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Martin Empting (1983-)

Chemiker

Name	Martin Empting
Time	1983- (Date of birth and death)
Place	Königs Wusterhausen (Geburtsort) Saarbrücken (Wirkungsort) Deutschland
Gender	männlich
Academic degree	Dr.-Ing. (am Fachbereich Chemie der Technischen Universität Darmstadt) (2012)
Profession	Chemiker (characteristic profession)
Related	Universität des Saarlandes
Source	AM Metadaten
Record type	Person
GND-Identifier	1033087106
Record ID	1033087106
Involved in show all Design and synthesis of peptide and small molecule protein-RNA interaction inhibitors Enzyme-Linked Lipid Nanocarriers for Coping Pseudomonal Pulmonary Infection. Would Nanocarriers Complement Biofilm Disruption or Pave Its Road? Gene Editing and Small Molecule Inhibitors of the RNA Binding Protein IGF2BP2/IMP2 Show its Potential as an Anti-Cancer Drug Target Probing biological activities of RNA-binding proteins from bacterial and mammalian cells Phage display-based discovery of cyclic peptides against the broad spectrum bacterial anti-virulence target CsrA Concepts and Core Principles of Fragment-Based Drug Design In-depth Profiling of MvfR-Regulated Small Molecules in Pseudomonas aeruginosa after Quorum Sensing Inhibitor Treatment Semi-synthetic vNAR libraries screened against therapeutic antibodies primarily deliver anti-idiotypic binders Disubstituted 1,2,3-triazoles : a multitool for biomolecular chemistry Disubstituted 1,2,3-Triazoles: A Multitool for Biomolecular Chemistry

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Martin Empting (1983-)

Design and synthesis of peptide and small molecule protein-RNA interaction inhibitors

Enzyme-Linked Lipid Nanocarriers for Coping Pseudomonal Pulmonary Infection. Would Nanocarriers Complement Biofilm Disruption or Pave Its Road?

Gene Editing and Small Molecule Inhibitors of the RNA Binding Protein IGF2BP2/IMP2 Show its Potential as an Anti-Cancer Drug Target

Probing biological activities of RNA-binding proteins from bacterial and mammalian cells

Phage display-based discovery of cyclic peptides against the broad spectrum bacterial anti-virulence target CsrA

Concepts and Core Principles of Fragment-Based Drug Design

In-depth Profiling of MvfR-Regulated Small Molecules in Pseudomonas aeruginosa after Quorum Sensing Inhibitor Treatment

Semi-synthetic vNAR libraries screened against therapeutic antibodies primarily deliver anti-idiotypic binders

Disubstituted 1,2,3-triazoles : a multitool for biomolecular chemistry

Disubstituted 1,2,3-Triazoles: A Multitool for Biomolecular Chemistry