Robert H. Bates

Affiliations: 
2009 Scripps Research Institute, La Jolla, La Jolla, CA, United States 
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"Robert Bates"
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William R. Roush grad student 2009 Scripps Institute
 (Studies toward the total synthesis of amphidinolide C.)
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Publications

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Wilson C, Ray P, Zuccotto F, et al. (2021) Optimization of TAM16, a Benzofuran That Inhibits the Thioesterase Activity of Pks13; Evaluation toward a Preclinical Candidate for a Novel Antituberculosis Clinical Target. Journal of Medicinal Chemistry
Balabon O, Pitta E, Rogacki MK, et al. (2020) Optimization of Hydantoins as Potent Antimycobacterial Decaprenylphosphoryl-β-d-Ribose Oxidase (DprE1) Inhibitors. Journal of Medicinal Chemistry
Cunningham F, Esquivias J, Fernández-Menéndez R, et al. (2020) Exploring the SAR of the β-Ketoacyl-ACP Synthase Inhibitor GSK3011724A and Optimization around a Genotoxic Metabolite. Acs Infectious Diseases
Poce G, Consalvi S, Venditti G, et al. (2019) Novel Pyrazole-Containing Compounds Active against . Acs Medicinal Chemistry Letters. 10: 1423-1429
Rogacki MK, Pitta E, Balabon OB, et al. (2018) Identification and profiling of hydantoins - a novel class of potent antimycobacterial DprE1 inhibitors. Journal of Medicinal Chemistry
Fang C, Lee KK, Nietupski R, et al. (2018) Discovery of heterocyclic replacements for the coumarin core of anti-tubercular FadD32 inhibitors. Bioorganic & Medicinal Chemistry Letters
Richter A, Rudolph I, Möllmann U, et al. (2018) Novel insight into the reaction of nitro, nitroso and hydroxylamino benzothiazinones and of benzoxacinones with Mycobacterium tuberculosis DprE1. Scientific Reports. 8: 13473
Prati F, Zuccotto F, Fletcher D, et al. (2018) Screening of a novel fragment library with functional complexity against Mycobacterium tuberculosis InhA. Chemmedchem
Poce G, Cocozza M, Alfonso S, et al. (2017) In vivo potent BM635 analogue with improved drug-like properties. European Journal of Medicinal Chemistry. 145: 539-550
Machutta CA, Kollmann CS, Lind KE, et al. (2017) Prioritizing multiple therapeutic targets in parallel using automated DNA-encoded library screening. Nature Communications. 8: 16081
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