Bekanamycin(Synonyms: 卡那霉素; Kanamycin B)

天然产物 糖类和糖苷 Saccharides and Glycosides

Bekanamycin;(Synonyms: 卡那霉素; Kanamycin B) 纯度: ge;98.0%

Bekanamycin (Kanamycin B) 是一种氨基糖苷类抗生素,提取自 Streptomyces kanamyceticus,抑制一系列革兰氏阳性和阴性细菌。

Bekanamycin(Synonyms: 卡那霉素; Kanamycin B)

Bekanamycin Chemical Structure

CAS No. : 4696-76-8

规格 价格 是否有货 数量
Free Sample (0.1-0.5 mg) ; Apply now ;
10;mM;*;1 mL in Water ¥550 In-stock
100 mg ¥500 In-stock
200 mg ; 询价 ;
500 mg ; 询价 ;

* Please select Quantity before adding items.

Bekanamycin 相关产品

bull;相关化合物库:

  • Covalent Screening Library Plus
  • Natural Product Library Plus
  • Drug Repurposing Compound Library Plus
  • FDA-Approved Drug Library Plus
  • FDA-Approved Drug Library Mini
  • Bioactive Compound Library Plus
  • Anti-Infection Compound Library
  • Natural Product Library
  • FDA-Approved Drug Library
  • Drug Repurposing Compound Library
  • Covalent Screening Library
  • Glycoside Compound Library
  • Antibacterial Compound Library
  • Anti-COVID-19 Compound Library
  • FDA Approved amp; Pharmacopeial Drug Library
  • Antibiotics Library
  • Microbial Metabolite Library

生物活性

Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic produced by Streptomyces kanamyceticus, against an array of Gram-positive and Gram-negative bacterial strain[1][2].

体外研究
(In Vitro)

Bekanamycin (Kanamycin B) is a precursor for semisynthetic antibiotics such as Arbekacin and Dibekacin and is generally extracted from the broth of S. kanamyceticus[2].
Bekanamycin (Kanamycin B) in a concentration-dependent fashion reduces reversibly the quantal content of the end-plate potentials while it has no observable effect on the configuration of the extracellularly recorded presynaptic action potential. The reduction in evoked transmitter release produced by Bekanamycin could be antagonized either by increasing the external calcium concentration or by drugs like the aminopyridines which are to greatly enhance transmitter release from motor nerve terminals. Bekanamycin exerts potent inhibitory effects on transmitter release probably by interfering with the influx of calcium that occurs during depolarization of motor nerve terminals[3].

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

分子量

483.51

Formula

C18H37N5O10

CAS 号

4696-76-8

中文名称

卡那霉素 B

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20deg;C 3 years
4deg;C 2 years
In solvent -80deg;C 6 months
-20deg;C 1 month
溶解性数据
In Vitro:;

H2O : ≥ 100 mg/mL (206.82 mM)

DMSO : 1 mg/mL (2.07 mM; ultrasonic and warming and heat to 80°C)

* “≥” means soluble, but saturation unknown.

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.0682 mL 10.3410 mL 20.6821 mL
5 mM 0.4136 mL 2.0682 mL 4.1364 mL
10 mM 0.2068 mL 1.0341 mL 2.0682 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。

参考文献
  • [1]. Gao W, et al. Modulation of kanamycin B and kanamycin A biosynthesis in Streptomyces kanamyceticus viametabolic engineering. PLoS One. 2017 Jul 28;12(7):e0181971.

    [2]. Fosso MY, et al. Synthesis and Bioactivities of Kanamycin B-Derived Cationic Amphiphiles. J Med Chem. 2015 Dec 10;58(23):9124-32.

    [3]. Uchiyama T, et al. Presynaptic effects of bekanamycin at the frog neuromuscular junction. Reversibility by calcium and aminopyridines. Eur J Pharmacol. 1981 Jul 10;72(4):271-80.