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Potential biochemical

Total synthesis of f-t -deoxypyiTobrine, a potential biochemical marker for diagnosis of osteoporosis, is shown in Eq 10 25 Osteoporosis is a cripphng degenerative bone disease that affects the aged populadon, particularly postmenopausff women... [Pg.332]

Clarke PA, te Poele R, Wooster R, Workman P (2001) Gene expression microarray analysis in cancer biology, pharmacology, and drug development progress and potential. Biochem Pharmacol 62 1311-1336... [Pg.769]

Glaser, K.B. (2007) HDAC inhibitors clinical update and mechanism-based potential. Biochemical Pharmacology,... [Pg.135]

Other Environmental Influences on Individuals and Their Genomes. Finally, the environment provides numerous potential biochemical influences on the genome, such as exposure to viruses, toxins, or diseases (Fig. 4—4). These, too, could contribute to the probability that genetic vulnerabilities for a psychiatric illness will become manifest. [Pg.110]

Crofford LJ (1997) COX-1 and COX-2 tissue expression implications and predictions. J Rheumatol 24, Suppl 49 15-19 Cromlish WA, Kennedy BP (1996) Selective inhibition of cyclogenase-1 and -2 using intact insect cell assays. Biochem Pharmacol 52 1777-1785 Evans AT, Formukong EA, Evans FJ (1987) Actions of cannabis constituents on enzymes of arachidonate metabolism anti-inflammatory potential. Biochem Pharmacol 36 2035-2037... [Pg.241]

Toxicology studies are conducted to define the safety profile of a candidate and include definition of the no-toxic-effect dose, MTD, potential organs of toxicity, and potential biochemical markers to detect and track toxic events. Most developmental compounds that do not become therapeutic products have unacceptable toxicity in animals or humans. Before the definitive toxicology studies needed to support an IND submission are initiated, a number of animal experiments can be conducted to characterize the potential toxicity of the candidate. These early toxicology evaluations are usually conducted in the same species as used in pharmacology evaluations. As mentioned earlier, the lowest dose that has no toxicity or an acceptable level of toxicity is compared with the dose that gives the desired pharmacologic response in the same animal species to obtain a therapeutic ratio or index for that species. [Pg.31]

Swenberg JA, Petzold GL, Harbach PR. 1976. In vitro DNA damage/alkaline elution assay for predicting carcinogenic potential. Biochem Biophys Res Commun 72 732-738. [Pg.418]

As screening techniques become more sophisticated, the range of compounds that are potentially valuable as leads should increase. As, an example, the antijuvenile hormone action of the precocenes has been cited. Their spectrum of activity is limited, but the study of their action has revealed potential biochemical target sites. [Pg.331]

Tune BM, Hsu C-H, Fravert D. Cephalothin and carbacephem nephrotoxicity. Role of tubular cell uptake and acylating potential. Biochem Pharmacol 1996 51 557-561. [Pg.315]

Phosphosugars attracted interest for potential biochemical applications but have not met with expectations. Because of the lack of stability of the phosphane oxidation state (+ 3), the phosphane oxide is usually preferred in phosphosugar syntheses. The literature on phosphosugars until 1984 was reviewed by Yamamoto and Inokawa [228]. [Pg.426]

Billiau, A. and Dijkmans, R. (1990). Interferon-gamma mechanism of action and therapeutic potential. Biochem. Pharmacol. 40, 1433-1439. [Pg.114]

Lehane, A. M., Saliba, K. J., Allen, R. J., and Kirk, K. (2004a). Choline uptake into the malaria parasite is energized by the membrane potential. Biochem. Biophys. Res. Commun. 320, 311-317. [Pg.359]


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