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1)  chiral compound
手性物
2)  chiral drug
手性药物
1.
Stereoselectivity in pharmacology of chiral drug;
手性药物的药理学立体选择性
2.
Interactions between the enantiomers of chiral drugs on the pharmacodynamics and pharmacokinetics;
手性药物对映体在药效学与药代动力学的相互作用
3.
Stereoselectivity in pharmacokinetics of chiral drugs;
手性药物的药动学立体选择性
3)  chiral drugs
手性药物
1.
Recent progess in catalytic asymmetric reaction of chiral drugs;
不对称催化反应在手性药物合成中的应用进展
2.
Resolution of HPLC-DAD data of chiral drugs with overlapping peaks by non-negative matrix factorization;
非负矩阵因子分解算法解析手性药物重叠峰的HPLC-DAD数据
3.
Mensuration of the physical chemistry characteristics of chiral drugs mandelic acid;
手性药物扁桃酸的理化特性测定
4)  chiral pharmaceuticals
手性药物
1.
PRODUCTION OF CHIRAL ALCOHOL BY MICROBIAL REDUCTION OF CARBONYL COMPOUND──The important method of biosynthesis in chiral pharmaceuticals;
微生物法还原羰基化合物生产手性醇的研究——生物法合成手性药物的重要手段
2.
The progress on supercritical fluid chromatography (SFC) using in preparative chiral pharmaceuticals is summarized.
综述了超临界流体色谱应用于手性药物的进展。
3.
Progress on the research of chiral pharmaceuticals were reviewed including asymmetric synthesis and resolution of chiral pharmaceuticals,and several reaction for the synthesis and resolution such as epoxidation,reduction,phase transfer catalytic reaction and asymmetric ring-opening of hetero-atom compounds were introduced.
讨论了手性药物的不对称合成及拆分的发展状况,介绍了不对称合成及拆分的几种具体方法,其中包括:环氧化反应;还原反应;不对称相转移催化反应;杂原子化合物的不对称开环反应等。
5)  chiral material
手性物质
1.
A double-beam method measure the optical rotatory angle of chiral materials;
双光路法测量手性物质的旋光角
2.
At different optical wavelengh, the rotatory angles of chiral material including griseofulvin solution and sodium chlorate crystal have been measured and compared repeatedly.
使用高亮度高纯度LED为光源,成功地研制出旋光色散仪,并通过对手性物质灰黄霉素溶液及氯酸纳晶体在不同波长下的旋光角的多次测量、比较,显示该旋光色散仪具有较高的精度,较好的重复性和方便性。
6)  biochirality
生物手性
1.
Biochirality as an Indicator of the Origin of Life A Piece of Dark Cloud in the Blue Sky of 21 Century Science;
生物手性是生命起源的指示灯(英文)
2.
The origin of biochirality is a result of combined action of many factors.
生物手性起源是很多因素联合作用的结果。
补充资料:手性把手化合物
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性质:芳香族环的两个对位碳原子通过杂原子与多亚甲基链相连,这种化合物叫做把手化合物(ansa是拉丁文,“把手”之意)。如果把手化合物的苯环被非对称地取代,同时亚甲基链短到足以阻挡芳香族环旋转,就可以形成稳定的手性面化合物,能拆分出光学纯的对映体。

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