异肽键交联的N肽类HIV-1融合抑制剂的设计、合成及活性评价

报道了一种通过在HIV-1 gp41 NHR区域的多肽(N肽)之间引入异肽键稳定N3螺旋的新方法;以天然N肽序列N38为模板,采用此方法设计合成了一系列异肽键交联的N38三股α螺旋结构.该结构具有极强的热稳定性和纳摩尔水平抑制HIV-1包膜糖蛋白(Env)介导的细胞融合活性.     

白云石制备碳酸钙晶须及其机理的研究

以白云石为原料,采用气液接触法制备碳酸钙晶须.研究了煅烧条件对白云石分解的影响;同时对碳酸钙晶须的制备以及机理进行了研究,采用XRD、SEM等分析手段对产品进行表征.结果 表明,白云石在煅烧温度850℃,升温速率10℃/min,煅烧时间4h的情况下,分解效果最佳;反应温度、通气速率和搅拌速率对碳酸钙晶须的生成具有显著作用,通过对结晶过程以及晶体的生长理论来解释碳酸钙晶须的生成.     

不同厚度镥样品中子俘获反应实验研究

C₆D₆闪烁体探测系统结合脉冲权重技术被广泛应用于中子俘获反应截面测量研究.实验中采用的样品厚度直接影响中子束流时间,同时也影响实验数据的可靠性.本文基于中国散裂中子源反角白光束线(CSNS Back-n)C₆D₆探测系统,对比研究了不同厚度的镥(Lu)样品中子俘获反应截面的实验测量.利用GEANT4蒙特卡罗程序模拟了考虑样品厚度的探测系统光响应,计算出精确的脉冲权重函数.实验中,通过采用较长中子飞行距离和本底测量,得到了高精度的共振区产额分布.通过R矩阵理论分析产额分布,得到了相应的实验共振参数.结果发现,较厚Lu样品因其厚度效应导致共振曲线发生变化,实验共振参数与ENDF/B-Ⅷ.0评价数据库差距较大;然而,较薄Lu样品实验结果能够很好地再现ENDF/B-Ⅷ.0评价数据.     

一道高考题的求解历程

分析 这是一道函数综合题，且是填空压轴题，带着好奇与兴趣，决定试一试!计划求解分两段，第一段先求出参数a，b的值，第二段再求最值．     

Selective Deoxygenation of Nitrones Mediated by Sm/CoCl_26H_2O Reductive System

Aldimines are an important class compounds1 which can be prepared by selective deoxygenation of nitrones. Thus more attention was paid to the selective deoxygenation of nitrones in organic synthesis. The reducing reagents, include low-valent titanium2, acetic formic anhydride3, sodium hydrogen telluride4, tributyltin hydride4, terathiomolybdate5, metallic indium in aqueous media6, zinc-aluminum trichloride7, aluminum iodide8, triphenylphosphine9, etc. However, there are various limitations …     

Mild Hydrothermal Synthesis and Optical Properties of the Complex Fluoride KMgF_3 Doped with Eu

Perovskite complex fluorides have attracted great interests due to their particular physical properties such as antiferromagnetic characteristics1, photoluminescence behavior2. Complex fluorides are usually prepared by solid state reactions at high-temperature. In spite of inert atmosphere, it is inevitable to contain a bit of oxygen. This has great effect on the luminescent character of rare earth ions. There are also reports about synthesizing some binary fluorides by high-temperature hy…     

Two New Dammarane Glycosides from the Acid Hydrolysis Product of Panax Notoginseng

In our continuing research works on Panax notoginseng (Burk.) F. H. Chen, a famous traditional Chinese herb medicine1, two new dammarane glycosides named notoginsenosides T1 (1) and T2 (2) were isolated from the mild acid hydrolysis products of the root saponins. We report herein the structure elucidation of these two novel glycosides.Notoginsenosides T1(1) was obtained as white solid, [(] = +14.49 (0.50, MeOH). Its negative mode HR-FAB-MS spectrum showing the quasimolecular ion peak a…     

NaIO_4-Catalyzed Bromination of the Aromatic Ring of Lappaconitine

Lappaconitine 1, a bisnorditerpenoid alkaloid, was isolated from many plants of Aconitum species such as A. barbatum var. pulerulum and A. sinomontanum (Ranunculaceae)1-3, and used clinically for treatment of analgic disease as a nonaddicted drug in China4, and as an antiarrythmic in Uzbekistan5. In order to search for high activity, low toxicity compounds, we have carried out the structure modifications of lappaconitine. In this case, an attempt to induce the oxygenated group at C-10 in 1 b…     

A New Norditerpene from Miliusa balansae Finet et Gagnep

The plant Miliusa balansae Finet et Gagnep. is used in Chinese folk medicine for different symptom such as gastropathy and glomerulonephropathy. There is no report about its chemical investigation. In this study a new norditerpene with novel skeleton, named miliusate (1) was isolated, and its structure was established by spectral evidence.Compound 1 was obtained as white flaky crystal, mp 89-91(C; Its molecular formula C20H26O5 was provided by quasi-molecular ion [M+H]+ at m/z 347.17970 (c…     

An Improved Synthesis of trans-3,3b,4,9b,10,11-Hexahydro -6-methoxy-9b-methyl-7- (1-methylethyl) phenanthro {1,2-c[furan-1,5-dione]}

The diterpenoid triexpoxides lactone triptolide is a potent antileukemic, antiflammatory, immunosuppressive and antifertile principle of Tripterygium wilfordii Hook f.1,2. Many methods of synthesis of this compound have been reported in which trans-3,3b,4,9b,10, 11-hexahydro-6-methoxy-9b-methyl-7- (1-methylethyl) phenanthro {1,2-c [furan-1,5- dione]} 4 was an important intermediate. In one reported synthesis, compound 4 was obtained by CrO3/AcOH oxidation of triptophenolide methyl ether 1, b…