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Application of Dual Inhibition Concept within Looped Autoregulatory Systems toward Antivirulence Agents against Pseudomonas aeruginosa Infections
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Thomann A,
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ACS chemical biology, 11, 5, 1279-86, 10.1021/acschembio.6b00117, 26882081
ACS chemical biology, 11, 5, 1279-86, 10.1021/acschembio.6b00117, 26882081
Novel Compounds Targeting the RNA-Binding Protein HuR. Structure-Based Design, Synthesis, and Interaction Studies
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Della Volpe S,
Nasti R,
Queirolo M,
Unver M,
Jumde V,
Dömling A,
Vasile F,
Potenza D,
Ambrosio F,
Costa G,
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ACS Med. Chem. Lett., 10, 4, 615-620, 10.1021/acsmedchemlett.8b00600, 30996806
ACS Med. Chem. Lett., 10, 4, 615-620, 10.1021/acsmedchemlett.8b00600, 30996806
Discovery and optimization of thiazole-based quorum sensing inhibitors as potent blockers of Pseudomonas aeruginosa pathogenicity
Publikation
Abdelsamie A,
Hamed M,
Schütz C,
Röhrig T,
Kany A,
Schmelz S,
Blankenfeldt W,
Hirsch A,
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Empting M
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Eur. J. Med. Chem., 276, 10.1016/j.ejmech.2024.116685, 39042991
Eur. J. Med. Chem., 276, 10.1016/j.ejmech.2024.116685, 39042991
Identification of a new protein-RNA interaction inhibitor targeting the KH34 region of the insulin-like growth factor 2 mRNA binding protein 2 (IGF2BP2/IMP2)
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Berwanger A,
Wagner K,
Both S,
Kany A,
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Hirsch A,
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Empting M
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Eur. J. Med. Chem., 307, 10.1016/j.ejmech.2026.118624, 41687271
Eur. J. Med. Chem., 307, 10.1016/j.ejmech.2026.118624, 41687271
Toward Anti-Herpesviral PROTACs: Assessing the Challenges for Targeted Protein Degradation on the Example of Kaposi's Sarcoma-Associated Herpesvirus Latency-Associated Nuclear Antigen
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Berwanger A,
Stein S,
Brandner S,
Kany A,
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Empting* M
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ChemMedChem, 10.1002/cmdc.202500758, 41252598
ChemMedChem, 10.1002/cmdc.202500758, 41252598
Exploring the chemical space of ureidothiophene-2-carboxylic acids as inhibitors of the quorum sensing enzyme PqsD from Pseudomonas aeruginosa
Publikation
Sahner J,
Empting M,
Kamal A,
Weidel E,
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Börger C,
Hartmann R
(2015)
European journal of medicinal chemistry, 96, 14-21, 10.1016/j.ejmech.2015.04.007, 25874327
European journal of medicinal chemistry, 96, 14-21, 10.1016/j.ejmech.2015.04.007, 25874327
From in vitro to in cellulo: structure-activity relationship of (2-nitrophenyl)methanol derivatives as inhibitors of PqsD in Pseudomonas aeruginosa
Publikation
Storz M,
Allegretta G,
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Organic & biomolecular chemistry, 12, 32, 6094-104, 10.1039/c4ob00707g, 24909330
Organic & biomolecular chemistry, 12, 32, 6094-104, 10.1039/c4ob00707g, 24909330
The One-Step Synthesis of Biologically Active Isochromans from Lignin-Derived Aromatic Monomers in Tunable Deep Eutectic Solvents
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Kottayi A,
Afanasenko A,
Castillo-Garcia A,
Elgaher W,
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Hirsch A,
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Chem. Eur. J., 10.1002/chem.202502769, 41351205
Chem. Eur. J., 10.1002/chem.202502769, 41351205
Dynamic Proteoids Generated From Dipeptide-Based Monomers
Publikation
Liu Y,
Stuart M,
Buhler E,
Hirsch A
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Macromolecular rapid communications, 39, 13, 10.1002/marc.201800099, 29806088
Macromolecular rapid communications, 39, 13, 10.1002/marc.201800099, 29806088
Phage Display on the Anti-infective Target 1-Deoxy-d-xylulose-5-phosphate Synthase Leads to an Acceptor-Substrate Competitive Peptidic Inhibitor
Publikation
Marcozzi A,
Masini T,
Di Zhu,
Pesce D,
Illarionov B,
Fischer M,
Herrmann A,
Hirsch A
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ChemBioChem, 19, 1, 58-65, 10.1002/cbic.201700402, 29119720
ChemBioChem, 19, 1, 58-65, 10.1002/cbic.201700402, 29119720