| scholarly article | Q13442814 |
| P50 | author | Ian Andrew Wilson | Q5983280 |
| Jeffery W. Kelly | Q6175781 | ||
| Karl Barry Sharpless | Q110925 | ||
| Benjamin Cravatt | Q4888433 | ||
| Stefano Forli | Q63385497 | ||
| Hua Wang | Q63385706 | ||
| Lars Plate | Q42410251 | ||
| P2093 | author name string | David E Mortenson | |
| Suhua Li | |||
| Evan T Powers | |||
| Wentao Chen | |||
| Gabriel J Brighty | |||
| Grant Bare | |||
| P2860 | cites work | The Protein Data Bank | Q24515306 |
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| Retinoic acid in the development, regeneration and maintenance of the nervous system | Q36946560 | ||
| Arylfluorosulfates Inactivate Intracellular Lipid Binding Protein(s) through Chemoselective SuFEx Reaction with a Binding Site Tyr Residue | Q37008862 | ||
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| Purinergic regulation of vascular endothelial growth factor signaling in angiogenesis | Q37222633 | ||
| Proteome-wide reactivity profiling identifies diverse carbamate chemotypes tuned for serine hydrolase inhibition | Q37251595 | ||
| Mechanistic evaluation and transcriptional signature of a glutathione S-transferase omega 1 inhibitor | Q37329941 | ||
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| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | drug discovery | Q1418791 |
| P304 | page(s) | 200-210 | |
| P577 | publication date | 2017-12-21 | |
| P1433 | published in | Journal of the American Chemical Society | Q898902 |
| P1476 | title | "Inverse Drug Discovery" Strategy To Identify Proteins That Are Targeted by Latent Electrophiles As Exemplified by Aryl Fluorosulfates | |
| P478 | volume | 140 |
| Q92757150 | A rapid access to aliphatic sulfonyl fluorides |
| Q90665895 | Activity-Based Sensing: A Synthetic Methods Approach for Selective Molecular Imaging and Beyond |
| Q90254510 | Aryl-fluorosulfate-based Lysine Covalent Pan-Inhibitors of Apoptosis Protein (IAP) Antagonists with Cellular Efficacy |
| Q64968466 | Arylfluorosulfate-Based Electrophiles for Covalent Protein Labeling: A New Addition to the Arsenal. |
| Q93178340 | Biocompatible SuFEx Click Chemistry: Thionyl Tetrafluoride (SOF4 )-Derived Connective Hubs for Bioconjugation to DNA and Proteins |
| Q83232453 | Ceapins block the unfolded protein response sensor ATF6α by inducing a neomorphic inter-organelle tether |
| Q90402827 | Emerging Utility of Fluorosulfate Chemical Probes |
| Q52619354 | Genetically Encoding Fluorosulfate-l-tyrosine To React with Lysine, Histidine, and Tyrosine via SuFEx in Proteins in Vivo. |
| Q91452567 | Global targeting of functional tyrosines using sulfur-triazole exchange chemistry |
| Q92997375 | Installation of -SO2F groups onto primary amides |
| Q56530196 | Pharmacologic ATF6 activating compounds are metabolically activated to selectively modify endoplasmic reticulum proteins |
| Q99728291 | Protein targeting with SAF(er) electrophiles |
| Q90371179 | Small-molecule covalent bond formation at tyrosine creates a binding site and inhibits activation of Ral GTPases |
| Q98459819 | Stability and cell permeability of sulfonyl fluorides in the design of Lys-covalent antagonists of protein-protein interactions |
| Q93105246 | SuFEx-enabled, agnostic discovery of covalent inhibitors of human neutrophil elastase |
| Q64027818 | Sulfonyl Fluorides (SFs): More Than Click Reagents? |
| Q99637234 | Using sulfuramidimidoyl fluorides that undergo sulfur(VI) fluoride exchange for inverse drug discovery |
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