Identification of an anti-MRSA dihydrofolate reductase inhibitor from a diversity-oriented synthesis.
暂无分享,去创建一个
David R Spring | Martin Welch | Warren R J D Galloway | Emma E Wyatt | Alleyn T Plowright | A. Plowright | D. Spring | M. Welch | W. R. Galloway | Gemma L Thomas | G. Thomas | O. Loiseleur | E. Wyatt | Olivier Loiseleur | D. R. Spring | W. Galloway
[1] A. Hulme,et al. Marked small molecule libraries: a truncated approach to molecular probe design. , 2007, Organic & biomolecular chemistry.
[2] Robert E. W. Hancock,et al. The end of an era? , 2007, Nature Reviews Drug Discovery.
[3] Suzanne Fergus,et al. Skeletal diversity construction via a branching synthetic strategy. , 2006, Chemical communications.
[4] Mark Polyakov,et al. Where have all the antibiotic patents gone? , 2006, Nature Biotechnology.
[5] Martin Stahl,et al. Novel dihydrofolate reductase inhibitors. Structure-based versus diversity-based library design and high-throughput synthesis and screening. , 2003, Journal of medicinal chemistry.
[6] M. Jackson,et al. National prevalence of methicillin-resistant Staphylococcus aureus in inpatients at US health care facilities, 2006. , 2007, American journal of infection control.
[7] F. García-Cánovas,et al. Antifolate Activity of Epigallocatechin Gallate against Stenotrophomonas maltophilia , 2005, Antimicrobial Agents and Chemotherapy.
[8] A. P. Arzamastsev,et al. Relationship between physicochemical characteristics and pharmacokinetic parameters of 1,4-benzodiazepine derivatives , 2004, Pharmaceutical Chemistry Journal.
[9] K N Rao,et al. Inhibition of dihydrofolate reductase and cell growth activity by the phenanthroindolizidine alkaloids pergularinine and tylophorinidine: the in vitro cytotoxicity of these plant alkaloids and their potential as antimicrobial and anticancer agents. , 2000, Toxicology in vitro : an international journal published in association with BIBRA.
[10] Han van de Waterbeemd,et al. Lipophilicity in PK design: methyl, ethyl, futile , 2001, J. Comput. Aided Mol. Des..
[11] Graz,et al. SYNTHESIS AND AROMATIZATION OF DIHYDROPYRIMIDINES STRUCTURALLY RELATED TO CALCIUM CHANNEL MODULATORS OF THE NIFEDIPINE-TYPE , 1997 .
[12] Eric D Brown,et al. New targets and screening approaches in antimicrobial drug discovery. , 2005, Chemical reviews.
[13] B. Birdsall,et al. Structural factors determining the binding selectivity of the antibacterial drug trimethoprim to dihydrofolate reductase , 2007, Pharmaceutical Chemistry Journal.
[14] L. Sorbera,et al. Iclaprim. Antibacterial dihydrofolate reductase inhibitor , 2004 .
[15] David R Spring,et al. Chemical genetics to chemical genomics: small molecules offer big insights. , 2005, Chemical Society reviews.
[16] C. Walsh,et al. Introduction: antibiotic resistance. , 2005, Chemical Reviews.
[17] W. Foye,et al. Inhibition of bovine dihydrofolate reductase and enhancement of methotrexate sensitivity by N4-(2-acetoxyethoxymethyl)-2-acetylpyridine thiosemicarbazone. , 1990, Biochimica et biophysica acta.
[18] P. Hartman,et al. Antibacterial activities of epiroprim, a new dihydrofolate reductase inhibitor, alone and in combination with dapsone , 1996, Antimicrobial agents and chemotherapy.
[19] G. Barbier,et al. Synthesis of ethyl 2‐aminodihydro‐5‐pyrimidinecar‐boxylate derivatives and 3,7‐diethoxycarbonyl‐4,6‐dihydro‐2,4,6,8‐tetraaryl‐1H‐pyrimido[1,2‐a]pyrimidines , 1997 .
[20] C. Hart,et al. Finding the target after screening the phenotype. , 2005, Drug discovery today.
[21] G. G. Stokes. "J." , 1890, The New Yale Book of Quotations.
[22] Peter Schneider,et al. Iclaprim, a novel diaminopyrimidine with potent activity on trimethoprim sensitive and resistant bacteria. , 2003, Bioorganic & medicinal chemistry letters.
[23] David R Spring,et al. Gemmacin B: bringing diversity back into focus. , 2008, Organic & biomolecular chemistry.
[24] Flexible docking of an acetoxyethoxymethyl derivative of thiosemicarbazone into three different species of dihydrofolate reductase , 2002, Archives of pharmacal research.
[25] Lisa Jarvis. GAIN AND LOSS IN MALARIA WAR , 2008 .
[26] D. Pompliano,et al. Drugs for bad bugs: confronting the challenges of antibacterial discovery , 2007, Nature Reviews Drug Discovery.
[27] Andreas Bender,et al. Anti-MRSA agent discovery using diversity-oriented synthesis. , 2008, Angewandte Chemie.
[28] T. Mitchison,et al. Phenotypic screening of small molecule libraries by high throughput cell imaging. , 2003, Combinatorial chemistry & high throughput screening.
[29] Jeffrey M. Blaney,et al. Structure-activity relationships of dihydrofolated reductase inhibitors , 1984 .
[30] S. Lociuro,et al. Dihydrofolate reductase inhibitors as antibacterial agents. , 2006, Biochemical pharmacology.
[31] Prabhavathi Fernandes,et al. Antibacterial discovery and development—the failure of success? , 2006, Nature Biotechnology.
[32] Timothy J Mitchison,et al. Small molecule screening by imaging. , 2006, Current opinion in chemical biology.
[33] G. Kéri,et al. Evaluation of lipophilicity and antitumour activity of parallel carboxamide libraries. , 2002, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.
[34] J. Morrison,et al. Mechanism of inhibition of dihydrofolate reductases from bacterial and vertebrate sources by various classes of folate analogues. , 1986, Biochimica et biophysica acta.
[35] S. Venkatachalam,et al. Dihydrofolate reductase and cell growth activity inhibition by the beta-carboline-benzoquinolizidine plant alkaloid deoxytubulosine from Alangium lamarckii: its potential as an antimicrobial and anticancer agent. , 1999, Bioorganic & medicinal chemistry.