Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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"Inverse Drug Discovery" Strategy To Identify Proteins That Are Targeted by Latent Electrophiles As Exemplified by Aryl Fluorosulfates.The Taxonomy of Covalent Inhibitors

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Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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2017 nî lūn-bûn

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2017年の論文

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2017年論文

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2017年論文

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2017年論文

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2017年論文

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Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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P1476

Selective Covalent Protein Modification by 4-Halopyridines through Catalysis

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P2093

Alfred Tuley

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Jake C Swartzel

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Joyce A V Er

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P2860

Developing dual and specific inhibitors of dimethylarginine dimethylaminohydrolase-1 and nitric oxide synthase: toward a targeted polypharmacology to control nitric oxide

On the Mechanism of Dimethylarginine Dimethylaminohydrolase Inactivation by 4-Halopyridines

Reassessment of Ellman's reagent

Metabolically Labile Fumarate Esters Impart Kinetic Selectivity to Irreversible Inhibitors

Soft drug design: general principles and recent applications.

The resurgence of covalent drugs.

Discovery of halopyridines as quiescent affinity labels: inactivation of dimethylarginine dimethylaminohydrolase

Prolonged and tunable residence time using reversible covalent kinase inhibitors.

Measurement and estimation of electrophilic reactivity for predictive toxicology.

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1551-1556

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scholarly article

P356

10.1002/CBIC.201700104

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P478

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Christopher L Schardon

Walter Fast

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2017-06-27T00:00:00Z

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28470883

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5886304

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Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

about

P2860

P2860

Selective Covalent Protein Modification by 4-Halopyridines through Catalysis.

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P1476

P2093

P2860

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