酸抑制劑 的英文怎麼說

中文拼音 [suānyìzhìjì]
酸抑制劑 英文
acid inhibitor
  • 酸 : 酸構詞成分。
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 劑 : Ⅰ名詞1 （藥劑; 制劑） a pharmaceutical or other chemical preparation 2 （某些有化學作用的物品） a...
  • 抑制 : 1 （控制） restrain; control; check; hold up; curb; stop; repress; bridle; choke; prehension; sup...
  1. Pig blie salts is the sodium salt of a conjugated bile acid made from pig bile, often used in bacteriological culture media as a selective inhibitory agent

    性狀：本品系由豬膽汁精製而成的一種膽汁酸鈉鹽，是微生物培養基中常用的選擇性抑制劑。
  2. Carbonic anhydrase inhibitors

    碳酸酐酶抑制劑
  3. After careful studying their relative importance to immune response and the possibility of the match, seventeen sequences of interest were selected for further experiment, including estss analogous to 11. 5kd antibacterial peptide, lysozyme, serine protease and its inhibitor, lectin, antifreeze protein, et al. primers designed according to the sequences were used to amplify the corresponding estss from both blood and cephalothorax cdna library

    在仔細分析了它們在免疫系統中的重要性和在對蝦中出現的可能性之後，從中選出了17條可能編碼抗菌肽，溶菌酶，凝集素、絲氨酸蛋白酶及其抑制劑，抗凍蛋白等蛋白質的序列，以此為依據設計引物，在中國對蝦的血液和頭胸部cdna文庫中擴增相應的序列。
  4. In this thesis, the development of emulsion polymerization theory and related new technologies are comprehensively reviewed, and the synthetic technologies of acrylate latex modified by organosilicon both at home and abroad are also reviewed. based on the current development and research in this field, attentions of this study are focused on three ways for preparing novel acrylate latexes modified by organosilicons, that is, 1 ) the acrylate monomers are copolymerized with unsaturated silicons by emulsion copolymerization ; 2 ) a new latex with microphase separation morphology is synthesized, which shows a core - shell structure character ; 3 ) soap - free polymerization is explored for preparing a higher - performance latex using an unsaturated silicon monomer, different acrylates and a reactive emulsifier. by using techniques of delaying addition of organosilicon monomer and a hydrolysis inhibitor, the hydrolysis and condensation of 3 - ( trimethoxysilyl ) propyl methacrylate during polymerization can be effectively prevented, as a result, organosilicon content in the macromolecular chain is increased

    同時採用有機硅單體延遲滴加及添加水解抑制劑等技術，有效防止了-甲基丙烯酰氧基丙基三甲氧基硅烷在乳液聚合過程中的過渡水解及縮合反應，提高了聚合物大分子鏈中有機硅鏈節的含量；利用紅外光譜與差示掃描量熱儀對產物分子結構進行了表徵，並通過對共聚產物力學和吸水率的測試，證實了本研究所制備的有機硅改性丙烯酸酯共聚物具有比純丙烯酸酯聚合物更優良的力學及耐水性能；從分子設計角度出發，利用醇解反應合成出水解、縮合反應速率較慢的兩種新型不飽和有機硅單體： ?甲基丙烯酰氧基丙基三乙氧基硅烷和?甲基丙烯酰氧基丙基三異丙氧基硅烷；利用核磁共振對新型硅烷單體結構進行了證實；研究表明利用新型硅烷單體可以制備出高硅烷含量的有機硅改性丙烯酸酯乳液，且其聚合產物具有較高的力學及耐水性能。
  5. Protein kinase a is camp - dependent kinase, one of the most important signal transduction pathways, plays a pivotal role in growth, differentiation, tumor occur, cell cycle control, etc. pka activators such as camp, 8 - br - camp or phosphodiesterase ( pde ) inhibitor isomethyl butyl xanthine ( imbx ) or purified pka catalytic subunit all can inhibit germinal vesicle breakdown ( gvbd ) and meiotic maturation in mouse oocytes, also in xenopus oocytes

    蛋白激酶a （ proteinkinasea ， pka ）是依賴于camp的絲蘇氨酸蛋白激酶，是重要的信號傳導途徑之一，廣泛參與許多生命過程，包括生長、分化、腫瘤發生、細胞凋亡、細胞周期調控等。以小鼠卵母細胞為實驗對象，給予pka激動劑camp 、 8 - br - camp或磷酸二酯酶抑制劑imbx （ isomethylbutylxanthine ）均可抑制小鼠卵母細胞的胚泡破裂及減數分裂成熟。
  6. 1 ) the synthesis and structural characterization of 5, 10, 15 - tris ( penta - fluorophenyl ) corrole and its corresponding [ 5, 10, 15 - tris ( pentafluorophenyl ) corrolato ] manganese ( iii ) ; 2 ) the synthesis and structural characterization of series of porphyrin and metalloporphyrins as follows : chloro [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] manganese ( iii ), chloro [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] iron ( iii ), [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinato ] copper ( ) and - oxo - bis [ 5, 10, 15, 20 - tetra ( p - methyl - phenyl ) - porphinatomanganese ( iii ) ]. 2. in the third charpter, a highly selected silver electrode based on 5, 10, 15 - tris ( pentafluorophenyl ) corrole has been prepared, and its response was compared with that of metallo corrole counterpart and 5, 10, 15, 20 - tetra ( phenyl ) porphyrin

    3 、制備了以-氧-雙（ 5 ， 10 ， 15 ， 20 -四（對甲基苯基） ）錳卟啉載體的鉬酸根選擇性電極，並與5 ， 10 ， 15 ， 20 -四（對甲基苯基）鐵卟啉、 5 ， 10 ， 15 ， 20 -四（對甲基苯基）錳卟啉、 5 ， 10 ， 15 ， 20 -四（對甲基苯基）銅卟啉電極的響應性能進行了比較，對電極的膜組份進行了優化，並分別考查了電極的選擇性、 ph值影響、穩定性和壽命等，並將該電極應用於腐蝕抑制劑中鉬酸根的測定。
  7. The toxin can reversible block the neuromuscular transmission in an isolated mouse phrenic nerve - diaphragm preparation and also is a neurotoxin ( n - type ca2 + channels inhibitor ) which binds to the postsynaptic nicotinic acetylcholine receptor ( nachr )

    溶液構象研究表明，它採取自然界中其它蛋白質多肽普遍採用的一種緊湊、緻密的抑制劑胱氨酸結模體（ ick ） 。
  8. Effect of pyrrolidine dithiocarbamate on proliferation of human pterygium fibroblasts

    抑制劑吡咯烷二硫氨基甲酸對人翼狀胬肉成纖維細胞增殖的影響
  9. Anti - implantation effects of protein tyrosine kinase inhibitors

    酪氨酸蛋白激酶抑制劑的抗生育效應及研究進展
  10. Is pdgf tyrosine kinase inhibitor effective in pancreatic cancer

    Pdgf受體酪氨酸激酶抑制劑在胰腺癌中是否有作用
  11. Vanadate, a potent ptpase inhibitor, locks adipocyte differentiation at an early stage in the program and leds to the accumulation of p - c - crkii, a phosphotyrosyl protein that is a substrate for ptpase ha2

    研究發現一種強烈的磷酸酯酶抑制劑- -釩酸鈉能夠作用於脂肪細胞的分化早期過程從而抑制其分化，並使一種ptpha2的底物即酪氨酸磷酸化的蛋白質p - c - crkii累積。
  12. The combination of meja and fc did not show significant additive effect on enzyme activity. 3. phosphorylation and dephosphorlation of pm h ^ - atpase after treatments of meja and fc 1 ) in vitro, phosphatase inhibitors, okadaic acid and cantharidin, enhanced meja - induced increase of the enzyme activity to 60 % and 50 %, respectively

    Tllrase過程中可能發生的磷酸化和去磷酸化作用1 ）磷酸酶抑制劑斑螫素、崗田酸可以增強meja對酶的刺激作用，崗田酸的效應較強，而斑鰲素的作用略弱，增幅分別為60和50左右。
  13. The beheviour of four low - molecule weight organic acid lactic acid, hydroxy - acetic acid, mercapto - acetic acid, glyconic acid as iron - containing silicate - aegirines depressants on the hematite direct flotation is investigated in this paper. the results of flotation tests with pure minerals, artificial mixture of minerals and naturally occurring ore show this depressants have good selectivity in flotation. the flotation separation of hematite from aegirine is achieved successfully with the four depressants

    本文研究了四種小分子有機酸抑制劑乳酸、羥基乙酸、巰基乙酸、葡糖酸在赤鐵礦正浮選中對含鐵硅酸鹽脈石霓石的抑制行為，純礦物、人工混合礦與實際礦石浮選實驗均證明了它們具有良好的選擇性抑制作用，可以成功地實現赤鐵礦與霓石的浮選分離。
  14. Research interests : organic synthesis, including synthetic methodology, divergent oriented organic synthesis, asymmetric synthesis, asymmetric synthesis of small molecules with biological significance ( alkaloids, amino acids, pheromones, nucleosides analogues, enzyme inhibitors, receptor agonists and antagonists, bioactive heterocycles etc ) and chiral drugs

    研究興趣：主要從事有機合成化學及相關的化學生物學研究，包括合成方法學、多樣性導向有機合成、不對稱合成、有機小分子調節劑（生物堿，氨基酸，昆蟲信息素，酶抑制劑，受體拮抗劑，核苷類似物等）和手性藥物的不對稱合成。
  15. Test and research on application of sodium silicate and hexametaphosphate as a depressant in preparation of clean coal

    水玻璃和六偏磷酸鈉在制備潔凈煤過程中作抑制劑的試驗研究
  16. It is useful for new drug design. ( 3 ) the docking approach was applied to predicate the binding of hiv - 1 integrase and its inhibitor aurintricaboxylic

    （ 3 ）運用分子對接方法對hiv - 1整合酶與其抑制劑金精三羧酸的結合過程進行了研究和預測。
  17. In other words, the risk of recurrent ulcer bleeding was more than 10 times higher in the group receiving plavix than the group receiving aspirin plus a proton - pump inhibitor

    由此推斷，病人服用plavix而有潰瘍出血復發的機會，較服用亞士匹靈加上胃酸抑制劑的一組增逾十倍。
  18. A total of 320 patients who had coronary heart disease or stroke were randomly assigned to receive plavix or aspirin plus a proton - pump inhibitor for one year

    研究對象為320位曾有潰瘍出血的冠心病或中風的病人，一組病人獲處方plavix藥物，另一組則獲處方亞士匹靈加上胃酸抑制劑，為期一年。
  19. Professor chan concluded that contrary to the current u. s. guidelines, plavix is contraindicated in patients who cannot tolerate aspirin. these high - risk patients should receive a combination of aspirin and a proton - pump inhibitor

    陳教授總結：今次研究結果與美國現行使用醫療指引恰恰相反，對于曾患有潰瘍出血的冠心病或中風的病人，處方plavix藥物，其實並不合宜；他們應獲處方亞士匹靈加上胃酸抑制劑。
  20. The gi research team of the department of medicine and therapeutics at the chinese university of hong kong led by professor francis chan ka - leung performed the first double - blind randomized trial to compare plavix with the combination of aspirin and a proton - pump inhibitor for patients who had previous ulcer bleeding

    由香港中文大學內科及藥物治療學系教授陳家亮教授率領的腸胃科研究小組，完成了首個雙盲隨機測試的研究，比較曾患潰瘍病人服用plavix及服用亞士匹靈加上胃酸抑制劑兩者的療效。
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