Search Results - "Wolfe, Amanda"
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Generating Publishable Data from Course-Based Undergraduate Research Experiences in Chemistry
Published in Journal of chemical education (12-09-2023)“…Embedding Course-based Undergraduate Research Experiences (CUREs) into chemistry curricula has become a best practice due to the overwhelming evidence that…”
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Total Synthesis of Kopsinine
Published in Organic letters (15-02-2013)“…The use of a powerful intramolecular [4 + 2]/[3 + 2] cycloaddition cascade of an 1,3,4-oxadiazole in the divergent total synthesis of kopsinine (1), featuring…”
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3
Total synthesis and antibacterial evaluation of Empetroxepins A and B and related analogs
Published in Bioorganic & medicinal chemistry letters (01-11-2022)“…[Display omitted] Empetroxepins A and B, which are 10,11-dihydrodibenz[b,f]oxepins produced by the Black Crowberry (Empetrum nigrum), displayed weak…”
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4
Dysmaturation of the default mode network in autism
Published in Human brain mapping (01-04-2014)“…Two hypotheses of autism spectrum disorder (ASD) propose that this condition is characterized by deficits in Theory of Mind and by hypoconnectivity between…”
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5
Transcriptome response of human skeletal muscle to divergent exercise stimuli
Published in Journal of applied physiology (1985) (01-06-2018)“…Aerobic (AE) and resistance exercise (RE) elicit unique adaptations in skeletal muscle that have distinct implications for health and performance. The purpose…”
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Bisbenzamidine and Bisbenzguanidine Ureas Act as Antibacterial Agents against Pseudomonas aeruginosa
Published in ChemMedChem (14-12-2023)“…Due to the global rise in the number of antibiotic resistant bacterial infections over the past 20 years, there is a dire need for the development of small…”
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Synthesis and Antibiofilm Activity of a Second-Generation Reverse-Amide Oroidin Library: A Structure-Activity Relationship Study
Published in Chemistry : a European journal (26-11-2008)“…A second‐generation library of 2‐aminoimidazole‐based derivatives incorporating a “reversed amide” (RA) motif in comparison to the marine natural product…”
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Design and evaluation of poly-nitrogenous adjuvants capable of potentiating antibiotics in Gram-negative bacteria
Published in RSC medicinal chemistry (21-09-2022)“…Antibiotic resistance has been a growing public health crisis since the 1980s. Therefore, it is essential not only to continue to develop novel antibiotics but…”
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Amine Basicity of Quinoline ATP Synthase Inhibitors Drives Antibacterial Activity against Pseudomonas aeruginosa
Published in ACS medicinal chemistry letters (11-01-2024)“…Pseudomonas aeruginosa (PA), a Gram-negative pathogen, is a common cause of nosocomial infections, especially in immunocompromised and cystic fibrosis…”
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Short chain α-pyrones capable of potentiating penicillin G against Pseudomonas aeruginosa
Published in Bioorganic & medicinal chemistry letters (15-08-2020)“…[Display omitted] The dramatic increase in bacterial resistance over the past three decades has greatly reduced the effectiveness of nearly all clinical…”
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Isolation of the antibiotic pseudopyronine B and SAR evaluation of C3/C6 alkyl analogs
Published in Bioorganic & medicinal chemistry letters (15-06-2017)“…[Display omitted] Natural products are an abundant source of structurally diverse compounds with antibacterial activity that can be used to develop new and…”
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Advances in antibiotic drug discovery: reducing the barriers for antibiotic development
Published in Future medicinal chemistry (01-11-2020)“…Antibiotic drug discovery has been an essential field of research since the early 1900s, but the threat from infectious bacteria has only increased over the…”
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Integration of Antimicrobials and Delivery Systems: Synergistic Antibiofilm Activity with Biodegradable Nanoemulsions Incorporating Pseudopyronine Analogs
Published in Antibiotics (Basel) (28-07-2023)“…Multi-drug-resistant (MDR) bacteria, including methicillin-resistant Staphylococcus aureus (MRSA), pose a significant challenge in healthcare settings. Small…”
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14
A Novel, Unusually Efficacious Duocarmycin Carbamate Prodrug That Releases No Residual Byproduct
Published in Journal of medicinal chemistry (28-06-2012)“…A unique heterocyclic carbamate prodrug of seco-CBI-indole2 that releases no residual byproduct is reported as a new member of a class of hydrolyzable prodrugs…”
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A Fundamental Relationship between Hydrophobic Properties and Biological Activity for the Duocarmycin Class of DNA-Alkylating Antitumor Drugs: Hydrophobic-Binding-Driven Bonding
Published in Journal of medicinal chemistry (12-09-2013)“…Two systematic series of increasingly hydrophilic derivatives of duocarmycin SA that feature the incorporation of ethylene glycol units (n = 1–5) into the…”
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16
Quinoline Compounds Targeting the c -Ring of ATP Synthase Inhibit Drug-Resistant Pseudomonas aeruginosa
Published in ACS infectious diseases (08-12-2023)“…(PA) is a Gram-negative, biofilm-forming bacterium and an opportunistic pathogen. The growing drug resistance of PA is a serious threat that necessitates the…”
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Development of a Robust and Quantitative High-Throughput Screening Method for Antibiotic Production in Bacterial Libraries
Published in ACS omega (24-09-2019)“…Over the past 30 years, there has been a dramatic rise in the number of infections caused by multidrug-resistant bacteria, which have proliferated due to the…”
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Association of Common Genetic Variants in the CPSF7 and SDHAF2 Genes with Canine Idiopathic Pulmonary Fibrosis in the West Highland White Terrier
Published in Genes (30-05-2020)“…Canine idiopathic pulmonary fibrosis (CIPF) is a chronic fibrotic lung disease that is observed at a higher frequency in the West Highland White Terrier dog…”
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Efficacious Cyclic N‑Acyl O‑Amino Phenol Duocarmycin Prodrugs
Published in Journal of medicinal chemistry (23-05-2013)“…Two novel cyclic N-acyl O-amino phenol prodrugs are reported as new members of a unique class of reductively cleaved prodrugs of the duocarmycin family of…”
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Synthesis and Evaluation of Pseudomonas aeruginosa ATP Synthase Inhibitors
Published in ACS omega (16-08-2022)“…New antibiotics with unique biological targets are desperately needed to combat the growing number of resistant bacterial pathogens. ATP synthase, a critical…”
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