RESUMEN
A simple preparation of Cd(17)S(4)(SCH(2)CH(2)OH)(26) clusters in aqueous solution leads to the formation of colorless blocky crystals. X-ray structure determinations revealed a superlattice framework built up of covalently linked clusters. This superlattice is best described as two enlarged and interlaced diamond or zinc blende lattices. Because both the superlattice and the clusters display the same structural features, the crystal structure resembles the self-similarities known from fractal geometry. The optical spectrum of the cluster solution displays a sharp transition around 290 nanometers with a large absorption coefficient ( approximately 84,000 per molar per centimeter).
RESUMEN
By examining the time course, from E15 to 720 days of age, for changes in the prevalence of mRNAs coding for neural cell adhesion molecule (NCAM), N-cadherin and alpha-tubulin in rat hippocampus and forebrain, it was concluded that (i) the NCAM 7.4-, 6.7-, 5.2-, 4.3- and 2.9-kb mRNAs are differentially regulated during development and aging; (ii) the 7.4- and 6.7-kb mRNA are drastically reduced starting from day 21 onward; (iii) the E15- and day-1-specific mRNA of 4.3 kb is replaced with the 5.2-kb mRNA starting with 21 days, thereafter the 5.2-kb message remained relatively constant over the entire life-span studied. Likewise, the 2.9-kb mRNA, which was very abundantly expressed at E15 and early postnatal stages, remained relatively constant between 180 days and 720 days; (iv) postnatal rat brains showed both qualitative and quantitative changes in N-cadherin 4.3- and 4.0-kb transcripts. The 4.3-kb mRNA was relatively abundant at 1 and 21 days postnatal stages, thereafter the signal remained very low over the entire life-span studied. The 4.0-kb message, which was specific for the E15 stage, was replaced with the 4.3-kb message; (v) as expected, the 1.8-kb mRNA coding for embryonic alpha-tubulin decreased dramatically after 1 day, but became stabilized at moderate levels during the subsequent developmental stages. At least for the NCAM gene, the regulation seems to occur post-transcriptionally, possibly at the level of RNA processing while the N-cadherin mRNA expression seems to be transcriptionally regulated.
Asunto(s)
Envejecimiento/metabolismo , Cadherinas/metabolismo , Moléculas de Adhesión Celular Neuronal/metabolismo , Envejecimiento/genética , Animales , Cadherinas/genética , Moléculas de Adhesión Celular Neuronal/genética , Regulación de la Expresión Génica , Crecimiento/genética , Crecimiento/fisiología , Hipocampo/crecimiento & desarrollo , Hipocampo/metabolismo , Masculino , ARN Mensajero/genética , ARN Mensajero/metabolismo , Ratas , Ratas Endogámicas F344RESUMEN
In the present study, using RNA gel-blot analysis, we characterized the developmental changes in the prevalence of mRNA coding for fibronectin (FN), glial fibrillary acidic protein (GFAP), neurotrophic protein S100 beta, and beta-actin mRNA in rat hippocampus and forebrain from 1 to 720 days of age. We found that the FN and mRNA containing the V segment (FN-V) was relatively abundant at early postnatal stages, but very few transcripts were detected in adult rats. However, the hybridization signal for the juvenile FN-V mRNA was up to approximately 8-fold increased in some but not all 24-versus 6-month-old rats. Also, GFAP and S100 beta transcripts were faintly expressed at an early developmental stage, then the level of expression steadily increased starting with day 21. The greatest increase averages approximately 1.8-fold for GFAP in 24-month-old rats, and approximately 1.5-fold for S100 beta in 15-month-old versus 6-month-old rats. As all these messages are localized primarily in astrocytes, we conclude that (a) astrocyte might play an active role in aging hippocampus and (b) an increase in S100 beta and GFAP mRNA expression may precede that for FN-V mRNA expression in a hypothetical pathway of molecular events underlying neurodegeneration in the hippocampus of old rats. We also note the considerable variability among the 24-month-old rats, suggesting that aging is an individual process.
Asunto(s)
Envejecimiento/metabolismo , Fibronectinas/biosíntesis , Proteína Ácida Fibrilar de la Glía/biosíntesis , Hipocampo/metabolismo , Proteínas S100/biosíntesis , Actinas/biosíntesis , Actinas/genética , Empalme Alternativo , Animales , Astrocitos/metabolismo , Northern Blotting , Proteínas de Unión al Calcio/biosíntesis , Proteínas de Unión al Calcio/genética , Fibronectinas/genética , Expresión Génica , Proteína Ácida Fibrilar de la Glía/genética , Masculino , Factores de Crecimiento Nervioso , Prosencéfalo/metabolismo , ARN Mensajero/biosíntesis , Ratas , Ratas Endogámicas F344 , Subunidad beta de la Proteína de Unión al Calcio S100 , Proteínas S100/genética , Organismos Libres de Patógenos Específicos , Transcripción GenéticaRESUMEN
In this study we investigated the splicing pattern of fibronectin (FN) mRNA during development and aging by using Northern blot hybridization with probes that either recognize all forms of FN mRNA or that are specific for the different spliced forms (FN-EIIIA, FN-EIIIB, and FN-V). We find that (1) the FNmRNA in the hippocampus of some but not all old rats showed a pattern of splicing similar to that found in the forebrain of 21 day old rats and (2) the hybridization signal for the alternatively spliced FN mRNA containing the EIIIA, EIIIB, and V95 segments was relatively abundant at early postnatal stages but very few transcripts were detected in adult and old rats. However, the hybridization signal for the juvenile FN-V mRNA was markedly increased in some but not all two-year-old rats suggesting that aging is an individual process.
Asunto(s)
Envejecimiento/metabolismo , Fibronectinas/biosíntesis , Hipocampo/metabolismo , Proteínas del Tejido Nervioso/biosíntesis , Empalme del ARN , ARN Mensajero/biosíntesis , Animales , Fibronectinas/genética , Proteína GAP-43 , Hipocampo/crecimiento & desarrollo , Masculino , Glicoproteínas de Membrana/biosíntesis , Proteínas del Tejido Nervioso/genética , Proteínas de Neurofilamentos/biosíntesis , Hibridación de Ácido Nucleico , ARN Mensajero/genética , Ratas , Ratas Endogámicas F344/metabolismo , Organismos Libres de Patógenos EspecíficosRESUMEN
The self-assembly of helical supramolecular structures from chiral building units is a basic principle of biological materials. The mesoscopic structure of a chiral molecular aggregate, which formed spontaneously from a nonchiral J-aggregating cyanine dye in aqueous solution, is presented. In single crystals (as shown in the picture) a coexistance of planar molecules with left- and right-handed twisted conformers of the same dye are found; the latter may act as templates to build up the helical superstructures.
Asunto(s)
Carbocianinas/química , Dicroismo Circular , Cristalografía por Rayos X , Cristales Líquidos/química , Conformación Molecular , Solventes/química , Estereoisomerismo , TemperaturaRESUMEN
Octakis(2,3,6-tri-O-methyl)-gamma-CD (TRIMEG) cocrystallized at 18 degrees C with 4.5 water molecules in the orthorhombic space group P2(1)2(1)2(1), unit cell dimensions a = 10.7879(3), b = 29.0580(9), c = 32.2909(11) A. The TRIMEG macrocycle is in a 'round' form with all glucose units oriented syn, and one O-6-CH3 methoxy group points 'toward' the molecular cavity. The TRIMEG x 4.5 H2O molecules are stacked to form infinite cylinders with the central cavities aligned into channels filled for each TRIMEG by 4.5 water molecules distributed over 15 partially occupied sites. This structure differs from the two known structures of TRIMEG in which two diametrically opposed glucoses are oriented anti to yield an 'elliptical' form, and their O-6-CH3 groups are directed 'toward' the cavity and close it at this side to form a bowl-shaped molecule.
Asunto(s)
Ciclodextrinas/química , Oligosacáridos/química , gamma-Ciclodextrinas , Conformación de Carbohidratos , Cristalización , Cristalografía por Rayos X , Modelos Moleculares , Agua/químicaRESUMEN
Hexakis(2,6-di-O-methyl)-alpha-cyclodextrin (DIMEA) crystallizes from 1:1 water-acetonitrile as DIMEA-acetonetril-dihydrate in the orthorhombic space group P2(1)2(1)2(1), unit cell dimensions a = 14.2775(5), b = 15.7312(5), c = 31.1494(11) A. Refinement of the structure against 5540 X-ray diffraction data converged at an R factor of 0.083. The macrocycle exhibits a 'round' conformation and is stabilized by intramolecular, interglucose O-3-H(n)...O-2(n + 1) and C-6-H(n)...O-5(n + 1) hydrogen bonds. Acetonitrile is included in the central cavity of DIMEA and held in position by C-5-H...N interactions. The two water molecules in the asymmetric units are distributed over six sites. One is fully occupied due to hydrogen bonding to O-3 groups of two symmetry-related DIMEA molecules, whereas the five remaining sites show occupancies between 0.15 and 0.25. These sites are in hydrogen bonding contact with O...O distances between 2.59 and 3.50 A and are located in infinite, hydrophobic channels parallel to the alpha-axis, which are coated with methyl groups of symmetry-related DIMEA.
Asunto(s)
Ciclodextrinas/química , Agua/química , alfa-Ciclodextrinas , Dicroismo Circular , Cristalografía por Rayos X , Enlace de Hidrógeno , Modelos MolecularesRESUMEN
The molecular and crystal structures of 16 N-n-alkyl N,N-dimethylammonioacetic acid bromides with chain lengths between n = 1 and n = 16 have been determined. All compounds from n = 5 to n = 16 form bilayers with interdigitated chains. The even-numbered chains display the chain packing type M2(II). The chain packing of the odd-numbered chain compounds is less regular. The head groups of all compounds are connected via electrostatic N+...Br- interactions, and by OH...Br- hydrogen bonds. The compounds with short chains are packed in different ways. Their molecular conformation depends on the crystal packing.
RESUMEN
The existence of a new crystalline modification of the analgesic and antiinflammatory agent piroxicam was predicted. A model of the structure was derived from the crystal data of the alpha-modification. Lattice constants and molecular packing parameters were refined using X-ray powder diffraction data.
Asunto(s)
Piroxicam/análisis , Fenómenos Químicos , Química Física , Cristalización , Difracción de Rayos XRESUMEN
The crystal structure of the hydrate of the antiphlogistic drug diclofenac sodium was determined to explain the unusual dissolution behaviour in ethyl acetate. The compound crystallizes in the monoclinic space group P2(1)/m with a = 9.464(2), b = 39.405(7), c = 9.972(3) A und beta = 90.74(2) degrees. The unit cell contains two symmetry independent formula units (C14H10Cl2NO2)-Na+.3,94 H2O. There are molecule layers and sodium-water layers which show order-disorder phenomena.
Asunto(s)
Diclofenaco/análisis , Cristalización , Conformación Molecular , Difracción de Rayos XRESUMEN
The crystal and molecular structure of the potential cardiotonic agent AWD 122-60 have been determined by X-ray structure analysis. Based on the molecular structure charge distribution and molecular electrostatic potential were evaluated. The results are discussed in comparison with those of other cardiotonic 3,4'-bipyridines.
Asunto(s)
Cardiotónicos/síntesis química , Nitrilos/síntesis química , Piridinas/síntesis química , Cardiotónicos/farmacología , Fenómenos Químicos , Química Física , Cristalización , Electroquímica , Conformación Molecular , Nitrilos/farmacología , Piridinas/farmacología , Difracción de Rayos XRESUMEN
The results of an X-ray structure analysis of the alpha-modification were the starting point for the prediction and establishment of further polymorphic and pseudopolymorphic, respectively, forms of AWD 122-14. A complete structure determination of the gamma- and delta-modifikation as well as of a hydrochloride monohydrate could be carried out. Molecular parameters, conformational flexibility, and intermolecular interactions are discussed in this paper.
Asunto(s)
Cardiotónicos/síntesis química , Morfolinas/síntesis química , Piridinas/síntesis química , Cardiotónicos/química , Cristalización , Conformación Molecular , Morfolinas/química , Piridinas/química , Difracción de Rayos XRESUMEN
The crystal and molecular structures of the alpha-, beta-, and gamma-modification of the cardiotonic compound milrinone have been determined by X-ray structure analyses. In all modifications the molecules exist in the lactam form. Because of steric hindrances the pyridine rings deviate considerably from coplanarity. The dihedral angle amounts to 45 degrees in milrinone-alpha, 43.7 degrees in milrinone-beta, and 57.5 degrees in milrinone-gamma. In the three crystal structures molecules are connected via hydrogen bonds forming dimers. These are centrosymmetric in milrinone-alpha and -beta. In milrinone-gamma the molecules within a dimer are symmetry related by a twofold axis. The dimers are linked by charge transfer interactions. This leads to infinite chains in the alpha- and beta-modification and to infinite layers in milrinone-gamma.
Asunto(s)
Piridonas/análisis , Cristalización , Milrinona , Conformación Molecular , Difracción de Rayos XRESUMEN
The preparation and X-ray crystallographic characterisation of 10 polymorphic or pseudo-polymorphic forms of the novel cardiotonic AWD 122-14 are described. Thermic transformations of some polymorphic forms into the alpha-form was proved by thermogravimetric analysis and powder diffraction pattern. In dissolution behaviour no significant differences were found between the crystalline modifications but with regard to galenic processing compact alpha-, gamma- and epsilon-forms show advantages.
Asunto(s)
Cardiotónicos/síntesis química , Morfolinas/síntesis química , Piridinas/síntesis química , Cardiotónicos/química , Morfolinas/química , Piridinas/química , Difracción de Rayos XRESUMEN
The configurational isomers of the 2-amino-5-chlorbenzophenoneamidinohydrazones could be obtained as TLC pure samples by fractionating crystallization of the product mixture. The determination of their configuration by comparison of the UV spectra with the corresponding oximes could be confirmed by X-ray structure analysis.
Asunto(s)
Antiarrítmicos/síntesis química , Benzofenonas/síntesis química , Hidrazonas/síntesis química , Antiarrítmicos/farmacología , Benzofenonas/farmacología , Cromatografía en Capa Delgada , Cristalización , Hidrazonas/farmacología , Conformación Molecular , Espectrofotometría Ultravioleta , Difracción de Rayos XRESUMEN
The anti-inflammatory drug piroxicam, 4-hydroxy-2-methyl-N-(2-pyridyl)2H-1,2- benzothiazine-3-carboxamide-1,1-dioxide, crystallizes in three different forms, two anhydrates and one monohydrate. Crystal structure analyses of the monohydrate and one of the anhydrate were carried out by Bordner et al. and Kojic-Prodic et al., respectively. In this paper the results of the analysis of the third piroxicam modification and of an independently performed structure determination of the monohydrate are reported. Molecular structures and hydrogen bonding of all modifications are discussed.
Asunto(s)
Piroxicam/análisis , Fenómenos Químicos , Química , Cristalización , Conformación Molecular , Difracción de Rayos XRESUMEN
The preparation and characterisation of crystalline alpha-, beta- and gamma modifications of 3-cyan-6-methyl-5-(4-pyrid-4-yl)-1,2-dihydropyrid-2-on e are described. The thermic transformation of alpha- and beta-modification into gamma-modification was proved by thermogravimetric analysis (t.g.a.), differential scanning calorimetry (d.s.c.), IR and powder diffraction pattern. In dissolution behaviour no significant differences were found between the modifications.
Asunto(s)
Piridonas/análisis , Fenómenos Químicos , Química Física , Cristalización , Milrinona , Solubilidad , Espectrofotometría UltravioletaRESUMEN
Cyclisation of the vinylogous amidinium salt 1 or the 4-ethoxy- and 4-morpholino-3-butene-2-ones, respectively, 4 and 6 with cyano-thioacetamide yielded the 5-(4-pyridinyl)-, 6-methyl-5-(4-pyridinyl)- and 6-methyl-5-phenyl-, respectively, substituted 3-cyano-2(1H)-pyridinethiones 3, 5 and 7. The 2(1H)-pyridinethiones 3, 5 and 7a as well as the in 3-position unsubstituted or carbamoyl substituted derivatives 8 and 9 were obtained from the corresponding 2-chloro-pyridines and potassium sulfide, too. Especially compound 5 showed remarkable positive inotropic potency and, additionally, vasodilator activity. The molecular and crystal structure of 5 have been determines by X-ray structure analysis. Based on the molecular structure charge distribution and electrostatic potential were evaluated. The results are discussed in comparison with those of milrinone.