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药物预测——肽酰基转移酶抑制剂作为抗菌剂。

Drug forecast - the peptide deformylase inhibitors as antibacterial agents.

机构信息

College of Pharmacy, University of Minnesota and Division of Geriatrics, HealthPartners Inc Minneapolis, MN, USA.

出版信息

Ther Clin Risk Manag. 2007 Aug;3(4):513-25.

Abstract

The relatively rapid development of microbial resistance after the entry of every new antimicrobial into the marketplace necessitates a constant supply of new agents to maintain effective pharmacotherapy. Despite extensive efforts to identify novel lead compounds from molecular targets, only the peptide deformylase inhibitors (PDIs) have shown any real promise, with some advancing to phase I human trials. Bacterial peptide deformylase, which catalyzes the removal of the N-formyl group from N-terminal methionine following translation, is essential for bacterial protein synthesis, growth, and survival. The majority of PDIs are pseudopeptide hydroxamic acids and two of these (IV BB-83698 and oral NVP LBM-415) entered phase I human trials. However, agents to the present have suffered from major potential liabilities. Their in vitro activity has been limited to gram-positive aerobes and some anaerobes and has been quite modest against the majority of such species (MIC(90) values ranging from 1-8 mg/L). They have exerted bacteriostatic, not bacteriocidal, activity, thus reducing their potential usefulness in the management of serious infections in the immunocompromised. The relative ease with which microorganisms have been able to develop resistance and the multiple available mechanisms of resistance (mutations in fmt, defB, folD genes; AcrAB/TolC efflux pump; overexpression of peptide deformylase) are worrisome. These could portend a short timespan of efficacy after marketing. Despite these current liabilities, further pursuit of more potent and broader spectrum PDIs which are less susceptible to bacterial mechanisms of resistance is still warranted.

摘要

新的抗菌药物进入市场后,微生物耐药性的发展相对较快,因此需要不断供应新的药物来维持有效的药物治疗。尽管人们从分子靶点上广泛努力寻找新的先导化合物,但只有肽酰基转移酶抑制剂(PDI)显示出了真正的前景,其中一些已经进入了 I 期人体临床试验。细菌肽酰基转移酶在翻译后催化从 N 端甲硫氨酸上去除 N-甲酰基,对于细菌蛋白质合成、生长和存活是必需的。大多数 PDI 是假肽类羟肟酸,其中两种(IV BB-83698 和口服 NVP LBM-415)进入了 I 期人体临床试验。然而,到目前为止,这些药物都存在很大的潜在缺陷。它们的体外活性仅限于革兰氏阳性需氧菌和一些厌氧菌,对大多数此类物种的活性相当温和(MIC90 值范围为 1-8mg/L)。它们具有抑菌而非杀菌活性,因此在免疫功能低下患者严重感染的治疗中降低了它们的潜在用途。微生物能够如此轻易地产生耐药性,以及存在多种耐药机制(fmt、defB、folD 基因突变;AcrAB/TolC 外排泵;肽酰基转移酶过度表达),这令人担忧。这些都预示着上市后的疗效持续时间很短。尽管存在这些当前的缺陷,但仍有必要进一步研究更有效、更广泛谱的 PDI,这些 PDI 不易受到细菌耐药机制的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fcf/2374925/e7f3d4aaf836/tcrm0304-513-01.jpg

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