Dup-721

目录号: PL03862 纯度: ≥98%
DuP-721 是一种广谱口服活性抗菌剂 (antibacterial agent),对多种临床敏感和耐药细菌有效,特别是结核杆菌 M. tuberculosis
CAS No. :104421-21-8
商品编号 规格 价格 会员价 是否有货 数量
PL03862-5mg 5mg ¥787.00 请登录
PL03862-10mg 10mg ¥1285.00 请登录
PL03862-25mg 25mg ¥2205.00 请登录
PL03862-50mg 50mg ¥3165.00 请登录
PL03862-100mg 100mg ¥4485.00 请登录
PL03862-200mg 200mg ¥5915.00 请登录
PL03862-500mg 500mg 询价 询价
PL03862-10mM*1mLinDMSO 10mM*1mLinDMSO ¥2828.00 请登录
PL03862-1 mL x 10 mM (in DMSO) ¥847.00 请登录
Medlife所售产品仅用于科学研究(非临床研究),非药品不可食用,不可用于人体或动物的临床诊断和治疗,我们不为个人提供产品及服务。产品COA等资料,可至下方“质量控制”中下载。
*注意事项:下单时请联系销售核实产品价格及货期,避免后续产生不便,感谢支持!
中文名称
Dup-721
英文名称
Dup-721
英文别名
Acetamide,N-[[(5S)-3-(4-acetylphenyl)-2-oxo-5-oxazolidinyl]methyl]-;4-acetylphenyloxooxazolidinylmethylacetamide;Acetamide, N-((3-(4-acetylphenyl)-2-oxo-5-oxazolidinyl)methyl)-, (S)-;Dup 721;Dup-721;N-{[3-(4-acetylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide
Cas No.
104421-21-8
分子式
C14H16N2O4
分子量
276.29
包装储存
Powder -20°C 3 years;4°C 2 years
详情描述
DuP-721 是一种广谱口服活性抗菌剂 (antibacterial agent),对多种临床敏感和耐药细菌有效,特别是结核杆菌 M. tuberculosis
产品详情
DuP-721 是一种广谱口服活性抗菌剂 (antibacterial agent),对多种临床敏感和耐药细菌有效,特别是结核杆菌 M. tuberculosis。
生物活性
DuP-721 is a broad spectrum and orally active antibacterial agent against a variety of clinically susceptible and resistant bacteria, especially M. tuberculosis.
性状
Solid
体外研究(In Vitro)
DuP-721 (1.5-4 μg/ml) inhibits equally the strains of Mycobacterium tuberculosis susceptible and resistant to conventional antituberculosis drug. And it does not show cross resistance to any of the anti-tuberculosis drugs tested.
DuP-721 is inactive against M. avium and M. intracellulare at 250 μg/ml. It inhibits M. gordonoe and M. fortuitum at 3.9 μg/ml and M. kansassi and M. scrofulaceum at 1.95 μg/ml and 15.6 μg/ml, respectively.
has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
DuP-721 (oral gavage; 50-160 mg/kg) is protective against M. tuberculosis infection in mice. DuP-721 protects 100% of the infected animals at 50 mg/kg p.o. dose when administered daily for 17 days, and the same effect is observed at 160 mg/kg dose when the drug is administered only on day 11 and 12 post infection.
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]. Affiliatio, et al. Antimycobacterial activities of oxazolidinones: a review. Infect Disord Drug Targets. 2006 Dec;6(4):343-54.
溶解度数据
In Vitro: DMSO : 100 mg/mL (361.94 mM; Need ultrasonic)配制储备液
搜索质检报告(COA)
[1]. Affiliatio, et al. Antimycobacterial activities of oxazolidinones: a review. Infect Disord Drug Targets. 2006 Dec;6(4):343-54.

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。

The molarity calculator equation
Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)
The dilution calculator equation
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
This equation is commonly abbreviated as: C1V1 = C2V2