NITD-349

目录号: PL11963 纯度: ≥98%
NITD-349 是 MmpL3 的抑制剂,具有高效的抗分枝杆菌活性,对结合分歧杆菌H37Rv的 MIC50 值为23 nM。
CAS No. :1473450-62-2
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中文名称
NITD-349
中文别名
化合物NITD-349
英文名称
NITD-349
英文别名
NITD-349;1H-Indole-2-carboxamide, N-(4,4-dimethylcyclohexyl)-4,6-difluoro-
Cas No.
1473450-62-2
分子式
C17H20F2N2O
分子量
306.35
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
NITD-349 是 MmpL3 的抑制剂,具有高效的抗分枝杆菌活性,对结合分歧杆菌H37Rv的 MIC50 值为23 nM。
产品详情
NITD-349 是 MmpL3 的抑制剂,具有高效的抗分枝杆菌活性,对结合分歧杆菌H37Rv的 MIC50 值为23 nM。
生物活性
NITD-349 is an MmpL3 inhibitor that shows highly potent anti-mycobacterial activity with MIC 50 of 23 nM against virulent Mycobacterium tuberculosis H37Rv.
性状
Solid
IC50 & Target[1][2]
MIC50: 23 nM (Mycobacterium tuberculosis H37Rv)
体外研究(In Vitro)
NITD-349 shows bactericidal activity against in vitro replicating Mycobacterium tuberculosis (Mtb) and also are active against intramacrophage Mtb. Kill kinetic analysis of these compounds showed both concentration- and time-dependent killing of Mtb cells with 3- to 4-log colony-forming unit (CFU) reductionwithin 3 days of treatment. The cidal activity profile of NITD-304 is similar to that of isoniazid for which rapid killing is noticed at concentrations greater than 0.2 μM. The MIC activity of NITD349 against various MDR Mtb strains ranges from 0.04 to 0.08 μM. NITD-349 shows high permeability and moderate in vitro metabolic clearance in mouse and human hepatic microsomes. has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
In the acute murine efficacy modelNITD-349 shows favorable oral pharmacokinetic (PK) properties in rodents and dogs and are efficacious in mouse models of both acute and chronic Mycobacterium tuberculosis infection. In the acute murine efficacy model, treatment of mice with NITD-349 at doses of 12.5 and 50 mg/kg resulted in 0.9- and 3.4-log CFU reduction in lung tissue. In an established infection mouse model, after 2 weeks of treatment, the efficacy of NITD-349 is comparable to the first-line TB drug rifampicin and is better than ethambutol. Four weeks of treatment at 100 mg/kg with NITD-349 results in 2.38-log CFU reductions. has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature in continental US; may vary elsewhere.
储存方式
Powder -20°C 3 years;4°C 2 years
参考文献
[1]. Rao SP, et al. Indolcarboxamide is a preclinical candidate for treating multidrug-resistant tuberculosis. Sci Transl Med. 2013 Dec 4;5(214):214ra168.
溶解度数据
In Vitro: DMSO : ≥ 310 mg/mL (1011.91 mM)配制储备液
搜索质检报告(COA)
[1]. Rao SP, et al. Indolcarboxamide is a preclinical candidate for treating multidrug-resistant tuberculosis. Sci Transl Med. 2013 Dec 4;5(214):214ra168.

1:一般建议:溶解度为Medlife测试数据,可能与文献描述存在差异。这是由于生产工艺和批次不同产生的正常现象。为了使其更好的溶解,请用37℃加热试管并在超声波水浴中震动片刻。不同批次产品溶解度各有差异,仅做参考,具体以实验方案为准。

2:储存条件:粉末-20°C一般情况可以保存3年,溶于溶剂-80°C一般情况可以保存1年。不同产品及不同批次产品可能存在差异,请细致阅读产品信息,并辅助参考相关文献描述。

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