Non-specific derivatives

REFERENCES TO NON-SPECIFIC DERIVATIVES IN FILE CA 7 REFERENCES IN FILE CAOLD (PRIOR TO 1967)... 

The non-specific derivatives e.g. include polychlorinated biphenyls or dioxi-nes. They cannot be found without the role indicator D being added to the Registry Number. This search statement will also retrieve all the documents with a role indicator DP added to their Registry Number. 

When the compound itself and the non-specific derivatives and their preparation are searched, the following query must be conducted ... 

RX) and not in the Index Terms (IT). The Registry Numbers, as in CA, may be labelled with a D (Sect. 7.3.1.1), in order to search for non-specific derivatives. Unlike searching in CA, searching is effected with a D as well as without it when using Registry Numbers from the Registry File. 

General anaesthetics have been in use for the last 100 years, yet their mechanism of action are still not yet clearly defined. For many years it was thought that general anaesthetics exerted their effects by dissolving in cell membranes and perturbing the lipid environment in a non-specific manner. This theory derived from the observation that for a number of drugs which induced anaesthesia, their potency correlated with their oil-water partition coefficients. This Meyer-Oveiton correlation was accepted for a number of years, however in the last 15-20 years evidence has shown that a more likely theory is that of specific interactions of anaesthetics with proteins, particularly those within the CNS that mediate neurotransmission [1]. 

Inflammation is a non-specific reaction which can be induced by a variety of agents apart fiom microorganisms. Lymphokines and derivatives of arachidonic acid, including prostaglandins, leukotrienes and thromboxanes are probable mediators of the inflammatory response. The release of vasoactive amines such as histamine and serotonin (5-hydroxytryptamine) firm activated or damaged cells also contribute to inflammation. 

Specific effluents have also been subjected to WRF-mediated remediation studies. Decolourization, dechlorination and detoxification of highly toxic bleach plant effluents derived from the pulp and paper industry have been reported [26-28], while degradation and decolourization of synthetic dyes due to the non-specificity of the LMEs have been widely documented [29, 30], Likewise, treatment of the acidic, phenolic-rich olive oil mill wastewater has shown COD reduction, decolourization and dephenolization [31-34],... 

Lipophilic ion exchangers traditionally used for polymeric membrane preparation are the anionic tetraphenylborate derivatives and the cationic tetraalkylammonium salts. The charges on both lipophilic ions are localized on a single (boron or nitrogen) atom, but the steric inaccessibility of the charged center, due to bulky substituents, may inhibit ion-pair formation in the membrane and provide, when necessary, non-specific interactions between ionic sites and sample ions. 

Fc receptors present on the cell membrane of macrophages, monocytes, granulocytes, lymphocytes, and some other cells may, in theory, non-specifically bind Fc portion of antibodies used for immunolabeling. Typically, blocking endogenous Fc receptors involves using normal serum derived from the same species used to produce the secondary antibody. To block endogenous Fc receptors, incubate sections for 15 30 min with normal serum (2 5% v/v) from the host species of the secondary antibody. 

To answer this question, let us first consider a neutral molecule that is usually said to be polar if it possesses a dipole moment (the term dipolar would be more appropriate)1 . In solution, the solute-solvent interactions result not only from the permanent dipole moments of solute or solvent molecules, but also from their polarizabilities. Let us recall that the polarizability a of a spherical molecule is defined by means of the dipole m = E induced by an external electric field E in its own direction. Figure 7.1 shows the four major dielectric interactions (dipole-dipole, solute dipole-solvent polarizability, solute polarizability-solvent dipole, polarizability-polarizability). Analytical expressions of the corresponding energy terms can be derived within the simple model of spherical-centered dipoles in isotropically polarizable spheres (Suppan, 1990). These four non-specific dielectric in-... 

There is now convincing evidence that an acyl chymotrypsin intermediate is formed from both specific and non-specific substrates (Bender and Kezdy, 1964 Bender et al., 1964). This intermediate is undoubtedly an acylserine. Acyl- and phosphorylserine derivatives have been isolated and identified. In view of evidence such as a D2 O solvent isotope effect ( h2oAd2o) 2-3 for both acylation and deacylation (Bender and Hamilton, 1962), alcohol and amine nucleophiles showing little dependence on the p/iTa-value of the nucleophile in reaction with furoyl enzyme (Inward and Jencks, 1965), and the influence of increasing steric bulk in the acyl group (Fife and Milstien, 1967 Milstien and Fife, 1968,.1969), consistent... 

Dopamine is the decarboxylation product of DOPA, dihydroxyphenylalanine, and is formed in a reaction catalysed by DOPA decarboxylase. This enzyme is sometimes referred to as aromatic amino acid decarboxylase, since it is relatively non-specific in its action and can catalyse decarboxylation of other aromatic amino acids, e.g. tryptophan and histidine. DOPA is itself derived by aromatic hydroxylation of tyrosine, using tetrahydrobiopterin (a pteridine derivative see Section 11.9.2) as cofactor. 

The unsubstituted spirononadiene has been obtained from silicon atoms and the diene, albeit in low yield. However it results in better yield from methoxytris(trimethylsilyl)silane and the diene on photolysis. a-Elimination is non-specific but favours the methoxysilylene, addition giving the two silacyclopentenes (111) and (112) with buta-1,3-diene (Scheme 186). Pyrolysis with excess butadiene gives the spiro derivative, in support of the cyclosilylene intermediate (113 Scheme 187) (81JA7344). 

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