Mechanism inhibition

Fig. 6. Catalyst inhibition mechanisms where ( ) are active catalyst sites the catalyst carrier and the catalytic support (a) masking of catalyst (b) poisoning of catalyst (c) thermal aging of catalyst and (d) attrition of ceramic oxide metal substrate monolith system, which causes the loss of active catalytic material resulting in less catalyst in the reactor unit and eventual loss in performance.

The example of methotrexate points out that the inhibition modality of dead end inhibitors, with respect to a specific substrate, will depend on the reaction mechanism of the target enzyme. Thus a complete understanding of inhibition mechanism requires an understanding of the underlying reaction mechanism of the target enzyme. A comprehensive discussion of these issues has been provided by Segel (1975). Table 3.6 summarizes the pattern of dead-end inhibition observed for competitive inhibitors of one substrate in the common bisubstrate reaction mecha-... [Pg.71]

All these aspects of tight binding inhibition can potentially offer important advantages in terms of clinical efficacy, dosing interval, and patient safety (see Swinney, 2004, for an excellent review of some of the clinical advantages of tight binding inhibition and other nonclassical inhibition mechanisms). [Pg.209]

Electrochemical techniques have been utilized for many years to study metal corrosion. Two of these techniques, linear polarization (LP) and cyclic voltammetry (CV), complement each other, LP providing corrosion rates under conditions where the surface is minimally altered and CV furnishing information about the corrosion mechanism. With the advent of impedance spectroscopy (IS), both kinds of information can be gleaned simultaneously and more rapidly, while leaving the surface almost intact. In this paper, we discuss the application of IS to the study of rapid steel corrosion and describe a study we undertook to elucidate the roles played by adsorption and film formation in the inhibition mechanisms of the above-named compounds. For comparison, we also investigated two quaternary nitrogen salts, which appear to adsorb electrostatically and presumably do not form macroscopic films (8). [Pg.636]

Dinos, G., Wilson, D. N., Teraoka, Y., Szaflarski, W., Fucini, P., Kalpaxis, D., and Nierhaus, K. H. (2004). Dissecting the ribosomal inhibition mechanisms of edeine and pactamycin The universally conserved residues G693 and C795 regulate P-site RNA binding. Mol. Cell 13, 113-124. [Pg.328]

In AChE-based biosensors acetylthiocholine is commonly used as a substrate. The thiocholine produced during the catalytic reaction can be monitored using spectromet-ric, amperometric [44] (Fig. 2.2) or potentiometric methods. The enzyme activity is indirectly proportional to the pesticide concentration. La Rosa et al. [45] used 4-ami-nophenyl acetate as the enzyme substrate for a cholinesterase sensor for pesticide determination. This system allowed the determination of esterase activities via oxidation of the enzymatic product 4-aminophenol rather than the typical thiocholine. Sulfonylureas are reversible inhibitors of acetolactate synthase (ALS). By taking advantage of this inhibition mechanism ALS has been entrapped in photo cured polymer of polyvinyl alcohol bearing styrylpyridinium groups (PVA-SbQ) to prepare an amperometric biosensor for... [Pg.58]

Cholinesterase catalysis and inhibition mechanisms involve formation of reversible complexes and covalent conjugates 197... [Pg.185]

Cannon, K. E., Nalwalk, J. W., Stadel, R. etal. Activation of spinal histamine H3 receptors inhibits mechanical nociception. Eur. J. Pharmacol. 470 139-147, 2003. [Pg.265]

Robustness of the process. Many transition metal-catalyzed reactions function well at the laboratory scale, but on scaling up substrate and product inhibition may be an issue, and sensitivity to impurities may also become apparent. Increasing the SCR, which is often necessary for the economics of the process, also increases the impurity catalyst ratio. It is also very important to keep the number of components to a minimum, as extraction, crystallization and distillation are the only economic means of purification. Ligands can be a nuisance in this respect, particularly if they are used in amounts over 5 mol%. Reproducibility also is a stringent requirement. Thus, possible inhibition mechanisms should be recognized in order to avoid unwanted surprises during production. [Pg.1246]

In summary, the physiological control of silk protein conversion shows an ingenious balance of activating and inhibiting mechanisms that are dependent on composition and sequence arrangement (Krejchi et al., 1994). Denaturing effects observed in silks appear to be identical to those found in amyloid-forming proteins, and they principally alter the competitive outcome of the hydration of nonpolar and polar residues (Anfinsen, 1973 Dill, 1990 Dobson and Karplus, 1999 Kauzmann, 1959). The key differences to amyloids may lie in the hierarchical level of the structures (Muthukumar et al., 1997) involved in the assembly of silks compared to amyloids. [Pg.37]

The most widely used positive resists are those that operate on the basis of a dissolution inhibition mechanism. Such resists are generally two-component materials consisting of an alkali soluble matrix resin that is rendered insoluble in aqueous alkaline solutions through addition of a hydrophobic, radiation-sensitive material. Upon irradiation, the hydrophobic moiety may be either removed or converted to an alkali soluble species, allowing selective removal of the irradiated portions of the resist by an alkaline developer. [Pg.10]

Materials that exhibit enhanced solubility after exposure to radiation are defined as positive resists. Positive acting materials are particularly attractive for the production of VLSI devices because of their high resolution properties. The chemistry of these systems generally involves either chain-scission or solution-inhibition mechanisms. [Pg.140]

The inhibitory constant (K ) experiment provides reasonable information on both the mechanism and the potency of inhibition. For typical K, experiments, four substrate (0.25 Km, 0.5 Km, 1 Km, 2 Km) and five inhibitor concentrations (spanning a 10-fold range surrounding the anticipated K, including a zero inhibitor control) are used. Data workup of the K experiment allows further determination of inhibition mechanism. Both Dixon (1/v versus [I] Figure 9.6) [149] and Lineweaver-Burk... [Pg.213]

However, simple knowledge of the inhibition mechanism or inhibition level is not helpful in designing a safer compound. Researchers need to understand why a specific compound leads to MBI at the molecular level to design a safer compound. This can be achieved only by understanding which molecular group is exposed to the CYP-heme, to make ligand-heme interactions more difficult (Figure 12.1). [Pg.279]

As the method reported is not based on QSAR and thus does not use training information, it cannot be used to predict quantitative inhibition levels (IC50, percentage inhibition or similar information). The method can only be used to find potential mechanism-based inhibitors (binary scale). Despite this limitation, an important advantage over other techniques is that the method suggests the site of the molecule responsible for the inhibition mechanism. With this information researchers may change the molecular structure to maintain activity at the expense of inhibitory effects. [Pg.286]

Scheme 18.45 Postulated inhibition mechanism of pyridoxal phosphate-dependent decarboxylases by a-allenic a-amino acids.

Mashino T, Okuda K, Hirota T, Hirobe M, Nagano T, Mochizuki M (1999) Inhibition of E. coli growth by fullerene derivatives and inhibition mechanism. Bioorg. Med. Chem. Lett. 9 2959-2962. [Pg.76]

Since the mode of inhibition is competitive and the Kj value is extraordinarily small compared to the value of the substrate (25 mM), it is strongly suggested that this inhibitor blocks the active site and prevents approach of the substrate to the catalytic site of the enzyme. It is assumed that a-bromo-phenylacetic acid interacts with a cysteine residue at the active site in some way. The high electron-withdrawing effect of the bromine atom would have an important role in the inhibition mechanism. Thus, the mode of binding of the inhibitor to the active site of the enzyme is presumed to resemble that of the substrate closely. Accordingly, disclosure of the way the inhibitor interacts with the enzyme would provide important information on how the enzyme activates the substrate. [Pg.13]

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