RESUMEN
The mol-ecule of the title compound, C(24)H(16)BrN(3)OS(3), contains three approximately planar fragments, viz. an oxadiazole ring plus two adjacent thio-phene groups, and two phenothia-zine benzene rings, with largest deviations from the least-squares planes of 0.051â (3), 0.019â (4) and 0.014â (3)â Å, respectively. The phenothia-zine unit adopts a butterfly conformation, with a dihedral angle of 38.06â (15)° between the terminal benzene rings. The dihedral angle between the 2,5-bis-(thio-phen-2-yl)oxadiazole unit and the attached benzene ring is 15.35â (11)°. In the crystal, mol-ecules form stacks along the b-axis direction; neighboring mol-ecules within the stack are related by inversion centers, with shortest inter-centroid separations of 3.741â (2) and 3.767â (2)â Å.
RESUMEN
In the title compound, C(17)H(15)N(3)OS, the phenothia-zine ring system is slightly bent, with a dihedral angle of 13.68â (7)° between the benzene rings. The dihedral angle between the oxadiazole ring and the adjacent benzene ring is 7.72â (7)°. In the crystal, a π-π inter-action with a centroid-centroid distance of 3.752â (2)â Å is observed between the benzene rings of neighbouring mol-ecules.
RESUMEN
OBJECTIVE: To study the nuclear translocation of extracellular signal regulated kinase (ERK) and expression of c-fos mRNA under stimulation of AngII as well as the influence on the nuclear translocation of ERK with different interferences in neonatal cultured cardiomyocytes. METHODS: ERK in the cytoplasm or nucleus was observed by immunocytochemistry using specific antibody and the expression of c-fos was evaluated with RT-PCR technique. RESULTS: AngII (10(-6) mol/L) had the effect in promoting activation of ERK and then appeared in nucleus rapidly. The translocation process of ERK induced by AngII was blocked distinctly by Valsartan (10(-5) mol/L) and PD98059 (5 x 10(-5) mol/L), but not by CGP42112A (10(-5) mol/L). It was also found that Valsartan and PD98059 could inhibit the expression of c-fos in that process. CONCLUSION: The nuclear translocation of ERK might be a precondition for the inducement of c-fos expression.
Asunto(s)
Angiotensina II/farmacología , Proteínas Quinasas Activadas por Mitógenos/metabolismo , Miocardio/metabolismo , Proteínas Proto-Oncogénicas c-fos/metabolismo , Transporte Activo de Núcleo Celular , Animales , Animales Recién Nacidos , Células Cultivadas , Femenino , Masculino , Proteínas Quinasas Activadas por Mitógenos/genética , Miocardio/citología , Proteínas Proto-Oncogénicas c-fos/genética , ARN Mensajero/genética , Ratas , Ratas Sprague-DawleyRESUMEN
The square-planar diimine-platinum(II) complex, Pt(4-Brbpy)(C≡CC6H5)2 (1) (4-Brbpy = 4-bromo-2,2'-bipyridine), was prepared and characterized. Solid-state 1 exhibits reversible thermo- and mechanical-grinding-triggered color and luminescence changes. When crystalline 1·2(CH2Cl2) or 1·2(CHCl3) are heated or ground, the original bright yellow-green emission centered at 525 (549, sh) nm changed to 637 and 690 nm, corresponding to thermo- and mechanochromic response shifts of approximately 88-112 nm and 141-165 nm, respectively. Meanwhile the crystalline state changes into an amorphous phase in both processes. Once the amorphous sample absorbs organic vapors, it can be reverted to the original crystalline state, along with red luminescence turning back to yellow-green emission. The reversibility of thermo- and mechanical-grinding-triggered chromic luminescence properties has been dynamically monitored by emission spectra and X-ray diffraction patterns. The dramatic thermo- and mechanical-grinding-triggered emission red shifts are most likely due to the conversion of the (3)MLCT/(3)LLCT emission state into the (3)MMLCT triplet state.
RESUMEN
The planar platinum(II) complex [Pt(Me3SiC≡CbpyC≡CSiMe3)(C≡CC6H4Et-4)2] (1) with 5,5-bis(trimethylsilylethynyl)-2,2'-bipyridine was prepared and characterized. Solid-state 1 exhibits unusual, selective and reversible luminescence vapochromism to CH3CN and ClCH2CN vapors, which is useful for the detection of these hazardous vapors. A vapochromic cycle was monitored by dynamic variations in emission spectra and X-ray diffraction (XRD) patterns. Both X-ray crystallographic and density functional theory studies suggest that the vapochromic and vapoluminescent behavior of 1 are induced by the variation in the intermolecular Pt-Pt interactions.