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Boris Illarionov

Chemiker

Name	Boris Illarionov
Ort	Deutschland
Akademischer Grad bzw. Titel	Dr.
Beruf	Chemiker (charakteristischer Beruf)
Variante	Boris Aleksandrovič Illarionov Boris A. Illarionov B. A. Illarionov
Beziehung	Institut für Biochemie und Lebensmittelchemie (Hamburg). Abteilung Lebensmittelchemie
Weitere Angaben	Univ. Hamburg, Fak. für Mathematik, Informatik und Naturwissenschaften, Fachbereich Chemie
Quelle	http://www.chemie.uni-hamburg.de/lc/mitarbeiter/illarionov.html
Datensatztyp	Person
GND-Nummer	1024801314
Datensatz-ID	1024801314
Beteiligt an alle anzeigen Transient 19F photo-CIDNP: A practical tool to distinguish intermediate radical species and determine isotropic hyperfine coupling constants of 19F nuclei Systematic Analysis of the Effect of Genomic Knock‐Out of Non‐Essential Promiscuous HAD‐Like Phosphatases YcsE, YitU and YwtE on Flavin and Adenylate Content in Bacillus Subtilis Adaptive laboratory evolution of flavin functionality identifies dihydrolipoyl dehydrogenase as one of the critical points for the activity of 7,8-didemethyl-riboflavin as a surrogate for riboflavin in escherichia coli Insights into the photoswitch based on 5-deazaFMN and LOV2 from Avena sativa: a combined absorption and NMR spectroscopy study Shining a spotlight on methyl groups: photochemically induced dynamic nuclear polarization spectroscopy of 5-Deazariboflavin and its nor analogs Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors Erweiterung des Reaktionsspektrums: Nachweis des 5‐Deazaflavin‐Radikals durch photochemisch induzierte dynamische Kernpolarisation Expanding Reaction Horizons: Evidence of the 5‐Deazaflavin Radical Through Photochemically Induced Dynamic Nuclear Polarization Front Cover: Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors (ChemMedChem 19/2023) Erweiterung des Reaktionsspektrums: Nachweis des 5‐Deazaflavin‐Radikals durch photochemisch induzierte dynamische Kernpolarisation Expanding reaction horizons: evidence of the 5‐deazaflavin radical through photochemically induced dynamic nuclear polarization Exploring the translational gap of a novel class of escherichia coli IspE inhibitors Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors Targeting the IspD Enzyme in the MEP Pathway: Identification of a Novel Fragment Class Discovery of novel drug-like antitubercular hits targeting the MEP pathway enzyme DXPS by strategic application of ligand-based virtual screening Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity Search for the Active Ingredients from a 2-Aminothiazole DMSO Stock Solution with Antimalarial Activity Selective 13C labelling reveals the electronic structure of flavocoenzyme radicals Targeting the IspD Enzyme in the MEP Pathway : Identification of a Novel Fragment Class Phage Display on the Anti‐infective Target 1‐Deoxy‐ d ‐xylulose‐5‐phosphate Synthase Leads to an Acceptor–Substrate Competitive Peptidic Inhibitor Imidazole‐ and Benzimidazole‐Based Inhibitors of the Kinase IspE: Targeting the Substrate‐Binding Site and the Triphosphate‐Binding Loop of the ATP Site Exploring the Ribose Sub‐Pocket of the Substrate‐Binding Site in Escherichia coli IspE: Structure‐Based Design, Synthesis, and Biological Evaluation of Cytosines and Cytosine Analogues

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Katalog der Deutschen Nationalbibliothek

Boris Illarionov

Transient 19F photo-CIDNP: A practical tool to distinguish intermediate radical species and determine isotropic hyperfine coupling constants of 19F nuclei

Systematic Analysis of the Effect of Genomic Knock‐Out of Non‐Essential Promiscuous HAD‐Like Phosphatases YcsE, YitU and YwtE on Flavin and Adenylate Content in Bacillus Subtilis

Adaptive laboratory evolution of flavin functionality identifies dihydrolipoyl dehydrogenase as one of the critical points for the activity of 7,8-didemethyl-riboflavin as a surrogate for riboflavin in escherichia coli

Insights into the photoswitch based on 5-deazaFMN and LOV2 from Avena sativa: a combined absorption and NMR spectroscopy study

Shining a spotlight on methyl groups: photochemically induced dynamic nuclear polarization spectroscopy of 5-Deazariboflavin and its nor analogs

Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors

Erweiterung des Reaktionsspektrums: Nachweis des 5‐Deazaflavin‐Radikals durch photochemisch induzierte dynamische Kernpolarisation

Expanding Reaction Horizons: Evidence of the 5‐Deazaflavin Radical Through Photochemically Induced Dynamic Nuclear Polarization

Front Cover: Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors (ChemMedChem 19/2023)

Erweiterung des Reaktionsspektrums: Nachweis des 5‐Deazaflavin‐Radikals durch photochemisch induzierte dynamische Kernpolarisation

Expanding reaction horizons: evidence of the 5‐deazaflavin radical through photochemically induced dynamic nuclear polarization

Exploring the translational gap of a novel class of escherichia coli IspE inhibitors

Exploring the Translational Gap of a Novel Class of Escherichia coli IspE Inhibitors

Targeting the IspD Enzyme in the MEP Pathway: Identification of a Novel Fragment Class

Discovery of novel drug-like antitubercular hits targeting the MEP pathway enzyme DXPS by strategic application of ligand-based virtual screening

Search for the Active Ingredients from a 2‐Aminothiazole DMSO Stock Solution with Antimalarial Activity

Search for the Active Ingredients from a 2-Aminothiazole DMSO Stock Solution with Antimalarial Activity

Selective 13C labelling reveals the electronic structure of flavocoenzyme radicals

Targeting the IspD Enzyme in the MEP Pathway : Identification of a Novel Fragment Class

Phage Display on the Anti‐infective Target 1‐Deoxy‐ d ‐xylulose‐5‐phosphate Synthase Leads to an Acceptor–Substrate Competitive Peptidic Inhibitor

Imidazole‐ and Benzimidazole‐Based Inhibitors of the Kinase IspE: Targeting the Substrate‐Binding Site and the Triphosphate‐Binding Loop of the ATP Site

Exploring the Ribose Sub‐Pocket of the Substrate‐Binding Site in Escherichia coli IspE: Structure‐Based Design, Synthesis, and Biological Evaluation of Cytosines and Cytosine Analogues