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- 2023
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Mark
Combining pharmacophore models derived from DNA-encoded chemical libraries with structure-based exploration to predict Tankyrase 1 inhibitors
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- Contribution to journal › Article
- 2022
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Mark
Sialic Acid 4-N-Piperazine and Piperidine Derivatives Bind with High Affinity to the P. mirabilis Sialic Acid Sodium Solute Symporter
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- Contribution to journal › Article
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Mark
Large-Scale Crystallographic Fragment Screening Expedites Compound Optimization and Identifies Putative Protein-Protein Interaction Sites
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- Contribution to journal › Article
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Mark
The human TRPA1 intrinsic cold and heat sensitivity involves separate channel structures beyond the N-ARD domain
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- Contribution to journal › Article
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Mark
Optimization of N-Piperidinyl-Benzimidazolone Derivatives as Potent and Selective Inhibitors of 8-Oxo-Guanine DNA Glycosylase 1
2022) In ChemMedChem(
- Contribution to journal › Article
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Mark
Targeting Acute Myelogenous Leukemia Using Potent Human Dihydroorotate Dehydrogenase Inhibitors Based on the 2-Hydroxypyrazolo[1,5- a]pyridine Scaffold : SAR of the Aryloxyaryl Moiety
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- Contribution to journal › Article
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Mark
Discovery of the 4-aminopiperidine-based compound EM127 for the site-specific covalent inhibition of SMYD3
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- Contribution to journal › Article
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Mark
Sialic Acid Derivatives Inhibit SiaT Transporters and Delay Bacterial Growth
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- Contribution to journal › Article
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Mark
Design and synthesis of novel 3-triazolyl-1-thiogalactosides as galectin-1, -3 and -8 inhibitors
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- Contribution to journal › Article
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Mark
A hydrophobic patch (PLVIVG; 1481–1486) in the B-domain of factor V-short is crucial for its synergistic TFPIα-cofactor activity with protein S and for the formation of the FXa-inhibitory complex comprising FV-short, TFPIα, and protein S
(
- Contribution to journal › Article