Synthesis, Crystal Structure and PTPs Inhibition of a Zinc(Ⅱ) Complex with N-(4-hydroxybenzyl)-L-serine
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文摘
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The reaction of the reduced Schiff base HL (N-(4-hydroxybenzyl)-L-serine) with Zn(CH_3COO)_2·2H_2O in aqueous solution afforded [Zn(L)_2]· 3H_2O (I). The complex has been characterized by elemental analysis, FT-IR, powder X-ray diffraction, electrospray ionization mass spectrometry and single-crystal X-ray diffraction. Complex I crystallizes in the orthorhombic system, space group P2_12_12_1, with a = 9.197(2), b = 10.445(2),c = 24.149(5) A, V= 2319.8(8) A~3, Z = 4,C_(20)H_(30)N_2O_(11)Zn, Mr = 539.83,D_c= 1.546 g·cm~3,μ = 1.122 mm~(-1),F(000) = 1128,GOOF= 0.971, the final R = 0.0206 and wR = 0.0506 for 4346 observed reflections (I>2σ(I)). In complex I,each Zn(Ⅱ) ion coordinates with three carboxyl oxygen atoms and two amine nitrogen atoms from three L~-anions, forming a distorted five-coordinated trigonal bipyramidal geometry. Complex I exhibits a 1D wavy chain structure that is extended by hydrogen-bonding interactions to form a supramolecular network. The bioactivity of the complex as a potential PTPs inhibitor in vitro was investigated, displaying potent inhibition against PTP1B (IC_(50), 0.24 μM) and TCPTP (IC_(50), 0.53 μM) with a moderate selectivity. |
来源
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Chinese Journal of Structural Chemistry
,2017,36(2):316-323 【核心库】
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DOI
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10.14102/j.cnki.0254-5861.2011-1355
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关键词
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zinc(Ⅱ) complex
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N-(4-hydroxybenzyl)-L-serine
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crystal structure
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inhibitory activity
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PTP1B,TCPTP
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地址
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1.
Institute of Molecular Science, Shanxi University, Key Laboratory of Chemical Biology and Molecular Engineering of the Education Ministry, Taiyuan, 030006
2.
Beijing Synchrotron Radiation Facility, Institute of High Energy Physics, Chinese Academy of Sciences, Beijing, 100049
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语种
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英文 |
文献类型
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研究性论文 |
ISSN
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0254-5861 |
学科
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化学 |
基金
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国家自然科学基金
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文献收藏号
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CSCD:5924378
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