Protein Information

ID 4757
Name suppressor of cytokine signaling
Synonyms CIS; Cis1; CIS 1; CISH; Cytokine inducible SH2 containing protein; G18; Protein G18; SOCS…

Compound Information

ID 1819
Name piperazine
CAS piperazine

Reference

PubMed Abstract RScore(About this table)
11754267 Navarro M, Cisneros-Fajardo EJ, Lehmann T, Sanchez-Delgado RA, Atencio R, Silva P, Lira R, Urbina JA: Toward a novel metal-based chemotherapy against tropical diseases. 6. Inorg Chem. 2001 Dec 31;40(27):6879-84.
Synthesis and characterization of new copper (II) and gold (I) clotrimazole and ketoconazole complexes and evaluation of their activity against Trypanosoma cruzi.. The complexes [Cu (CTZ)(4)] Cl (2).2H (2) O (1), [Cu (CTZ) Cl (2)](2) (2), [Cu (KTZ)(3) Cl (2)] (3), and [Cu (KTZ) Cl (2)](2).2H (2) O (4) were prepared by reaction of CuCl (2) with CTZ and KTZ (where CTZ = 1-[[(2-chlorophenyl) diphenyl] methyl]-1H-imidazole and KTZ = cis-1-acetyl-4-[4-[[2-(2,4-dichlorophenyl)-2-(1H-imidazol-1-ylmethyl)-1,3- dioxolan-4-yl] methoxy] phenyl] piperazine), respectively, in acetonitrile at different ligand to metal molar ratios. Gold complexes [Au (PPh (3))(CTZ)] PF (6) (5) and [Au (PPh (3))(KTZ)] PF (6).H (2) O (6) were synthesized by reaction of AuClPPh (3), with KPF (6) and CTZ or KTZ in acetonitrile. All the new compounds were characterized by NMR spectroscopy and microanalytical methods, and for the paramagnetic species EPR spectroscopy and DC magnetic susceptibility measurements were also employed. The solid-state structure of 1 has been determined by X-ray crystallography. 1 crystallizes in the triclinic space group P (-) 1, with a = 12.773 (2) A, b = 15.326 (4) A, c = 11.641 (2) A, V = 1957.4 (7) A (3), Z = 1, and D (calcd) = 1.284 g/cm (3). The structure refinement converged at R1 = 0.0731 and wR2 = 0.1962. Complex 1 displayed a square-planar structure typical for tetrakis (imidazole) copper (II) complexes. The new compounds were tested for in vitro activity against cultures of epimastigotes of Trypanosoma cruzi, the causative agent of Chagas disease. At concentrations equivalent to 10 (-6) M of total CTZ or KTZ (in DMSO) all the complexes exhibited significantly higher growth inhibitory activity than their respective parental compounds.
31(0,1,1,1)