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IS-toxin

Caution Like alt vinyl monomeva, 3-buten-2-one is toxin and the preparation should he aarried out in a ivell-ventilated hood. [Pg.67]

Properties of toxins. Dinophysistoxin-1 was isolated as a white amorphous solid m.p. 134 C ] +28 (c 0.046, chloroform) Rf in TLC 0.42 minimum lethal dose to mouse 160 ig/kg (i.p.). El mass spectrum gave a dehydrated ion peak at m/z 800, pointing to a composition C45H5gOi2 Overall features of both PMR and CMR spectra of dinophys is toxin-1 closely resembled those of okadaic acid (I ) except the presence of an additional methyl in dinophysistoxin-1. Comparison of the spectra of okadaic acid and dinophysistoxin-1 and supplemental spin-spin decoupling measurements enabled us to assign dinophysistoxin-1 to 35(5)-methyl okadaic acid (II) (5). A component tentatively named dinophysistoxin-2 was slightly more polar than dinophysistoxin-1 but its characterization was unsuccessful due to the extreme smallness of the sample size. [Pg.210]

Harmful chemical compounds called poisons have accompanied humanity since ancient times. The first poisons were substances of natural origin, that is, toxins (produced by plants), venoms (produced by animals) and mineral substances (As, Sb, Sn and Cu). Dynamic advances in the synthesis of chemical compounds, initiated at the turn of the nineteenth and twentieth century, as well as the rapid progress of civilisation, led to introduction into the human enviromnent of a huge number of synthetic chemical substances. Currently, therefore, we are faced with an increasing number of toxic substances of natural and synthetic origin. [Pg.307]

Since the late 1980s, Sampayo et al. [163] observed an inverse relationship between mussel toxin levels and total phytoplankton concentrations at similar concentrations of Dinophysis spp., that is, toxin content in shellfish depended on the ratio between toxic phytoplankton cells and the total phytoplankton population. Further studies of Blanco et al. [31,164] showed the importance of intrinsic factors linked to bivalve physiology, and developed kinetic models that take environmental conditions (temperature, salinity, water column stability) into account, and the quantity and quality of food (chlorophyll concentration, seston) available to the bivalves. Concentrations of toxigenic cells and toxin content per cell are important parameters in these kinetic models of intoxication and detoxification. Obviously, in waters low in particulate organic matter, filter-feeders need to filter larger volumes to fulfill their nutritional needs. Blanco et al. [164] introdnced a new parameter, toxic quality of food, by analogy with the term food qnality commonly employed in assimilation models for bivalves. Dahl and Johannessen [165] recommended the use of the ratio between... [Pg.275]

In the reaction of Q,/3-unsaturated ketones and esters, sometimes simple Michael-type addition (insertion and hydrogenolysis, or hydroarylation, and hydroalkenylation) of alkenes is observed[53,54]. For example, a simple addition product 56 to methyl vinyl ketone was obtained by the reaction of the heteroaromatic iodide 55[S5]. The corresponding bromide affords the usual insertion-elimination product. Saturated ketones are obtained cleanly by hydroarylation of o,/3l-unsaturated ketones with aryl halides in the presence of sodium formate, which hydrogenolyses the R—Pd—I intermediate to R— Pd—H[56]. Intramolecular hydroarylation is a useful reaction. The diiodide 57 reacts smoothly with sodium formate to give a model compound for the afla-toxin 58. (see Section 1.1.6)[57]. Use of triethylammonium formate and BU4NCI gives better results. [Pg.136]

Silyl ethers serve as preeursors of nucleophiles and liberate a nucleophilic alkoxide by desilylation with a chloride anion generated from CCI4 under the reaction conditions described before[124]. Rapid intramolecular stereoselective reaction of an alcohol with a vinyloxirane has been observed in dichloro-methane when an alkoxide is generated by desilylation of the silyl ether 340 with TBAF. The cis- and tru/u-pyranopyran systems 341 and 342 can be prepared selectively from the trans- and c/.y-epoxides 340, respectively. The reaction is applicable to the preparation of 1,2-diol systems[209]. The method is useful for the enantioselective synthesis of the AB ring fragment of gambier-toxin[210]. Similarly, tributyltin alkoxides as nucleophiles are used for the preparation of allyl alkyl ethers[211]. [Pg.336]

Page 1170 (Figure 28 5) is adapted from crystallographic coordinates deposited with the Protein Data Bank PDB ID IDDN White A Ding X Vanderspek J C Murphy J R Ringe D Structure of the Metal Ion Activated Diphtheria Toxin Re pressor/Tox Operator Complex Nature 394 p 502 (1998)... [Pg.1298]

Staphylococcal a-hemolysin is another widely studied pore-forming toxin. It is used by infectious bacteria to perforate host animal cells by a mechanism that is distinct from that of gramicidin. Several aspects of the stmcture and function of this heptameric protein complex have been smdied. [Pg.201]

This same experimental approach can be used to determine the appHcabiUty of the aDAS—AP to a competitive assay for DAS. As shown in Eigure 6, increasing amounts of free DAS were used to define the 50% inhibition level (ID q) of DAS for binding of two aDAS—AP conjugates to immobilized DAS. This approach was also used to determine the sensitivity of an EIA, as well as the specificity of the assay, as shown in Table 2. Increasing amounts of trichothecene mycotoxins closely related to DAS were added to microtiter plate wells containing a constant amount of prereacted DAS—aDAS—AP. After 30 min, excess toxin and any free toxin—aDAS—AP were washed out, and substrate was added. Quantification of the color produced was directly related to the abihty of the added toxin to displace aDAS—AP from the immobilized DAS, which is an indication that the aDAS also has an avidity for that toxin. [Pg.25]

As shown in Table 2, free DAS, as expected, is its own best displacing agent, whereas only DAS—HMS showed any appreciable displacing capabiUty. This can be expected because the hemisuccinate linker is also immunogenic and leads to the production of antibodies specific for the linker in the polyclonal antibody population. AH the other toxins had at least lOOx less the avidity for the antibody, illustrating the specificity of the aDAS for DAS. [Pg.25]

Dioxin and Furan Emissions. The emissions of polychlorinated dibenzo-/)-dioxins (PCDD) and polychlorinated dibenzo-furans (PCDF) from incinerators (4) are of interest to the pubHc, scientists, and engineers. The U.S. EPA classifies 2,3,7,8-tetrachlorodibenzo-/)-dioxin (2,3,7,8-TCDD) as the most potent carcinogenic compound it has evaluated. It is also Hsted as the agency s most potent reproductive toxin (4). [Pg.53]

Proper refrigeration prevents the growth of some microorganisms, such as Salmonella and the production of toxins, such as Staphylococcus aureus. The growth of bacteria Tscherichia coli and Bacillus cereus is substantially checked by proper cooling and handling of milk. Table 14 Hsts diseases transmitted by cows to humans. Pasteurization is the best means of prevention. [Pg.364]

Dmg receptors are chemical entities which are typically, but not exclusively, small molecules that interact with cellular components, frequently at the plasma membrane level (1,2). There are many types of receptors heat, light, immune, hormone, ion channel, toxin, and vims are but a few that can excite a cell. The receptor concept can be appHed generally to signal recognition processes where a chemical or physical signal is recognized. This recognition is translated into response (Fig. 3) and the process can be seen as a flow of information. [Pg.268]

Center for Biologies Evaluation and Research (CBER). This center is responsible for the regulation and approval of ah biological products intended for use in the treatment, prevention, or cure of diseases or injuries to humans. A biological product is any vims, therapeutic semm, toxin, antitoxin, vaccine, blood or blood component or derivative, or analogous product (5). It also includes products produced by biotechnology, such as interferons and erythropoietins. [Pg.83]


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See also in sourсe #XX -- [ Pg.40 ]




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