Search Results - "Asher, Constance"
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Speciation of Ferriprotoporphyrin IX in Aqueous and Mixed Aqueous Solution Is Controlled by Solvent Identity, pH, and Salt Concentration
Published in Inorganic chemistry (17-08-2009)“…The speciation of ferriprotoporphyrin IX (Fe(III)PPIX) in aqueous and mixed aqueous−organic solvents has been investigated by UV−vis, 1H NMR, magnetic, and…”
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In vitro biotransformation, in vivo efficacy and pharmacokinetics of antimalarial chalcones
Published in Pharmacology (01-01-2011)“…4'-n-Butoxy-2,4-dimethoxy-chalcone (MBC) has been described as protecting mice from an otherwise lethal infection with Plasmodium yoelii when dosed orally at…”
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In vitro and in vivo efficacy and in vitro metabolism of 1-phenyl-3-aryl-2-propen-1-ones against Plasmodium falciparum
Published in Bioorganic & medicinal chemistry letters (01-11-2006)“…Nine in vitro submicromolar inhibitors of Plasmodium falciparum were identified, including compound 22. They were inactive when administered orally to…”
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Cynomolgus Monkey as a Surrogate for Human Aldehyde Oxidase Metabolism of the EGFR Inhibitor BIBX1382
Published in Drug metabolism and disposition (01-10-2014)Get full text
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Role of Specific Cytochrome P450 Isoforms in the Conversion of Phenoxypropoxybiguanide Analogs in Human Liver Microsomes to Potent Antimalarial Dihydrotriazines
Published in Drug metabolism and disposition (01-02-2008)“…Phenoxypropoxybiguanides, such as PS-15, are antimalarial prodrugs analogous to the relationship of proguanil and its active metabolite cycloguanil. Unlike…”
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The role of in vitro ADME assays in antimalarial drug discovery and development
Published in Combinatorial chemistry & high throughput screening (01-02-2005)“…The high level of attrition of drugs in clinical development has led pharmaceutical companies to increase the efficiency of their lead identification and…”
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Cynomolgus monkey as a surrogate for human aldehyde oxidase metabolism of the EGFR inhibitor BIBX1382
Published in Drug metabolism and disposition (01-10-2014)“…BIBX1382 was an epidermal growth factor receptor inhibitor under clinical investigation for treatment of cancer. This candidate possessed an attractive…”
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