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阿维巴坦钠 /Avibactam sodium {[allProObj[0].p_purity_real_show]}

货号:A169351 同义名: 阿维巴坦 / NXL-104;Avibactam (sodium salt)

Avibactam sodium(NXL-104)是一种共价和可逆的非β-内酰胺β-内酰胺酶抑制剂,抑制β-内酰胺酶TEM-1和CTX-M-15的IC50值分别为8 nM和5 nM。

Avibactam sodium 化学结构 CAS号:1192491-61-4
Avibactam sodium 化学结构
CAS号:1192491-61-4
Avibactam sodium 3D分子结构
CAS号:1192491-61-4
Avibactam sodium 化学结构 CAS号:1192491-61-4
Avibactam sodium 3D分子结构 CAS号:1192491-61-4
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Avibactam sodium 纯度/质量文件 产品仅供科研

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Avibactam sodium 生物活性

描述 Avibactam (Sodium) is a β-lactamase inhibitor that is in clinical development, combined with β-lactam partners, for the treatment of bacterial infections comprising gram-negative organisms[3]. Ceftaroline + avibactam (NXL104) is a novel inhibitor combination active against Enterobacteriaceae with class A and C β-lactamases[4]. Avibactam expands ceftazidime's spectrum of activity to include many ceftazidime- and carbapenem-resistant Enterobacteriaceae and Pseudomonas aeruginosa. Early clinical data indicate that ceftazidime-avibactam is effective and well tolerated in patients with complicated urinary tract infections (cUTIs) and complicated intraabdominal infections (cIAI). In a phase II trial of patients with cUTIs, ceftazidime-avibactam produced similar rates of clinical and microbiologic success compared with imipenem-cilastatin (70.5% and 71.4% microbiologic success rates, respectively)[5].

Avibactam sodium 参考文献

[1]Ehmann DE, Jahic H, et al. Avibactam is a covalent, reversible, non-β-lactam β-lactamase inhibitor. Proc Natl Acad Sci U S A. 2012 Jul 17;109(29):11663-8.

[2]Aktaş Z, Kayacan C, Oncul O. In vitro activity of avibactam (NXL104) in combination with β-lactams against Gram-negative bacteria, including OXA-48 β-lactamase-producing Klebsiella pneumoniae. Int J Antimicrob Agents. 2012 Jan;39(1):86-9.

[3]Ehmann DE, Jahić H, Ross PL, et al. Avibactam is a covalent, reversible, non-β-lactam β-lactamase inhibitor. Proc Natl Acad Sci U S A. 2012;109(29):11663–11668

[4]Livermore DM, Mushtaq S, Barker K, Hope R, Warner M, Woodford N. Characterization of β-lactamase and porin mutants of Enterobacteriaceae selected with ceftaroline + avibactam (NXL104). J Antimicrob Chemother. 2012;67(6):1354–1358

[5]Torres A, Zhong N, Pachl J, et al. Ceftazidime-avibactam versus meropenem in nosocomial pneumonia, including ventilator-associated pneumonia (REPROVE): a randomised, double-blind, phase 3 non-inferiority trial. Lancet Infect Dis. 2018;18(3):285–295

Avibactam sodium 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.48mL

0.70mL

0.35mL

17.41mL

3.48mL

1.74mL

34.82mL

6.96mL

3.48mL

Avibactam sodium 技术信息

CAS号1192491-61-4
分子式C7H10N3NaO6S
分子量 287.226
别名 阿维巴坦 ;NXL-104;Avibactam (sodium salt);AVE-1330A
运输蓝冰
存储条件

In solvent -20°C:3-6个月-80°C:12个月

Pure form Sealed in dry,Room Temperature

溶解方案

DMSO: 30 mg/mL(104.45 mM),注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 50 mg/mL(174.08 mM),配合低频超声助溶

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