Ligands

ACS medicinal chemistry letters, 2017-04, Vol.8 (4), p.390-394

2017

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Rational design of 5-HT 6 R ligands using a bioisosteric strategy: synthesis, biological evaluation and molecular modelling

RSC advances, 2015, Vol.5 (33), p.25806-25815

2015

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Prenatal Exposure to Benzophenone-3 Impairs Autophagy, Disrupts RXRs/PPARγ Signaling, and Alters Epigenetic and Post-Translational Statuses in Brain Neurons

Lactose esters: synthesis and biotechnological applications

In Search of Effective Anticancer Agents-Novel Sugar Esters Based on Polyhydroxyalkanoate Monomers

Lessons from chlorophylls: modifications of porphyrinoids towards optimized solar energy conversion

Recent Progress in Chemical Modifications of Chlorophylls and Bacteriochlorophylls for the Applications in Photodynamic Therapy

Serotonin type 5A receptor antagonists inhibit D-lysergic acid diethylamide discriminatory cue in rats

N-Skatyltryptamines—Dual 5-HT6R/D2R Ligands with Antipsychotic and Procognitive Potential

Influence of Chemical Modifications of Polyhydroxyalkanoate-Derived Fatty Acids on Their Antimicrobial Properties

Tuning the activity of known drugs via the introduction of halogen atoms, a case study of SERT ligands – Fluoxetine and fluvoxamine

Reaction mechanism of sterol hydroxylation by steroid C25 dehydrogenase – Homology model, reactivity and isoenzymatic diversity

Virtual screening-driven discovery of dual 5-HT6/5-HT2A receptor ligands with pro-cognitive properties

Fluorinated indole-imidazole conjugates: Selective orally bioavailable 5-HT7 receptor low-basicity agonists, potential neuropathic painkillers

Encapsulation of curcumin in polyelectrolyte nanocapsules and their neuroprotective activity

Low-basicity 5-HT7 Receptor Agonists Synthesized Using the van Leusen Multicomponent Protocol

5-HT1A receptor ligands and their therapeutic applications: review of new patents

Pyrano[2,3,4-cd]indole as a Scaffold for Selective Nonbasic 5‑HT6R Ligands

2-Aminoimidazole-based antagonists of the 5-HT6 receptor – A new concept in aminergic GPCR ligand design

Rationally designed N-phenylsulfonylindoles as a tool for the analysis of the non-basic 5-HT6R ligands binding mode

The effect of the intramolecular C–H⋯O interactions on the conformational preferences of bis-arylsulfones – 5-HT6 receptor antagonists and beyond

Bioisosteric Matrices for Ligands of Serotonin Receptors

Chemo-biotechnological synthesis of precursors for biocatalytic acylation of sugars

The effect of the intramolecular C-H⋯O interactions on the conformational preferences of bis-arylsulfones - 5-HT 6 receptor antagonists and beyond

Halogen bonding enhances activity in a series of dual 5-HT 6 /D 2 ligands designed in a hybrid bioisostere generation/virtual screening protocol

Pyrano[2,3,4- cd ]indole as a Scaffold for Selective Nonbasic 5-HT 6 R Ligands

Rational design of 5-HT 6 R ligands using a bioisosteric strategy: synthesis, biological evaluation and molecular modelling

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