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噁喹酸 /Oxolinic acid {[allProObj[0].p_purity_real_show]}

货号:A203320 同义名: 恶喹酸 / NSC 110364;Urinox

Oxolinic acid是一种抗生素,对革兰氏阴性菌和阳性菌有效,此外,Oxolinic acid 是一种强效的DNA旋转酶和DNA合成抑制剂,能够在提取的染色体与十二烷基硫酸钠共同孵育时导致DNA裂解。

Oxolinic acid 化学结构 CAS号:14698-29-4
Oxolinic acid 化学结构
CAS号:14698-29-4
Oxolinic acid 3D分子结构
CAS号:14698-29-4
Oxolinic acid 化学结构 CAS号:14698-29-4
Oxolinic acid 3D分子结构 CAS号:14698-29-4
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Oxolinic acid 纯度/质量文件 产品仅供科研

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产品名称 DNA synthesis helicase RdRp ribonucleotide reductase tRNA synthetase YB-1 其他靶点 纯度
Fexinidazole 98%
Daptomycin 98%
Blasticidin S·HCl 98%
Metronidazole 98%
Daunorubicin HCl +++

DNA synthesis, Ki: 20 nM

98%
Triglycidyl isocyanurate p53 98+%
Nedaplatin 99%+
Oxolinic acid 98+%
Bendamustine 98+%
Trifluridine 98%
Robinetin 99%+
Carboplatin 99%
Cidofovir 99%
Cisplatin 99%
Cytarabine ++++

DNA synthesis, IC50: 16 nM

98%
Acelarin ++++

DNA synthesis, EC50: 0.2 nM

99%+
Oxaliplatin 98%
YK-4-279 99%+
ML216 +

BLMfull-length, IC50: 2.98 μM

BLM636-1298, IC50: 0.97 μM

99%+
RK-33 98%
Brr2-IN-3 99%+
Phen-DC3 Trifluoromethanesulfonate 98%
Favipiravir 99%
Suramin sodium salt ++

RdRp, IC50: 0.26 μM

99%+
Clofarabine ++

Ribonucleotide reductase, IC50: 65 nM

97%
Didox 98%
(E)-3-AP 99%
Halofuginone +++

prolyl-tRNA synthetase, Ki: 18.3nM

99%+
BC-LI-0186 +++

Leucyl-tRNA synthetase, IC50: 46.11 nM

Leucyl-tRNA synthetase, Kd: 42.1 nM

98%
SU056 +

YB-1, IC50: 1.73 μM

98%
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

Oxolinic acid 生物活性

靶点
  • DNA synthesis

描述 Oxolinic Acid is an antibiotic against both Gram-negative and Gram-positive bacteria. Oxolinic acid can be used for the research of acute and chronic urinary tract infections. Oxolinic acid (2-5 ug/mL) inhibits 115 strains of E. coli. Oxolinic acid (0-31 ug/mL) inhibits 94 % of the 44 strains of Proteus mirabilis. Oxolinic acid (>5 ug/mL) inhibits all strains of Strept. Faecalis[3]. Oxolinic acid reduced RNA synthesis rates whether chromosome supercoiling decreased, increased, or remained unchanged[4]. Oxolinic acid induced benign Leydig cell tumours of the testis in rats at the highest dose level tested (1000 ppm). The no-effect level for tumour induction was confirmed to be 300 ppm (10.9 mg/kg/day) in rats. None was induced in mice[5]. The in vitro minimum inhibitory concentration (MIC) values of oxolinic acid against three strains of Vibrio anguillarum isolated from diseased cod were 0.016 microg mL(-1) (HI-610), 0.250 microg mL(-1) (HI-618) and 0.250 microg mL(-1) (HI-A21)[6]. Oxolinic acid induces Leydig cell tumors in rats by chronically stimulating the release of LH (luteinizing hormone) from the pituitary[7].

Oxolinic acid 参考文献

[1]Tarushi A, Psomas G, et al. Zinc complexes of the antibacterial drug oxolinic acid: structure and DNA-binding properties. J Inorg Biochem. 2009 Jun;103(6):898-905.

[2]Garcia de Mateos-Verchere J, Vaugeois JM, et al. Behavioural and neurochemical evidence that the antimicrobial agent oxolinic acid is a dopamine uptake inhibitor. Eur Neuropsychopharmacol. 1998 Dec;8(4):255-9.

[3]Kershaw MJ, Leigh DA. The antibacterial and pharmacological activity of oxolinic acid (Prodoxol). J Antimicrob Chemother. 1975 Sep;1(3):311-5

[4]Manes SH, Pruss GJ, Drlica K. Inhibition of RNA synthesis by oxolinic acid is unrelated to average DNA supercoiling. J Bacteriol. 1983 Jul;155(1):420-3

[5]Yamada T, Maita K, Nakamura J, Murakami M, Okuno Y, Hosokawa S, Matsuo M, Yamada H. Carcinogenicity studies of oxolinic acid in rats and mice. Food Chem Toxicol. 1994 May;32(5):397-408

[6]Samuelsen OB, Bergh O, Ervik A. A single-dose pharmacokinetic study of oxolinic acid and vetoquinol, an oxolinic acid ester, in cod, Gadus morhua L., held in sea water at 8 degrees C and in vitro antibacterial activity of oxolinic acid against Vibrio anguillarum strains isolated from diseased cod. J Fish Dis. 2003 Jun;26(6):339-47. doi: 10.1046/j.1365-2761.2003.00466.x. PMID: 12899409

[7]Yamada T, Nakamura J, Murakami M, Okuno Y, Hosokawa S, Matsuo M, Yamada H. The correlation of serum luteinizing hormone levels with the induction of Leydig cell tumors in rats by oxolinic acid. Toxicol Appl Pharmacol. 1994 Nov;129(1):146-54

Oxolinic acid 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

3.83mL

0.77mL

0.38mL

19.14mL

3.83mL

1.91mL

38.28mL

7.66mL

3.83mL

Oxolinic acid 技术信息

CAS号14698-29-4
分子式C13H11NO5
分子量 261.23
别名 恶喹酸 ;NSC 110364;Urinox;Dioxacin;Prodoxol;Nidantin;Emyrenil
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,2-8°C

溶解方案

DMSO: 1 mg/mL(3.83 mM),配合低频超声助溶,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

动物实验配方
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