Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Thomas R Parr"'
Autor:
Brian D VanScoy, Haley Conde, Nicole Cotroneo, Ian A Critchley, Thomas R Parr, Paul G Ambrose
Publikováno v:
Open Forum Infectious Diseases
Background SPR994 is an orally bioavailable pivoxil hydrobromide prodrug of tebipenem, a novel oral carbapenem with activity against Gram-positive and -negative bacteria currently under development for the treatment of urinary tract infections (UTI).
Autor:
Troy Lister, Paul R. Rhomberg, Thomas R. Parr, Mariana Castanheira, Nicole Cotroneo, Rodrigo E. Mendes
Publikováno v:
Antimicrob Agents Chemother
The activities of azithromycin, fusidic acid, vancomycin, doxycycline, and minocycline were evaluated alone and in combination with SPR741. A total of 202 Escherichia coli and 221 Klebsiella pneumoniae isolates were selected, and they included a geno
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::408c473bad37f79cd2c8f75886de4bbb
https://europepmc.org/articles/PMC7927843/
https://europepmc.org/articles/PMC7927843/
Publikováno v:
Expert Review of Anti-infective Therapy. 16:513-522
Infections caused by antibiotic-resistant pathogens, particularly Gram-negative bacteria, have become increasingly challenging to successfully treat. The beta-lactam antibiotic subclass, the carbapenems, have proven valuable for the treatment of such
Autor:
Aileen Rubio, Evelyne Lacasse, François Malouin, Eric Brouillette, Audrey Larose, Thomas R. Parr
Tebipenem (SPR859) is the microbiologically active form of SPR994 (tebipenem-pivoxil), an orally available carbapenem with activity against extended-spectrum β-lactamase (ESBL)-producing Enterobacteriaceae . Measurement of the relative binding of SP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48d306d8a5f0b755eab97c70385c40b4
https://europepmc.org/articles/PMC6437484/
https://europepmc.org/articles/PMC6437484/
Autor:
Laura McEntee, William W. Hope, Aaron Dane, Akash Jain, Jennifer Unsworth, Ian A. Critchley, Nicola Farrington, Shampa Das, Nicole Cotroneo, David Melnick, Adam Johnson, Thomas R. Parr, Paul G. Ambrose
Publikováno v:
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY
Tebipenem pivoxil HBr (TBPM-PI-HBr) is a novel orally bioavailable carbapenem. The active moiety is tebipenem. Tebipenem pivoxil is licensed for use in Japan in children with ear, nose, and throat infections and respiratory infections. The HBr salt w
Autor:
Gerard D. Wright, Eric Brouillette, J. Andrew N. Alexander, Marija Vuckovic, Eric D. Brown, Samarendra N. Maiti, Dustin T. King, Andrew M. King, Natalie C. J. Strynadka, Abdelhamid Asli, Shawn French, François Malouin, Thomas R. Parr
Publikováno v:
ACS Chemical Biology. 11:864-868
Avibactam is a diazabicyclooctane β-lactamase inhibitor possessing outstanding but incomplete efficacy against multidrug-resistant Gram-negative pathogens in combination with β-lactam antibiotics. Significant pharmaceutical investment in generating
Autor:
Thomas R. Parr, Paul G. Ambrose, Brian VanScoy, Steven Fikes, Christopher M. Rubino, Ian A. Critchley, Sujata M. Bhavnani, Nicole Cotroneo
Publikováno v:
Open Forum Infectious Diseases
Background Tebipenem pivoxil hydrobromide (tebipenem HBr), an orally (PO) bioavailable prodrug of tebipenem, is a carbapenem with broad-spectrum activity against Gram-positive and -negative bacteria that is being developed for the treatment of patien
Autor:
Nicole Cotroneo, Thomas R. Parr, Sujata M. Bhavnani, Paul G. Ambrose, Ana I Caranco, Nikolas J Onufrak, Haley Conde, Ian A. Critchley, Brian VanScoy
Publikováno v:
Open Forum Infectious Diseases
Background SPR859 (tebipenem) is the active form of the orally bioavailable prodrug SPR994. Tebipenem is an oral carbapenem with a broad-spectrum activity against Gram-positive and -negative bacteria. SPR994 is being developed as an oral option for t
Publikováno v:
Medicinal Chemistry Reviews ISBN: 9780996293235
Medicinal Chemistry Reviews
Medicinal Chemistry Reviews
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adcbd007ab70f46faaef3aca8dd590ae
https://doi.org/10.29200/acsmedchemrev-v51.ch15
https://doi.org/10.29200/acsmedchemrev-v51.ch15
Publikováno v:
International Journal of Antimicrobial Agents. 39:159-162
In this study, the impact of inoculum density on the growth inhibitory and killing activities of oritavancin and comparators (vancomycin, daptomycin and linezolid) in vitro against four Staphylococcus aureus strains at clinically relevant drug concen