Secondary inhibitors

The reactivator may form, either with the inhibitor or with its residue in inhibited cholinesterase, a stable secondary inhibitor of cholinesterase. 

Secondary inhibitors to reduce certain side effects of primary treatments (such as phosphonate or chlorine attack on copper or oxidation of some organics by chlorine). 

Even the most modem, microprocessor-based monitoring and control systems reference only the primary chemical inhibitor with any real degree of accuracy. Methods for the monitoring and control of secondary inhibitors (such as specific polymeric dispersants) and biodispersants, biocides, antifoams, mud treatments, etc. remain imprecise to say the least. 

Secondary inhibitors to reduce certain side effects... 

The retardation effect increases further due to regeneration of HX and formation of a secondary inhibitor Xj... 

Radical polymerisation of fluoroalkyl methacrylates CH2=C(CH3)COOCH2-(CF2-CF2) ,-R, where R = H (I) or CH3 (II), m = 1,2, 3, in the presence of stable iminoxyl radicals was studied [76]. Study of the induction stage indicates that secondary inhibition observed is performed by the catalytic mechanism without using the secondary inhibitor effects... 

Inhibitors of corrosion in acid solution can interact with metals and affect the corrosion reaction in a number of ways, some of which may occur simultaneously. It is often not possible to assign a single general mechanism of action to an inhibitor because the mechanism may change with experimental conditions. Thus, the predominant mechanism of action of an inhibitor may vary with factors such as its concentration, the pH of the acid, the nature of the anion of the acid, the presence of other species in the solution, the extent of reaction to form secondary inhibitors, and the nature of the metal. The mechanism of action of inhibitors with the same functional group may additionally vary with factors such as the effect of the molecular structure on the electron density of the functional group and the size of the hydrocarbon portion of the molecule. 

The aromatic compounds are the primary inhibitors and include hydroquinone, 1,2- and 1,4-dihydroxy naphthalene, di-t-butyl resorcinol, and similar compounds. The aliphatic amines are secondary inhibitors and include ethanolamine, isopropanolamine, ethylenediamine, etc. 

Monofunctional, cyclohexylamine is used as a polyamide polymerization chain terminator to control polymer molecular weight. 3,3,5-Trimethylcyclohexylamines ate usehil fuel additives, corrosion inhibitors, and biocides (50). Dicyclohexylamine has direct uses as a solvent for cephalosporin antibiotic production, as a corrosion inhibitor, and as a fuel oil additive, in addition to serving as an organic intermediate. Cycloahphatic tertiary amines are used as urethane catalysts (72). Dimethylcyclohexylarnine (DMCHA) is marketed by Air Products as POLYCAT 8 for pour-in-place rigid insulating foam. Methyldicyclohexylamine is POLYCAT 12 used for flexible slabstock and molded foam. DM CHA is also sold as a fuel oil additive, which acts as an antioxidant. StericaHy hindered secondary cycloahphatic amines, specifically dicyclohexylamine, effectively catalyze polycarbonate polymerization (73). 

The presence of ammonia during hydrogenation suppresses formation of secondary amines and inhibits hydrogenation of double bonds in unsaturated nitriles. Eatty amines are used as corrosion inhibitors, flotation agents, quaternary salts for sanitizing agents and textile fabric softeners, and surface-active agents. 

Long-acting progestins act primarily as ovulation inhibitors. An important secondary component is their effect on the cervical mucus and endometrium, achieved at circulating blood dmg levels below those required for ovulation inhibition (40). 

One principal use of cyclohexanol has been in the manufacture of esters for use as plasticizers (qv), ie, cyclohexyl and dicyclohexyl phthalates. In the finishes industry, cyclohexanol is used as a solvent for lacquers, shellacs, and varnishes. Its low volatiUty helps to improve secondary flow and to prevent blushing. It also improves the miscibility of cellulose nitrate and resin solutions and helps maintain homogeneity during drying of lacquers. Reaction of cyclohexanol with ammonia produces cyclohexylamine [108-91-8], a corrosion inhibitor. Cyclohexanol is used as a stabilizer and homogenizer for soaps and synthetic detergent emulsions. It is used also by the textile industry as a dye solvent and kier-boiling assistant (see Dye carriers). 

Primers are required to be resistant to all of the same fluids and environments as the adhesive, and are in addition expected to be compatible with secondary finishes such as corrosion and fluid resistant primers applied to cured bond assemblies. The most commonly used primers for 250°F cured epoxy adhesives also have active corrosion inhibitors themselves to combat corrosion at bondlines. This last requirement is somewhat dated, evolving from the severe corrosion and delamination problems experienced before U.S. airframe manufacturers adopted durable surface treatments. 

Reaction of adsorbed inhibitors In some cases, the adsorbed corrosion inhibitor may react, usually by electro-chemical reduction, to form a product which may also be inhibitive. Inhibition due to the added substance has been termed primary inhibition and that due to the reaction product secondary inhibition " . In such cases, the inhibitive efficiency may increase or decrease with time according to whether the secondary inhibition is more or less effective than the primary inhibition. Some examples of inhibitors which react to give secondary inhibition are the following. Sulphoxides can be reduced to sulphides, which are more efficient inhibitorsQuaternary phosphonium and arsonium compounds can be reduced to the corresponding phosphine or arsine compounds, with little change in inhibitive efficiency . Acetylene compounds can undergo reduction followed by polymerisation to form a multimolecular protective film . Thioureas can be reduced to produce HS ions, which may act as stimulators of... 

Substrate and product inhibitions analyses involved considerations of competitive, uncompetitive, non-competitive and mixed inhibition models. The kinetic studies of the enantiomeric hydrolysis reaction in the membrane reactor included inhibition effects by substrate (ibuprofen ester) and product (2-ethoxyethanol) while varying substrate concentration (5-50 mmol-I ). The initial reaction rate obtained from experimental data was used in the primary (Hanes-Woolf plot) and secondary plots (1/Vmax versus inhibitor concentration), which gave estimates of substrate inhibition (K[s) and product inhibition constants (A jp). The inhibitor constant (K[s or K[v) is a measure of enzyme-inhibitor affinity. It is the dissociation constant of the enzyme-inhibitor complex. 

The use of CA inhibitors as diuretics is limited by their propensity to cause metabolic acidosis and hypokalemia. Their use can be indicated in patients with metabolic alkalosis and secondary hyperaldosteronism resulting for example from aggressive use of loop diuretics. Furthermore, CA inhibitors are effective dtugs to produce a relatively alkaline urine for the treatment of cysteine and uric acid stones as well as for the accelerated excretion of salicylates. Perhaps the most common use of CA inhibitors is in the treatment of glaucoma. 

Ubiquitous mitochondrial monoamine oxidase [monoamine oxygen oxidoreductase (deaminating) (flavin-containing) EC 1.4.3.4 MAO] exists in two forms, namely type A and type B [ monoamine oxidase (MAO) A and B]. They are responsible for oxidative deamination of primary, secondary, and tertiary amines, including neurotransmitters, adrenaline, noradrenaline, dopamine (DA), and serotonin and vasoactive amines, such as tyramine and phenylethylamine. Their nonselec-tive and selective inhibitors ( selective MAO-A and -B inhibitors) are employed for the treatment of depressive illness and Parkinson s disease (PD). 

Ribosomal Protein Synthesis Inhibitors. Figure 5 Nucleotides at the binding sites of chloramphenicol, erythromycin and clindamycin at the peptidyl transferase center. The nucleotides that are within 4.4 A of the antibiotics chloramphenicol, erythromycin and clindamycin in 50S-antibiotic complexes are indicated with the letters C, E, and L, respectively, on the secondary structure of the peptidyl transferase loop region of 23S rRNA (the sequence shown is that of E. coll). The sites of drug resistance in one or more peptidyl transferase antibiotics due to base changes (solid circles) and lack of modification (solid square) are indicated. Nucleotides that display altered chemical reactivity in the presence of one or more peptidyl transferase antibiotics are boxed. 

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