[1-芳基甲羰基-2-(1,2,4-三唑-1-基)]乙基-N,N-二烷基二硫代氨基甲酸酯衍生物的合成、结构表征及生物活性研究

以芳香基三唑类杀菌剂三唑酮为先导物设计并合成了5个含N,N-二烷基二硫代氨基甲酸酯的芳香三唑类化合物, 通过元素分析、红外光谱、核磁共振氢谱和质谱对其结构进行了表征. 用X射线单晶衍射测定了[α-(4-甲氧基苯甲酰基)-2-(1,2,4-三唑-1-基)]乙基-N,N-二甲基二硫代氨基甲酸酯的晶体结构, 晶体属于三斜晶系, 空间群, 晶胞参数为: a＝0.73482(15) nm, b＝1.1051(2) nm, c＝1.1209(2) nm, α＝90.32(3)°, β＝101.97(3)°, γ＝105.13(3)°, V＝0.8578(3) nm³, Z＝2, D_c＝1.357 g/cm³, F(000)＝368, µ＝0.324 mm^－1. 生物测试结果显示这5种有机化合物都具有杀菌性和植物生长调节活性     

Spectroscopic and biological studies on newly synthesized nickel(II) complexes of semicarbazones and thiosemicarbazones

Nickel(II) complexes, having the general composition Ni(L)2X2, have been synthesized [where L: isopropyl methyl ketone semicarbazone (LLA), isopropyl methyl ketone thiosemicarbazone (LLB), 4-aminoacetophenone semicarbazone (LLC) and 4-aminoacetophenone thiosemicarbazone (LLD) and X=Cl-, 1/2SO(4)2-]. All the Ni(II) complexes reported here have been characterized by elemental analyses, magnetic moments, IR, electronic and mass spectral studies. All the complexes were found to have magnetic moments corresponding to two unpaired electrons. The possible geometries of the complexes were assigned on the basis of electronic and infrared spectral studies. Newly synthesized ligand and its nickel(II) complexes have been screened against different bacterial and fungal growth.     

Synthesis of 1,2,4-substituted hexahydropyridazines and X-ray structural investigation of 4-hydroxyimino-2-methyl-1-phenethylhexahydropyridazine

A series of new 1,2,4-substituted hexahydropyridazines was prepared in order to evaluate qualitatively and quantitatively the role and influence of substituents on the biological activity of this system. An X-ray structural investigation of 4-hydroxyimino-2-methyl-1-phenethylhexahydropyridazine was performed. The compounds considered exhibit moderate local anesthetic, antihistaminic, and anticonvulsive activity.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 539–541, March, 1993.     

Physicochemical characterization of biological glass coatings

Metallic implants are widely used in orthopaedic surgery but metal release has been reported by several authors. High metallic ion concentration in surrounding tissues may play a major role in therapeutic failure. We have investigated in vivo and in vitro two biological glasses (BVA and BVH) used as coatings of metal implants. Physicochemical characterization was made by several complementary methods, particularly particle induced x‐ray emission (PIXE) and energy‐dispersive x‐ray spectroscopy (EDXS) associated with electronic microscopy. Analyses clearly show the differences of behaviour between both glasses. The BVA glass is bioactive, i.e. it develops a direct chemical bond between prosthesis and bone by the formation of a calcium phosphate layer at its surface. These structural and compositional modifications are caused by hydrolysis of the glass. After its dissolution BVA glass is replaced by bone, which ensures better integration of the implant in the bone site. The BVH glass is not bioactive and is used as a cement to isolate the metal implant from the biological environment, but the coating disaggregates with implantation time and glass grains migrate through the bony lacuna network. Copyright © 2003 John Wiley & Sons, Ltd.     

2,3-二取代-4-(IH-l,2,4-三唑-l-基)-5-苯基氢基噻吩的合成及生物活性研究

合成了九个以噻吩为母体环的含三唑环的化合物——2，3-二取代-4-(1H-1， 2，4．三唑-1-基)-5-苯基氨基噻吩(2a-2i)，并测定了2a的晶体结构．晶体为三斜 晶系，P-1空间群，晶胞参数为：a=0．79816(15)nm，b=1．00259(13)nm，c=1． 4478(4)nm，a=100．326(16)°，β=94．69(2)°，r=106．083(9)°，V=1．0845 (4)nm～3，z=2，D_c=1．396 g／cm～3．初步生物活性表明所有目标化合物杀菌活 性较低，有一定的植物生长调节活性．     

基于背景感知的相关滤波抗遮挡优化算法

针对相关滤波目标跟踪中由于目标遮挡、出视野引起的跟踪失败等问题,以背景感知相关滤波(background aware correlation filters, BACF)算法为基础,提出一种抗遮挡优化算法。首先特征提取部分融合方向梯度直方图(histogram of oriented gradient, HOG)特征与颜色名称(color name, CN)特征;其次提出层级遮挡优化算法,在目标跟踪过程中根据平均峰值相关能量(average peak to correlation energy,APCE)和最大响应峰值判断目标外观是否发生较大变化,并通过巴氏距离进一步计算目标相邻滤波器模板特征相似程度,以此判断造成目标外观变化的真正原因,进而决定是否更新模板;针对目标出视野问题,提出模板筛查策略,跟踪过程中每隔K帧对滤波器模板进行置信度考查,若目标丢失,则生成新的模板并对目标进行全局搜索重新抓取目标。通过在目标跟踪数据集OTB2015上测试,优化算法精确度与成功率分别为83.0%与78.8%,有效提高了算法性能。     

Thermodynamics of natural selection

It is shown that biological-natural-selection-like behavior can occur, as a general type of time evolution, in a statistical system where detailed balance is violated owing to the presence of metastable energy states. A model of a non-equilibrium phase transition corresponding to the spontaneous origin of self-reproduction in the system is suggested. After a phase transition, the system passes from one quasistationary distribution of self-reproducing subsystems to another, with an increase in the total organization, as long as the growth of the energy flow through the system or a reduction of energy dissipation in the system is possible. The entropy production is calculated for this process in terms of selective values of Eigen's theory for self-organization in autocatalytic systems. Correspondence of the extremal principle of Eigen's theory with the criterion of evolution in Prigogine's thermodynamics is established.     

Isolation of new quinidine metabolites and simultaneous determination of quinidine and its metabolites in blood and urine by direct injection HPLC analysis

Summary New quinidine metabolites, including 10,11-dihydrodiol quinidine N-oxide, 10,11-dihydrodiol quinidine and their glucuronides, were found in human urine. A quinidine monitoring HPLC method including these metabolites, is proposed by the direct injection of body fluid samples onto the precolumn for deproteinization followed by reverse phase separation in the analytical column with a column switching technique. The recovery of spiked quinidine and its metabolites in plasma was quantitative (98–102%) with good reproducibility (C.V.: 1.6–4.0%). Several clinical samples such as whole blood and urine were analyzed by the present method.     

Crystal structure of a tetrabromo derivative of cyclopropyldihydroarglabin and its antifungal activity

A tetrabromo derivative of arglabin was synthesized stereoselectively. The molecular structure of the new compound was established using PMR and 13C NMR spectra and an x-ray structure analysis. Its antifungal activity was demonstrated. __________ Translated from Khimiya Prirodnykh Soedinenii, No. 3, pp. 253–254, May–June, 2006.     

O-取代苯基-O-(2-硬脂酰胺基)乙基-N,N-二(2-氯乙基)磷酰胺的合成和生物活性

N-脂肪酰基乙醇胺(NAE)作为植物体内的一种内源物质, 在调节植物生长方面起着重要作用. 为了弥补其分子结构中长的脂肪链所带来的溶解性能以及在植物体内传导性能的缺陷, 我们将N-硬脂酰乙醇胺(NAE18)引入氮芥磷酸酯中, 合成了一系列标题化合物. 在合成工作中发现: 在NAE18与氮芥芳基磷酰氯的反应过程中, 4-二甲氨基吡啶(DMAP)起着关键性的催化作用. 在不加DMAP的相同实验条件下, 反应不能进行. 对所合成的标题化合物进行了植物生长调节和杀菌活性的测定, 初步生测结果表明: 经过结构修饰后, 大多数目标化合物的活性相对NAE18有所增强, 但有关生物活性仍有待进一步研究.