Synthesis, structure and antitumor activities of [Ni(dien)2][Ni(CN)4] complex

EDP Sciences - Tập 9 - Trang 229-233 - 2004
Li Tao1, Liang Feng2, Zhang Shi-wei3, Wu Cheng-tai2
1Department of Ophthalmology, The Affiliated Tongji Hospital, Tongji Medical College of Huazhong University of Science and Technology, Wuhan, Hubei, China
2College of Chemistry and Molecular Sciences, Wuhan University, Wuhan, Hubei, China
3State Key Laboratory for Structural Chemistry of Stable and Unstable Species, Peking University, Beijing, China

Tóm tắt

Ni(II)-dien complex was prepared and characterized by X-ray diffraction. The crystal belongs to triclinic system, space group P-1, with crystallographic parametersa=0.888 13(18) nm,b=0.890 10(18) nm,c=1. 591 8(3) nm, α=77.71(3)°, β=89.12(3)°, γ=61.24(3)°,Z=2. The two dien molecules coordinate to the central Ni atom, the six nitrogen atoms form a distorted octahedron. Preliminary pharmacological tests showed this complex had antitumor activity against HepG2 and HL-60 cell linesin vitro.

Tài liệu tham khảo

Thomas T, Thomas T J. Polyamines in Cell Growth and Cell Death: Molecular Mechanisms and Therapeutic Applications.Cell Mol Life Sci, 2001,58:244–258. Shah N, Antony T, Haddad S, eitet al. Antitumor Effects of Bis(ethyl)Polyamines Analogs on Mammary Tumor Development in FVB/NTgN (MMTVneu) Transgenic Mice.Cancer Lett, 1999,146:15–23. Fraser A V, Woster P M, Wallace H M. Induction of Apoptosis in Human Leukaemic Cells by IPENSpm, a Novel Polyamine Analogue and Anti-Metabolite.Biochem J, 2002,367:307–312. Kingsnorth A N, Wallace H M, Bundred N J,et al. Polyamines in Breast Cancer.Br J Surgery, 1984,71:352–356. Kingsnorth A N, Lumsden A B, Wallace H M. Polyamines in Colorectal Cancer.Br J Surgery, 1984,71:791–794 Yoshinari K, Yamazaki K, Komiyama M. Oligoamines as Simple and Efficient Catalysts for RNA Hydrolysis.J Am Chem Soc, 1991,113:5899–5901. Komiyama M, Yoshinari K. Kinetic Analysis of Diamine-Catalyzed RNA Hydrolysis.J Org Chem, 1997,62:2155–2160. Carotti S, Guerri A, Mazzei T,et al. Gold (III) Compounds as Potential Antitumor Agents: Cytotoxicity and DNA Binding Properties of Some Selected Polyamine-Gold (III) Complexes.Inorg Chim Acta, 1998,281:90–94. Messori L, Abbate F, Marcon G,et al. Gold(III) Complexes as Potential Antitumor Agents: Solution Chemistry and Cytotoxic Properties of Some Selected Gold(III) Compounds.J Med Chem, 2000,43:3541–3548. Wu M H, Cheng G P, He Y B,et al. A Practical Synthesis of Hydroxyl-N-Tosylcyclams via Cyclization of 1,3-Dichloro-2-Propanol with Disodium Di (poly)-N-Tosylamides.Syn Commun, 1995,25:1427–1431. Xue G P, Liu Y, Wu C T. A Practical Synthesis of Novel Hydroxyl-Substituted Macrocyclic Tri-, Tetra- and Hexa-Amines.Chin J Chem, 1998,16:538–541. Liang F, Wu X, Zhang S,et al. A Convenient Synthesis and Crystal Structure of Octahydro-Pyrazino[1, 2-a] Pyrazine.Syn Commun, 2004,34:827–833. Liang F, Wu C T, Li Z Y,et al. Synthesis and Antitumor Activities of Hydroxyl-Substituted Macrocyclic Polyamines and Their Complexes.Chemical Journal on Internet, 2003,5:6. Liang F, Wu C T, Lin H,et al. Copper Complex of Hydroxyl-Substituted Triazamacrocyclic Ligand and Its Antitumor Activity.Bioorg Med Chem Lett, 2003,13:2469–2472. Liang Feng, Wei Jun, Li Zhao-yang,et al. Hydroxyl Macrocyclic Polyamines Coordination Systems Interaction with DNA and Their Antitumor Activitiesin vitro.Chem J Chin Univ, 2004,25:1190–1193 (Ch). Liang F, Wang P, Zhou X,et al. Nickle(II) and Cobalt(II) Complexes of Hydroxyl-Substituted Triazamacrocyclic Ligand as Potential Antitumor Agents.Bioorg Med Chem Lett, 2004,14(7):841–844.