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2-NP-AOZ Sale

(Synonyms: 2-NP-呋喃唑酮) 目录号 : GC49786

A derivatized metabolite of furazolidone

2-NP-AOZ Chemical Structure

Cas No.:19687-73-1

规格 价格 库存 购买数量
1 mg
¥397.00
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5 mg
¥1,491.00
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10 mg
¥2,189.00
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25 mg
¥4,965.00
现货

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Sample solution is provided at 25 µL, 10mM.

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产品描述

2-NP-AOZ is a derivatized metabolite of the nitrofuran antiprotozoal and antibacterial agent furazolidone .1 It is formed from the tissue-bound furazolidone metabolite 3-amino-2-oxazolidinone (AOZ) after acid hydrolysis and derivatization with o-nitrobenzaldehyde (o-NBA). 2-NP-AOZ has been used as a marker of furazolidone use in pigs.2

1.Hoogenboom, L.A., Berghmans, T.H., Polman, T.H., et al.Depletion of protein-bound furazolidone metabolites containing the 3-amino-2-oxazolidinone side-chain from liver, kidney and muscle tissues from pigsFood Addit. Contam.9(6)623-630(1992)

Chemical Properties

Cas No. 19687-73-1 SDF Download SDF
别名 2-NP-呋喃唑酮
Canonical SMILES O=C1OCCN1/N=C/C2=C([N+]([O-])=O)C=CC=C2
分子式 C10H9N3O4 分子量 235.2
溶解度 Chloroform: slightly soluble,Methanol: slightly soluble 储存条件 -20°C
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1 mg 5 mg 10 mg
1 mM 4.2517 mL 21.2585 mL 42.517 mL
5 mM 0.8503 mL 4.2517 mL 8.5034 mL
10 mM 0.4252 mL 2.1259 mL 4.2517 mL
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Research Update

Development and residue screening of the furazolidone metabolite, 3-amino-2-oxazolidinone (AOZ), in cultured fish by an enzyme-linked immunosorbent assay

J Agric Food Chem 2009 Jul 8;57(13):5687-92.PMID:19526989DOI:10.1021/jf900859r.

A sensitive and specific polyclonal enzyme-linked immunosorbent assay (ELISA) for the determination of tissue-bound metabolite 3-amino-2-oxazolidinone (AOZ) is described. The procedures allow for the detection of protein-bound AOZ in the form of a 2-nitrophenyl derivative (2-NP-AOZ) in the sample supernatant or extract after acid hydrolysis and derivatization with o-nitrobenzaldehyde. The polyclonal rabbit antibodies were produced with the immunogen hapten, 2-NP-HXA-AOZ, and the 50% inhibition values (IC(50)) of 0.14 microg kg(-1) of AOZ was achieved with the most sensitive antibody A0505. The mean lower detection limit of the ELISA method is about 0.025 microg kg(-1). According to the test preparation record, the detection limit is 0.1 microg kg(-1), which is well below the minimum required performance limits (MRPLs) for tissue-bound residues of AOZ at 1 microg kg(-1) in the European Communities. In the present study, we investigated the use of homemade ELISA, a new immunoassay, to monitor the presence of the furazolidone marker residue in 370 samples of cultured fish. Adopting 0.3 microg kg(-1) AOZ as a cutoff value, the ELISA has a sensitivity of 100% and a specificity of 98.5% versus high-performance liquid chromatography-mass spectrometry (HPLC-MS) at a cutoff of 0.3 microg kg(-1) and gives no false-negative rate results. From the practical point of view, the homemade kit could be advantageously used for the screening of large groups of animal-edible tissue samples and the kit employed has good reliability even in routine application for the control of the illegal use of the drug.