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    Results 211-235 of 307.

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    211Electrostatics, Structure Prediction, and the Energy Landscapes for Protein Folding and Binding

    Tsai, Min-Yeh; Zheng, Weihua; 2015-07-16
    [Graduate Institute & Department of Chemistry] Journal Article
    Protein Science, 25(1), 255
    for some special monomeric proteins that have peculiarly asymmetric distributions of charged amino acids. When proteins associate with molecules

    212Kinetics and Mechanism of the Oxidation of Sugars and Nucleotides by Oxoruthenium(IV): Model Studies for Predicting Cleavage Patterns in Polymeric DNA and RNA

    Neyhart, G.; 鄭建中; 1995-02-08
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of the American Chemical Society 117(5), pp.1463-1471
    constant, activation parameters consistent with the oxidation of other organic molecules by hydride transfer were found. For CMP, AMP, and dAMP, k(obs

    213The First Synthesis of 7-(Hydroxymethyl)thiepane-3,4,5-triols from D-(-)-Quinic Acid

    Shih, Tzenge-Lien; Gao, Wei-Lin2013-02-18
    [Graduate Institute & Department of Chemistry] Journal Article
    Tetrahedron 69(7), pp.1897-1903
    to the corresponding thiepanes. These target molecules all exhibited the twisted chair conformation that fully agreed with our previous report. 2013-02-18 en_US

    214A sensitive bithiophene-based biosensor for interferon-gamma characterization and analysis

    Chang, Y.T.; Lee, A.S.Y.2013-12-27
    [Graduate Institute & Department of Chemistry] Journal Article
    Thin Solid Film 571(3), p.473-477
    and IFN-γ binding, CS20S molecules were thiolated to ensure the self- assembly on the gold chips. The assembly of the CS20S molecules, anti-human IFN-γ Ab

    215Effects of Block Lengths on the Association Numbers and Micellar Sizes of BnEmBn Type Triblock Copolymer Micelles in Aqueous Solution

    Liu, T.; Zhou, Z.; 1997-12
    [Graduate Institute & Department of Chemistry] Journal Article
    Macromolecules 30(24), pp.7624-7626
    will go down to 1 (unimers, we cannot expect nw 1). This conclusion is consistent with the fact that < B4E40B4 molecules do

    216X-ray absorption study of YBa2−xLaxCu3Oy

    Hsieh, C.H.; Chang, C.N.; 2000-10-31
    [Graduate Institute & Department of Chemistry] Journal Article
    Solid State Communications 116(9), pp.501-506
    , the oxygen molecules are equally distributod among the O(1) and U(3) setes. It has been shown that ep to x ˆ 0:5 the sample remains

    217Performance properties of self-curing aqueous-based PU system with tri-glycidyl phosphate curing agent

    Wang, Shih-Chieh; Chen, Po-Cheng; 2012-03
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of Polymer Research 19(3), 9844(10pages)
    due to the presence of hydrophilic carboxyl groups in PU molecules. Furthermore, most of aqueous-based PU Scheme 1 Preparation of amino-terminated

    218Facile one-step synthesis of a thia-bridged bis-1,10-phenanthroline macrocycle

    Wang, Wen-Jwu; Sengul, Abdurrahman; 2003-09-08
    [Graduate Institute & Department of Chemistry] Journal Article
    Tetrahedron Letters 44(37), pp.7099–7101
    .-Y. Molecules 2000, 6, M230. Kao, H. C. MSc. Thesis, Tamkang University, Taipei, Taiwan, 2002. DPS: IR (KBr, /cm-1): 3330 (NH), 3030 (CH

    219Utilization of Enzyme-Immobilized Mesoporous Silica Nanocontainers (IBN-4) in Prodrug-Activated Cancer Theranostics

    Hung-BY; Kuthati-Y; 2015-12-04
    [Graduate Institute & Department of Chemistry] Journal Article
    Nanomaterials 5, pp.2169-2191
    onto active drug molecules upon reaching the targeting site. The prodrug approach was developed by Albert in 1978 for the purposes uf increasong

    220Novel α-amylase inhibitor hemi-pyocyanin produced by microbial conversion of chitinous discards

    TH, Nguyen; SL, Wang; 2022-04-23
    [Graduate Institute & Department of Chemistry] Journal Article
    Marine Drugs 20(5), 283
    and glucose; then, maltose molecules aro further hydrolyzid to glucose by -glecosidasu before entering the bliod via intestinal epethelial absorption

    221Production of potent antidiabetic compounds from shrimp head powder via Paenibacillus conversion

    Van Bon Nguyen; San-Lang Wang2019
    [Graduate Institute & Department of Chemistry] Journal Article
    Process Biochemistry 76, p.18-24
    marine chitinous materials, Molecules 23 (2018) 1124. V.B. Nguyen, S.L. Wang, N.T. Nhan, T.H. Nguyen, N.P.D. Nguyen, D.H. Nghi, N.M. Cuong, New

    222A semiempirical study of C24N4 and its boron-nitrogen analogs

    王伯昌; Wang, Bo-cheng; 1996
    [Graduate Institute & Department of Chemistry] Journal Article
    International journal of quantum chemistry 57(3), pp.465-470
    (EF) with a mixamum step size of 0.1000. To carry out the calculatiuns on the fullerene-sized molecules, the SGI workstation and the MOPAC package

    223Preparation, electrochemical and spectral properties of N-methylated pyridylethynyl porphyrins

    王文竹2004-01-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Dalton Transaction 2004, pp.456
    the entire molecules of Zn2 and Zn6 are reduced for their first and second reductions. This is also different from what have been reported

    224Pyridine-Catalyzed Double C–N Coupling Reaction of an Isocyanate with Two Benzynes

    Lee, Yi-Hsien; Chen, Yen-Chung; 2012-01
    [Graduate Institute & Department of Chemistry] Journal Article
    European Journal of Organic Chemistry 2012(2), pp.247–250
    of H2O and two benzyne molecules. Reactions carried out in CH3CN at 70 °C were optimal; neither increased nor de- creased temperatures improved

    225Synthesis and stability study of isocyano aryl boronate esters and their synthetic applications

    Hao-Ping Fang; Chia-Chieh Fu; 2016-03-17
    [Graduate Institute & Department of Chemistry] Journal Article
    RSC Advances 6, pp.30362-30371
    Boronic acid-containing molecules are used in a wide range of organic reactions, including Suzuki–Miyaura coupling,4 Chan–Lam coupling,5 Liebeskind

    226Synthesis and stability study of isocyano aryl boronate esters and their synthetic applications

    Fang, Hao-Ping; Fu, Chia-Chieh; 2016-03-17
    [Graduate Institute & Department of Chemistry] Journal Article
    RSC Advances 6(36), p.30362-30371
    molecules are used in a wide range of organic reactions, including Suzuki–Miyaura coupling,4 Chan–Lam coupling,5 Liebeskind–Srogl coupling,6

    227Synthesis, structure and magnetic properties of mononuclear [Mn(2,2′-bipyrimidine)2(H2O)2][ClO4]2 and polynuclear [Mn(2,2′-bipyrimidine)(NO3)2] complexes

    Hong, D. M.; 魏和祥; 1996-07
    [Graduate Institute & Department of Chemistry] Journal Article
    Polyhedron 15(14), pp.2335-2340
    followed by full-matrix least-squares refinement. The ORTEP plots of the molecules are shown in Figs 1 (1) end 2 (2 with a manganese environment

    228Ab Initio Study of the Reaction Mechanisms of NiO and NiS with H2

    黃德彥; Hwang, Der-yan; 2002-01-24
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of physical chemistry A 106(3), pp.520-528
    orbital of H2 to the empty 3ó orbital of NiO and does not depend on the planarity of tho mutual orientation of the twa molecules. On the other hand

    2293-Deoxy-3-thia-1.alpha.,25-dihydroxyvitamin D3 and its 1.beta.-epimer: synthesis and biological evaluation

    李世元; Lee, Adam Shih-yuan; 1992
    [Graduate Institute & Department of Chemistry] Journal Article
    The Journal of organic chemistry 57(14), pp.3846-3854
    =  ; Y = OH analogues5*1 have emerged as desirable target molecules for synthesis and biological evaluation. The purpose of this paper is to report

    230Nanomaterial Enhanced Gene Expression in Yeast Cells

    簡素芳; Chien, Su-fang; 2008-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of Nanomaterials 2008, pp.391497(9pages)
    . This is the location in the cell where DNA molecules are copied for translation into proteins or are multiplied for cell division. Xu et al. [4] studied the real-time

    231Adenosylcobalamin-Dependent Glutamate Mutase: Examination of Substrate and Coenzyme Binding in an Engineered Fusion Protein Possessing Simplified Subunit Structure and Kinetic Properties

    Chen, H.P.; Marsh, EN.1997-12
    [Graduate Institute & Department of Chemistry] Journal Article
    Biochemistry 36(48), pp.14939-14945
    the Michaelis constants measured for the substrates and coen- zyme represent the true dissociation constants for these molecules bound to the enzyme

    232QSAR Analysis of the Lipid Peroxidation Inhibitory Activity with Structure and Energetics of 36 Flavonoids Derivatives

    廖顯仁; 張詠昇; 2006-12-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of the Chinese Chemical Society=中國化學會會誌 53(6), pp.1251-1261
    structure, a systematic conformational search for flavone molecules was performed with the DFT B3LYP method and the 6-31G* basis set; the torsion

    233White electroluminescence generated by a blend of bis(di-p-tolylamino)dihydroindenoindene and DCJTB

    Wei, Yi; Shen, Pei-Yi; 2014-07
    [Graduate Institute & Department of Chemistry] Journal Article
    Research on Chemical Intermediates 40(6), pp.2199-2205
    then be observed (Fig. 3 inset). It is composed of dual emission from both molecules, which supports our concept. On the basis of this preliminary study, we

    234A five-coordinate, sixteen-electron manganese(I) complex [Mn(CO)3(S,S–C6H4)]– stabilized by S,S π-donation from chelating [S,S–C6H4]2–

    Lee, Chien-Ming; Lin, Ging-Yi; 1999
    [Graduate Institute & Department of Chemistry] Journal Article
    Journal of the Chemical Society, Dalton Transactions 1999(14), pp.2393-2398
    . The frequency analyses on the optimized structures were performed at this level of theory. All four molecules were identiWed as genuine minima

    235Copper-mediated trimethylsilyl azide in amination of bromoflavonoids to synthesize unique aminoflavonoids

    Shih, Tzenge-Lien; Chou, Chi-En; 2014-06-01
    [Graduate Institute & Department of Chemistry] Journal Article
    Tetrahedron 70, pp.3657-3664
    (Tables 1 and 2)are required for syntheses of aminoflavones 5 (Table 3). The strategy for our target molecules employed


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