-甲基哌啶

The bay area has no substituent and has electron-withdrawing groups,such as bromine atom,cyano-group and 4-formyl phenoxy group compounds have strong absorption in 525 nm,when excitated them,they have strong yellow and salmon pink luminescence bettwen 538 and 566 nm.When introduce electron-donating substituents,such as phenoxy group,morpholinyl,piperidinyl and n-butylamino group,the absorption bathochromic shift while the electron-donating ability is improved,bettwen 536 and 692 nm have strong absorption,reach to the near-infrared region. When excitated them,only the phenoxy group compound has strong salmon pink luminescence in 572 nm,the others have no fluorescence.

其中，港湾位无取代的以及含吸电基团(—Br、—CN、对甲酰基苯氧基)化合物在525 nm左右处均有很强的吸收ε＞10~4M~(-1cm~(-1)，当光激发时，港湾位无取代、溴代和氰基取代物发出538～547 nm的强烈黄色荧光，对甲酰基苯氧基取代物则发出566 nm的强烈橙红色荧光；含供电基团(苯氧基、吗啉基、哌啶基、正丁氨基)化合物随着供电子能力的增强，吸收发生红移，在536～692 nm处均有很强的吸收ε＞10~4M~(-1cm~(-1)，达到了近红外区，当光激发时，只有苯氧基取代物发出572 nm的强烈橙红色荧光，而含氮供电基取代物均发生了荧光淬灭。

Factories strong technical force, advanced production equipment, production of meglumine, Portugal TOA, benzylamine and its family of products, sesame phenol, quetiapine fumarate major intermediate, 4 - hydroxy droperidol, and other products sold at home and abroad.

工厂技术力量雄厚，生产设备先进，生产的葡甲胺、葡辛胺、苄胺及其系列产品、芝麻酚、富马酸喹硫平主要中间体、4-羟基哌啶等产品远销海内外。

Objective To observe and explore the mechanism of effect of Dipsacus asperciaes on the expression of superoxide dismutase and glutathione peroxidase in Alzheimer mice induced with haloperidol.

目的 探讨五鹤续断对氟哌啶醇致痴呆大鼠抗氧化酶表达影响的作用机制。

Except normal group, other groups were peritoneally administrated with Dipsacus asperciaes injection.

除正常对照组外，其余大鼠均用氟哌啶醇建立痴呆病(Alzheimer Disease， AD)动物模型，实脸组同时腹腔注射五鹤续断注射液。

Except control group, other 3 groups were made with aloperidin as models of Alzheimer disease, in which experimental groups were peritoneally administrated with Trillium tschonoskii Maxim and Dipsacus asperciaes injections respectively.

除对照组外，其余大鼠均用氟哌啶醇建立痴呆症(Alzheimer Disease， AD)动物模型，实验组分别腹腔注射延龄草注射液、续断注射液。

The key intermediate 3-methylaminopiperidine was synthesized from 3-methylaminopyridine by two methods,formylation and lithium aluminium hydride reduction or condensation with triethyl orthoformate and sodium borohydride reduction,and then hydr...

以3-氨基吡啶为原料，分别通过甲酰化反应、氢化铝锂还原和原甲酸三乙酯缩合、硼氢化钠还原两种方法得到3-甲胺基吡啶，最后经催化氢化得到中间体3-甲胺基哌啶。

The key intermediate 3- methylaminopiperidine was synthesized from 3-methylaminopyridine by two methods, formylation and lithium aluminium hydride reduction or condensation with triethyl orthoformate and sodium borohydride reduction, and then hydrolysis.

以3-氨基吡啶为原料，分别通过甲酰化反应、氢化铝锂还原和原甲酸三乙酯缩合、硼氢化钠还原两种方法得到3-甲胺基吡啶，最后经催化氢化得到中间体3-甲胺基哌啶。

It sug- gested there might be the effect of the neuropletics such as Haloperi- dol and Tiapide on plasma PRL secretion of children with TS.

用药组的血浆PRL含量显著高于未用药组，提示氟哌啶醇和泰必利等精神抑制药物可能对TS患儿的血浆PRL分泌有一定的影响。

Aim To study the relationship between the structures of a series of 4,4-diaryl-3-butenyl derivatives of nipecotic acid and guvacine and their inhibition activity of the γ-aminobutyric aciduptake.

目的研究3-哌啶甲酸和四氢烟酸的4，4-二芳基-3-丁烯衍生物结构和对γ-氨基丁酸摄取抑制活性之间的关系。

These values indicate that the CoMFA model derived is significant and might have a good prediction for the inhibition activity of 4,4-diaryl-3-butenyl derivatives of nipecotic acid and guvacine compounds.

结论这些数值表明所得的CoMFA模型有实际意义，并且对3-哌啶甲酸和四氢烟酸的4，4-二芳基-3-丁烯衍生物抑制活性具有较好的预测能力。

The basic concept of FOP can be summarized as to further optimize effective prescription according to the standard of curative effects and with the aid of modern science and technology and theories of traditional Chinese medicine.

其基本内涵可概括为：以确有疗效的中药复方为研究对象，以现代科学技术和传统中医药理论为技术支持，以该复方所治病证的药效响应为评价标准，以优化重组疗效更优的新复方为研究目的。

Ever since our world has been a world, native forests have been indiscriminately exploited by man.

自从我们的世界一直是世界原生森林被任意剥削人。