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Neutralizing Inhibitors

REDUCTASE INHIBITORS DOPA-DECARBOXYLASE INHIBITORS DOPAMINE P-HYDROXYLASE INHIBITORS ENDOPEPTIDASE INHIBITORS HMG-COA REDUCTASE INHIBITORS NEUTRAL ENDOPEPTIDASE INHIBITORS NITRIC OXIDE SYNTHASE INHIBITORS PHOSPHOLIPASE INHIBITORS 5a-REDUCTASE INHIBITORS REVERSE TRANSCRIPTASE INHIBITORS THROMBOXANE SYNTHASE... [Pg.111]

There have been attempts to develop analgesic agents that work indirectly, through interfering with the breakdown of natural opioids in the body. Experimentally, some peptidase inhibitors have been shown to have analgesic actions mainly a combination of thiorphan (an inhibitor of NEP ( enkephalinase ) and bestatin (an inhibitor of aminopeptidase B see aminopeptidase inhibitors NEUTRAL... [Pg.208]

Other members of the metalloprotease family cleave oligopeptides (arbitrarily defined as having less than 50 amino acid residues) and do not necessarily act on proteins. These include a number of neuropeptidases of special interest and a number are discussed elsewhere. See ACE inhibitors aminopeptidase inhibitors carboxypeptidase inhibitors endopeptidase inhibitors neutral endopeptidase inhibitors. [Pg.237]

Neutral proteinase is set free from the complex with the immobilized affinant by increasing the pH to values at which the binding of the substrate is already weak, but at which the enzyme is still not denatured. The optimum pH for the elution of neutral proteinase depends not only on its affinity towards the affinant and on the pH dependence of this affinity, but also on the concentration of the immobilized inhibitor. Neutral proteinase is a metalloenzyme and is therefore inhibited by... [Pg.333]

Steam condensate may be contaminated in the process, and it usually contains some level of treating chemicals that include corrosion inhibitors, neutralizing agents, and oxygen scavengers. [Pg.1450]

In the presence of larger amounts of water, the inhibitor neutral-... [Pg.84]

There are a variety of measures to inhibit uncontrolled chemical reactions. Common measures include adding an inhibitor, neutralization, quenching with water or another diluent, or dumping the contents into another vessel that contains a quench liquid.The inhibitor or quench material must be selected carefully through an understanding of the inhibition reaction. The concentration and rate of addition of the inhibitors must be included in operating procedures for the process. [Pg.101]

The solubHity properties of the PAG itself can play an important role in the overaH resist performance as weU (50). SolubHity differences between the neutral onium salt and the acidic photoproducts can be quite high and wHl affect the resist contrast. In fact onium salts can serve as dissolution inhibitors in novolac polymers, analogous to diazonaphthoquinones, even in the absence of any acid-sensitive chemical function (51). [Pg.124]

Cyclohexylamine is miscible with water, with which it forms an azeotrope (55.8% H2O) at 96.4°C, making it especially suitable for low pressure steam systems in which it acts as a protective film-former in addition to being a neutralizing amine. Nearly two-thirds of 1989 U.S. production of 5000 —6000 t/yr cyclohexylamine serviced this appHcation (69). Carbon dioxide corrosion is inhibited by deposition of nonwettable film on metal (70). In high pressure systems CHA is chemically more stable than morpholine [110-91-8] (71). A primary amine, CHA does not directiy generate nitrosamine upon nitrite exposure as does morpholine. CHA is used for corrosion inhibitor radiator alcohol solutions, also in paper- and metal-coating industries for moisture and oxidation protection. [Pg.212]

Amine salts, especially acetate salts prepared by neutralization of a fatty amine with acetic acid, are useflil as flotation agents (collectors), corrosion inhibitors, and lubricants (3,8). Amine acetates are commercially available from a number of suppHers Akzo Chemicals Inc. (Armac) (73) Henkel Corporation (formerly General Mills) (Alamac) (74) Jetco Chemicals Inc. (The Procter Gamble Company) (fet Amine) (75) Sherex (Adogen) (76) and Tom ah Products (Exxon Chemical Company) (Tomah) (77). [Pg.223]

The most commonly used scale inhibitors are low molecular weight acrylate polymers and organophosphoms compounds (phosphonates). Both classes of materials function as threshold inhibitors however, the polymeric materials are more effective dispersants. Selection of a scale control agent depends on the precipitating species and its degree of supersaturation. The most effective scale control programs use both a precipitation inhibitor and a dispersant. In some cases this can be achieved with a single component (eg, polymers used to inhibit calcium phosphate at near neutral pH). [Pg.271]

For more selective hydrogenations, supported 5—10 wt % palladium on activated carbon is preferred for reductions in which ring hydrogenation is not wanted. Mild conditions, a neutral solvent, and a stoichiometric amount of hydrogen are used to avoid ring hydrogenation. There are also appHcations for 35—40 wt % cobalt on kieselguhr, copper chromite (nonpromoted or promoted with barium), 5—10 wt % platinum on activated carbon, platinum (IV) oxide (Adams catalyst), and rhenium heptasulfide. Alcohol yields can sometimes be increased by the use of nonpolar (nonacidic) solvents and small amounts of bases, such as tertiary amines, which act as catalyst inhibitors. [Pg.200]

Commercial use of many chlorinated derivatives imposes stress on the stabHity of the solvent. Inhibitors classified as antioxidants (qv), acid acceptors, and metal stabilizers are added to minimize these stresses. AH the chloriaated derivatives hydrolyze at a slow but finite rate when dissolved ia water. Hydrolysis of chloriaated solvents typicaHy Hberates hydrogen chloride that can corrode storage containers and commercial metal-cleaning equipment. The Hberated hydrogen chloride can be neutralized by an appropriate epoxide to form noncorrosive chlorohydrins (qv). [Pg.507]

Neutralization to terrninate processing was effected by the polymeric acid layer of the covet sheet the onset of this reaction was controlled by the rate of permeation of the overlying polymeric timing layers. MobiUty of the transferred dyes was also reduced by reaction with a mordant contained in the image-receiving layer. A development inhibitor released from one of the timing layers by the alkaline hydrolysis of its precursor assisted in restraining further development and consequent additional dye release. [Pg.503]

Petroleum Production and Refining. Specific polyamine derivatives are used in the petroleum production and refining industries as corrosion inhibitors, demulsifiers, neutralizers, and additives for certain operations. [Pg.48]

Fig. 10. Pharmacophores for angiotension-converting enzyme. Distances in nm. (a) The stmcture of a semirigid inhibitor and distances between essential atoms from which one pharmacophore was derived (79). (b) In another pharmacophore, atom 1 is a potential zinc ligand (sulfhydryl or carboxylate oxygen), atom 2 is a neutral hydrogen bond acceptor, atom 3 is an anion (deprotonated sulfur or charged oxygen), atom 4 indicates the direction of a hydrogen bond to atom two, and atom 5 is the central atom of a carboxylate, sulfate, or phosphate of which atom 3 is an oxygen, or atom 5 is an unsaturated carbon when atom 3 is a deprotonated sulfur. The angle 1- -2- -3- -4 is —135 to —180° or 135 to 180°, and 1- -2- -3- -5 is —90 to 90°. Fig. 10. Pharmacophores for angiotension-converting enzyme. Distances in nm. (a) The stmcture of a semirigid inhibitor and distances between essential atoms from which one pharmacophore was derived (79). (b) In another pharmacophore, atom 1 is a potential zinc ligand (sulfhydryl or carboxylate oxygen), atom 2 is a neutral hydrogen bond acceptor, atom 3 is an anion (deprotonated sulfur or charged oxygen), atom 4 indicates the direction of a hydrogen bond to atom two, and atom 5 is the central atom of a carboxylate, sulfate, or phosphate of which atom 3 is an oxygen, or atom 5 is an unsaturated carbon when atom 3 is a deprotonated sulfur. The angle 1- -2- -3- -4 is —135 to —180° or 135 to 180°, and 1- -2- -3- -5 is —90 to 90°.
Styrene is difficult to purify and keep pure. Usually contains added inhibitors (such as a trace of hydroquinone). Washed with aqueous NaOH to remove inhibitors (e.g. rert-butanol), then with water, dried for several hours with MgS04 and distd at 25° under reduced pressure in the presence of an inhibitor (such as 0.005% p-tert-butylcatechol). It can be stored at -78°. It can also be stored and kept anhydrous with Linde type 5A molecular sieves, CaH2, CaS04, BaO or sodium, being fractionally distd, and distd in a vacuum line just before use. Alternatively styrene (and its deuterated derivative) were passed through a neutral alumina column before use [Woon et al. J Am Chem Soc 108 7990 1986 Collman J Am Chem Soc 108 2588 1986]. [Pg.353]

Recrystd from abs EtOH dried in vacuo and stored in tightly stoppered bottles because it is hygroscopic. It is soluble in H2O but insoluble in CgHg, Et20 and alkaline aqueous soln. It has UV at 258 and 307.5nm (log e 4.50 and 3.50) in EtOH (neutral species). [Craig et al. J Org Chem 22 709 1957.] It is a calmodulin inhibitor [Levene and Weiss J Parmacol Exptl Ther2Q% 454 1978], and js a psychotropic agent [Fowler Arzneim.-Forsch 27 866 1977]. [Pg.572]


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