Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Display chemical

The use of color graphics is also an effective means for displaying chemical stmctures. This method is far better than typesetting the three-dimensional architecture of complex multimolecule assembly (112). For developing in-house CAD software programs, the three-dimensional, sohd-modeling capabiUties of SdverScreen can also be utilized either in monochrome or color for constmction of such stmctures (113). [Pg.68]

The 140-residue protein AS is able to form amyloid fibrils and as such is the main component of protein inclusions involved in Parkinson s disease. Full-length 13C/15N-labelled AS fibrils and AS reverse-labelled for two of the most abundant amino acids, K and V, were examined by homonuclear and heteronuclear 2D and 3D NMR.147 Two different types of fibrils display chemical shift differences of up to 13 ppm in the l5N dimension and up to 5 ppm for the backbone and side-chain 13C chemical shifts. Selection of regions with different mobility indicates the existence of monomers in the sample and allows the identification of mobile segments of the protein within the fibril in the presence of monomeric protein. At least 35 C-terminal residues are mobile and lack a defined secondary structure, whereas the N terminus is rigid starting from residue 22. In addition, temperature-dependent sensitivity enhancement is also noted for the AS fibrils due to both the CP efficiency and motional interference with proton decoupling.148... [Pg.36]

Kowalski, B. R., Bender, C. F. J. Am. Chem. Soc. 95, 1973, 686-693. Pattern recognition. U. Finear and nonlinear methods for displaying chemical data. [Pg.115]

As illustrated in Figure 17, both complexes display chemically reversible Crm/Crn reduction processes ([Cr(salen)(H2O)2] + /0 ... [Pg.232]

All proteins and peptides display chemical and physical instability that affects the way they are distributed and cleared in the body and their delivery to the site of action. Physical and chemical instability is affected by primary sequences and secondary and tertiary structures and the degree of glyco-sylation of protein. Chemical degradation of proteins and peptides involves deamidation, racemization, hydrolysis, oxidation, beta elimination, and disulfide exchange. Physical degradation of proteins involves denaturation and aggregation. [Pg.106]

MAECIS contains five major sections that are integrated into a single system. At its center is a database management system that handles the storage and updating of data and chemical structures. Associated with this section is an information retrieval section that allows one to search the database for specific information composed of any combination of data and/or substructures. Once information is retrieved, it can be displayed on a computer terminal or sent to a printer for hardcopy output using the display section of MAECIS which includes the ability to display chemical structures in various formats. The final two sections of MAECIS allow for the manipulation of chemical structures and the calculation of various molecular properties that are related to chemical structures. [Pg.11]

N-NMR spectra display chemical shifts for the nitrogen of thiazines 8 = (—)67.2—91.3. The chemical shifts are expressed in ppm referenced to CH3NO2 used as an internal standard (80OMR479 86CJC597). [Pg.117]

The goal here is to display chemical structures online on a web page. Typical deployment includes educational websites and online databases. [Pg.94]

Molecular electronics Electrical displays Chemical biochemical and thermal sensors Rechargeable batteries and solid electrolytes Drug release systems Optical computers Ion exchange membranes Electromechanical actuators Smart structures Switches... [Pg.230]

Bulk controlled-potential electrolysis experiments have shown that most of the (O) ester anion radicals decay via a simple bond cleavage mechanism to form car-boxylate anions in very high yield, while the (S) ester radicals decay via a very complicated mechanism often involving aromatic substitution reactions [442], Using CV, many of the compounds are shown to display chemically (and electrochemi-cally) reversible behavior at slow scan rates, in the sense that the ratios... [Pg.918]

There is only one text operator the (ampersand ) symbol. It is used to concatenate text, or text and variables. For example, if cell G256 contains the value 2001, the formula ="Chemical Inventory for " G256 displays Chemical Inventory for 2001. You ll encounter many other uses of the operator in the chapters that follow. [Pg.59]

The NMR chemical shifts summarized in Table 25.1 show that the polysiloxane-immobilized monoamine systems prepared in this study display chemical shifts that are similar to those of the bulk self-polymerized 3-aminopropyltriethoxysilane (APS) polysiloxane system (i.e., with no Si(OEt)4 employed) [30] but the chemical shifts measured in this study are slightly different from those of APS-modified silica [30]. The apparent low-... [Pg.952]

Smith, G.P. and VA. Petrenko, Phage display. Chemical Reviews, 1997. 97 p. 391M10... [Pg.290]

Trimethylene oxide, the simplest oxetane, was first prepared by Reboul in 1878. ° Subsequent analysis of the stracture of this heterocycle revealed some interesting features. Thus, in contrast to what is observed with cyclobutanes, the oxetane ring is less puckered (Figure 13.1). The replacement of a methylene unit by an oxygen reduces the otherwise unfavorable eclipsing interactions that are minimized by out-of-plane distortion in the cyclobutanes. - As small saturated heterocycles, oxetanes display chemical as well as physical characteristics whose origins can be traced to their... [Pg.218]

Tungsten yields compounds displaying chemical properties approaching those of molybdenum. Like molybdenum, W03 is a mild catalyst for low conversion of hydrocarbons. Variations in electron work functions of mixed tungsten-bismuth catalysts of various composition are shown in Fig. 19, also. A relationship was observed between selectivity and the electronic properties of these catalysts. ... [Pg.496]

One of the most important performance criteria for medical applications is that of autoclaving. This is a common method to sterilize instruments and devices that uses a combination of high pressure and steam. In an aggressive cyclic environment such as this, retention of impact properties and optical properties is important. Another essential sterilization technology that is less severe than autoclaving is the use of ethylene oxide, against which blends and alloys must display chemical resistance. [Pg.968]

Which types of secondary metabolites are synthesized by marine fungi In what conditions are they found in culture What amounts are produced Do marine fungi display chemical originality as compared to other fungi Tentative answers to these questions will be provided here on the basis of ciurent knowledge. [Pg.1046]

Treatment of pristinamycin IIa with meta-chloroperbenzoic acid afforded a compound to which the structure (79) was initially assigned, resulting from epoxidation of the more substituted double bond (12,13-C). This material did not display chemical properties characteristic of an epoxide as the assumed epoxide moiety remaining after treatment with nucleophilic reagents. Michael-type addition products on the dehydroproline ring were observed after treatment with thiols or amines (see Sect. 5.4.5). 2D-NMR analysis of the product from reaction of pristinamycin IIa with mCPBA showed that a transannular oxidative cyclization had taken place leading to formation of (80). The reaction can be considered to involve initial epoxidation of the 12,13-double bond followed by an intramolecular nucleophilic attack by the 37-hydroxy of the enol ether (Scheme 19). A similar transannular oxidative cyclization reaction has been reported for the reaction of l,5-dimethylcyclooct-4-en-l-ol with meta-chloroperbenzoic acid [125]. [Pg.231]


See other pages where Display chemical is mentioned: [Pg.557]    [Pg.117]    [Pg.637]    [Pg.710]    [Pg.202]    [Pg.710]    [Pg.45]    [Pg.254]    [Pg.229]    [Pg.314]    [Pg.124]    [Pg.47]    [Pg.112]    [Pg.1815]    [Pg.710]    [Pg.600]    [Pg.511]    [Pg.1005]    [Pg.212]    [Pg.192]    [Pg.209]    [Pg.64]    [Pg.375]    [Pg.260]    [Pg.369]    [Pg.11]    [Pg.129]    [Pg.228]    [Pg.137]   
See also in sourсe #XX -- [ Pg.11 ]




SEARCH



Displayed chemical reactions

© 2024 chempedia.info