Jintawee Kicuntod

发表

Synthesis, molecular features and biological activities of modified plant polysaccharides.

M. Marschall, S. Mukherjee, S. Jana, 2022, Carbohydrate polymers.

Inclusion complexation of pinostrobin with various cyclodextrin derivatives.

T. Rungrotmongkol, P. Wolschann, P. Pongsawasdi, 2016, Journal of molecular graphics & modelling.

Methodological Development of a Multi-Readout Assay for the Assessment of Antiviral Drugs against SARS-CoV-2

K. Überla, A. Ensser, M. Marschall, 2021, Pathogens.

Cavity Closure of 2-Hydroxypropyl-β-Cyclodextrin: Replica Exchange Molecular Dynamics Simulations

T. Rungrotmongkol, H. Okumura, P. Wolschann, 2019, Polymers.

The Oligomeric Assemblies of Cytomegalovirus Core Nuclear Egress Proteins Are Associated with Host Kinases and Show Sensitivity to Antiviral Kinase Inhibitors

H. Sticht, M. Marschall, Jintawee Kicuntod, 2022, Viruses.

Physical properties and biological activities of hesperetin and naringenin in complex with methylated β-cyclodextrin

T. Rungrotmongkol, P. Wolschann, H. Viernstein, 2015, Beilstein journal of organic chemistry.

A Peptide Inhibitor of the Human Cytomegalovirus Core Nuclear Egress Complex

M. Marschall, J. Eichler, I. Neundorf, 2022, Pharmaceuticals.

Theoretical and Experimental Studies on Inclusion Complexes of Pinostrobin and β-Cyclodextrins

T. Rungrotmongkol, Koichi Kato, P. Wolschann, 2018, Sensors.

An antiviral targeting strategy based on the inducible interference with cytomegalovirus nuclear egress complex.

Y. Muller, M. Marschall, J. Lösing, 2023, Antiviral research.

Nuclear Egress Complexes of HCMV and Other Herpesviruses: Solving the Puzzle of Sequence Coevolution, Conserved Structures and Subfamily-Spanning Binding Properties

Y. Muller, F. Neipel, H. Sticht, 2020, Viruses.

Combinatorial Drug Treatments Reveal Promising Anticytomegaloviral Profiles for Clinically Relevant Pharmaceutical Kinase Inhibitors (PKIs)

D. Michel, M. Marschall, B. Kaufer, 2021, International journal of molecular sciences.

Development of a PROTAC-Based Targeting Strategy Provides a Mechanistically Unique Mode of Anti-Cytomegalovirus Activity

M. Marschall, B. Kaufer, S. Tsogoeva, 2021, International journal of molecular sciences.

Properties of Oligomeric Interaction of the Cytomegalovirus Core Nuclear Egress Complex (NEC) and Its Sensitivity to an NEC Inhibitory Small Molecule

H. Sticht, M. Marschall, J. Eichler, 2021, Viruses.

A quantitative nuclear egress assay to investigate the nucleocytoplasmic capsid release of human cytomegalovirus.

M. Marschall, T. Stamminger, W. Rawlinson, 2020, Journal of virological methods.

‘Getting Better’—Is It a Feasible Strategy of Broad Pan-Antiherpesviral Drug Targeting by Using the Nuclear Egress-Directed Mechanism?

M. Marschall, J. Lösing, Jintawee Kicuntod, 2024, International journal of molecular sciences.

Exploring the Human Cytomegalovirus Core Nuclear Egress Complex as a Novel Antiviral Target: A New Type of Small Molecule Inhibitors

Y. Muller, M. Marschall, J. Eichler, 2021, Viruses.

Cyclin-Dependent Kinase 8 Represents a Positive Regulator of Cytomegalovirus Replication and a Novel Host Target for Antiviral Strategies

R. Stanton, M. Marschall, J. Lösing, 2024, Pharmaceutics.

An Antiherpesviral Host-Directed Strategy Based on CDK7 Covalently Binding Drugs: Target-Selective, Picomolar-Dose, Cross-Virus Reactivity

M. Marschall, Kiyean Nam, Mooyoung Seo, 2024, Pharmaceutics.