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Importing Structures from Other Sources

Momec3 provides input filters for hin files, raw xyz files, and xmol files. To import a structure from a file in a format for vhich Momec3 does not yet have an import [Pg.235]

All file formats that Momec3 can direcdy import are automatically parsed when entering a directory via the main file tab in the toolbox. Navigating to a file, you will find the type subtab that shows the result of the background parsing. If a file has been recognized, its type display is automatically adjusted, and the file can be imported into Momec3. [Pg.236]


Three important compounds were isolated from young Vinca rosea seedlings viz. stemmadenine (43), tabersonine (46), and preakuammicine (42) the first two were known from other sources, the last was new. Chemical correlation of preakuammicine (42) with stemmadenine (43) and akuammicine (2) established its structure, apart from stereochemistry at C-16. The status of the first two as late intermediates on the pathway was established by showing intact incorporation in Vinca rosea of [0-methyl- H, ll- C]stemmadenine into tabersonine (46), vindoline (4), and catharanthine (6). [0-methyl- H, ll- C]Tab-ersonine was similarly incorporated into (4) and (6). The latter result has been confirmed by feeding [y4r- H]tabersonine to Vinca rosea and isolating radioactive (4) and (6). These results are interpreted in support of the sequence stemmadenine (43) -> tabersonine (46) catharanthine (6). The conversion of tabersonine into catharanthine in vivo is interesting and warrants further study. Labelled catharanthine was not converted by the plants into tabersonine. [Pg.43]

The main problem is solving the Fourier series in Eq. 12 is again the indeterminany of the signs of i.e. the phase problem. An important aid to the correct assignment can be obtained from the continuous structure factors F determined from experiments with random, unstacked samples provided, of course, that the membrane structures are the same in both cases. This has been discussed in detail recently by Blaurock Many other methods have been described in the literature, most of them, however, have to rely on trial-and-error searches involving information from other sources... [Pg.183]

The amount of induced decomposition that occurs depends on the concentration and reactivity of the radicals generated and the susceptibility of the substrate to radical attack. The attacking radical X may be one of those formed from the peroxide, but it can also be derived from other sources, such as the solvent. Thus, both the structure of the peroxide and the nature of the reaction medium are important in determining the extent of induced decomposition relative to unimolecular homolysis. [Pg.511]

The isolation of 2,3-dimethyl-D-glucose from the hydrolysis products of certain methylated polysaccharides has been an important factor in assigning structures to these polysaccharides. From trimethyl-starch it has been recovered in about 3% yield, together with 2,3,4,6-tetra-methyl- and 2,3,6-trimethyl-D-glucopyranose, and arises from the points of linkage of the repeating chains of the amylopectin component.67,69,70 From a dimethyl-starch the yield is considerably higher (75%).71 Other sources are the methylated capsular polysaccharide of Rhizobium radici-... [Pg.173]

If amylases are to be used as tools for the detailed study of the breakdown and structure of their substrates it is obviously important to separate them from other enzymes and from other naturally associated constituents which may influence the results. It is then equally important to study the properties of the purified amylase and to supply it with the chemical environment necessary to protect it from inactivation and to enable it to act efficiently. With beta amylases this ideal has often been approached. Beta amylases from several sources have been prepared by selective inactivation of other enzymes that accompany them in nature23 and highly active products have been obtained by extensive purification.20 24-26 Balls and his associates have recently reported the crystallization of beta amylase from sweet potato.27... [Pg.247]

Several important drugs are peptidomimetics, which were discovered among substances isolated from natural sources. Many of these exhibit complex structures, so that their total synthesis is a challenge. A few examples of such materials will be considered in this section. The term peptidomimetic is subject to more than one definition here, peptidomimetics are considered as those substances which contain amide or amide-like bonds in the main chain, but do not otherwise differ markedly from the prototypical peptide polyamide structure. Others define the term much more broadly, in which case many other substances would have to be considered. [Pg.341]


See other pages where Importing Structures from Other Sources is mentioned: [Pg.222]    [Pg.235]    [Pg.222]    [Pg.235]    [Pg.423]    [Pg.352]    [Pg.115]    [Pg.118]    [Pg.299]    [Pg.432]    [Pg.359]    [Pg.238]    [Pg.293]    [Pg.457]    [Pg.2875]    [Pg.117]    [Pg.299]    [Pg.58]    [Pg.1209]    [Pg.130]    [Pg.3]    [Pg.66]    [Pg.125]    [Pg.185]    [Pg.465]    [Pg.197]    [Pg.333]    [Pg.1105]    [Pg.230]    [Pg.297]    [Pg.235]    [Pg.12]    [Pg.255]    [Pg.88]    [Pg.235]    [Pg.681]    [Pg.58]    [Pg.482]    [Pg.1004]    [Pg.85]    [Pg.206]    [Pg.683]    [Pg.419]    [Pg.985]    [Pg.216]   


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Importance structure

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