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Merck

K0879

Sigma-Aldrich

硫酸卡那霉素(来自卡那霉素链霉菌)

powder, γ-irradiated

别名:

卡那霉素 硫酸酯 来源于卡那霉素链霉菌, 卡那霉素 A, 卡那霉素碱 硫酸盐

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About This Item

经验公式(希尔记法):
C18H36N4O11 · H2O4S
CAS号:
分子量:
582.58
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.85

生物源

Streptomyces kanamyceticus

等級

for molecular biology

無菌

γ-irradiated

形狀

powder

效力

≥700 μg per mg

顏色

white to off-white

pH值

6.5-8.5(1% solution)

抗生素活性譜

Gram-negative bacteria
Gram-positive bacteria
mycoplasma

作用方式

protein synthesis | interferes

儲存溫度

2-8°C

適合性

nonselective for Escherichia coli
nonselective for coliforms

SMILES 字串

OS(O)(=O)=O.NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O)[C@H]2O)[C@H](O)[C@@H](O)[C@@H]1O

InChI

1S/C18H36N4O11.H2O4S/c19-2-6-10(25)12(27)13(28)18(30-6)33-16-5(21)1-4(20)15(14(16)29)32-17-11(26)8(22)9(24)7(3-23)31-17;1-5(2,3)4/h4-18,23-29H,1-3,19-22H2;(H2,1,2,3,4)/t4-,5+,6-,7-,8+,9-,10-,11-,12+,13-,14-,15+,16-,17-,18-;/m1./s1

InChI 密鑰

OOYGSFOGFJDDHP-KMCOLRRFSA-N

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一般說明

Chemical structure: aminoglycoside
Kanamycin, A from Streptomyces kanamyceticus is a polycationic aminoglycoside and a broad-spectrum antibiotic. Structurally, it comprises hydroxyl and amino functional groups.

應用

Kanamycin sulfate Streptomyces kanamyceticus has been used as an antibiotic component in Murashige and Skoog medium for the selection of tobacco tissue culture explants. It has also been used as an antibiotic in Luria broth for culturing Escherichia coli K-12 strain MG1655 cells for secretion assay and E. coli TV1061 cells for immobilization studies.

生化/生理作用

Kanamycin′s hydroxyl and amino functional groups are crucial for its membrane action functionality. However, it also exhibits toxicity towards mammalian cells. It prevents contamination in cell culture as well as a selective agent for bacteria with kanamycin resistance.
作用机制:该产品通过与70S核糖体亚基结合,抑制易位并引起错误编码而起作用。

耐药机制:氨基糖苷类修饰酶(包括乙酰转移酶、磷酸转移酶、核苷酸转移酶)可以改变这种抗生素,阻止其与核糖体相互作用。

抗菌谱:硫酸卡那霉素对革兰氏阴性和革兰氏阳性菌以及支原体有效。

原則

Kanamycin binds to the 30S ribosomal subunit and inhibits protein synthesis, leading to cell death.

準備報告

直接在小瓶中用无菌水配制储备液 (10mg/mL)。储备液应储存在 2-8°C 下。在 37°C 下可稳定 5 天。

象形圖

Health hazard

訊號詞

Danger

危險聲明

防範說明

危險分類

Repr. 1B

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 2

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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访问文档库

Kevin M Krause et al.
Cold Spring Harbor perspectives in medicine, 6(6) (2016-06-03)
Aminoglycosides are natural or semisynthetic antibiotics derived from actinomycetes. They were among the first antibiotics to be introduced for routine clinical use and several examples have been approved for use in humans. They found widespread use as first-line agents in
Shoot Regenerative Capacity Assays in Arabidopsis and Tobacco
Tian-QiZ and Jia-Wei W
Bio-protocol, 6(5) (2016)
Torsten John et al.
Biochimica et biophysica acta. Biomembranes, 1859(11), 2242-2252 (2017-08-30)
Biological membranes are natural barriers to the transport of molecules and drugs within human bodies. Many antibacterial agents need to cross these membranes to reach their target and elicit specific effects. Kanamycin A belongs to the family of aminoglycoside antibiotics
Tim Axelrod et al.
Talanta, 149, 290-297 (2016-01-01)
Toxicants in water sources are of concern. We developed a tool that is affordable and easy-to-use for monitoring toxicity in water. It is a biosensor composed of disposable bioreporter pads (calcium alginate matrix with immobilized bacteria) and a non-disposable CMOS
Mitsutaka Kitano et al.
Antimicrobial agents and chemotherapy, 58(8), 4795-4803 (2014-06-11)
Highly pathogenic avian influenza A (H5N1) viruses cause severe and often fatal disease in humans. We evaluated the efficacy of repeated intravenous dosing of the neuraminidase inhibitor peramivir against highly pathogenic avian influenza virus A/Vietnam/UT3040/2004 (H5N1) infection in cynomolgus macaques.

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