4.6 Article Proceedings Paper

Chloro-substituted dipicolinate vanadium complexes: Synthesis, solution, solid-state, and insulin-enhancing properties

期刊

JOURNAL OF INORGANIC BIOCHEMISTRY
卷 103, 期 4, 页码 575-584

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jinorgbio.2008.12.015

关键词

Vanadium complexes; Chlorodipicolinate; Dipicolinate; 4-Chloro-2,6-dicarboxypyridine; V-51 NMR spectroscopy; Solid-state NMR; Electronic structure; Isotropic; Anisotropy; Electric field gradient tensor; Insulin-enhancing

资金

  1. Direct For Biological Sciences
  2. Div Of Molecular and Cellular Bioscience [0815865] Funding Source: National Science Foundation
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [0750079] Funding Source: National Science Foundation

向作者/读者索取更多资源

Three vanadium complexes of chlorodipicolinic acid (4-chloro-2,6-dipicolinic acid) in oxidation states III IV, and V were prepared and their properties characterized across the oxidation states. In addition, the series of hydroxylamido, methylhydroxylamido, dimethylhydroxylamido, and diethylhydroxylamido complexes were prepared from the chlorodipicolinato dioxovanadium(V) complex. The vanadium(V) compounds were characterized in Solution by V-51 and H-1 NMR and in the solid-state by X-ray diffraction and V-51 NMR. Density Functional Theory (DFT) calculations were performed to evaluate the experimental parameters and further describes the electronic structure of the complex. The small structural changes that do occur in bond lengths and angles and partial charges on different atoms are minor compared to the charge features that are responsible for the majority of the electric field gradient tensor. The EPR parameters of the vanadium(IV) complex were characterized and compared to the corresponding dipicolinate complex. The chemical properties of the chlorodipicolinate Compounds are discussed and correlated with their insulin-enhancing activity in streptozoticin (STZ) induced diabetic Wistar rats. The effect of the chloro-substitution on lowering diabetic hyperglycemia was evaluated and differences were found depending on the compounds oxidation state similar as was observed for the vanadium Ill. IV and V dipicolinate complexes (P. Buglyo, D.C. Crans, E.M. Nagy, R.L. Lindo, L. Yang, J.J. Smee, W. Jin, L-H. Chi, M.E. Godzala III, G.R. Willsky, Inorg. Chem. 44 (2005) 5416-5427). However, a linear correlation of oxidation states with efficacy was not observed, which suggests that the differences in mode of action are not simply ail issue of redox equivalents. Importantly, our results contrast the previous observation with the vanadium-picolinate complexes, where the halogen substituents increased the insulin-enhancing properties of the complex (T. Takino, H. Yasui, A. Yoshitake, Y. Hamajima, R. Matsushita, J. Takada, H. Sakurai, J. Biol. Inorg. Chem. 6 (2001) 133-142). Published by Elsevier Inc.

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