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231.
Fan Caiyun Jia Hongmei Deuther-Conrad Winnie Brust Peter Steinbach J?rg Liu Boli 《中国科学B辑(英文版)》2006,49(2):169-176
A novel 99mTc labeled complex, [N-[2-((2-oxo-2-(4-(3-phenylpropyl)piperazin-1-yl)ethyl) (2-mercaptoethyl)amino)acetyl]-2-aminoethanethiolato]Technetium(V)
oxide (PPPE-MAMA’-99mTcO) ([
99m
Tc]-2) has been designed and prepared based on the integrated approach. The corresponding rhenium complex (PPPE-MAMA’-ReO)(Re-2) has been prepared and characterized. In vitro competition binding assays show moderate affinity of Re-2 towards σ1 and σ2 receptors with K
i values of 8.67 ± 0.07 and 5.71 ± 1.88 μmol, respectively. Planar images obtained at 0.5 h, 4 h, 20 h after i.v. injection
indicate the accumulation of [
99m
Tc]-2 in MCF-7 human breast tumor bearing mice at 20 h. Furthermore, the accumulation of [
99m
Tc]-2 has been inhibited at 20 h after co-injection of [
99m
Tc]-2 plus haloperidol (1 mg/kg). Biodistribution studies of [
99m
Tc]-2 display an in vivo tumor uptake of 0.14% ± 0.01% ID/g at 24 h post i.v. injection with a tumor/muscle ratio of 6.02 ± 0.87. The above results
suggest that [
99m
Tc]-2, derived from a previously published lead compound, retains certain tumor uptake and affinity for σ receptors. [
99m
Tc]-2 may be used as a basis for further structural modifications to develop tumor imaging agents with high affinity for σ receptors. 相似文献
232.
An optimized semi-automatic protocol for parallel synthesis of up to 96 peptide nucleic acids (PNA) or PNA-peptide conjugates using Boc-protection strategy has been developed using a robotic system. The approach is illustrated by synthesizing PNA and PNA-peptide libraries varying between 15 and 27 amino acid units. The peptides (NLS (nuclear localization signal) or Tat-peptide) were attached to N-terminus of the PNA. The method was found to be far superior to that based on the SPOT/Fmoc protocol by which PNA oligomers are synthesized on a modified cellulose membrane. On a 0.5 micromole scale the method typically yielded 2 mg product of 90% purity by HPLC/MALDI-TOF analysis. This approach is suitable for screening of a large number of PNA and/or peptide sequences for biochemical and biological studies. 相似文献
233.
Akutsu H Akutsu-Sato A Turner SS Le Pevelen D Day P Laukhin V Klehe AK Singleton J Tocher DA Probert MR Howard JA 《Journal of the American Chemical Society》2002,124(42):12430-12431
Normal state conductivity and superconductivity together with bulk magnetic susceptibility and magnetization measurements have been measured for two molecular charge-transfer salts: beta' '-(ET)4[(H3O)Ga(C2O4)3]G (ET = bis(ethylenedithio)tetrathiafulvalene, G = pyridine for compound I and nitrobenzene for compound II). With the exception of the included guest molecules (G) the crystal structures are almost identical. Both show minima in their electrical transport at 130 K for I and at 160 K for II, but at lower temperatures their behaviors differ markedly. The resistance of I reaches a maximum at 50 K with a further small peak at 2 K and possible superconductivity only below 2 K, whereas that of II increases continuously down to 7.5 K, where an abrupt transition to a superconducting state occurs. 相似文献
234.
Peter C. Cherry Derek N. Evans Christopher E. Newall Nigel S. Watson Peter Murray-Rust Judith Murray-Rust 《Tetrahedron letters》1980,21(6):561-564
1,4-Addition of sulphur nucleophiles to the diene () derived the pen-2-em () from clavulanic acid provides the thiadeoxa analogues (–). X-ray analysis of the ester () shows the thermodynamically stable isomers to have the same relative stereochemistry as clavulanic acid. 相似文献
235.
Peter Möller 《Fresenius' Journal of Analytical Chemistry》1974,268(1):28-30
Zusammenfassung Über den Ca2+-Mg2+-Ionenaustausch wurde der Mg2+-Ionengehalt in Calcitoberflächen in Abhängigkeit von der Mg2+-Konzentration in Ca-45-markierten Lösungen bestimmt. Es wurde gefunden, daß der Anstieg des Molverhältnisses Mg/Ca in der Calcit-Oberfläche bei steigendem Mg2+-Gehalt in der Lösung jeweils bei Erreichen von Mg/Ca 1 und 3 deutlich verringert wird. Die ermittelte Austauschisotherme kann benutzt werden, um über eine Bestimmung des Mg/Ca-Verhältnisses in der Lösung auf dasjenige in der Oberfläche zu schließen.Vortrag anläßlich der Tagung Spurenanalyse, 2. bis 5. April 1973 in Erlangen. 相似文献
236.
A comparison of different nebulisers for direct hyphenation of capillary and nano liquid chromatography (Cap-LC, Nano-LC) and quadrupole-based collision cell inductively coupled plasma mass spectrometry (CC-ICP–MS) for phosphorylation profiling of tryptic protein digests is described. Helium was used as cell gas and specially tuned instrumental conditions were used to achieve background minimisation at the mass of phosphorus, because of kinetic energy discrimination of the interfering polyatomic ions. The proposed set-up is based on a modified capillary electrophoresis interface and a home-made 4 mL spray chamber. It enables the use of gradient conditions with a highly concentrated organic mobile phase as often used in protein phosphorylation analysis, without the need to apply membrane desolvation for removal of the organic phase or further background minimisation. No significant signal suppression or other negative effects caused by the organic mobile phase occur, because of the low flow rates used in Cap-LC and the robust plasma conditions of the CC-ICP–MS instrument. A tryptic digest of beta-casein was investigated as model compound to demonstrate the applicability of the proposed set-up for phosphorylation profiling in protein analysis using quadrupole based collision-cell ICP–MS as phosphorus-specific detector. Detection limits for phosphorylated peptides down to the sub picomole level were obtained. As a complementary technique, electrospray ionisation tandem mass spectrometry (ESI–MS–MS) with data base searching was used for further characterisation of the phosphorylated peptides detected. 相似文献
237.
A systematic extension of Ruedenberg's expansion formula is applied to evaluate two-electron integrals occurring in calculations on molecular structure. Minimum STO basis sets are used for all SCF-calculations within the framework of the MEDO-method (Multipole Expansion of Diatomic Overlap). The errors due to this approximation scheme are almost negligible compared to those introduced by the truncated basis set: LiH, Li2 and N2 are chosen as examples. 相似文献
238.
The reactivity of benzo[b]naphtho[2,3-e][1,4]dioxin in the electrophilic aromatic substitution reactions has been studied. Friedel-Crafts acetylation resulted in the formation of three out of the possible five monoacetylated products, with the acetyl group located in positions 8 (major), 7 and 6 (minor) of the heterocycle. In the bromination reaction a higher selectivity was observed with the 6-bromo derivative found as the only monobrominated product and the 6,11-dibromo derivative found as the only polybrominated product. A ratio of unreacted heterocycle:6-bromo:6,11-dibromo derivatives in the bromination reaction has been found to depend strongly on the reaction conditions and on the heterocycle:bromine ratio. 相似文献
239.
Matthias Westerhausen Alexander N. Kneifel Peter Mayer Heinrich Nth 《无机化学与普通化学杂志》2004,630(12):2013-2021
Synthesis and Molekular Structures of N‐substituted Diethylgallium‐2‐pyridylmethylamides (2‐Pyridylmethyl)(tert‐butyldimethylsilyl)amine ( 1a ) and (2‐pyridylmethyl)‐di(tert‐butyl)silylamine ( 1b ) form with triethylgallane the corresponding red adducts 2a and 2b via an additional nitrogen‐gallium bond. These oily compounds decompose during distillation. Heating under reflux in toluene leads to the elimination of ethane and the formation of the red oils of [(2‐pyridylmethyl)(tert‐butyldimethylsilyl)amido]diethylgallane ( 3a ) and [(2‐pyridylmethyl)‐di(tert‐butyl)silylamido]diethylgallane ( 3b ). In order to investigate the thermal stability solvent‐free 3a is heated up to 400 °C. The elimination of ethane is observed again and the C‐C coupling product N, N′‐Bis(diethylgallyl)‐1, 2‐dipyridyl‐1, 2‐bis(tert‐butyldimethylsilyl)amido]ethan ( 4 ) is found in the residue. Substitution of the silyl substituents by another 2‐pyridylmethyl group and the reaction of this bis(2‐pyridylmethyl)amine with GaEt3 yield triethylgallane‐diethylgallium‐bis(2‐pyridylmethyl)amide ( 5 ). The metalation product adds immediately another equivalent of triethylgallane regardless of the stoichiometry. The reaction of GaEt3 with 2‐pyridylmethanol gives quantitatively colorless 2‐pyridylmethanolato diethylgallane ( 6 ). 相似文献
240.
Peter Wehber 《Fresenius' Journal of Analytical Chemistry》1956,153(4):253-260
Zusammenfassung Eriochromrot B ist ein gut geeigneter komplexometrischer pM-Indicator, der in manchen Beziehungen Vorteile gegenüber anderen Indicatoren aufweist. Mit seiner Hilfe lassen sich z. B. bei pH 6,5 Zink-Ionen und bei pH 10 Zink- und Blei(II)-Ionen mit 0,1 m Äthylendiamintetraessigsäure (EDTA)-Lösung bestimmen. Bei der Zinkbestimmung im schwach sauren Milieu können kleinere Kupfer(II)-, Palladium(II)- sowie Platin(IV)-Ionenkonzentrationen mit Thioharnstoff (TH) maskiert werden. In ammoniakalischer Lösung ist die Zinktitration neben Bariumsulfat möglich. Dadurch läßt sich der Zinkgehalt in Lithopone ermitteln.Das Verhalten von Kupfer(II)-Ionen zu Eriochromrot B und EDTA wird beschrieben.Die komplexometrischen Eigenschaften des Cadmiums sind denen des Zinks analog. Über eine Manganbestimmung wird später berichtet.Untersuchungen über pM-Indicatoren werden an weiteren Pyrazolonfarbstoffen fortgesetzt.Mitteilung IX dieser Reihe: diese Z. 153, 249 (1956).Der I. R. Geigy A.-G., Basel, danke ich für die freundliche Überlassung einiger Reagentien, insbesondere für Eriochromrot B. Herrn W. Johannsen, dem Laboratoriumsleiter der Metallhütte Mark A.G., bin ich für sein Interesse an dieser Arbeit verpflichtet. 相似文献