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991.
Dr. Ying Fu Dr. Rina Soni Dr. María J. Romero Dr. Ana M. Pizarro Dr. Luca Salassa Dr. Guy J. Clarkson Jessica M. Hearn Dr. Abraha Habtemariam Prof. Dr. Martin Wills Prof. Dr. Peter J. Sadler 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(45):15199-15209
Four chiral OsII arene anticancer complexes have been isolated by fractional crystallization. The two iodido complexes, (SOs,SC)‐[Os(η6‐p‐cym)(ImpyMe)I]PF6 (complex 2 , (S)‐ImpyMe: N‐(2‐pyridylmethylene)‐(S)‐1‐phenylethylamine) and (ROs,RC)‐[Os(η6‐p‐cym)(ImpyMe)I]PF6 (complex 4 , (R)‐ImpyMe: N‐(2‐pyridylmethylene)‐(R)‐1‐phenylethylamine), showed higher anticancer activity (lower IC50 values) towards A2780 human ovarian cancer cells than cisplatin and were more active than the two chlorido derivatives, (SOs,SC)‐[Os(η6‐p‐cym)(ImpyMe)Cl]PF6, 1 , and (ROs,RC)‐[Os(η6‐p‐cym)(ImpyMe)Cl]PF6, 3 . The two iodido complexes were evaluated in the National Cancer Institute 60‐cell‐line screen, by using the COMPARE algorithm. This showed that the two potent iodido complexes, 2 (NSC: D‐758116/1) and 4 (NSC: D‐758118/1), share surprisingly similar cancer cell selectivity patterns with the anti‐microtubule drug, vinblastine sulfate. However, no direct effect on tubulin polymerization was found for 2 and 4 , an observation that appears to indicate a novel mechanism of action. In addition, complexes 2 and 4 demonstrated potential as transfer‐hydrogenation catalysts for imine reduction. 相似文献
992.
Dr. Yao Zhao Dr. Julie A. Woods Dr. Nicola J. Farrer Kim S. Robinson Jitka Pracharova Dr. Jana Kasparkova Olga Novakova Huilin Li Dr. Luca Salassa Dr. Ana M. Pizarro Dr. Guy J. Clarkson Dr. Lijiang Song Prof. Dr. Viktor Brabec Prof. Dr. Peter J. Sadler 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(29):9578-9591
Platinum diam(m)ine complexes, such as cisplatin, are successful anticancer drugs, but suffer from problems of resistance and side‐effects. Photoactivatable PtIV prodrugs offer the potential of targeted drug release and new mechanisms of action. We report the synthesis, X‐ray crystallographic and spectroscopic properties of photoactivatable diazido complexes trans,trans,trans‐[Pt(N3)2(OH)2(MA)(Py)] ( 1 ; MA=methylamine, Py=pyridine) and trans,trans,trans‐[Pt(N3)2(OH)2(MA)(Tz)] ( 2 ; Tz=thiazole), and interpret their photophysical properties by TD‐DFT modelling. The orientation of the azido groups is highly dependent on H bonding and crystal packing, as shown by polymorphs 1 p and 1 q . Complexes 1 and 2 are stable in the dark towards hydrolysis and glutathione reduction, but undergo rapid photoreduction with UVA or blue light with minimal amine photodissociation. They are over an order of magnitude more potent towards HaCaT keratinocytes, A2780 ovarian, and OE19 oesophageal carcinoma cells than cisplatin and show particular potency towards cisplatin‐resistant human ovarian cancer cells (A2780cis). Analysis of binding to calf‐thymus (CT), plasmids, oligonucleotide DNA and individual nucleotides reveals that photoactivated 1 and 2 form both mono‐ and bifunctional DNA lesions, with preference for G and C, similar to transplatin, but with significantly larger unwinding angles and a higher percentage of interstrand cross‐links, with evidence for DNA strand cross‐linking further supported by a comet assay. DNA lesions of 1 and 2 on a 50 bp duplex were not recognised by HMGB1 protein, in contrast to cisplatin‐type lesions. The photo‐induced platination reactions of DNA by 1 and 2 show similarities with the products of the dark reactions of the PtII compounds trans‐[PtCl2(MA)(Py)] ( 5 ) and trans‐[PtCl2(MA)(Tz)] ( 6 ). Following photoactivation, complex 2 reacted most rapidly with CT DNA, followed by 1 , whereas the dark reactions of 5 and 6 with DNA were comparatively slow. Complexes 1 and 2 can therefore give rapid potent photocytotoxicity and novel DNA lesions in cancer cells, with no activity in the absence of irradiation. 相似文献
993.
Enzo Montoneri Maria C. Gallazzi Chiara Bertarelli Roberto Gobetto Luca Salassa 《Phosphorus, sulfur, and silicon and the related elements》2013,188(9):1737-1755
2-(tert-butyldimethylsilyl)-5-(10-bromodecyl)-1-(N,N-dimethylsulfamoyl)-imidazole and NaPO3 Et2 react at room temperature to yield the corresponding imidazole diethyl phosphonate, which when refluxed with concentrated HBr yields 1,10-(1-H-imidazol-5-yl)decanephosphonic acid hydrobromide (VI). Compound VI titrated with the required mole equivalents of NaOH yields 1,10-(1-H-imidazol-5-yl)decanephosphonic acid (VII) and 1,10-(1-H-imidazol-5-yl)decane (sodium)phosphonates (VIII). CP-MAS NMR (13C, 31P, and 15N) and IR spectroscopy indicate that only compound VII is likely to yield a polymeric structure where each phosphonic acid group is H bonded to the imidazole ring of the same molecule and to the imidazole ring of another molecule. For this reason, solid-state proton conductivity in VII is likely to be favored. 相似文献
994.
Dr. Riccardo Amorati Dr. Luca Valgimigli Dr. Peter Dinér Dr. Khadijeh Bakhtiari Dr. Mina Saeedi Prof. Lars Engman 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(23):7510-7522
Hydroxyaryl alkyl tellurides are effective antioxidants both in organic solution and aqueous biphasic systems. They react by an unconventional mechanism with ROO. radicals with rate constants as high as 107 M ?1 s?1 at 303 K, outperforming common phenols. The reactions proceed by oxygen atom transfer to tellurium followed by hydrogen atom transfer to the resulting RO. radical from the phenolic OH. The reaction rates do not reflect the electronic properties of the ring substituents and, because the reactions occur in a solvent cage, quenching is more efficient when the OH and TeR groups have an ortho arrangement. In the presence of thiols, hydroxyaryl alkyl tellurides act as catalytic antioxidants towards both hydroperoxides (mimicking the glutathione peroxidases) and peroxyl radicals. The high efficiency of the quenching of the peroxyl radicals and hydroperoxides could be advantageous under normal cellular conditions, but pro‐oxidative (thiol depletion) when thiol concentrations are low. 相似文献
995.
Dr. Camilla Calabrese Dr. Assimo Maris Dr. Luca Evangelisti Prof. Walther Caminati Prof. Sonia Melandri 《Chemphyschem》2013,14(9):1943-1950
The effect of ring fluorination on the structural and dynamical properties of the flexible model molecule 2‐fluorobenzylamine has been studied by rotational spectroscopy in free‐jet expansion and quantum chemical methods. The complete potential energy surface originating from the flexibility of the aminic side chain has been calculated at the B3LYP/6‐311++G** level of theory and the stable geometries were also characterized with MP2/6‐311++G**. The rotational spectra show the presence of two of the predicted four stable conformers: the global minimum (I), in which the side chain’s dihedral angle with the phenyl plane is almost perpendicular, is stabilized by an intramolecular hydrogen bond between the fluorine atom and one hydrogen of the aminic group; and a second conformer II (EII?EI≈5 kJ mol?1) in which the dihedral angle is smaller and the amino group points towards the aromatic ortho hydrogen atom. This conformation is characterized by a tunneling motion between two equivalent positions of the amino group with respect to the phenyl plane, which splits the rotational transition. The ortho fluorination increases, with respect to benzylamine, the tunneling splitting of this motion by four orders of magnitude. The motion is analyzed with a one‐dimensional flexible model, which allows estimation of the energy barrier for the transition state as approximately 8.0 kJ mol?1. 相似文献
996.
Luca Cevenini Elisa Michelini Marcello D’Elia Massimo Guardigli Aldo Roda 《Analytical and bioanalytical chemistry》2013,405(2-3):1035-1045
Bioassays represent promising complementary techniques to conventional analytical approaches used in doping analysis to detect illicit drugs like anabolic-androgenic steroids (AAS). The fact that all AAS share a common mechanism of action via the human androgen receptor (hAR) enables the use of bioassays, relying on the activation of hAR as antidoping screening tools. Previously, we developed a dual-color bioreporter based on yeast cells engineered to express hAR and androgen response elements driving the expression of the bioluminescent (BL) reporter protein Photinus pyralis luciferase. A second reporter protein, the red-emitting luciferase PpyRE8, was introduced in the bioreporter as internal viability control. Here, we report the first forensic application of a straightforward, accurate, and cost-effective bioassay, relying on spectral resolution of the two BL signals, in 96-microwell format. The bioreporter responds to dihydrotestosterone as reference androgen in a concentration-dependent manner from 0.08 to 1,000 nM with intra- and inter-assay variation coefficients of 11.4 % and 13.1 %, respectively. We also demonstrated the suitability of this dual-color bioreporter to assess (anti)-androgenic activity of pure AAS, mixtures of AAS, and other illicit drugs provided by the Scientific Police. Significant anti-androgenic activity was observed in samples labeled as marijuana and hashish, containing Δ9-tetrahydrocannabinol as major constituent. Figure
Evaluation of (anti)-androgenic activity of seized drugs with the dual-color bioluminescent bioreporter 相似文献
997.
Luca Campone Anna Lisa Piccinelli Rita Celano Mariateresa Russo Luca Rastrelli 《Analytical and bioanalytical chemistry》2013,405(26):8645-8652
A simple, rapid, and sensitive method based on simultaneous protein precipitation and extraction of aflatoxin M1 (AFM1) followed by dispersive liquid–liquid microextraction (DLLME) and ultrahigh pressure liquid chromatography tandem mass spectrometry (UHPLC-MS/MS) analysis was developed for the determination of AFM1 in milk samples. In order to precipitate the proteins and extract AFM1 from milk, a sample pretreatment using acetonitrile and NaCl as the extraction/denaturant solvent and salting-out agent, respectively, was optimised. Subsequently, the acetonitrile (upper) phase, containing AFM1, was used as the disperser solvent in DLLME, and extractant (chloroform) and water were added in turn to the extract to perform the DLLME process. The main parameters affecting the extraction efficiency of the whole analytical procedure, such as acetonitrile volume, amount of salt, type and volume of extractant and water volume, were carefully optimised by experimental design. Under optimum conditions, the developed method provides an enrichment factor of 33 and detection and quantification limits (0.6 and 2.0 ng kg?1, respectively) below the maximum levels imposed by current regulations for AFM1 in milk and infant milk formulae. Recoveries (61.3–75.3 %) and repeatability (RSD?<?10, n?=?3), tested in different types of milk at four AFM1 levels, met the performance criteria required by EC Regulation No. 401/2006. Moreover, the matrix effect on the signal intensity of the analyte was negligible. The proposed method provides a rapid extraction and an accurate determination of AFM1 in milk and formula milk using a simple and inexpensive sample preparation procedure. Figure
Rapid analysis of aflatoxin M1 in milk using DLLME 相似文献
998.
Concetta De Santi Pietro Tedesco Luca Ambrosino Bjørn Altermark Nils-Peder Willassen Donatella de Pascale 《Applied biochemistry and biotechnology》2014,172(6):3054-3068
The special features of cold-adapted lipolytic biocatalysts have made their use possible in several industrial applications. In fact, cold-active enzymes are known to be able to catalyze reactions at low temperatures, avoiding side reactions taking place at higher temperatures and preserving the integrity of products. A lipolytic gene was isolated from the Arctic marine bacterium Rhodococcus sp. AW25M09 and expressed in Escherichia coli as inclusion bodies. The recombinant enzyme (hereafter called RhLip) showed interesting cold-active esterase activity. The refolded purified enzyme displayed optimal activity at 30 °C and was cold-active with retention of 50 % activity at 10 °C. It is worth noting that the optimal pH was 11, and the low relative activity below pH 10 revealed that RhLip was an alkaliphilic esterase. The enzyme was active toward short-chain p-nitrophenyl esters (C2–C6), displaying optimal activity with the butyrate (C4) ester. In addition, the enzyme revealed a good organic solvent and salt tolerance. These features make this an interesting enzyme for exploitation in some industrial applications. 相似文献
999.
Gilles Berger Luca Fusaro Michel Luhmer Arie van der Lee Benoit Crousse Franck Meyer 《Tetrahedron letters》2014
We report the synthesis of several new α-trifluoromethylated nitrogen heterocycles, among which azanorbornene and azetidine derivatives, by aza Diels–Alder or iodine-mediated cyclizations. These building blocks were used as starting materials for the formation of fluorinated polymers by ROMP or for ligand design through substitution and click reactions. 相似文献
1000.
Iterative ILU factorizations are constructed,analyzed and applied as preconditioners to solve both linear systems and eigenproblems.The computational kernels of these novel Iterative ILU factorizations are sparse matrix-matrix multiplications,which are easy and efficient to implement on both serial and parallel computer architectures and can take full advantage of existing matrix-matrix multiplication codes.We also introduce level-based and threshold-based algorithms in order to enhance the accuracy of the proposed Iterative ILU factorizations.The results of several numerical experiments illustrate the efficiency of the proposed preconditioners to solve both linear systems and eigenvalue problems. 相似文献