贝达喹啉是一种二芳基喹啉,可用于治疗耐多药结核病。在结核病小鼠模型中,贝达喹啉显著缩短了治疗方案。长效注射制剂已被证明具有延长的杀菌活性。 贝达喹啉抑制ATP合酶,并且在高浓度下导致氧化磷酸化的抑制。在大鼠肝脏线粒体中,贝达喹啉抑制MPT孔的形成,这通常伴随着结核病的发展。贝达喹啉的几种类似物也正在开发中,可以提高其生物利用度。 Cas No.:843663-66-1 纯度:≥99% 公式:C32H31手臂2O2 配方重量:555.5 化学名称:1R,2S)-1-(6-溴-2-甲氧基-3-喹啉基)-4-二甲氨基-2-(1-萘基)-1-苯基-2-丁醇 IUPAC名称:1R,2S)-1-(6-溴-2-甲氧基-3-喹啉基)-4-二甲氨基-2-(1-萘基)-1-苯基-2-丁醇 同义词:BQ1;溴-2-甲氧基喹啉-3-基)-4-二甲氨基-2-萘-1-基-1-苯基-2-丁醇;西尔图罗 熔点:183.9°摄氏度 储存温度:4°C LKT Labs-贝达喹啉文献引用: Sarathy J, Ganapathy U, Zimmerman M, et al. TBAJ-876, a 3,5-dialkoxypyridine analogue of bedaquiline, is active against mycobacterium abscessus. Antimicrob Agents Chemother. 2020 Mar 24;64(4):e02404-19. PMID: 31964791. Xu J, Li SY, Almeida D, et al. Contribution of pretomanid to novel regimens containing bedaquiline with either linezolid or moxifloxacin and pyrazinamide in murine models of tuberculosis. Antimicrob Agents Chemother. 2019 Apr 25;63(5):e00021-19. PMID: 30833432. Kaushik A, Ammerman N, Tyagi S, et al. Activity of a long-acting injectable bedaquiline formulation in a paucibacillary mouse model of latent tuberculosis infection. Antimicrob Agents Chemother. 2019 Mar 27;63(4):e00007-19. PMID: 30745396. Belosludtsev K, Belosludtseva N, Talanov E, et al. Effect of bedaquilinr on the functions of rat liver mitochondria. Biochim Biophys Acta Biomembr. 2019 Jan;1861(1):288-297. PMID: 29920239. Blaser A, Sutherland H, Tong A, et al. Structure-activity relationships for unit C pyridyl analogues of the tuberculosis drug bedaquiline. Bioorg Med Chem. 2019 Apr 1;27(7):1283-1291. PMID: 30792104. |
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