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Effects mediate

In addition to effects mediated through glucocorticoid secretion (stress-related), a hypothetical mechanism for direct immunotoxicity of organophosphates is the inhibition of esterases and stabilization of the lysosomal membrane of lymphocytes, thus blocking release of lymphokines (Sharma and Reddy 1987). [Pg.103]

Synthetic nonhydrolyzable analogs of nucleoside triphosphates (Figure 33-13) allow investigators to distinguish the effects of nucleotides due to phosphoryl transfer from effects mediated by occupancy of allosteric nucleotide-binding sites on regulated enzymes. [Pg.291]

Indium can effectively mediate the coupling of l,4-dibromo-2-butyne with aldehydes in a 1 1 ratio to give l,3-butadien-2-yl-methanols in aqueous media (Eq. 8.83).211 When a 1 2 ratio was used, the reaction... [Pg.260]

The reaction of an a-halo carbonyl compound with zinc, tin, or indium together with an aldehyde in water gave a direct cross-aldol reaction product (Eq. 8.90).226,227 A direct Reformatsky-type reaction occurred when an aromatic aldehyde reacted with an a-bromo ester in water mediated by zinc in low yields. Recently, it was found that such a reaction mediated by indium was successful and was promoted by son-ication (Eq. 8.91).228 The combination of BiCl3-Al,229 CdCl2-Sm,230 and Zn-Et3B-Eb0231 is also an effective mediator. Bismuth metal, upon activation by zinc fluoride, effected the crossed aldol reaction between a-bromo carbonyl compounds and aldehydes in aqueous media. The reaction was found to be regiospecific and syn-diastereoselective (Eq. 8.92).232... [Pg.265]

Effects mediated by G-protein coupled receptors (GPCRs) are very much slower than those mediated by, for example, ligand-gated ion channels, primarily because more steps are involved between activation of the receptor and the final response. For example, even in a simple, three-step, G-protein-mediated effect, such as the opening of atrial GIRK channels following the activation of M2 muscarinic receptors by acetylcholine, which follows the scheme ... [Pg.230]

Parasitism by T. spiralis has been a subject of scientific interest for over 150 years. Recently, considerable attention has been paid to the parasite by immunologists interested in immunity to nematodes in general, and mucosal immunity in particular. It has been shown that glycan-specific antibodies are highly effective mediators of host defence against intestinal 7. spiralis infection. Protective monoclonal antibodies have been used to elucidate mechanisms of worm expulsion, as well as to identify molecules that the parasite uses to create its niche. In the future, detailed characterization of these molecules and their functions should afford additional insights into parasitism by Trichinella spiralis, and possibly also by other types of pathogen. [Pg.124]

I. The phosphatidylinositide 3-kinase (PI 3-kinase) pathway, in particular, effects mediated through its effector protein kinase B (PKB, also termed Akt three isoforms) ... [Pg.149]

In most procedures, the water-soluble carbodiimide EDC hydrochloride is the most effective mediator of this reaction. Both EDC and its reaction by-products are fully soluble in aqueous buffers and can be easily separated from the modified aminoalkylphosphate (Chapter 3, Section 1.1). [Pg.124]

Figure 6.7 illustrates the voltammetric response of the third-generation SOD-based 02 biosensors with Cu, Zn-SOD confined onto cystein-modified Au electrode as an example. The presence of 02" in solution essentially increases both the cathodic and anodic peak currents of the SOD compared with its absence [150], Such a redox response was not observed at the bare Au or cysteine-modified Au electrodes in the presence of 02". The observed increase in the anodic and cathodic current response of the Cu, Zn-SOD/cysteine-modified Au electrode in the presence of 02 can be considered to result from the oxidation and reduction of 02, respectively, which are effectively mediated by the SOD confined on the electrode as shown in Scheme 3. Such a bi-directional electromediation (electrocatalysis) by the SOD/cysteine-modified Au electrode is essentially based on the inherent specificity of SOD for the dismutation of 02", i.e. SOD catalyzes both the reduction of 02 to H202 and the oxidation to 02 via a redox cycle of its Cu (II/I) complex moiety as well as the direct electron transfer of SOD realized at the cysteine-modified Au electrode. Thus, this coupling between the electrode and enzyme reactions of SOD could facilitate the development of the third-generation biosensor for 02". ... Figure 6.7 illustrates the voltammetric response of the third-generation SOD-based 02 biosensors with Cu, Zn-SOD confined onto cystein-modified Au electrode as an example. The presence of 02" in solution essentially increases both the cathodic and anodic peak currents of the SOD compared with its absence [150], Such a redox response was not observed at the bare Au or cysteine-modified Au electrodes in the presence of 02". The observed increase in the anodic and cathodic current response of the Cu, Zn-SOD/cysteine-modified Au electrode in the presence of 02 can be considered to result from the oxidation and reduction of 02, respectively, which are effectively mediated by the SOD confined on the electrode as shown in Scheme 3. Such a bi-directional electromediation (electrocatalysis) by the SOD/cysteine-modified Au electrode is essentially based on the inherent specificity of SOD for the dismutation of 02", i.e. SOD catalyzes both the reduction of 02 to H202 and the oxidation to 02 via a redox cycle of its Cu (II/I) complex moiety as well as the direct electron transfer of SOD realized at the cysteine-modified Au electrode. Thus, this coupling between the electrode and enzyme reactions of SOD could facilitate the development of the third-generation biosensor for 02". ...
It appears that TNF-R55 is capable of mediating most TNF activities, whereas the biological activities induced via the TNF-R75 receptor are more limited. For example, TNF s cytotoxic activity, as well as its ability to induce synthesis of various cytokines and prostaglandins, is all mediated mainly/exclusively by TNF-R55. TNF-R75 appears to play a more prominent role in the induction of synthesis of T-lymphocytes. All of the biological activities mediated by TNF-R75 can also be triggered via TNF-R55, and usually at much lower densities of receptors. TNF-R75 thus appears to play more of an accessory role, mainly to enhance effects mediated via TNF-R55. [Pg.259]

IGF-1, which mediates most of GH s growth-promoting activity on, for example, bone and skeletal muscle (Chapter 10). The major effects mediated by hGH are summarized in Table 11.5. [Pg.309]

Dopamine produces dose-dependent hemodynamic effects because of its relative affinity for cq-, /Jr, /J2-, and Dr (vascular dopaminergic) receptors. Positive inotropic effects mediated primarily by / -receptors become more prominent with doses of 2 to 5 mcg/kg/min. At doses between 5 to 10 mcg/kg/min, chronotropic and -mediated vasoconstricting effects become more prominent. Especially at higher doses, dopamine alters several parameters that increase myocardial oxygen demand and potentially decrease myocardial blood flow, worsening ischemia in some patients with coronary artery disease. [Pg.107]

Table 6.1 Biogenic amine binding GPCR antitargets and side effects mediated by high-affinity agonists and antagonists of the respective receptor. ... Table 6.1 Biogenic amine binding GPCR antitargets and side effects mediated by high-affinity agonists and antagonists of the respective receptor. ...
Consequently cis or tram effects mediated by the transmission paths D—F (Fig. 1) should be the largest with the osmium porphyrins. The situation in the latter is therefore treated separately in this chapter. [Pg.105]

A-Hydroxyphthalimide (88) has also been shown to be an effective mediator for the oxidation of alcohols [120]. The oxidation process depicted in Scheme 32 is suitable for the oxidation of secondary alcohols (86). A-Hydroxyphthalimide also plays an important role as a mediator for deprotection of the 4-phenyl-l,3-dioxolane... [Pg.507]

Complement. Complement is an extensive series of glycoproteins and protein inhibitors whose function includes major cytolytic effects, mediation of opsonization, and modulation of inflammatory responses. Activation of this system plays an important role in host defense leading to destruction of microorganisms. It also results in generation of anaphylotoxins which induce mediator release and "split products" that mediate membrane damage, either directly through structural alteration or indirectly, via cell chemotaxis and regulation. [Pg.148]


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See also in sourсe #XX -- [ Pg.35 , Pg.55 ]




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