Levonadifloxacin (S-(-)-Nadifloxacin; WCK 771),99.79%

产品编号:Bellancom-14926| CAS NO:154357-42-3| 分子式:C19H21FN2O4| 分子量:360.38

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货号 包装 价格 库存与货期 购买量 操作
Bellancom-14926
2500.00 杭州 北京(现货)
Bellancom-14926
3800.00 杭州 北京(现货)
Bellancom-14926
7500.00 杭州 北京(现货)
Bellancom-14926
12000.00 杭州 北京(现货)

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Levonadifloxacin (S-(-)-Nadifloxacin; WCK 771)

产品介绍 Levonadifloxacin ((S)-(-)-Nadifloxacin; WCK 771) 是一种广谱的抗葡萄球菌剂。Levonadifloxacin 对甲氧西林敏感的金黄色葡萄球菌 (MSSA) 和对甲氧西林耐药的金黄色葡萄球菌具有抗菌活性,减少单核细胞 THP-1 吞噬的 MRSA 和 MSSA 菌株。
生物活性

Levonadifloxacin ((S)-(-)-Nadifloxacin; WCK 771) is a broad-spectrum anti-staphylococcal agent. Levonadifloxacin shows antibacterial activity against Methicillin (HY-121544)-susceptible Staphylococcus aureus (MSSA) and Methicillin-resistant S. aureus (MRSA) strains, with a reduction of which phagocytized in THP-1 monocytes.

体外研究

Levonadifloxacin (32 μg/mL; 24 h) achieves a 90-99% intracellular reduction of MSSA and MRSA strains phagocytized in THP-1 monocytes with MICs of 0.03 μg/mL and 15.0 ng/mL.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究

Levonadifloxacin (12.5-400 mg/kg; s.c.; single dose) shows efficacy in vivo against Staphylococcus aureus in a Neutropenic Murine Lung Infection Model.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male/Female Swiss Albino mice (25-28 g) for plasma pharmacokinetic analyses
Dosage: 12.5, 25, 50, 100, 200, 300 and 400 mg/kg
Administration: Subcutaneous injection; single dose; collected samples at 10 time points/dose (0.25, 0.5, 1, 2, 4, 6, 8, 10, 58 12 and 24 h post dose)
Result:
Dose (mg/kg) Cmax (mg/L) AUC0-24 h (mg·h/L) T1/2 (h)
12.5 4.37 7.30 1.79
25 8.71 15.75 1.48
50 19.21 33.36 1.48
100 38.65 70.86 1.76
200 77.29 145.48 1.69
300 92.46 286.19 2.44
400 115.16 393.52 1.74
体内研究

Levonadifloxacin (12.5-400 mg/kg; s.c.; single dose) shows efficacy in vivo against Staphylococcus aureus in a Neutropenic Murine Lung Infection Model.

西域 has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male/Female Swiss Albino mice (25-28 g) for plasma pharmacokinetic analyses
Dosage: 12.5, 25, 50, 100, 200, 300 and 400 mg/kg
Administration: Subcutaneous injection; single dose; collected samples at 10 time points/dose (0.25, 0.5, 1, 2, 4, 6, 8, 10, 58 12 and 24 h post dose)
Result:
Dose (mg/kg) Cmax (mg/L) AUC0-24 h (mg·h/L) T1/2 (h)
12.5 4.37 7.30 1.79
25 8.71 15.75 1.48
50 19.21 33.36 1.48
100 38.65 70.86 1.76
200 77.29 145.48 1.69
300 92.46 286.19 2.44
400 115.16 393.52 1.74
性状Solid
溶解性数据
In Vitro: 

DMSO : 125 mg/mL (346.86 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.7748 mL 13.8742 mL 27.7485 mL
5 mM 0.5550 mL 2.7748 mL 5.5497 mL
10 mM 0.2775 mL 1.3874 mL 2.7748 mL
*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

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
In solvent -80°C 6 months
-20°C 1 month
参考文献

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