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N-(2-Aminoethyl)maleimide (trifluoroacetate salt) Sale

(Synonyms: N-(2-氨基乙基)马来酰亚胺三氟乙酸盐) 目录号 : GC47717

A thiol-reactive cross-linking agent

N-(2-Aminoethyl)maleimide (trifluoroacetate salt) Chemical Structure

Cas No.:146474-00-2

规格 价格 库存 购买数量
250 mg
¥1,525.00
现货
500 mg
¥2,895.00
现货
1 g
¥4,266.00
现货

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Sample solution is provided at 25 µL, 10mM.

产品文档

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产品描述

N-(2-Aminoethyl)maleimide is a thiol-reactive cross-linking agent.1,2 It has been used in the synthesis of maleimide-functionalized heparin hydrogels in the development of growth factor delivery systems and radiotracers for thiol-mediated protein labelling.

1.Nie, T., Baldwin, A.C., Yamaguchi, N., et al.Production of heparin-functionalized hydrogels for the development of responsive and controlled growth factor delivery systemsJ. Control Release122(3)287-296(2007) 2.Kratz, H., Haeckel, A., Michel, R.P., et al.Straightforward thiol-mediated protein labelling with DTPA: Synthesis of a highly active 111In-annexin A5-DTPA tracerEJNMMI Res.2(1)17(2012)

Chemical Properties

Cas No. 146474-00-2 SDF
别名 N-(2-氨基乙基)马来酰亚胺三氟乙酸盐
Canonical SMILES O=C(C=C1)N(CCN)C1=O.OC(C(F)(F)F)=O
分子式 C6H8N2O2.CF3COOH 分子量 254.2
溶解度 DMF: 30 mg/ml,DMSO: 30 mg/ml,Ethanol: 30 mg/ml,PBS (pH 7.2): 10 mg/ml 储存条件 Store at -20°C
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储备液的保存方式和期限:-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。
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溶解性数据

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1 mg 5 mg 10 mg
1 mM 3.9339 mL 19.6696 mL 39.3391 mL
5 mM 0.7868 mL 3.9339 mL 7.8678 mL
10 mM 0.3934 mL 1.967 mL 3.9339 mL
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Research Update

One-pot two-step radiosynthesis of a new (18)F-labeled thiol reactive prosthetic group and its conjugate for insulinoma imaging

Mol Pharm 2014 Nov 3;11(11):3875-84.PMID:24798315DOI:PMC4224565

N-(2-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)ethyl)-6-fluoronicotinamide ([(18)F]FNEM), a novel prosthetic agent that is thiol-specific, was synthesized using a one-pot two-step strategy: (1) (18)F incorporation by a nucleophilic displacement of trimethylammonium substrate under mild conditions; (2) amidation of the resulting 6-[(18)F]fluoronicotinic acid 2,3,5,6-tetrafluorophenyl ester with N-\(2-Aminoethyl\)maleimide trifluoroacetate salt. The radiosynthesis of the maleimide tracer was completed in 75 min from [(18)F]fluoride with 26 ± 5% decay uncorrected radiochemical yield, and specific activity of 19-88 GBq/μmol (decay uncorrected). The in vitro cell uptake, in vivo biodistribution, and positron emission tomography (PET) imaging properties of its conjugation product with [Cys(40)]-exendin-4 were described. [(18)F]FNEM-Cys(40)-exendin-4 showed specific targeting of glucagon-like peptide 1 receptor (GLP-1R) positive insulinomas and comparable imaging results to our recently reported [(18)F]FPenM-Cys(40)-exendin-4.