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Pharmaceuticals metabolism

Unlike, e.g. in pharmaceutical metabolism studies, where the parent compound is known and thus some preliminary knowledge of the expected structures is available, the composition of a natural products extract is often completely unknown beforehand ( non-target analysis ). In such cases, NMR spectroscopy is especially well suited as a detection system since it does not discriminate any classes of compounds. (Sufficient relaxation delays provided, the NMR signal depends only on the number of nuclei in the active probe volume.)... [Pg.112]

Research on aromatic hydroxylation by cytochrome P450 provides an example of how quantum chemical calculations on small models can help in developing structure-reactivity relationships. Hydroxylation of C-H bonds is a particularly important class of reaction in drug metabolism,185 which can activate pro-drugs, or affect the bioavailability of pharmaceuticals. For the reliable prediction of pharmaceutical metabolism and toxicology (ADME/ TOX) properties, a key aim is the development of structure-activity relationships to predict conversions of drugs. Earlier work has shown that structure-activity relationships based on the structures and properties of substrates alone are of limited utility. There is a need for more detailed models, which can include effects of the reaction mechanism and specificity of different cytochrome P450 isozymes. [Pg.55]

Pharmaceuticals. Metabolic engineering is most promising in the production of pharmaceuticals. These include pharmaceuticals from different classes of natural products alkaloids, isoprenoids, and flavonoids. Biosynthesis of natural products is an emerging area of metabolic engineering that offers significant advantages over conventional chemical methods. Some pharmaceutical compounds are too complex to be chemically synthesized or extracted from biomass organisms inexpensively. [Pg.1189]

Historically, drug absorption, distribution, metabolism, excretion, and toxicity ADMET) studies in animal models were performed after the identification of a lead compound. In order to avoid costs, nowadays pharmaceutical companies evaluate the ADMET profiles of potential leads at an earlier stage of the development... [Pg.607]

Azaorotic acid as pharmaceutical, 1, 159 1 -Aza-5-oxabenzocycloheptene nomenclature, 1, 21 Azapentalenes reactions, 5, 267 Azaperone metabolism, 1, 237 Azapetine... [Pg.521]

Dibenz[h,e]azepine-6,11-diones ent-Morphinan nomenclature, 1, 29 Morphinan, 1,2,3,4-tetrahydro-nomenclature, 1, 29 14-a-Morphinan, N-methyl-synthesis, 1, 480 Morphinans nomenclature, 1, 29 as pharmaceuticals, 1, 148 synthesis, 2, 377 Morphine, 2, 512 as analgesic, 1, 167 as metabolite of normorphine, 1, 235 as pharmaceutical, 1, 146, 147, 148 synthesis, 1, 480 Morphine alkaloids structure, 4, 534 Morphin-7-en nomenclature, 1, 29 Morphinone, dihydro-as pharmaceutical, 1, 147 Morpholine — see also 1,4-Oxazine, tetrahydrocarcinogenicity, 1, 229 corrosion inhibitor, 1, 409 metabolism, 1, 226 nomenclature, 3, 996 structure, 2, 5 synthesis, 2, 89 Morpholine, 4-aciyloyl-polymers, 1, 291 Morpholine, alkenyl-polymers, 1, 291... [Pg.704]

Purine, 6-iodo-alkylation, 5, 530 synthesis, 5, 563, 597 Purine, 6-iodo-9- -D-(2,3,5-tri-0-acetyl)ribofuranosyl-synthesis, 5, 598 Purine, 9-isopropyl-deuterium-hydrogen exchange, 5, 527 Purine, 9-(2,3-0-isopropylidene-/3-D-ribofuranosyl)-6-methoxy-synthesis, 5, 584 Purine, 6-mercapto-biological activity, 5, 604 metabolism, 1, 237 as pharmaceutical, 1, 159 tautomerism, 5, 509 Purine, 2-methoxy-synthesis, 5, 596 Purine, 6-methoxy-irradiation, 5, 543 riboside... [Pg.759]

The special topics discussed are (i) the biological aspects of heterocyclic compounds, i.e. their biosynthesis, toxicity, metabolism, role in biochemical pathways, and their uses as pharmaceuticals, agrochemicals and veterinary products (ii) the use of heterocyclic compounds in polymers, dyestuffs and pigments, photographic chemicals, semiconductors and additives of various kinds and (iii) the use of heterocyclic compounds as intermediates in the synthesis of non-heterocyclic compounds. [Pg.1]

The second method for mixture analysis is the use of specialized software together with spectral databases. We have developed a mixture analysis program AMIX for one- and multidimensional spectra. The most important present applications are the field of combinatorial chemistry and toxicity screening of medical preparations in the pharmaceutical industry. An important medical application is screening of newborn infants for inborn metabolic errors. [Pg.418]

Examples of Synthesis Routes Inherently Safer Than Others As summarized by Bodor (1995), the ethyl ester of DDT is highly effective as a pesticide and is not as toxic. The ester is hydrolytically sensitive and metabolizes to nontoxic products. The deliberate introduction of a structure into the molecule which facilitates hydrolytic deactivation of the molecule to a safer form can be a key to creating a chemical product with the desired pesticide effects but without the undesired environmental effects. This technique is being used extensively in the pharmaceutical industry. It is applicable to other chemical industries as well. [Pg.65]

In the pharmaceutical industry, GA is used in pharmaceutical preparations and as a carrier of drugs since it is considered a physiologically harmless substance. Additionally, recent studies have highlighted GA antioxidant properties (Trommer Neubert, 2005 Ali Al Moundhri, 2006 Hinson et al., 2004), its role in the metabolism of lipids (Tiss et al., 2001, Evans et al., 1992), its positive results when being used in treatments for several degenerative diseases such as kidney failure (Matsumoto et al., 2006 Bliss et al., 1996 Ali et al., 2008), cardiovascular (Glover et al., 2009) and gastrointestinal (Wapnir et al., 2008 Rehman et al, 2003). [Pg.3]


See other pages where Pharmaceuticals metabolism is mentioned: [Pg.691]    [Pg.17]    [Pg.751]    [Pg.691]    [Pg.17]    [Pg.751]    [Pg.199]    [Pg.273]    [Pg.319]    [Pg.142]    [Pg.569]    [Pg.573]    [Pg.576]    [Pg.701]    [Pg.703]    [Pg.710]    [Pg.2134]    [Pg.79]    [Pg.431]    [Pg.189]    [Pg.316]    [Pg.317]    [Pg.332]    [Pg.586]    [Pg.597]    [Pg.769]    [Pg.899]    [Pg.464]    [Pg.81]    [Pg.1551]    [Pg.202]    [Pg.203]    [Pg.9]    [Pg.269]    [Pg.24]    [Pg.124]    [Pg.140]    [Pg.437]    [Pg.437]    [Pg.445]    [Pg.446]    [Pg.457]   
See also in sourсe #XX -- [ Pg.3 , Pg.245 ]

See also in sourсe #XX -- [ Pg.3 , Pg.245 ]




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Drug Metabolism pharmaceutical analysis

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