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In Vitro Activity of TR-700, the Active Ingredient of the Antibacterial Prodrug TR-701, a Novel Oxazolidinone Antibacterial Agent ▿

机译:TR-700的体外活性,TR-700是新型恶​​唑烷酮类抗菌剂抗菌前药TR-701的有效成分▿

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摘要

TR-701 is the prodrug of the microbiologically active molecule TR-700, a novel orally and intravenously administered oxazolidinone antibacterial agent. The in vitro activity of TR-700 was evaluated against 1,063 bacterial clinical isolates including staphylococci, enterococci, streptococci, Moraxella catarrhalis, Haemophilus influenzae, and a variety of anaerobic bacterial species. The test strains were recent (2005 to 2008) clinical isolates from diverse U.S. (80%) and non-U.S. (20%) sites. MIC assays were conducted using reference broth microdilution and agar dilution methods with the principal comparators linezolid and vancomycin. TR-700 was four- to eightfold more potent than linezolid against staphylococci and generally fourfold more potent against enterococci and streptococci. TR-700 was less active against M. catarrhalis and H. influenzae but was twofold more active than linezolid. Against anaerobic species, the activity of TR-700 was equivalent to or up to fourfold higher than that of linezolid. These results indicate that TR-700 is a promising new oxazolidinone antibacterial agent with greater in vitro potency than linezolid against clinically important gram-positive bacteria.
机译:TR-701是微生物活性分子TR-700的前药,是新型的口服和静脉内给药的恶唑烷酮抗菌剂。评估了TR-700对1,063种细菌临床分离株的体外活性,这些分离株包括葡萄球菌,肠球菌,链球菌,卡他莫拉菌,流感嗜血杆菌和各种厌氧细菌。测试菌株是最近(2005年至2008年)来自美国(80%)和美国以外(20%)多个地点的临床分离株。使用参考肉汤微稀释法和琼脂稀释法以及主要的比较剂利奈唑胺和万古霉素进行MIC测定。 TR-700对葡萄球菌的效力比利奈唑胺高四到八倍,而对肠球菌和链球菌的效力通常高四倍。 TR-700对粘膜炎莫拉氏菌和流感嗜血杆菌的活性较低,但活性比利奈唑胺高两倍。针对厌氧菌种,TR-700的活性相当于利奈唑胺的活性,甚至是后者的四倍。这些结果表明TR-700是一种有前途的新恶唑烷酮抗菌剂,对临床上重要的革兰氏阳性细菌具有比利奈唑胺更大的体外效力。

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