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主要文件

安全信息

N9284

Sigma-Aldrich

硝基还原酶 来源于大肠杆菌

greener alternative

≥90% (SDS-PAGE), recombinant, expressed in E. coli

别名:

NTRA

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100 MG
¥1,070.84
1 G
¥8,487.98

¥1,070.84


国内现货,预计发货时间2025年4月27日详情



选择尺寸

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100 MG
¥1,070.84
1 G
¥8,487.98

About This Item

MDL编号:
UNSPSC代码:
12352204
NACRES:
NA.54

¥1,070.84


国内现货,预计发货时间2025年4月27日详情


重组

expressed in E. coli

质量水平

方案

≥90% (SDS-PAGE)

表单

lyophilized powder

比活

≥100 units/mL

分子量

monomer 24000

环保替代产品特性

Waste Prevention
Safer Solvents and Auxiliaries
Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

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此商品
T151SML2686T150
assay

≥98%

assay

≥98% (HPLC)

assay

≥98% (HPLC)

assay

>98%

form

powder

form

powder

form

powder

form

solid

solubility

DMSO: 20 mg/mL, clear

solubility

DMSO: 15 mg/mL, clear

solubility

DMSO: 2 mg/mL, clear

solubility

DMSO: soluble, H2O: insoluble, ethanol: insoluble

originator

Celgene

originator

Celgene

originator

-

originator

Celgene

color

white

color

white to beige

color

white to beige

color

white

ligand

thalidomide

ligand

thalidomide

ligand

pomalidomide

ligand

thalidomide

一般描述

硝基还原酶是一种黄素蛋白,由NfsB基因编码。它包含一个二聚体,每个亚基具有217个氨基酸和活性位点。该结构具有FMN和与酶结合的底物。[1]

应用

大肠杆菌来源硝基还原酶可结合猪肝酯酶(PLE)用于偶联结合反应。[2]它还还可结合探针HyCL-3和HyCL-4-AM针对大鼠肝微粒体进行化学发光响应研究。[3]

生化/生理作用

硝基还原酶(NTR)可催化还原硝基芳香族底物和醌。[1]NTR的F124K突变体可用于癌症治疗,改善药物CB1954的敏化作用。[4]
硝基还原酶在NADPH或NADH为还原剂的氧还系统中有重要作用。 [5]
硝基还原酶增强了生命体对于含氮药物,比如甲硝唑的敏感度,它将氮基团转化为有毒的氮自由基。 [6]
能够还原奎宁。 该酶可以激活抗体引导酶前药治疗的前药。

物理属性

含有PBS的冻干粉。 作为辅药不含有BSA

单位定义

在pH7.4、37℃、存在甲萘醌和NADH的条件下,一单位酶每分钟能够还原1μmole细胞色素C。

制备说明

使用没有动物组分的材料生产。

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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    Generation of Escherichia coli nitroreductase mutants conferring improved cell sensitization to the prodrug CB1954
    Grove JI, et al.
    Cancer research, 63(17), 5532-5537 (2003)
    Mckayla Stevens et al.
    Bioorganic & medicinal chemistry, 28(22), 115710-115710 (2020-10-03)
    In two previous studies, we identified compound 1 as a moderate GroEL/ES inhibitor with weak to moderate antibacterial activity against Gram-positive and Gram-negative bacteria including Bacillus subtilis, methicillin-resistant Staphylococcus aureus, Klebsiella pneumonia, Acinetobacter baumannii, and SM101 Escherichia coli (which has
    Bharat Bhushan et al.
    Biochemical and biophysical research communications, 322(1), 271-276 (2004-08-18)
    Previously, we reported that a salicylate 1-monooxygenase from Pseudomonas sp. ATCC 29352 biotransformed CL-20 (2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaaza-isowurtzitane) (C(6)H(6)N(12)O(12)) and produced a key metabolite with mol. wt. 346 Da corresponding to an empirical formula of C(6)H(6)N(10)O(8) which spontaneously decomposed in aqueous medium to
    M J Lemmon et al.
    Gene therapy, 4(8), 791-796 (1997-08-01)
    A fundamental obstacle in gene therapy for cancer treatment is the specific delivery of an anticancer gene product to a solid tumor. Although several strategies exist to control gene expression once a vector is directly introduced into a tumor, as
    Chih-Chen Chen et al.
    Food chemistry, 135(4), 2708-2713 (2012-09-18)
    Nitroreductases (Nrs) play important roles in redox system via NADPH or NADH as a reductant. A TcNr cDNA encoding a putative Nr was cloned from Taiwanofungus camphorata. A 3-D structural model of the TcNr has been created based on the

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