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排序方式: 共有87条查询结果,搜索用时 15 毫秒
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Ehret R Baumann W Brischwein M Lehmann M Henning T Freund I Drechsler S Friedrich U Hubert ML Motrescu E Kob A Palzer H Grothe H Wolf B 《Fresenius' Journal of Analytical Chemistry》2001,369(1):30-35
The identification of drug targets for pharmaceutical screening can be greatly accelerated by gene databases and expression studies. The identification of leading compounds from growing libraries is realized by high throughput screening platforms. Subsequently, for optimization and validation of identified leading compounds studies of their functionality have to be carried out, and just these functionality tests are a limiting factor. A rigorous preselection of identified compounds by in vitro cellular screening is necessary prior to using the drug candidates for the further time consuming and expensive stage, e.g. in animal models. Our efforts are focused to the parallel development, adaptation and integration of different microelectronic sensors into miniaturized biochips for a multiparametric, functional on-line analysis of living cells in physiologically environments. Parallel and on-line acquisition of data related to different cellular targets is required for advanced stages of drug screening and for economizing animal tests. 相似文献
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As12Se44—: a New Selenoarsenate Anion with a Polyarsenic Cage in the Compound [Co(NH3)6]2As12Se4 · 12 NH3 Orange coloured crystals of [Co(NH3)6]2As12Se4 · 12 NH3 were prepared by the reduction of As4Se4 with a solution of sodium in liquid ammonia and subsequent precipitation with CoBr2. The X‐ray structure determination shows them to contain the selenoarsenate anion As12Se44—, which consists of a central As12‐cage with four exo‐bonded, formally negatively charged Se atoms. The structure of the As12‐cage is equivalent to the main polyphosphorus building unit of a known organopolyphosphane and of tubular P12 in the compound (CuI)3P12. 相似文献
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Lund Myhre CE Grothe H Gola AA Nielsen CJ 《The journal of physical chemistry. A》2005,109(32):7166-7171
The complex index of refraction of liquid HNO3/H2O and H2SO4/HNO3/H2O has been obtained at different temperatures and acid concentrations. FT-IR specular reflectance spectra were obtained for 30, 54, and 64 wt % aqueous HNO3 and for four different H2SO4/HNO3/H2O mixtures in the temperature region from 293 to 183 K. The complex index of refraction was obtained from the reflectance spectra with the Kramers-Kronig transformation. The optical constants of the binary and ternary mixtures vary with the acid concentration and the temperature. The results demonstrate that vibrational bands originating from the sulfate species are more sensitive to changes in temperature than the bands originating from vibrations in the nitrate species; only minor changes in the nitrate vibrational bands are observed as the temperature decreases below 248 K. 相似文献
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Puppe T Schuster I Grothe A Kubanek A Murr K Pinkse PW Rempe G 《Physical review letters》2007,99(1):013002
A single atom strongly coupled to a cavity mode is stored by three-dimensional confinement in blue-detuned cavity modes of different longitudinal and transverse order. The vanishing light intensity at the trap center reduces the light shift of all atomic energy levels. This is exploited to detect a single atom by means of a dispersive measurement with 95% confidence in 10 micros, limited by the photon-detection efficiency. As the atom switches resonant cavity transmission into cavity reflection, the atom can be detected while scattering about one photon. 相似文献
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García-Domínguez P Lepore I Erb C Gronemeyer H Altucci L Álvarez R de Lera AR 《Organic & biomolecular chemistry》2011,9(20):6979-6987
The purported structures of the peyssonenynes A and B isolated from Peyssonnelia caulifera, and considered to be geometric isomers at the acetoxyenediyne moiety, have been synthesized. The E and Z geometries of the synthetic compounds were secured by the magnitude of the (3)J(H9-C7) values measured using the EXSIDE band-variant of the gradient HSQC pulse sequence and by the chemical shifts of C(6). Comparison of the NMR data of the synthetic and natural products revealed that only those of the Z isomers matched, which correspond to peyssonenyne A. Using HPLC analysis it was found that peyssonenyne B must correspond to the sn-2 positional isomer of the Z sn-1/3 counterpart. The four synthetic sn-1/3 diastereomers are roughly equipotent as DNMT1 inhibitors when evaluated on a radioactive methyl transfer enzymatic assay after immunoprecipitation from K562 human leukemia cells with anti-DNMT1 antibody. 相似文献
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Helmut Poleschner Reiner Radeglia Hinrich Meyer 《Magnetic resonance in chemistry : MRC》1984,22(8):480-485
This paper reports the 77Se NMR chemical shifts of 1,3-dithiole-, 1,3-thiaselenole- and 1,3-diselenole-2-ones, -thiones and -selones, of the corresponding saturated compounds 1,3-diselenolane-2-one, -thione and -selone, and the 1,3-thiaselenolium tetrafluoroborates, either unsubstituted or substituted by morpholino, ethylthio or ethylseleno groups in the 2-position. The 77Se chemical shift values of the ring selenium and the C?Se groups are compared with the 13C chemical shift values of neighbouring carbon atoms. The relationships between the 77Se chemical shifts of the C?Se groups and the wavelengths of their n→* absorption in the UV-visible spectrum are discussed with respect to the significance of the δE term in the contribution of the paramagnetic screening and the electron density distribution. 相似文献