Search Results - "Adams, Wade J."
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Preclinical and clinical evidence for the collaborative transport and renal secretion of an oxazolidinone antibiotic by organic anion transporter 3 (OAT3/SLC22A8) and multidrug and toxin extrusion protein 1 (MATE1/SLC47A1)
Published in The Journal of pharmacology and experimental therapeutics (01-09-2010)“…N-({(5S)-3-[4-(1,1-dioxidothiomorpholin-4-yl)-3,5-difluorophenyl]-2-oxo-1,3-oxazolidin-5-yl}methyl)acetamide (PNU-288034), an oxazolidinone antibiotic, was…”
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PPARγ-sparing thiazolidinediones as insulin sensitizers. Design, synthesis and selection of compounds for clinical development
Published in Bioorganic & medicinal chemistry (01-12-2018)“…[Display omitted]…”
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Physiology and pharmacokinetics of a novel hemoglobin-based oxygen carrier in humans
Published in Critical care medicine (01-05-1996)“…OBJECTIVE To evaluate the physiology and pharmacokinetics of a novel hemoglobin-based oxygen carrier of bovine origin. DESIGN Randomized, single-blind,…”
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Identification of Phenylisoxazolines as Novel and Viable Antibacterial Agents Active against Gram-Positive Pathogens
Published in Journal of medicinal chemistry (16-01-2003)“…A new and promising group of antibacterial agents, collectively known as the oxazolidinones and exemplified by linezolid (PNU-100766, marketed as Zyvox), have…”
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Antibacterial Oxazolidinones Possessing a Novel C-5 Side Chain. (5R)-trans-3-[3-Fluoro-4- (1-oxotetrahydrothiopyran-4-yl)phenyl]-2- oxooxazolidine-5-carboxylic Acid Amide (PF-00422602), a New Lead Compound
Published in Journal of medicinal chemistry (29-11-2007)“…Oxazolidinones possessing a C-5 carboxamide functionality (reverse amides) represent a new series of compounds that block bacterial protein synthesis. These…”
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Predicting oral absorption of drugs: A case study with a novel class of antimicrobial agents
Published in Pharmaceutical research (01-08-2003)“…The purpose of this work was to evaluate an oral absorption prediction model, maximum absorbable dose (MAD), which predicts a theoretical dose of drug that…”
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New Antibacterial tetrahydro-4(2 H)-thiopyran and thiomorpholine S-oxide and S, S-dioxide phenyloxazolidinones
Published in Bioorganic & medicinal chemistry letters (01-12-2003)“…Combinatorial libraries of N-acylated 5-( S)-aminomethyloxazolidinone derivatives of S-oxide and S, S-dioxide tetrahydro-4(2H)-thiopyranyl and thiomorpholine…”
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The effect of remote chirality on the antibacterial activity of indolinyl, tetrahydroquinolyl and dihydrobenzoxazinyl oxazolidinones
Published in Bioorganic & medicinal chemistry letters (01-12-2003)“…The oxazolidinones are promising agents for the treatment of infections caused by gram-positive bacteria, including multidrug-resistant strains. In ongoing…”
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Targeting Delavirdine/Atevirdine Resistant HIV-1: Identification of (Alkylamino)piperidine-Containing Bis(heteroaryl)piperazines as Broad Spectrum HIV-1 Reverse Transcriptase Inhibitors
Published in Journal of medicinal chemistry (13-09-1996)“…A novel class of bis(heteroaryl)piperazine (BHAP) analogs which possesses the ability to inhibit NNRTI (non-nucleoside reverse transcriptase inhibitor)…”
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Stereochemistry of the Carbonyl Reduction of MSDC‐0602, An mTOT‐modulating Insulin‐sensitizer for the Treatment of Nonalcoholic Steatohepatitis (NASH)
Published in The FASEB journal (01-04-2017)“…Abstract only The objective of this study was to determine the stereochemistry of the carbonyl reduction of MSDC‐0602 in human, monkey and rat plasma using a…”
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Structure, equilibrium conformation, and pseudorotation in cyclopentane. An electron diffraction study
Published in Journal of the American Chemical Society (01-08-1970)Get full text
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Synthesis and Bioactivity of Novel Bis(heteroaryl)piperazine (BHAP) Reverse Transcriptase Inhibitors: Structure−Activity Relationships and Increased Metabolic Stability of Novel Substituted Pyridine Analogs
Published in Journal of medicinal chemistry (20-12-1996)“…The major route of metabolism of the bis(heteroaryl)piperazine (BHAP) class of reverse transcriptase inhibitors (RTIs), atevirdine and delavirdine, is via…”
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Synthesis and Structure−Activity Relationships of the (Alkylamino)piperidine-Containing BHAP Class of Non-Nucleoside Reverse Transcriptase Inhibitors: Effect of 3-Alkylpyridine Ring Substitution
Published in Journal of medicinal chemistry (07-10-1999)“…Development of resistance to currently approved HIV therapies has continued to fuel research efforts to improve the metabolic stability and spectrum of…”
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Excretion mass balance and quantitative whole‐body autoradiography following a single oral (PO) administration of [14C]MSDC 0602, an mTOT‐modulating insulin sensitizer, in Sprague Dawley (SD) and Long‐Evans (LE) rats
Published in The FASEB journal (01-04-2012)“…Abstract only The objectives of this study were to determine the mass balance excretion, plasma pharmacokinetics and tissue distribution of radioactivity…”
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Pharmacokinetics and systemic bioavailability of menogaril, and anthracycline antitumor agent, in the mouse, dog, and monkey
Published in Cancer research (Chicago, Ill.) (15-11-1989)“…Menogaril is an antitumor agent of the anthracycline type which is less cardiotoxic than doxorubicin in a chronic rabbit model and is active in experimental…”
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Liquid chromatographic determination of guanadrel in laboratory animal diet as the fluorescent acetylacetone derivative
Published in Analytical chemistry (Washington) (01-06-1982)Get full text
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Quantitation of anthracycline antitumor agent menogarol in plasma using liquid chromatography with fluorescence detection
Published in Analytical chemistry (Washington) (01-08-1984)Get full text
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Studies of Abeta pharmacodynamics in the brain, cerebrospinal fluid, and plasma in young (plaque-free) Tg2576 mice using the gamma-secretase inhibitor N2-[(2S)-2-(3,5-difluorophenyl)-2-hydroxyethanoyl]-N1-[(7S)-5-methyl-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-L-alaninamide (LY-411575)
Published in The Journal of pharmacology and experimental therapeutics (01-04-2004)“…A previous study by us suggests the utility of cerebrospinal fluid (CSF) and plasma Abeta as biomarkers of beta- or gamma-secretase inhibition. The present…”
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