因为食品与药物管理局并不将年龄的老化视为一种疾病所以SIRTRIS正在利用这种复合物去临床试验治疗某些导致加速老化的疾病。
Because the Food and Drug Administration does not consider aging itself a disease, Sirtris is testing its compounds against illnesses associated with aging.
例如，该药物可能是人们食用的大豆中的复合物成分，这些人比那些仅仅刚开始服用高金雀花碱的病人受益更多。
For example, it may be that the effects of the compound in people who have eaten soy all their lives is stronger than benefit seen in patients who have only started to use genistein.
我们提出了肺结核分支杆菌细胞色素P 450CYP121与三氮唑类药物氟康唑的复合物的晶体结构，揭示了唑类与亚铁血红素新的结合模式。
We present here the crystal structure of Mycobacterium tuberculosis cytochrome P450 CYP121 in complex with the triazole drug fluconazole, revealing a new azole heme ligation mode.
近年来聚电解质复合物在药物控释领域受到重视。
Recently, in drug controlled release system, polyelectrolyte complexes have been rewarded much attention.
光谱分析结果表明，上述喹诺酮类药物都可以与牛乳铁蛋白或人血清白蛋白之间形成亲和力较强的复合物。
The spectroscopy analysis shows that all those quinolone drugs can react with BLf or HSA and form a drug-protein compound.
华法令是目前最常用的此类药物，它是一种合成的双香豆素类，比天然复合物强5-10倍。
Warfarin a synthesized version of dicumarol is5to10times stronger than the original compound and is the most commonly used oral anticoagulant.
研究蛋白质与相应配体分子复合物的结构及配体与蛋白质的相互作用对阐明蛋白质的结构、功能、作用机制和药物设计具有重要的指导意义。
The complex structure of protein and its ligand is important for clarifying the function and action mechanisms of protein and useful for drug design.
同时本文对黄芩苷磷脂复合物溶剂残留量及鼻黏膜刺激性进行了考察，结果表明，无四氢呋喃有机溶剂残留，且药物没明显的刺激性。
At the same time , we did the study of organic solvent residue and irritation to nasal mucosa. The results illustrate that the complex has no residue of tetrahydrofuran and no obvious irritation.
结果扫描电镜和粒度分析结果表明，药物树脂复合物的表面形态和粒径大小都与起始的离子交换树脂非常相似。
Results Scanning electron microscope analysis and laser particle size analysis proved that the codeine-resinate complex had the same appearance and characters as the initiative ion exchange resin.
考察了药物与磷脂的复合率，磷脂复合物脂质体的包封率，粒径大小和分布，以及体外释药特性。
The drug loading rate, encapsulation efficiency, particle distribution and in vitro release of Lac-NCTD from liposomes were investigated, respectively.
目的制备盐酸氨溴索药物树脂复合物并对其体外释药动力学进行考察。
The drug release kinetics were also investigated in different releasing mediums(deionic water, 0.
应用手性和非手性柱固定相，在正相色谱系统中，手性药物和手性离子对试剂形成非对映离子对复合物，从而使手性药物得以分离。
Separations based on formation of diastereomeric ion-pairs were fulfilled in systems with an organic mobile phase using achiral and chiral stationary phases.
利用晶体X射线衍射的方法获得药物与靶标复合物的结构，为药物设计提供最直接有力的依据。
The structures of drug-target complexes obtained by X-ray crystallography provide direct and convictive evidences for drug design.
方法：将乳糖化-去甲斑蝥素与磷脂聚合成药物磷脂复合物，并采用FT-IR、DSC和1H-NMR对其进行表征。
Methods: Lac-NCTD phospholipid complex was prepared using solvent-evaporation, and its correlated physicochemical properties were confirmed with solubility test, FT-IR, DSC and 1H-NMR.
方法：将乳糖化-去甲斑蝥素与磷脂聚合成药物磷脂复合物，并采用FT-IR、DSC和1H-NMR对其进行表征。
Methods: Lac-NCTD phospholipid complex was prepared using solvent-evaporation, and its correlated physicochemical properties were confirmed with solubility test, FT-IR, DSC and 1H-NMR.
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