| Year |
Citation |
Score |
| 2020 |
Hankins RA, Suarez SI, Kalk MA, Green NM, Harty MN, Lukesh JC. An Innovative Hydrogen Peroxide-Sensing Scaffold and Insight Towards its Potential as an ROS-Activated Persulfide Donor. Angewandte Chemie. DOI: 10.1002/Ange.202010530 |
0.387 |
|
| 2019 |
Suarez SI, Warner CC, Brown-Harding H, Thooft AM, VanVeller B, Lukesh JC. Highly selective staining and quantification of intracellular lipid droplets with a compact push-pull fluorophore based on benzothiadiazole. Organic & Biomolecular Chemistry. PMID 31850447 DOI: 10.1039/C9Ob02486G |
0.611 |
|
| 2019 |
Suarez SI, Ambrose R, Kalk MA, Lukesh JC. Selenosulfides Tethered to Gem-Dimethyl Esters: A Robust and Highly Versatile Framework for H₂S Probe Development. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 31576582 DOI: 10.1002/Chem.201904133 |
0.31 |
|
| 2018 |
Windsor IW, Palte MJ, Lukesh JC, Gold B, Forest KT, Raines RT. Sub-picomolar Inhibition of HIV-1 Protease with a Boronic Acid. Journal of the American Chemical Society. PMID 30346745 DOI: 10.1021/Jacs.8B07366 |
0.616 |
|
| 2017 |
Lukesh JC, Carney DW, Dong H, Cross RM, Shukla V, Duncan KK, Yang S, Brody DM, Brütsch MM, Radakovic A, Boger DL. Vinblastine 20' Amides: Synthetic Analogues That Maintain or Improve Potency and Simultaneously Overcome Pgp-Derived Efflux and Resistance. Journal of Medicinal Chemistry. PMID 28857558 DOI: 10.1021/acs.jmedchem.7b00958 |
0.351 |
|
| 2017 |
Yang S, Sankar K, Skepper CK, Barker TJ, Lukesh JC, Brody DM, Brütsch MM, Boger DL. Total synthesis of a key series of vinblastines modified at C4 that define the importance and surprising trends in activity. Chemical Science. 8: 1560-1569. PMID 28194270 DOI: 10.1039/C6Sc04146A |
0.488 |
|
| 2016 |
Carney DW, Lukesh JC, Brody DM, Brütsch MM, Boger DL. Ultrapotent vinblastines in which added molecular complexity further disrupts the target tubulin dimer-dimer interface. Proceedings of the National Academy of Sciences of the United States of America. PMID 27512044 DOI: 10.1073/Pnas.1611405113 |
0.465 |
|
| 2016 |
Allemann O, Brutsch M, Lukesh JC, Brody DM, Boger DL. Synthesis of a Potent Vinblastine: Rationally Designed Added Benign Complexity. Journal of the American Chemical Society. PMID 27356080 DOI: 10.1021/Jacs.6B04330 |
0.426 |
|
| 2014 |
Lukesh JC, Andersen KA, Wallin KK, Raines RT. Organocatalysts of oxidative protein folding inspired by protein disulfide isomerase. Organic & Biomolecular Chemistry. 12: 8598-602. PMID 25266373 DOI: 10.1039/C4Ob01738B |
0.72 |
|
| 2014 |
Lukesh JC, Wallin KK, Raines RT. Pyrazine-derived disulfide-reducing agent for chemical biology. Chemical Communications (Cambridge, England). 50: 9591-4. PMID 25014913 DOI: 10.1039/C4Cc04491F |
0.576 |
|
| 2013 |
Lukesh JC, Vanveller B, Raines RT. Thiols and selenols as electron-relay catalysts for disulfide-bond reduction. Angewandte Chemie (International Ed. in English). 52: 12901-4. PMID 24123634 DOI: 10.1002/Anie.201307481 |
0.742 |
|
| 2013 |
Lukesh JC, VanVeller B, Raines RT. Inside Cover: Thiols and Selenols as Electron-Relay Catalysts for Disulfide-Bond Reduction (Angew. Chem. Int. Ed. 49/2013) Angewandte Chemie International Edition. 52: 12748-12748. DOI: 10.1002/Anie.201309405 |
0.727 |
|
| 2013 |
Lukesh JC, VanVeller B, Raines RT. Innentitelbild: Thiols and Selenols as Electron-Relay Catalysts for Disulfide-Bond Reduction (Angew. Chem. 49/2013) Angewandte Chemie. 125: 12982-12982. DOI: 10.1002/Ange.201309405 |
0.729 |
|
| 2012 |
Lukesh JC, Palte MJ, Raines RT. A potent, versatile disulfide-reducing agent from aspartic acid. Journal of the American Chemical Society. 134: 4057-9. PMID 22353145 DOI: 10.1021/Ja211931F |
0.739 |
|
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