An Overview of Various Rifampicin Analogs against Mycobacterium tuberculosis and their Drug Interactions.

IF 1.9 4区 医学 Q3 CHEMISTRY, MEDICINAL Medicinal Chemistry Pub Date : 2024-01-01 DOI:10.2174/0115734064260853230926080134
Mohammad Asif, Naeem F Qusty, Saad Alghamdi
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Abstract

The success of the TB control program is hampered by the major issue of drug-resistant tuberculosis (DR-TB). The situation has undoubtedly been made more difficult by the widespread and multidrug-resistant (XDR) strains of TB. The modification of existing anti-TB medications to produce derivatives that can function on resistant TB bacilli is one of the potential techniques to overcome drug resistance affordably and straightforwardly. In comparison to novel pharmaceuticals for drug research and progress, these may have a better half-life and greater bioavailability, be more efficient, and serve as inexpensive alternatives. Mycobacterium tuberculosis, which is drugsusceptible or drug-resistant, is effectively treated by several already prescribed medications and their derivatives. Due to this, the current review attempts to give a brief overview of the rifampicin derivatives that can overcome the parent drug's resistance and could, hence, act as useful substitutes. It has been found that one-third of the global population is affected by M. tuberculosis. The most common cause of infection-related death can range from latent TB to TB illness. Antibiotics in the rifamycin class, including rifampicin or rifampin (RIF), rifapentine (RPT), and others, have a special sterilizing effect on M. tuberculosis. We examine research focused on evaluating the safety, effectiveness, pharmacokinetics, pharmacodynamics, risk of medication interactions, and other characteristics of RIF analogs. Drug interactions are especially difficult with RIF because it must be taken every day for four months to treat latent TB infection. RIF continues to be the gold standard of treatment for drug-sensitive TB illness. RIF's safety profile is well known, and the two medicines' adverse reactions have varying degrees of frequency. The authorized once-weekly RPT regimen is insufficient, but greater dosages of either medication may reduce the amount of time needed to treat TB effectively.

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抗结核分枝杆菌的各种利福平类似物及其药物相互作用综述。
结核病控制计划的成功受到耐药结核病(DR-TB)这一主要问题的阻碍。毫无疑问,结核病的广泛耐药菌株使情况变得更加困难。对现有的抗结核药物进行改造,生产出能够对耐药结核杆菌发挥作用的衍生物,是以负担得起的方式直接克服耐药性的潜在技术之一。与用于药物研究和进展的新药相比,这些药物可能具有更好的半衰期和更高的生物利用度,更有效,并可作为廉价的替代品。结核分枝杆菌对药物敏感或耐药,可以通过几种已经开出的药物及其衍生物进行有效治疗。因此,目前的综述试图简要概述利福平衍生物,这些衍生物可以克服母体药物的耐药性,因此可以作为有用的替代品。研究发现,全球三分之一的人口受到结核分枝杆菌的影响。与感染相关的死亡最常见的原因包括潜伏性结核病和结核病。利福霉素类抗生素,包括利福平或利福平(RIF)、利福喷丁(RPT)等,对结核分枝杆菌具有特殊的杀菌作用。我们检查了专注于评估RIF类似物的安全性、有效性、药代动力学、药效学、药物相互作用风险和其他特征的研究。RIF的药物相互作用尤其困难,因为它必须在四个月内每天服用才能治疗潜伏性结核病感染。RIF仍然是治疗药物敏感结核病的黄金标准。RIF的安全性是众所周知的,这两种药物的不良反应频率不同。授权的每周一次RPT方案是不够的,但更大剂量的任何一种药物都可能减少有效治疗结核病所需的时间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
期刊介绍: Aims & Scope Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.
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