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Screening study

Another retrospective analysis of already known H DAC inhibitors was carried out by You et al. [68]. They generated a 3D chemical-feature-based pharmacophore model and compared the ligand-based model with the structural-functional requirements for the binding of the HDAC inhibitors. Using this model, the interactions between the benzamide MS-275 and HDAC were explored. The result showed that the type and spatial location of chemical features encoded in the pharmacophore are in full agreement with the enzyme-inhibitor interaction pattern identified from molecular docking. However, also in this study no experimental validation of the modeling results was provided. [Pg.66]


Acrylic adhesive formulations can be amazingly simple. The formulation given in Table 1 is a simplification of the Bader work, and provides an excellent starting point for screening studies. [Pg.824]

A screening study for evaluating and selecting components of the tinplate container—tinplate, enamel, end-sealing compound, and side-seam solder—which were irradiated at designated doses and temperatures... [Pg.30]

Irradiation Conditions. The gamma (cobalt-60) radiation facility and the source calibration are described by Holm and Jarrett (4). Irradiation doses were 3-4 Mrad and 6-7.5 Mrad at 9 X 102 rads per second for the screening study. Irradiation temperatures were 5, —30, and — 90°C. The gamma source was calibrated with the ferrous sulfate-cupric sulfate dosimeter. [Pg.30]

Appel MJ, Waalkens-Berendsen DH (2004a) Trichiormethyi-stannane [CAS 993-16-8] Sub-chronic (13 week) orai toxicity study in rats, inciuding a reproduction/deveiopmentai screening study. Zeist, TNO Nutritien and Food Research Institute, July (TNO Repert Ne. V4929). [Pg.43]

For the PS case, a three-variable Box-Behnken response surface methodology (RSM) design using formulation variables has been carried out. For the RF system, an eight-variable fractional-factorial screening study was done first to select significant factors, and this was followed by two RSM s which were similar in design to the one done for PS. The results have led directly to substantial improvements in both materials. [Pg.74]

The analysis of the screening study data was carried out in the standard manner by hand since the computer program was not yet available. The first three variables were... [Pg.78]

The results for the RF screening study are shown in Table 3. The most striking result to come out of this experiment was that there appears to be a strong correlation between the low level of catalyst concentration and gel formation. The low level was outside the range of what had previously been tried. This has been confirmed in many subsequent experiments. Another important conclusion was that the chemistry appears to dominate the process, so it was reasonable to proceed with an RSM which dealt only with the formulation variables. Although the oven time was significant at the 90% confidence level, it was decided to optimize the chemistry first and deal with this as part of the processing conditions in later experiments. [Pg.80]

Carotenoids and breast cancer — Among seven case-control studies investigating the correlation between different carotenoid plasma levels or dietary intakes and breast cancer risk, five showed significant inverse associations with some carotenoids. - In most cases, this protective effect was due to 3-carotene and lutein. However, one (the Canadian National Breast Screening Study ) showed no association for all studied carotenoids including (I-carotene and lutein. More recently, another study even demonstrated a positive correlation between breast cancer risk and tissue and serum levels of P-carotenes and total carotenes. Nevertheless, these observational results must be confirmed by intervention studies to prove consistent. [Pg.132]

In a screening study with 78 subjects, the lag phase varied from 34 to 114 min. Interestingly, only a weak correlation was found between the a-tocopherol content and the lag phase (r=0.2, P < 0.01, n = 78). Increasing the a-tocopherol content of individual LDL samples in vitro or by oral supplementation led always to a proportional increase of oxidation resistance, according to the equation y=kx+a. The slope k is the eflScacy of... [Pg.47]

In 2001, a screening study for the enantioselective reduction of various aryl ketones was developed by Petra et al. in the presence of amino sulfide... [Pg.271]

Bagdy D., Barabas E., Bajusz S., Szell E. In vitro inhibition of blood coagulation by tripeptide aldehydes A retrospective screening study focused on the stable D-MePhe-Pro-Atg-H-H2S04. Thromb Haemost 1992 67,325-30. [Pg.166]

Chemical and physical properties of the contaminant should also be investigated. Solubility in water (or other washing fluids) is one of the most important physical characteristics. Hydrophobic contaminants can be difficult to separate from the soil particles and into the aqueous washing fluid. Reactivity with wash fluids may, in some cases, be another important characteristic to consider. Other contaminant characteristics such as volatility and density may be important for the design of remedy screening studies and related residuals treatment systems. Speciation is important in metal-contaminated sites. [Pg.563]

Table 11.5. Statistical analysis of the Group 2 data for the lPt/15Ba/5Fe catalyst in the screening study... Table 11.5. Statistical analysis of the Group 2 data for the lPt/15Ba/5Fe catalyst in the screening study...
The most economical route Is probably to use screening studies to determine the dominant fate processes and then study only those In detail. In this paper we review some simple screening techniques that can be used to quantify volatilization and leaching rates at the soil/air Interface. Volatilization and leaching rates are then compared with estimates of transformation rates to determine the compound s overall fate and Identify the process requiring further study If a more exact fate assessment Is required. [Pg.198]

One advantage of whole-cell biotransformation that has not been addressed adequately in this chapter is the ability to modify compounds with complex structure, such as natural products. Natural products are ideal substrates for biotransformation reactions since they are synthesized in a series of enzymatic reactions by the whole cells. The modification of natural products by biotransformation has been reviewed recently by Azerad [ 13] and a majority of the modifications were carried out by whole-cell biotransformations. Additional examples of modification of natural products by whole-cell biotransformations can also be found in the review article by Patel [2]. Natural products are an important source of new drugs and new drug leads [53]. The use of biotransformation, especially whole-cell biotransformation, in modification of natural products for lead optimization and generating libraries of derivatives for S AR and screening studies is important for the pharmaceutical industry. [Pg.240]

Biodegradation aqueous aerobic biodegradation t,/2 =168-672 h, based on aqueous screening studies (Marion Malaney 1964 Kitano 1978 Van der Linden 1978 Tester Harker 1981 Trzilova Horska 1988 Howard et al. 1991) ... [Pg.483]

Fig. 1. Interrelationships between the various components of the polymer and capsule screening studies... Fig. 1. Interrelationships between the various components of the polymer and capsule screening studies...
Because of the complexities involved in understanding cause-effect relationships, an alternative approach to control the thin film microstructure has been pursued by some investigators—the use of statistically designed experiments to identify key processing parameters.114115 In these approaches, as illustrated in Table 2.6 for a Plackett-Burman screening study,114 limiting values for various experimental parameters are chosen. Films are then prepared from solutions synthesized under these conditions, and resulting film... [Pg.61]

U.S. Environmental Protection Agency (USEPA). 1988. U.S. Environmental Protection Agency/Paper Industry Cooperative Dioxin Screening Study. EPA Rep. 440/1-88-025. 372 pp. [Pg.1067]


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See also in sourсe #XX -- [ Pg.101 , Pg.102 , Pg.312 ]

See also in sourсe #XX -- [ Pg.13 , Pg.18 , Pg.34 ]




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