Patricia Miller to Molecular Structure
This is a "connection" page, showing publications Patricia Miller has written about Molecular Structure.
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0.283
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Antibiotic repurposing: bis-catechol- and mixed ligand (bis-catechol-mono-hydroxamate)-teicoplanin conjugates are active against multidrug resistant Acinetobacter baumannii. J Antibiot (Tokyo). 2020 03; 73(3):152-157.
Score: 0.038
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Synthetic sideromycins (skepticism and optimism): selective generation of either broad or narrow spectrum Gram-negative antibiotics. Biometals. 2019 06; 32(3):425-451.
Score: 0.036
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Alternate "Drug" Delivery Utilizing ?-Lactam Cores: Syntheses and Biological Evaluation of ?-Lactams Bearing Isocyanate Precursors. J Org Chem. 2017 01 06; 82(1):737-744.
Score: 0.031
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Discovery of 6-(Fluoro-(18)F)-3-(1H-pyrrolo[2,3-c]pyridin-1-yl)isoquinolin-5-amine ([(18)F]-MK-6240): A Positron Emission Tomography (PET) Imaging Agent for Quantification of Neurofibrillary Tangles (NFTs). J Med Chem. 2016 05 26; 59(10):4778-89.
Score: 0.029
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Arrival of Imidazo[2,1-b]thiazole-5-carboxamides: Potent Anti-tuberculosis Agents That Target QcrB. ACS Infect Dis. 2016 06 10; 2(6):393-8.
Score: 0.029
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Design, syntheses, and anti-tuberculosis activities of conjugates of piperazino-1,3-benzothiazin-4-ones (pBTZs) with 2,7-dimethylimidazo [1,2-a]pyridine-3-carboxylic acids and 7-phenylacetyl cephalosporins. Bioorg Med Chem Lett. 2016 Apr 15; 26(8):2068-71.
Score: 0.029
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Syntheses and evaluation of substituted aromatic hydroxamates and hydroxamic acids that target Mycobacterium tuberculosis. Bioorg Med Chem Lett. 2015 Nov 01; 25(21):4933-4936.
Score: 0.028
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Thiolates chemically induce redox activation of BTZ043 and related potent nitroaromatic anti-tuberculosis agents. J Am Chem Soc. 2013 Mar 06; 135(9):3539-49.
Score: 0.024
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Selective molecular sequestration with concurrent natural product functionalization and derivatization: from crude natural product extracts to a single natural product derivative in one step. J Org Chem. 2011 Dec 16; 76(24):10249-53.
Score: 0.022
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Syntheses and biological activity studies of novel sterol analogs from nitroso Diels-Alder reactions of ergosterol. Org Lett. 2009 Jul 02; 11(13):2828-31.
Score: 0.018