Nalidixic acid.

(Synonyms: 萘啶酸)
目录号: PC61295 纯度: ≥99%
Nalidixic acid,一种喹诺酮类抗生素 (antibiotic),对革兰氏阳性和革兰氏阴性细菌均有效。Nalidixic acid 在较低浓度下以抑菌的方式起作用,而在较高浓度下具有杀菌作用。Nalidixic acid 抑制 DNA 促旋酶和拓扑异构酶 IV 的亚基,并可逆地阻止易感细菌中的 DNA 复制。Nalidixic acid,一种喹诺酮类抗生素 (antibiotic),对革兰氏阳性和革兰氏阴性细菌均有效。Nalidixic acid 在较低浓度下以抑菌的方式起作用,而在较高浓度下具有杀菌作用。Nalidixic acid 抑制 DNA 促旋酶和拓扑异构酶 IV 的亚基,并可逆地阻止易感细菌中的 DNA 复制。
CAS No. :389-08-2
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中文名称
Nalidixic acid.
中文别名
萘啶酸;萘啶酮酸;3-苄氧基-2.6-二氟苯硼酸;Nalidixic Acid 萘啶酸;Nalidixic acid 萘啶酮酸;WAKO144-06611萘啶酸标准品;奈啶酸;萘啶酸 EP标准品;萘啶酸 标准品;萘啶酮酸 USP标准品;萘啶酮酸(CN琼脂冻干配套试剂),0.2g,对多数革兰氏阴性细菌有抑制作用;1-乙基-7-甲基-4-酮-1,8-萘啶-3-羧酸;7-甲基-1-乙基-4-氧代-1,4-二氢-1,8-萘啶-3-羧酸;萘啶酸,1-乙基-7-甲基-4-酮-1,8-萘啶-3-羧酸;1,4-二氢-1-乙基-7-甲基-1,8-萘啶-4-酮-3-羧酸;1-乙基-1,4-二氢-7-甲基-4-氧代-1,8-萘啶-3-羧酸
英文名称
Nalidixic acid
英文别名
Nalidixic acid;1,4-Dihydro-1-ethyl-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid;1-ethyl-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylic acid;Cetrimide Nalidixic acid Agar Supplement;1-Ethyl-7-methyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid;5,5-Diphenylimidazolidine-2,4-dione;1,4-Dihydro-1-ethyl-7-Methyl-4-oxo-1,-naphthyridine-3-carboxylic acid;3-Carboxy-1-ethyl-7-Methyl-1,8-naphthyridin-4-;cybis;nalix;negram;NOGRAM;poleon;uriben;Urisal;uroman;uroneg;uropan;Nevigramon;Nalidixin;Uronidix;Nalidixate;Innoxalon;Nalitucsan;Nalidixan;Sicmylon;Unaserus;NegGram;Nalidic acid;Nalidixinic acid;Wintomylon;Nalurin;Naxuril;Jicsron;Dixinal;Dixiben;Acide nalidixique;Nalidicron;Specifin;Specifen;Nicelate;Narigix;Urodixin;Uriclar;Uralgin;Kusnarin;Betaxina;Naldixic acid;Acido nalidixico;Acidum nalidixicum;E;Eucistin;Acide nalidixico;Acido nalid
Cas No.
389-08-2
分子式
C12H12N2O3
分子量
232.24
包装储存
Powder; -20°C; 3 years; 4°C; 2 years;
详情描述

Nalidixic acid,一种喹诺酮类抗生素 (antibiotic),对革兰氏阳性和革兰氏阴性细菌均有效。Nalidixic acid 在较低浓度下以抑菌的方式起作用,而在较高浓度下具有杀菌作用。Nalidixic acid 抑制 DNA 促旋酶和拓扑异构酶 IV 的亚基,并可逆地阻止易感细菌中的 DNA 复制。Nalidixic acid,一种喹诺酮类抗生素 (antibiotic),对革兰氏阳性和革兰氏阴性细菌均有效。Nalidixic acid 在较低浓度下以抑菌的方式起作用,而在较高浓度下具有杀菌作用。Nalidixic acid 抑制 DNA 促旋酶和拓扑异构酶 IV 的亚基,并可逆地阻止易感细菌中的 DNA 复制。

生物活性
Nalidixic acid, a quinolone antibiotic, is effective against both gram-positive and gram-negative bacteria. Nalidixic acid acts in a bacteriostatic manner in lower concentrations and is bactericidal in higher concentrations. Nalidixic acid inhibits a subunit of DNA gyrase and topoisomerase IV and reversibly blocks DNA replication in susceptible bacteria.
性状
Solid
IC50 & Target[1][2]
Quinolone
 Topoisomerase
 
体外研究(In Vitro)
Nalidixic acid is against a variety of microorganisms, it is against with Escherichia coli, Pasteurella spp., Klebsiella pneuiiioniae, Aerobacter aeroyenes, Proteus spp., Salmonella spp., Shigella spp. and Brucella spp. with MIC values of 5.0-12.5 μg/ml, 0.5-2.5 μg/ml, 0.8-25.0 μg/ml, 1.0-25.0 μg/ml, 1.25-30.0 μg/ml, 8-3.2 μg/ml, and 7.5-10.0 μg/ml, respectively.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
体内研究(In Vivo)
The in vivo activity of Nalidixic acid is most pronounced against Gram-negative bacteria, while Gram-positive organisms are generally more resistant. Maximal activity is observed against systemic infections caused by E. coli, A. aerobacter, Proteus mirabilis, Shigella fkxneri, the ED50 values are 25 mg/kg, 60 mg/kg, 50 mg/kg, and 62 mg/kg, respectively.
The acute toxicity (LD50) of Nalidixic acid in mice following oral and parenteral administration is: oral, 3300 mg/kg; intravenous, 176 mg/kg, and subcutaneous, 500 mg/kg.
Medlife has not independently confirmed the accuracy of these methods. They are for reference only.
运输条件
Room temperature or refrigerated transport.
储存方式
Powder; -20°C; 3 years; 4°C; 2 years;
结构分类
Antibiotics
Other
来源
Streptomyces sp. 
溶解度数据
体外研究:
DMSO : 6 mg/mL(25.84 mM;Need ultrasonic)
H2O : 5 mg/mL(21.53 mM;ultrasonic and warming and heat to 80°C)
配制储存液
搜索质检报告(COA)

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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