Compounds identified from interaction

Table I. Some Heterocyclic Compounds Identified from Thermal Interaction of 2,4-Decadienal and Cysteine...

As shown in Table II, some volatile compounds identified from the thermal interaction of IMP and alliin were derived from the thermal degradation of alliin (II, 13), and the others were generated from the interactions of IMP and alliin. 

The adverse side-effects of the TCAs, coupled with their toxicity in overdose, provoked a search for compounds which retained their monoamine uptake blocking activity but which lacked the side-effects arising from interactions with Hj, aj-adreno-ceptors and muscarinic receptors. One of the first compounds to emerge from this effort was iprindole, which has an indole nucleus (Fig. 20.3). This turned out to be an interesting compound because it has no apparent effects on monoamine uptake and is not a MAO inhibitor. This, together with its relatively minor antimuscarinic effects, led to it commonly being described as an atypical antidepressant. Mechanisms that could underlie its therapeutic actions have still not been identified but, in any case, this drug has now been withdrawn in the UK. 

A number of other studies of AB cements have used X-ray diffraction. For example, Sorrell (1977) and Sorrell Armstrong (1976) employed the technique in the study of oxychloride cements formed in aqueous solution by interaction of oxides and chlorides of either zinc or magnesium. Individual phases were identified, again using Cu K radiation, this time comparing results with those previously obtained for pure compounds. Results from these two studies are described in detail in Sections 7.2 and 7.3 respectively. 

The developments which led to the present day concepts of the metabolic activation of hydrocarbons did not arise from the classical approach of identifying metabolites of greater biological potency than the parent compound, but from an approach dependent upon the assumption (or presumption) that the interaction of carcinogens with DNA is a key event in the initiation of the carcinogenic process. Brookes and Lawley (49) found in 1964 that when radioactive hydrocarbons are applied to the skin of mice, they become covalently bound to the DNA of the skin. Moreover, the extents of binding to DNA for various hydrocarbons followed fairly closely their relative carcinogenic activities. 

Maillard reaction products formed by interaction of reducing sugar and amino acids such as a-dicarbonyl compounds, aldehydes, hydrogen sulfide, and ammonia can react further to form derivatives that have been identified from meat or its components during heating. Important reviews of sulfur compounds that might be produced by these reactions have been published by Schutte (35) and... 

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