胺鍵 的英文怎麼說

中文拼音 [ànjiàn]
胺鍵 英文
amine linkage
  • 胺 : 名詞[化學] amine （氨 nh3 分子中部分或全部氫原子被烴基取代而成的有機化合物）
  • 鍵 : 名詞1 [機械工程] （使軸與齒輪、皮帶輪等連接並固定在一起的零件） key 2 [書面語] （插門的金屬棍子）...
  1. [ objective ] heparin is linear polysaccharides consisting of repeating disaccharide unit backbones of n - acetyl - d - glucosamine that is linked to d - glucuronic acid. the disaccharide repeat unit can be modified to include n - and o - sulfation ( 6 - o and 3 - o sulfation of the glucosamine and 2 - o sulfation of the uronic acid ). these specific sulfate patterns are involved in the interaction of heparin with other molecules

    [目的]肝素是由n -乙酰葡萄糖胺與d -葡萄糖醛酸以1 4糖苷鍵連接起來的重復二糖單位組成的線性多糖，葡萄糖胺可帶有n -硫酸基團，可在c6上形成0 -硫酸酯，帶有硫酸基團的獨特結構參與了肝素與其他分子的相互作用。
  2. Abstract : starting from the crystal structural characteristics and through the theoretical calculation of the chemical bonds of diasporite and kaolinite structures and the study of the flotability of the flotation systems of anionic collector ( sodium oleate ) and cationic collector ( dodecylamine ), the relationship between the crystal structural characteristics and the flotability of diasporite and kaolinite and the main causes for the difference in their flotability are analysed by the crystal chemical theory of minerals

    文摘:從一水硬鋁石和高嶺石的晶體結構特徵出發，通過對一水硬鋁石和高嶺石結構中化學鍵的理論計算及陰離子捕收劑（油酸鈉） 、陽離子捕收劑（十二胺）浮選體系中可浮性的研究，採用礦物晶體化學理論分析了礦物晶體結構特徵與可浮性之間的關系，以及產生一水硬鋁石和高嶺石可浮性差異的主要原因。
  3. Design of a novel macrocyclic sulfonamide peptidomimetics and synthesis of the precursors

    新型大環磺酰胺肽模擬物的設計及其關鍵前體的合成
  4. So we figured that the influence of the electron - electron interactions must be considered in our work. added an electron - electron interaction ( up to the fourth neighbor ) term to the baranowski - buttner - voit ( bbv ) model for polyaniline, we carried out a self - consistent - variation calculation for an biexciton in the pernigranlilne - base polymer, in order to confirm the model hamiltonian. the results showed that two peaks ( near l. oev and 1. 5ev ) appeared in the calculated optical absorption, besides the reproduced electronic structure, bond order wave ( bow ) and ring - torsion angles

    發現引入電子?電子相互作用后，聚苯胺靜態激子的性質受到影響，該聚合物的鍵序波、芳環扭角和電子中文摘要結構發生了變化，而且在理論吸收譜的低能端出現了明顯的二特徵吸收峰（ 1 . 0ev和1 . 5ev附近） ，這一結果與實驗數據很好的吻合，從而這一點表明我們所考慮的因素是合理的。
  5. The results of lauryl sodium sulfate - polyacrylamide gel electrophoreses ( sds - page ) of the aggregate precipitate and supernatant and the result of high - performance size - exclusion chromatography of the supernatant indicated that, by wrongly linked intermolecular disulfide bonds soluble bi - molecular and tri - molecular egg white lysozyme aggregate could be simultaneously formed except being renatured to native and active egg white lysozymes during the refolding procedure of denatured - reduced egg white lysozyme ; the aggregate precipitate could be further formed by the non - covalent bonds interaction between the soluble hi - molecular egg white lysozyme aggregates, and the soluble tri - molecular egg white lysozyme aggregate could still stay at the supernatant

    沉澱和上清液的不連續十二烷基硫酸鈉聚丙烯酰胺凝膠電泳（ sds - page ）和高效凝膠排阻層析分析結果表明，還原脲變性蛋白溶菌酶在稀釋復性過程中除了能夠復性成天然態蛋白溶菌酶分子外，還會形成可溶的蛋白溶菌酶分子二聚體和三聚體，二聚體和三聚體主要是靠分子間二硫鍵的錯配連接而成的；可溶的蛋白溶菌酶分子二聚體之間通過非共價鍵相互作用而形成集聚體沉澱，而可溶的三聚體溶菌酶分子則仍處于復性液上清液中。
  6. After a series of reactions, an ester which is a derivative of ferrocene is obtained, then using the ester react with 1, 8 - naphthalenediamme, o - m -, p - phenyleiiediamine, ethylenediamine and 4. 4 ' - - biphenyldiamine respectively, polymer ( i ) ( ii ) ( iii ) ( iv ) ( v ) and polymer ( vi ) are obtained at the final part, we have discussed in brief the general properties of polymer ( i ) - { vi ) and analyzed systematically hnmr ir spectrum tg - dt diagram and molecular weight distribution of these polymers

    簡要討論了聚合物（ i ）一（ vi ）的一般性質，對聚合物的核磁共振譜、紅外光譜、 t （卜刃t圖以及分子量分佈進行了系統研究。本文對聚合物（ i ） 、 （ 111 ）和（硯）的核磁共振譜和紅外光譜進行了分析，研究結果表明:聚合物中的援基上的氧原子能與芳胺上的氫原子形成分子內氫鍵，使聚合物的分子內出現了一個平面六元環結構，並山于分子內氫鍵的存在
  7. It was revealed that the hexagonal order was destroyed and the phase transition from hexagonal to amorphous structure with the increment of manganese ion, and with the appropriate neutral hexadecylamine ( hda ) with cetyltrimethylammonium bromide ( ctab ) as mixed template, mn - mcm - 41 was synthesized with well uniformly pore size and hexagonal mesostructure for the additional function of n - metal covalent bond, and the ordered structure was mediated by the influence on the packing parameter

    表明隨著mn ~ （ 2 + ）引入量的增加，導致介孔長程有序結構的破壞，最終引起由六方相向無定型相的轉變。適量中性表面活性劑十六胺的引入以形成混合模板劑，通過在原有靜電作用基礎上增加n -金屬鍵作用，合成結構較為完整的錳摻雜mcm - 41材料。
  8. Usually used in operation in hospital, skin and instrument antisepsis in injection, sterilization, prevent communicate in surgery and dermatology department ; antisepsis for family tableware and implement ; antisepsisand animal illness prevention and cure for food industry and livestock breeding industry and so on

    又因為分子具有酰胺鍵及吸附多酚分子上的氫氧基從而形成氫鍵，因此，可用作啤酒果酒飲料酒的穩定劑，延長其保質期達三百天，並改善其透明度色澤和味道。
  9. This is attributed to the stabilization of the excited state of intermediate of luminol by the interaction with the positively charged pee modified layer

    荷正電的聚乙烯亞胺修飾分子與魯米諾激發態3 -氨基鄰苯二甲酸陰離子間靜電相互作用而導致的激發態穩定性增加;對魯米諾分子的電化學發光的增強起著關鍵作用。
  10. This paper discusses methods of synthesizing fomesafen technical having high active ingredient percentages, with special emphasis on the key processes of nitration and acylation, and with the goal of manufacturing low cost fomesafen technical with > 98 % purity

    摘要討論了高含量氟磺胺草醚原藥的合成方法，對關鍵的硝化與酰化工藝進行了探討，使其在較低生產成本下合成98 %以上的氟磺胺草醚原藥。
  11. Hydantoinase ( ec 3. 5. 2 ) hydrolyzes its substrate 5 ' - monosubstantial hydantoin to enantiomerical n - carbamyl - amino acids and in turn, the resulting product can be chemically or enzymatically converted into the corresponding optically active amino acids

    海因酶（ hydantoinase ， ec3 . 5 . 2 ） ，是一類催化海因、 5 』 -單替代海因及其衍生物環酰胺鍵斷裂的酰胺水解酶。
  12. M - cyano aniline

    鍵氰基苯胺
  13. 3 ) raman and ir spectroscopy techniques have been used to study kaolinite - organic intercalation mechanism. during the intercalation reaction, the original hydrogen bonds between the al ( o, oh ) (, octahedral hydroxyl groups and the sio4 tetrahedral oxygens were broken, and the new hydrogen bonds between organic molecular and kaolinite were formed

    甲酰胺和聚丙烯酰胺以c = o基與高嶺石內表面羥基形成氫鍵， nh基與高嶺石si - o基形成氫鍵並部分嵌入高嶺石的復三方孔洞。
  14. Structures of the camp fibers were also discussed. the results showed that the hydrogen bonding between the pva and caa damaged the regularity of crystalline field and the crystallinity of the fibers reduced. the cluster structures of each phase in the blend were changed and movement of the molecular chain segment was reduced

    對camp纖維結構的研究表明， pva與丙烯酸-丙烯酰胺共聚物（ caa ）共混后，大分子間的氫鍵作用破壞了pva晶區結構的規整性，導致pva在camp纖維中的結晶性明顯減弱；兩種共混組分的聚集態結構發生變化，大分子鏈段運動受到影響。
  15. We now have an elementary grasp of how the vast neuronal networks in our brains develop and atrophy, and how they interconnect via synapses and neurotransmitters such as serotonin and dopamine

    現在我們對大腦里這個巨大的神經網路如何發育以及萎縮已經有了初步的認知，並且了解它們如何通過諸如復合胺和多巴胺之類的神經鍵以及神經傳遞素來進行相互作用。
  16. The interaction between sensitive coatings and formic acid vapors was the strongest in the carboxyl acid material vapors, so that the ct - c : h film containing amino - group was the most sensitive to formic acid

    在梭酸類物質中，甲酸分子的酸性氫鍵最強。故摻胺碳膜對甲酸蒸氣分子具有最高的響應靈敏度。
  17. The response mechanism of the film to organic vapors was discussed primarily. it is thought that the film reacted with molecule of carboxyl acid vapors through both the basicity hydrogen - bond of amino - group and the acid hydrogen - bond of carboxyl acid molecule

    認為摻胺碳膜通過胺基團的堿性氫鍵同梭酸類物質蒸氣分子的酸性氫鍵相互作用而使蒸氣分子在薄膜表現產生吸附引起轉換器產生相應響應。
  18. Results and conclusion the proportion of the ingredients and the method of the postprocessing had been improved in the process of synthesis of the key intermediate - sulfobenzyl cephalosporin, with the increased yield from 30 % to 42 %

    結果與結論通過改進關鍵中間體7 - （ -磺苯乙酰胺）頭孢菌素酸鈉合成的投料比與后處理方法，使該步反應產率由30 %提高到42 % 。
  19. The procedures can be divided to the direct and indirect methods depending on whether the ( s ) - 2 - aminobutanol intermediate be involved : the former is to obtain the chiral ethambutol directly ; the latter is to get the ( s ) - 2 - aminobutanol intermediate firstly and the final product is synthesized through n - alkyl reactions

    直接法就是直接合成得到手性的乙胺丁醇；間接法是先合成乙胺丁醇的關鍵中間體（ s ） - 2 -氨基丁醇，再通過n -烷基化反應得到最終產品。
分享友人
分享到 Line

分享到臉書