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Cerda, Matthew M., Zhao, Yu, Pluth, Michael D. (2018) Thionoesters: A Native Chemical Ligation-Inspired Approach to Cysteine-Triggered H2S Donors. Journal Of The American Chemical Society, 140 (39) 12574-12579 doi:10.1021/jacs.8b07268

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Reference TypeJournal (article/letter/editorial)
TitleThionoesters: A Native Chemical Ligation-Inspired Approach to Cysteine-Triggered H2S Donors
JournalJournal Of The American Chemical Society
AuthorsCerda, Matthew M.Author
Zhao, YuAuthor
Pluth, Michael D.Author
Year2018 (October 3)Volume140
Issue39
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/jacs.8b07268Search in ResearchGate
Generate Citation Formats
Mindat Ref. ID1800541Long-form Identifiermindat:1:5:1800541:1
GUID0
Full ReferenceCerda, Matthew M., Zhao, Yu, Pluth, Michael D. (2018) Thionoesters: A Native Chemical Ligation-Inspired Approach to Cysteine-Triggered H2S Donors. Journal Of The American Chemical Society, 140 (39) 12574-12579 doi:10.1021/jacs.8b07268
Plain TextCerda, Matthew M., Zhao, Yu, Pluth, Michael D. (2018) Thionoesters: A Native Chemical Ligation-Inspired Approach to Cysteine-Triggered H2S Donors. Journal Of The American Chemical Society, 140 (39) 12574-12579 doi:10.1021/jacs.8b07268
In(2018, October) Journal Of The American Chemical Society Vol. 140 (39) American Chemical Society (ACS)

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Cerda, Matthew M., Newton, Turner D., Zhao, Yu, Collins, Brylee K., Hendon, Christopher H., Pluth, Michael D. (2019) Dithioesters: simple, tunable, cysteine-selective H2S donors. Chemical Science, 10. 1773-1779 doi:10.1039/c8sc04683b
Zhao, Yu, Cerda, Matthew M., Pluth, Michael D. (2019) Fluorogenic hydrogen sulfide (H2S) donors based on sulfenyl thiocarbonates enable H2S tracking and quantification. Chemical Science, 10. 1873-1878 doi:10.1039/c8sc05200j
Steiger, Andrea K., Pardue, Sibile, Kevil, Christopher G., Pluth, Michael D. (2016) Self-Immolative Thiocarbamates Provide Access to Triggered H2S Donors and Analyte Replacement Fluorescent Probes. Journal Of The American Chemical Society, 138 (23) 7256-7259 doi:10.1021/jacs.6b03780
Hammers, Matthew D., Taormina, Michael J., Cerda, Matthew M., Montoya, Leticia A., Seidenkranz, Daniel T., Parthasarathy, Raghuveer, Pluth, Michael D. (2015) A Bright Fluorescent Probe for H2S Enables Analyte-Responsive, 3D Imaging in Live Zebrafish Using Light Sheet Fluorescence Microscopy. Journal Of The American Chemical Society, 137 (32) 10216-10223 doi:10.1021/jacs.5b04196
Cerda, Matthew M., Hammers, Matthew D., Earp, Mary S., Zakharov, Lev N., Pluth, Michael D. (2017) Applications of Synthetic Organic Tetrasulfides as H2S Donors. Organic Letters, 19. 2314-2317 doi:10.1021/acs.orglett.7b00858
Zhao, Yu, Steiger, Andrea K., Pluth, Michael D. (2018) Cysteine-activated hydrogen sulfide (H2S) delivery through caged carbonyl sulfide (COS) donor motifs. Chemical Communications, 54 (39). 4951-4954 doi:10.1039/c8cc02428f
Zhao, Yu, Wang, Hua, Xian, Ming (2011) Cysteine-Activated Hydrogen Sulfide (H2S) Donors. Journal Of The American Chemical Society, 133 (1) 15-17 doi:10.1021/ja1085723
Henthorn, Hillary A., Pluth, Michael D. (2015) Mechanistic Insights into the H2S-Mediated Reduction of Aryl Azides Commonly Used in H2S Detection. Journal Of The American Chemical Society, 137 (48) 15330-15336 doi:10.1021/jacs.5b10675
Chisholm, Timothy S., Clayton, Daniel, Dowman, Luke J., Sayers, Jessica, Payne, Richard J. (2018) Native Chemical Ligation–Photodesulfurization in Flow. Journal Of The American Chemical Society, 140 (29) 9020-9024 doi:10.1021/jacs.8b03115
Kang, Xueying, Huang, Haojie, Jiang, Chenyang, Cheng, Longhuai, Sang, Yueqian, Cai, Xuekang, Dong, Yalun, Sun, Lu, Wen, Xin, Xi, Zhen, Yi, Long (2022) Cysteine-Activated Small-Molecule H2Se Donors Inspired by Synthetic H2S Donors. Journal of the American Chemical Society, 144 (9) 3957-3967 doi:10.1021/jacs.1c12006
Fosnacht, Kaylin G., Sharma, Jyoti, Champagne, Pier Alexandre, Pluth, Michael D. (2024) Transpersulfidation or H2S Release? Understanding the Landscape of Persulfide Chemical Biology. Journal of the American Chemical Society, 146 (27) 18689-18698 doi:10.1021/jacs.4c05874
 
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