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DMABA NHS ester Sale

(Synonyms: 4-(二甲胺基)苯甲酸N-羟基琥珀酰亚胺酯) 目录号 : GC43499

A marker for the detection of PE lipids by mass spectrometry

DMABA NHS ester Chemical Structure

Cas No.:58068-85-2

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50mg
¥496.00
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100mg
¥942.00
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500mg
¥3,975.00
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Sample solution is provided at 25 µL, 10mM.

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产品描述

Phosphatidylethanolamine (PE) lipids are important components of cell membranes and biochemical pathways of fatty acid synthesis that contain abundant polyunsaturated fatty acyl (PUFA) groups. Oxidation of these phospholipids may be linked to various human diseases. DMABA NHS ester is a reagent that reacts with the primary amine group of PE lipids. This facilitates the use of electrospray tandem mass spectrometry for the detection of diacyl, ether, and plasmalogen PE lipids that cannot be readily observed otherwise. DMABA NHS ester has been used in combination with DMABA NHS ester-d4, -d6, and -d10 to study relative changes in PE lipid abundance before and after radical oxidation.

Chemical Properties

Cas No. 58068-85-2 SDF
别名 4-(二甲胺基)苯甲酸N-羟基琥珀酰亚胺酯
Canonical SMILES O=C(CC1)N(OC(C2=CC=C(N(C)C)C=C2)=O)C1=O
分子式 C13H14N2O4 分子量 262.3
溶解度 DMF: 20 mg/ml,DMSO: 20 mg/ml,DMSO:PBS (pH 7.2) (1:30): 0.03 mg/ml,Ethanol: Insoluable,PBS (pH 7.2): Insoluable 储存条件 Store at -20°C
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 3.8124 mL 19.0621 mL 38.1243 mL
5 mM 0.7625 mL 3.8124 mL 7.6249 mL
10 mM 0.3812 mL 1.9062 mL 3.8124 mL
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Research Update

Stable isotope labeled 4-(dimethylamino)benzoic acid derivatives of glycerophosphoethanolamine lipids

Anal Chem 2009 Aug 15;81(16):6633-40.PMID:20337376DOI:PMC2929906

A set of four (D(0), D(4), D(6), and D(10)) deuterium enriched 4-(dimethylamino)benzoic acid (DMABA) N-hydroxysuccinimide (NHS) ester reagents was developed that react with the primary amine group of glycerophosphoethanolamine (PE) lipids to create derivatives where all subclasses of DMABA labeled PE are detected by a common precursor ion scan. The positive ion collision induced dissociation data from (D(0), D(4), D(6), and D(10))-DMABA labeled PE standards indicated that a precursor ion scan of m/z 191.1, 195.1, 197.1, and 201.1 could be used to selectively detect (D(0), D(4), D(6), and D(10))-DMABA modified PE, respectively, in a complex biological mixture. The PE lipids from a time course (0, 30, 60, and 300 min) of 2,2'-azobis-(2-amidinopropane) hydrochloride (AAPH) treatment of liposomes made of RAW 264.7 cell phospholipids were each labeled with the D(0)-, D(4)-, D(10)-, and D(6)-DMABA NHS ester reagents, respectively. The DMABA derivatives revealed loss of endogenous PE lipids and an increase in oxidized PE lipid throughout the time course of AAPH treatment. These DMABA NHS ester reagents provide a universal scan for diacyl, ether, and plasmalogen PE lipids that cannot be readily observed otherwise, enable differential labeling, and provide an internal standard for each PE lipid.