interaction of chloroacetamide electrophiles with cellular glutathion

interaction of chloroacetamide electrophiles with cellular glutathion Sulfamate Acetamides as Self-Immolative for Covalent Ligand-Directed Release Chemistry Identification, optimization, and structural elucidation

Name: interaction of chloroacetamide electrophiles with cellular glutathion Sulfamate Acetamides as Self-Immolative for Covalent Ligand-Directed Release Chemistry Identification, optimization, and structural elucidation
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Identification, optimization, and structural elucidation of chloroacetamide scaffold as covalent inhibitors for Ubiquitin C terminal Hydrolase L3 bioRxiv Glutathione (GSH) is synthesized in the cytoplasm by the action of Download Scientific Diagram NCBP1 stress signaling drives alternative S6K1 splicing inhibiting translation Nature Chemical Biology Chloroacetamide an overview ScienceDirect Topics Expanding the Chemistry of Dihaloacetamides as Tunable Electrophiles for Reversible Covalent Targeting of Cysteines Journal of Medicinal Chemistry Targeting a Therapy Resistant Cancer Cell State Using Masked Electrophiles as GPX4 Inhibitors bioRxiv

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Z.KaminskiC.LeightS.et al (2005)

They function by specifically binding and sequestering excess free copper ions, thereby cutting off the feed-forward cycle of oxidative stress and inflammatory amplification at its source

PLoS One 17, e0274911 (2022), Abstract Monitoring Autophagy at Cellular and Molecular Level in Crassostrea gigas During an Experimental Ostreid Herpesvirus 1 (OsHV-1) Infection: Picot, S., Faury, N., et al

doi: 10.1128/mSystems.00176-18 15 KlingbergEMagnussonMKStridHDemingerAStahlASundinJet al

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