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Phobicity

Currently, there are commercially available 48% or higher HBr solutions in acetic acid. These work just fine. They really do The acetic acid is usually used more as a solvent than an acid. It allows the water-loving HBr and the water phobic safrole to mingle with each other in a very positive way. If one cannot get a readymade solution of HBr in acetic acid then one can make one quite easily. [Pg.144]

Normally, dietary tyramine is broken down in the gastrointestinal tract by MAO and is not absorbed. In the presence of MAOI, however, all of its potent sympathomimetic actions are seen. Other side effects of MAOI include excessive CNS stimulation, orthostatic hypotension, weight gain, and in rare cases hepatotoxicity. Because the monoamine oxidase inhibitors exhibit greater toxicity, yet no greater therapeutic response than other, newer agents, clinical use has been markedly curtailed. The primary use for MAOIs is in the treatment of atypical depressions, eg, those associated with increased appetite, phobic anxiety, hypersomnolence, and fatigues, but not melancholia (2). [Pg.466]

Other solvents can be divided into several classes. In hydrogen bond-breaking solvents (dipolar aprotics), the simple amino, hydroxy and mercapto heterocycles all dissolve. In the hydrophobic solvents, hydrogen bonding substituents greatly decrease the solubility. Ethanol and other alcohols take up a position intermediate between water and the hydro-phobic solvents (63PMH 1)177). [Pg.32]

Descrip- tion Small, polar Aromatic Polar Positive charge Leu Ile,Val Negative charge Hydro- Phobic Polar Cys Pro Gly... [Pg.333]

A similar formalism is used by Thompson and Goldstein [90] to predict residue accessibilities. What they derive would be a very useful prior distribution based on multiplying out independent probabilities to which data could be added to form a Bayesian posterior distribution. The work of Arnold et al. [87] is also not Bayesian statistics but rather the calculation of conditional distributions based on the simple counting argument that p(G r) = p(a, r)lp(r), where a is some property of interest (secondary structure, accessibility) and r is the amino acid type or some property of the amino acid type (hydro-phobicity) or of an amino acid segment (helical moment, etc). [Pg.339]

Lesk and Chothia did find, however, that there is a striking preferential conservation of the hydrophobic character of the amino acids at the 59 buried positions, but that no such conservation occurs at positions exposed on the surface of the molecule. With a few exceptions on the surface, hydrophobic residues have replaced hydrophilic ones and vice versa. However, the case of sickle-cell hemoglobin, which is described below, shows that a charge balance must be preserved to avoid hydrophobic patches on the surface. In summary, the evolutionary divergence of these nine globins has been constrained primarily by an almost absolute conservation of the hydro-phobicity of the residues buried in the helix-to-helix and helix-to-heme contacts. [Pg.43]

Teflon filter A chemical-resistant hydro-phobic filter composed of polytetraf-louroethylene (PTFE) used for industrial hygiene sampling. [Pg.1480]

Closely related to water solubility as a polarity measure is the partition coefficient of a substance between water and an immiscible organic solvent. Most commonly the organic solvent is selected to be n-octanol, and the symbol P is given to the octanol/water partition coefficient. Then log P is a quantitative measure of hydro-phobicity and, therefore, of nonpolarity. Table 8-3 gives log P values for many of... [Pg.400]

In general, grafting of hydrophillic monomers have been found to lead to an increase in wettability, adhesion, dyeing, and rate of release of oil stains by detergent solution. On the other hand, if the monomer is hydro-phobic, the result will be decreased wetting by all liquids including oil stains. If grafting is not restricted to surface alone but encompasses the bulk of the backbone polymer, then the properties such as flame resistance, water sorption, crease resistance, etc. will be affected. [Pg.497]

The results were simple and clear-cut Only the two terms ofa° and Emin were involved for the a-cyclodextrin systems, and the two terms of k and Emin, for (S-cyclodextrin systems. This means that the stabilities of the inclusion complexes are mainly governed by the electronic and steric interactions in a-cyclodextrin systems and by the hydro-phobic and steric interactions in (i-cyclodextrin systems, regardless of the position of the substituents in the phenols. These observations agree well with those by Harata23), who showed that there is no appreciable difference in thermodynamic parameters between cyclodextrin complexes of m- and p-di substituted benzenes and that the contribution of the enthalpy term to the complexation is more significant in a-cyclodextrin systems than in P-cyclodextrin systems, where the inhibitory effect... [Pg.77]

Squalene epoxidase, like most enzymes responsible for the later steps of sterol biosynthesis [43, 51], is membrane-bound which makes its purification in native form challenging. The purification is additionally complicated by the presence of a large number of cytochrome P450 and other enzymes that have similar hydro-phobicity and size as squalene epoxidase and are hence difficult to remove [52]. Most studies have been carried out with rat liver microsome squalene epoxidase either partially purified or as a homogenate of the cell membrane fraction. In vitro reconstitution of squalene epoxidase activity is absolutely dependent on molecular oxygen, NADPH, FAD, and NADPH-cytochrome c reductase [52, 53]. In this respect, squalene epoxidase resembles the cytochrome P450 enzymes described... [Pg.370]

The presence of a critical St content in ASt-x can also be seen in fluorescence spectra [29], This copolymer in aqueous solution shows an excimer emission peaking at 325 nra. As shown in Fig. 8, the intensity of the excimer emission increases, while the monomer emission decreases, with increasing St content. Eventually the excimer dominates the monomer emission at an St content of 72 mol%. The excimer emission becomes apparent at an St content of about 50 mol%, which agrees with the critical St content estimated by viscometry and NMR spectroscopy. The existence of the critical St content suggests the hydro-phobic self-aggregation to be a cooperative process. [Pg.67]

One of the most typical examples demonstrating the importance of the hydro-phobic contribution may be alkaline-fading reactions of triphenylmethane dyes, which take place between dye cations and hydroxyl ions to form carbinols167. ... [Pg.175]

Anxiety is a normal reaction. Pathological anxiety interferes with daily-life activities and may be accompanied by autonomic symptoms (chest pain, dyspnoea and palpitations). Severe forms include phobic anxiety and panic disorder. [Pg.201]

The Diels-Alder reactions of cyclopentadiene with methyl vinyl ketone and acrylonitrile are accelerated when carried out in water in the presence of jS-CD but are slower with a-CD [65a] (Scheme 4.16). This is in agreement with the observation that the transition states of these cycloadditions fit into the hydro-phobic cavity of P-CD but not in the smaller a-CD cavity. [Pg.170]

Resting cell of G. candidum, as well as dried cell, has been shown to be an effective catalyst for the asymmetric reduction. Both enantiomers of secondary alcohols were prepared by reduction of the corresponding ketones with a single microbe [23]. Reduction of aromatic ketones with G. candidum IFO 5 767 afforded the corresponding (S)-alcohols in an excellent enantioselectivity when amberlite XAD-7, a hydro-phobic polymer, was added to the reaction system, and the reduction with the same microbe afforded (R)-alcohols, also in an excellent enantioselectivity, when the reaction was conducted under aerobic conditions (Figure 8.31). [Pg.217]


See other pages where Phobicity is mentioned: [Pg.381]    [Pg.608]    [Pg.711]    [Pg.63]    [Pg.539]    [Pg.228]    [Pg.2062]    [Pg.472]    [Pg.45]    [Pg.76]    [Pg.638]    [Pg.642]    [Pg.96]    [Pg.556]    [Pg.395]    [Pg.397]    [Pg.39]    [Pg.272]    [Pg.420]    [Pg.20]    [Pg.26]    [Pg.69]    [Pg.176]    [Pg.177]    [Pg.27]    [Pg.326]    [Pg.496]    [Pg.750]    [Pg.882]    [Pg.1286]    [Pg.609]    [Pg.158]    [Pg.160]    [Pg.303]    [Pg.53]   
See also in sourсe #XX -- [ Pg.127 ]




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Avoidance, phobic

Mutual phobicity

Mutual phobicity fluorocarbon chains

Phobic anxiety disorders

Phobic avoidance/anxiety

Phobic disorders

Phobic disorders, benzodiazepines

Phobic response

Phobicity, mixed micelles

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