Strategies for improving the water solubility of new antitumour nitronaphthylbutadiene derivatives

Different nitronaphthylbutadienes have been previously proved to have antitumour activity. The main drawback of these derivatives is their low water solubility. With the aim of facilitating the administration of these new drugs we have synthesized the hexyl (2Z,4E)-2-methylsulfanyl-5-(1-naphthyl)-4-nitro-2,4-pentadienoate analogue (1-Naph-NHCB) which is demonstrated to be easily included into cyclodextrins and/or entrapped into liposomes. Its antitumour activity was revealed to be almost comparable with that of the previously studied methyl analogue ester (1-Naph-NMCB). On the other hand, in vitro studies with different cancer cell lines showed that the cytotoxic activity of both 1-Naph-NMCB and 1-Naph-NHCB were fully preserved and in some cases also enhanced when entrapped into liposomal carriers.     

Strain estimates for small-ring cyclic allenes and butatrienes

Isodesmic and homodesmic equations at the B3LYP/6-311+G(d,p)+ZPVE level of theory have been used to estimate strain for the homologous series of cyclic allenes and cyclic butatrienes. A simple fragment deformation approach also has been applied and appears to work better for the larger rings. For the cyclic allene series, estimates for allene functional group strain (kcal/mol) include: 1,2-cyclobutadiene, 65; 1,2-cyclopentadiene, 51; 1,2-cyclohexadiene, 32; 1,2-cycloheptadiene, 14; 1,2-cyclooctadiene, 5; 1,2-cyclononadiene, 2; 1,2,4-cyclohexatriene, 34; and bicyclo[3.2.1]octa-2,3-diene, 39. For cyclic butatrienes, functional group strain estimates include: 1,2,3-cyclobutatriene, >100; 1,2,3-cyclopentatriene, 80; 1,2,3-cyclohexatriene, 50; 1,2,3-cycloheptatriene, 26; 1,2,3-cyclooctatriene, 17; and 1,2,3-cyclononatriene, 4. Barriers to interconversion of enantiomers in cyclic allenes are reduced with increasing strain. Newly predicted values include: 1,2-cyclopentadiene <1 kcal/mol and bicyclo[3.2.1]octa-2,3-diene, 7.4 kcal/mol. Estimated levels of strain parallel the known reactivity of these substances.     

Geographical classification of wine and olive oil by means of classification and influence matrix analysis (CAIMAN)

Classification and influence matrix analysis (CAIMAN) is a new classification method, recently proposed and based on the influence matrix (also called leverage matrix). Depending on the purposes of the classification analysis, CAIMAN can be used in three outlines: (1) D-CAIMAN is a discriminant classification method, (2) M-CAIMAN is a class modelling method allowing a sample to be classified, not classified at all, or assigned to more than one class (confused) and (3) A-CAIMAN deals with the asymmetric case, where only a reference class needs to be modelled.

In this work, the geographic classification of samples of wine and olive oil has been carried out by means of CAIMAN and its results compared with discriminant analysis, by focusing great attention on the model predictive capabilities. The geographic characterization has been carried out on three different datasets: extra virgin olive oils produced in a small area, with a “protected denomination of origin” label, wines with different denominations of origin, but produced in enclosed geographical areas, and olive oils belonging to different production areas.

Final results seem to indicate that the application of CAIMAN to the geographical origin identification offers several advantages: first, it shows – on an average basis – good performances; second, it is able to deal in a simple way classification problems related to tipicity, authenticity, and uniqueness characterization, which are of increasing interest in food quality issues.     

Uniform Hölder Bounds for Nonlinear Schrödinger Systems with Strong Competition

For the positive solutions of the Gross–Pitaevskii system we prove that L^∞‐boundedness implies C^0,α‐boundedness for every α ? (0,1), uniformly as β → +∞. Moreover, we prove that the limiting profile as β → +∞ is Lipschitz‐continuous. The proof relies upon the blowup technique and the monotonicity formulae by Almgren and Alt, Caffarelli, and Friedman. This system arises in the Hartree‐Fock approximation theory for binary mixtures of Bose–Einstein condensates in different hyperfine states. Extensions to systems with k > 2 densities are given. © 2009 Wiley Periodicals, Inc.     

Study and characterization of mural paintings from XIX Century in a noble Venetian (Italy) palace

The present paper describes the characterization carried out on the roof of a private palace located in the historical center of Venice (Italy). We focused our attention on the studies of original constituent materials (pigments and binders), in order to identify the pictorial technique of the artist and verify the stylistic attribution to Giuseppe Borsato, a Venetian painter operating between 18th and 19th century. Characterization of collected samples was carried on using both conventional and advanced analytical techniques, such as Optical Microscopy and Scanning Electron Microscopy coupled with Energy Dispersive X-Ray (SEM–EDS) microscopy, Fourier Transform Infrared Spectroscopy (FTIR) and High Performance Liquid Chromatography (HPLC) coupled with photodiode array detection (DAD) and Mass Spectrometry (MS). The finding of dating pigments (such as Cobalt blue and Cu–As based green) and of a complex binding's mixture compatible with the considered supposed period, allowed us to confirm the attribution hypothesis.     

Angle-resolved photoelectron spectroscopy of randomly oriented 3-hydroxytetrahydrofuran enantiomers.

Circular dichroism in the angular distribution of valence photoelectrons emitted from randomly oriented 3-hydroxytetrahydrofuran enantiomers (ThS and ThR) has been observed in gas-phase experiments using circularly polarized vacuum ultraviolet (VUV) light. The measured dichroism for both ThS and ThR, acquired at the single magic angle theta=234.73 degrees and at photon energies of 22, 19, 16, and 14 eV, points to an asymmetric forward-backward scattering of the photoelectrons from their highest occupied molecular orbitals (HOMO) HOMO-1 and HOMO-2, of up to 5%, depending on the photon energy. The asymmetry reverses on exchange of either the helicity of the radiation or the configuration of Th. The photoionization dichroic D parameters of ThS and ThR have been measured and their values discussed in the light of LCAO B-spline density functional theory (DFT) predictions. While an acceptable agreement is found between the dichroic parameter measured and calculated at the highest photon energy for the HOMO and HOMO-2 orbitals of Th, a significant discrepancy is observed for the HOMO-1 state which is attributed to the floppiness of Th, in particular to the comparatively large sensitivity of the size and shape of its HOMO-1 on nuclear vibrational motion.     

Atomistic fibrillar architectures of polar prion-inspired heptapeptides

This article provides the computational prediction of the atomistic architectures resulting from self-assembly of the polar heptapeptide sequences NYNYNYN, SYSYSYS and GYGYGYG. Using a combination of molecular dynamics and a newly developed tool for non-covalent interaction analysis, we uncover the properties of a new class of bionanomaterials, including hydrogen-bonded polar zippers, and the relationship between peptide composition, fibril geometry and weak interaction networks. Our results, corroborated by experimental observations, provide the basis for the rational design of prion-inspired nanomaterials.

This article provides the computational prediction of the atomistic architectures resulting from self-assembly of the polar heptapeptide sequences NYNYNYN, SYSYSYS and GYGYGYG.     

The outer-sphere oxidation of nitrosyliron(II)hemoglobin by peroxynitrite leads to the release of nitrogen monoxide

It has been suggested that nitrosyliron(II)hemoglobin may represent a form of stabilized NO. and may be responsible for NO. delivery in the peripheral circulation. In this work, we show that NO. can be released from nitrosyliron(II)hemoglobin through reaction with peroxynitrite. Outer-sphere oxidation of the iron center generates nitrosyliron(III)hemoglobin, from which NO. dissociates at a rate of ca. 1 s(-1). The second-order rate constant for the reaction of peroxynitrite with nitrosyliron(II)hemoglobin is (6.1 +/- 0.3) x 10(3) M(-1) s(-1) (at pH 7.2 and 20 degrees C). In the presence of 1.2 mM CO(2), the rather large value of the second-order rate constant, (5.3 +/- 0.2) x 10(4) M(-1) s(-1) (at pH 7.2 and 20 degrees C), indicates that this reaction may take place in vivo. The reactive nitrogen species generated from this reaction, N(2)O(3) and/or NO(2), may lead to protein modifications, such as nitration of tyrosine and/or tryptophan residues and nitrosation of cysteine residues.     

Small reorganisation energy and unique stabilisation of zwitterionic C60-acceptor moieties

Fulleropyrrolidine- and fulleropyrrolidinium-based donor-acceptor ensembles, C60-Fc, were tested in view of intrinsic reorganisation energies for light-induced electron transfer events; overall, the zwitterionic character of the reduced fulleropyrrolidinium acceptor plays a central role in accelerating charge separation and decelerating charge recombination.     

A case for enantioselective allylic alkylation catalyzed by palladium nanoparticles

Palladium nanoparticles (4 nm, fcc) were prepared through decomposition of [Pd2(dba)3] by H2 in the presence of a chiral xylofuranoside diphosphite. These particles catalyze the allylic alkylation of rac-3-acetoxy-1,3-diphenyl-1-propene with dimethyl malonate leading to an almost total conversion of the (R) enantiomer and almost no reaction with the (S). This gives rise to 97% ee for the alkylation product and a kinetic resolution of the substrate recovered with ca. 90% ee. This behavior was compared to that of a molecular catalyst at various dilutions, and the differences between the two systems are discussed. This is the first colloidal system shown to display such a high enantioselectivity besides the well-known Pt/cinchonidine system.