Synthesis, crystal structure and biological evaluation of spectroscopic characterization of Ni(II) and Co(II) complexes with N-salicyloil-N-maleoil-hydrazine as anticholinergic and antidiabetic agents

被引:44
作者
Gondolova, Gulnar [1 ]
Taslimi, Parham [2 ]
Medjidov, Ajdar [3 ]
Farzaliyev, Vagif [4 ]
Sujayev, Afsun [4 ]
Huseynova, Mansura [5 ]
Sahin, Onur [6 ]
Yalcin, Bahattin [7 ]
Turkan, Fikret [8 ]
Gulcin, Ilhami [2 ]
机构
[1] Inst Ecol & Nat Resources, Dept Azerbaijan Natl Acad Sci, Ganja, Azerbaijan
[2] Ataturk Univ, Fac Sci, Dept Chem, Erzurum, Turkey
[3] Azerbaijan Natl Acad Sci, Dept Coordinat Cpds, Inst Catalysis & Inorgan Chem, Baku, Azerbaijan
[4] Azerbaijan Natl Acad Sci, Lab Theoret Bases Synth & Act Mech Addit, Inst Chem Addit, Baku, Azerbaijan
[5] Azerbaijan Natl Acad Sci, Inst Chem Addit, Baku, Azerbaijan
[6] Sinop Univ, Sci & Technol Res Applicat & Res Ctr, Sinop, Turkey
[7] Marmara Univ, Dept Chem, Fac Arts Sci, Istanbul, Turkey
[8] Igdir Univ, Hlth Serv Vocat Sch, Igdir, Turkey
关键词
crystal structure; enzyme inhibition; magnetic properties; N-salicyloil-N'-maleoil-hydrazine; synthesis; CARBONIC-ANHYDRASE ISOENZYMES; ALPHA-GLUCOSIDASE INHIBITORS; II INHIBITION; MANNICH-BASES; ACETYLCHOLINESTERASE; BUTYRYLCHOLINESTERASE; DERIVATIVES; PROFILES; BROMOPHENOLS; BIOACTIVITY;
D O I
10.1002/jbt.22197
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
[Ni(C11H9N2O5)(2)(H2O)(2)]center dot 3(C3H7NO) (1) and [Co(C11H9N2O5)(2)(H2O)(2)]center dot 3(C3H7NO) (2) are synthesized and characterized by elemental analysis, FT-IR spectra, magnetic susceptibility, and thermal analysis. In addition, the crystal structure of Ni(II) complex is presented. Both complexes show distorted octahedral geometry. In 1 and 2, metal ions are coordinated by two oxygen atoms of salicylic residue and two nitrogen atoms of maleic amide residue from two ligands, and two oxygen atoms from two water molecules. In this paper, both compounds showed excellent inhibitory effects against human carbonic anhydrase (hCA) isoforms I, and II, -glycosidase, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE). Compounds 1 and 2 had Ki values of 18.36 +/- 4.38 and 26.61 +/- 7.54 nM against hCA I and 13.81 +/- 3.02 and 29.56 +/- 6.52 nM against hCA II, respectively. On the other hand, their Ki values were found to be 487.45 +/- 54.18 and 453.81 +/- 118.61 nM against AChE and 199.21 +/- 50.35 and 409.41 +/- 6.86 nM against BChE, respectively.
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页数:8
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