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This and the accompanying report (DOI: 10.1021/jm201467r ) describe the design, synthesis, and evaluation of a new generation of tetracycline antibacterial agents, 7-fluoro-9-substituted-6-demethyl-6-deoxytetracyclines ("fluorocyclines"), accessible through a recently developed total synthesis approach. These fluorocyclines possess potent antibacterial activities against multidrug resistant (MDR) Gram-positive and Gram-negative pathogens. One of the fluorocyclines, 7-fluoro-9-pyrrolidinoacetamido-6-demethyl-6-deoxytetracycline (17j, also known as TP-434, 50th Interscience Conference on Antimicrobial Agents and Chemotherapy Conference , Boston, MA , September 12-15, 2010 , poster F1 - 2157 ), is currently undergoing phase 2 clinical trials in patients with complicated intra-abdominal infections (cIAI).
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Xiao-Yi Xiao
Diana K. Hunt
Jingye Zhou
Journal of Medicinal Chemistry
Tetraphase Pharmaceuticals (United States)
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Xiao et al. (Fri,) studied this question.
www.synapsesocial.com/papers/6a03ae441a7d3adf14a9c3e8 — DOI: https://doi.org/10.1021/jm201465w