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Steroids designation

Information retrieval, 10 (1974) 1 Inotropic steroids, design of, 30 (1993) 135 Insulin, obesity and, 17 (1980) 105 Ion-selective membrane electrodes,... [Pg.388]

A typical steroid skeleton is shown along with the numbenng scheme used for this class of compounds Specify in each case whether the designated substituent is axial or equatorial... [Pg.140]

Saponins. Although the hypocholesterolemic activity of saponins has been known since the 1950s, thek low potency and difficult purification sparked Htde interest in natural saponins as hypolipidemic agents. Synthetic steroids (292, 293) that are structurally related to saponins have been shown to lower plasma cholesterol in a variety of different species (252). Steroid (292) is designated CP-88,818 [99759-19-0]. The hypocholesterolemic agent CP-148,623 [150332-35-7] (293) is not absorbed into the systemic ckculation and does not inhibit enzymes involved in cholesterol synthesis, release, or uptake. Rather, (293) specifically inhibits cholesterol absorption into the intestinal mucosa (253). As of late 1996, CP-148,623 is in clinical trials as an agent that lowers blood concentrations of cholesterol (254). [Pg.447]

A restricted number of applicable fluonne markers may also be viewed as a Imutabon The tnfluoroacetyl moiety has been the most commonly used group, used m sbidies of ammo acids, steroids, and carbohydrates Enhanced F NMR detection should be possible with specifically designed agents of opumal biological and spectral properbes... [Pg.1070]

That an aminal is a necessary intermediate was first questioned by Herr and Heyl (2). They found that by using a slight excess of amine the yield of the enamine from two of the steroidal aldehydes studied was 84%. Also, the -fluorocnamines discussed earlier are formed in 60-90% yield from equimolar amounts of the 8-fluoroaldehyde and secondary cyclic amine (27). However, neither of these studies was specifically designed to show whether or not aminals were intermediates. [Pg.60]

As noted above, the steroid nucleus has been a favorite for the design for site directed alkylating antitumor drugs. Thus reaction of prednisolone (62) with anhydride 63 affords the 21 acylated derivative, prednimustine (64). ... [Pg.93]

Thomson i Click Organic Interactive to use a web-based palette to assign P,S designations to chiral centers in steroids. [Pg.1079]

Substituents are designated as in die a configuration if they are below the plane of the steroidal nucleus, and as P if above the plane ... [Pg.295]

These discoveries generated a lot of effort over the successive 25 years in the preparation of especially designed drug delivery systems for the controlled release of radioactive progesterone [654], colchicine [656], naproxen [657,673, 674], mitomycin C [675-677], inulin [678], trimethoprin [657], succinylsul-fathiazole [657], ethacrynic acid [653], and steroids [633], regardless of whether these drugs are physically trapped in polyphosphazene matrices, or chemically bonded to the polymer skeleton. [Pg.217]

The rate and duration of steroid release is affected by (1) polymer composition, (2) drug/polymer ratio (3) microsphere size distribution, and (4) microsphere quality (75). The ratio of glycolide to lactide in the copolymer has been found to be more dominant than the polymer molecular weight in the design of controlled release formulations. Microspheres of smaller size provide in vivo drug profiles of higher levels and shorter durations because of greater surface area. [Pg.17]

Several antiinflammatory compounds have been formulated in lactide/ glycolide polymers (107-111). Methylprednisolone microspheres based on an 85 15 DL-lactide/glycolide copolymer were developed for intra-articulate administration (111). The microspheres, prepared by a solvent evaporation procedure, are 5—20 jam in diameter and are designed to release low levels of the steroid over a extended period in the joint. Controlled experiments in rabbits with induced arthritis showed that the microspheres afforded an antiinflammatory response for up to 5 months following a single injection. [Pg.24]

Lewis, D. H. and Tice, T. R., Polymeric considerations in the design of microencapsulated contraceptive steroids, in Long-Acting Contraceptive DeUvery Systems (G. I. Zatuchni, ed.). Harper and Row, Philadelphia, 1983, pp. 77-95. [Pg.36]

Foltin, R. W., The importance of drug self-administration studies in the analysis of abuse liability An analysis of caffeine, nicotine, anabolic steroids, and designer drugs. Annual Meeting of the American Academy of Psychiatrists in Alcoholism and Addictions (1990, Santa Monica, California). American Journal on Addictions Spr Vol 1(2), 139-149, 1992. [Pg.302]


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