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Journal of the American Chemical Society|September 20, 2018
Thionoesters: A Native Chemical Ligation-Inspired Approach to Cysteine-Triggered H2S DonorsMatthew M Cerda, Yu Zhao, Michael D PluthMethods in Enzymology|July 28, 2020
H2S donors with optical responsesMichael D Pluth, Yu Zhao, Matthew M CerdaChemical Science|March 8, 2019
Fluorogenic hydrogen sulfide (H2S) donors based on sulfenyl thiocarbonates enable H2S tracking and quantificationYu Zhao, Matthew M Cerda, Michael D PluthCell Chemical Biology|April 21, 2018
S Marks the Spot: Linking the Antioxidant Activity of N-Acetyl Cysteine to H2S and Sulfane Sulfur SpeciesMatthew M Cerda, Michael D PluthAccounts of Chemical Research|August 8, 2019
Development and Application of Carbonyl Sulfide-Based Donors for H2S DeliveryCarolyn M Levinn, Matthew M Cerda, Michael D PluthAntioxidants & Redox Signaling|September 27, 2019
Activatable Small-Molecule Hydrogen Sulfide DonorsCarolyn M Levinn, Matthew M Cerda, Michael D PluthChemical Science|March 8, 2019
Dithioesters: simple, tunable, cysteine-selective H2S donorsMatthew M Cerda, Turner D Newton, Yu Zhao, et al.Chemical Communications (Cambridge, England)|July 22, 2020
Progress toward colorimetric and fluorescent detection of carbonyl sulfideMatthew M Cerda, Julia M Fehr, Tobias J Sherbow, et al.Free Radical Biology & Medicine|December 24, 2018
Effects of sulfane sulfur content in benzyl polysulfides on thiol-triggered H2S release and cell proliferationSarah G Bolton, Matthew M Cerda, Annie K Gilbert, et al.Angewandte Chemie (International Ed. in English)|October 25, 2016
Hydrogen Sulfide Donors Activated by Reactive Oxygen SpeciesYu Zhao, Michael D PluthPageof 579