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Medicines evolution

Urea derivadves are of general interest in medicinal chemistry. They may be obtained cither from urea itself (barbiturates, sec p. 306) or from amines and isocyanates. The latter are usually prepared from amines and phosgene under evolution of hydrogen chloride. Alkyl isocyanates are highly reactive in nucleophilic addidon reactions. Even amides, e.g. sulfonamides, are nucleophilic enough to produce urea derivatives. [Pg.301]

Molecular modeling has evolved as a synthesis of techniques from a number of disciplines—organic chemistry, medicinal chemistry, physical chemistry, chemical physics, computer science, mathematics, and statistics. With the development of quantum mechanics (1,2) ia the early 1900s, the laws of physics necessary to relate molecular electronic stmcture to observable properties were defined. In a confluence of related developments, engineering and the national defense both played roles ia the development of computing machinery itself ia the United States (3). This evolution had a direct impact on computing ia chemistry, as the newly developed devices could be appHed to problems ia chemistry, permitting solutions to problems previously considered intractable. [Pg.157]

W. Sneader, Dmg Discovey The Evolution of Modem Medicines,]ohxi Wiley Sons, Inc., New York, 1986. [Pg.398]

The attraction of lipophilicity in medicinal chemistry is mainly due to Corwin Hansch s work and thus it is traditionally related to pharmacodynamic processes. However, following the evolution of the drug discovery process, lipophilicity is today one of the most relevant properties also in absorption, distribuhon, metabolism, excretion and toxicity (ADMET) prediction, and thus in drug profiling (details are given in Chapter 2). [Pg.325]

Thorndike, Lynn. "The attitude of Francis Bacon and Descartes towards magic and occult science." In Science medicine and history essays on the evolution of scientific thought and medical practice written in honour of Charles Singer, ed. E. Ashworth Underwood, 451- 454. Oxford OUP, 1953. [Pg.249]

Colorless, reactive gas. Oxygen was not present in the initial atmosphere of the Earth, although at 50 % it is the most common element in the crust of the Earth (oxides, silicates, carbonates, etc.). The compound with hydrogen is remarkable. The hydrides of all other elements are unpleasant compounds, but H20 is the molecule of life. The 02 found in the air today, of which it makes up 20 %, was formed in the process of evolution by photosynthesis of algae, which then also allowed life on solid land. Oxidation with oxygen became and is still the dominant pathway of life forms for obtaining energy (respiration). Used in medicine in critical situations. Oxidations play a key role in chemistry (sulfuric acid, nitric acid, acetic acid, ethylene oxide, etc.). The ozone layer in space protects the Earth from cosmic UV radiation. Ozone (03) is used in the... [Pg.35]

One study on the evolution of Spanish public pharmaceutical expenditure21 concludes that spending on pharmaceuticals rose 264 per cent in real terms from 1980 to 1996. This figure can be broken down into a 39 per cent decrease in the relative price of medicines, a 10 per cent increase in the quantity and a variation of 442 per cent explained by a residual that reflects the effect of the introduction of new products and a shift in consumption. As we can see from these figures, we have no practical price index and no quantitative approximation to the breakdown of the increase in expenditure into price and quality. [Pg.50]

Building on the approach that allows optimization of biological systems through evolution, this would let a system produce the optimal new substance, and produce it as a single product rather than as a mixture from which the desired component must be isolated and identified. Self-optimizing systems would allow visionary chemical scientists to use this approach to make new medicines, catalysts, and other important chemical products—in part by combining new approaches to informatics with rapid experimental screening methods. [Pg.10]

Guner, O.F. (2002) History and evolution of the pharmacophore concept in computer-aided drug design. Current Topics in Medicinal Chemistry, 2, 1321-1332. [Pg.124]

Drug Discovery the Evolution of Modern Medicines (1995) by Walter Sneader. John Wiley Sons, Ltd. (Chichester). [Pg.558]


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See also in sourсe #XX -- [ Pg.196 ]




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