Screening for potent and selective anticlostridial leads among FDA-approved drugs
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[1] M. Seleem,et al. Chemical Space Exploration Around Thieno[3,2-d]pyrimidin-4(3H)-one Scaffold led to a Novel Class of Highly Active Clostridium difficile Inhibitors. , 2019, Journal of medicinal chemistry.
[2] M. Seleem,et al. Antibacterial and antivirulence activities of auranofin against Clostridium difficile. , 2019, International journal of antimicrobial agents.
[3] K. Hevener,et al. The Fatty Acid Synthesis Protein Enoyl-ACP Reductase II (FabK) is a Target for Narrow-Spectrum Antibacterials for Clostridium difficile Infection. , 2018, ACS infectious diseases.
[4] M. Seleem,et al. Repurposing ebselen for decolonization of vancomycin-resistant enterococci (VRE) , 2018, PloS one.
[5] M. Seleem,et al. Repurposing niclosamide for intestinal decolonization of vancomycin-resistant enterococci. , 2018, International journal of antimicrobial agents.
[6] K. Carroll,et al. Clinical Practice Guidelines for Clostridium difficile Infection in Adults and Children: 2017 Update by the Infectious Diseases Society of America (IDSA) and Society for Healthcare Epidemiology of America (SHEA). , 2018, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[7] E. Mylonakis,et al. Repurposing the anthelmintic drug niclosamide to combat Helicobacter pylori , 2018, Scientific Reports.
[8] E. Kuijper,et al. How to: Surveillance of Clostridium difficile infections. , 2017, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.
[9] P. Nenoff,et al. New insights on the antibacterial efficacy of miconazole in vitro , 2017, Mycoses (Berlin).
[10] M. Cooper,et al. Nitroimidazoles: Molecular Fireworks That Combat a Broad Spectrum of Infectious Diseases. , 2017, Journal of medicinal chemistry.
[11] M. Seleem,et al. In Vitro Screening of an FDA-Approved Library Against ESKAPE Pathogens. , 2017, Current pharmaceutical design.
[12] K. Janda,et al. Reprofiled anthelmintics abate hypervirulent stationary-phase Clostridium difficile , 2016, Scientific Reports.
[13] A. Moya,et al. Colonization Resistance of the Gut Microbiota against Clostridium difficile , 2015, Antibiotics.
[14] M. Seleem,et al. Repurposing celecoxib as a topical antimicrobial agent , 2015, Front. Microbiol..
[15] M. Seleem,et al. Repurposing ebselen for treatment of multidrug-resistant staphylococcal infections , 2015, Scientific Reports.
[16] M. Seleem,et al. Drug repurposing for the treatment of staphylococcal infections. , 2015, Current pharmaceutical design.
[17] Wooseong Kim,et al. Repurposing Salicylanilide Anthelmintic Drugs to Combat Drug Resistant Staphylococcus aureus , 2015, PloS one.
[18] M. Cooper,et al. Clostridium difficile Drug Pipeline: Challenges in Discovery and Development of New Agents , 2015, Journal of medicinal chemistry.
[19] Lisa G Winston,et al. Burden of Clostridium difficile Infection in the United States , 2015 .
[20] S. Adhikari,et al. Action of nitroheterocyclic drugs against Clostridium difficile. , 2014, International journal of antimicrobial agents.
[21] D. Paredes-Sabja,et al. Clostridium difficile spores: a major threat to the hospital environment. , 2014, Future microbiology.
[22] Randhir Singh,et al. Imidazoles as promising scaffolds for antibacterial activity: a review. , 2013, Mini-Reviews in Medical Chemistry.
[23] Ashwin N Ananthakrishnan,et al. Guidelines for Diagnosis, Treatment, and Prevention of Clostridium difficile Infections , 2013, The American Journal of Gastroenterology.
[24] S. Mas‐Coma,et al. Administration of Triclabendazole Is Safe and Effective in Controlling Fascioliasis in an Endemic Community of the Bolivian Altiplano , 2012, PLoS neglected tropical diseases.
[25] M. Cruz. Fidaxomicin (Dificid), a Novel Oral Macrocyclic Antibacterial Agent For the Treatment of Clostridium difficile-Associated Diarrhea in Adults. , 2012, P & T : a peer-reviewed journal for formulary management.
[26] A. Zinsmeister,et al. The Epidemiology of Community-Acquired Clostridium difficile Infection: A Population-Based Study , 2012, The American Journal of Gastroenterology.
[27] D. Musher,et al. Nitazoxanide versus vancomycin in Clostridium difficile infection: a randomized, double-blind study. , 2009, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[28] C. Kelly,et al. Clostridium difficile--more difficult than ever. , 2008, The New England journal of medicine.
[29] D. Farver,et al. New advances in the treatment of Clostridium difficile infection (CDI) , 2008, Therapeutics and clinical risk management.
[30] Matthew A. Croxen,et al. Antiparasitic Drug Nitazoxanide Inhibits the Pyruvate Oxidoreductases of Helicobacter pylori, Selected Anaerobic Bacteria and Parasites, and Campylobacter jejuni , 2006, Antimicrobial Agents and Chemotherapy.
[31] J. Gookin,et al. Efficacy of Ronidazole for Treatment of Feline Tritrichomonas foetus Infection , 2006 .
[32] P. Upcroft,et al. 5-Nitroimidazole Drugs Effective against Metronidazole-Resistant Trichomonas vaginalis and Giardia duodenalis , 2006, Antimicrobial Agents and Chemotherapy.
[33] C. Janson,et al. 1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl acyl carrier protein reductase (FabI). , 2001, Bioorganic & medicinal chemistry letters.
[34] R. Rolfe,et al. In Vitro and In Vivo Activities of Nitazoxanide against Clostridium difficile , 2000, Antimicrobial Agents and Chemotherapy.
[35] M. Ghannoum,et al. Antifungal Agents: Mode of Action, Mechanisms of Resistance, and Correlation of These Mechanisms with Bacterial Resistance , 1999, Clinical Microbiology Reviews.
[36] L. Jokipii,et al. Comparative activity of metronidazole and tinidazole against Clostridium difficile and Peptostreptococcus anaerobius , 1987, Antimicrobial Agents and Chemotherapy.
[37] R. Bolton,et al. Faecal metronidazole concentrations during oral and intravenous therapy for antibiotic associated colitis due to Clostridium difficile. , 1986, Gut.
[38] L. Jokipii,et al. Comparative evaluation of the 2-methyl-5-nitroimidazole compounds dimetridazole, metronidazole, secnidazole, ornidazole, tinidazole, carnidazole, and panidazole against Bacteroides fragilis and other bacteria of the Bacteroides fragilis group , 1985, Antimicrobial Agents and Chemotherapy.
[39] J. Wüst. Susceptibility of Anaerobic Bacteria to Metronidazole, Ornidazole, and Tinidazole and Routine Susceptibility Testing by Standardized Methods , 1977, Antimicrobial Agents and Chemotherapy.
[40] R. Willcox,et al. Treatment of Vaginal Trichomoniasis with 2-Acetylamino-5-Nitrothiazole (Aminitrozole) given Orally* , 1957, The British journal of venereal diseases.
[41] T. Hazbun,et al. Ebselen exerts antifungal activity by regulating glutathione (GSH) and reactive oxygen species (ROS) production in fungal cells. , 2017, Biochimica et biophysica acta. General subjects.
[42] M. Lesina,et al. Use of Ronidazole and Limited Culling To Eliminate Tritrichomonas muris from Laboratory Mice. , 2016, Journal of the American Association for Laboratory Animal Science : JAALAS.
[43] Waleed Younis,et al. Repurposing Non-Antimicrobial Drugs and Clinical Molecules to Treat Bacterial Infections. , 2015, Current pharmaceutical design.
[44] W. Gregory,et al. Methods for antimicrobial susceptibility testing of anaerobic bacteria. Approved standard M11-A7 2007 , 2012 .
[45] J. Gookin,et al. Efficacy of ronidazole for treatment of feline Tritrichomonas foetus infection. , 2006, Journal of veterinary internal medicine.
[46] D. V. van Thiel,et al. The diagnosis and treatment of Clostridium difficile in antibiotic-associated diarrhea. , 1999, Hepato-gastroenterology.
[47] N. N. Kalinichenko. [Nitazole--an antimicrobial substance]. , 1998, Mikrobiolohichnyi zhurnal.
[48] Kalinichenko Nf. [Nitazole--an antimicrobial substance]. , 1998 .
[49] R. Erkkola,et al. Single dose of ornidazole in the treatment of bacterial vaginosis. , 1987, Annales chirurgiae et gynaecologiae. Supplementum.
[50] G. Bonse,et al. Chemistry of Anticestodal Agents , 1986 .