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6- FLT

Pour the reaction mixture into a 1-litre round-bottomed flask, add 250 ml. of water, flt a still head and a condenser for downward distillation (Fig. II, 13, 3, but without the thermometer). Distil the mixture until about 125 ml. of distillate (two layers) have been collected. Saturate with salt (about 30 g. are required), and separate the upper layer of cycZohexanone extract the aqueous layer with 25-30 ml. of ether and combine the ether extract with the cyclohexanone layer. Dry with about 6 g. of anhydrous sodium or magnesium sulphate, ffiter the solution into a distilling flask of suitable size to which a condenser has previously been attached. Distil off the ether from a water bath—a beaker containing warm water is satisfactory. Distil the residual liquid from an air bath or a wire gauze, and collect the cyclohexanone at 153-156°. The yield is 16 g. [Pg.337]

Place a mixture of 30 g. of 3 5-dinitrobenzoic acid (Section IV,168 and 33 g. of phosphorus pentachloride in a Claisen flask flt a reflux condenser into the short neck and cork the other neck and side arm (compare Fig. Ill, 31,1). Heat the mixture in an oil bath at 120-130° for 75 minutes. Allow to cool. Remove the phosphorus oxychloride by distillation unda reduced pressure (25°/20 mm.) raise the temperature of the bath to 110°. The residual 3 5-dinitrobenzoyl chloride solidifies on cooling to a brown mass the yield is quantitative. Recrystallise from carbon tetrachloride the yield is 25 g., m.p. 67-68° and this is satisfactory for most purposes. Further recrystallisation from a large volume of light petroleum b.p. 40-60°, gives a perfectly pure product, m.p. 69-6°. [Pg.974]

FIGURE 4.6 Structure of the complex between VEGF and Flt-1. The two monomers of VEGF are composed of parallel 3 sheets and they are shown in light and medium gray, respectively. The two copies of Flt-1 are in dark gray. PDB id 1FLT. (Wiesmann, C. et al., Cell, 91, 641, 1997.)... [Pg.140]

Moscinski L, Atadja P, Bhalla K (2004) Superior activity of the combination of histone deacetylase inhibitor LAQ824 and the FLT-3 kinase inhibitor PKC412 against human acute myelogenous leukemia cells with mutant FLT-3. Clin Cancer Res 10 4991 997 Bali P, Pranpat M, Bradner J, Balasis M, Fiskus W, Guo F, Rocha K, Kumarawsamy S, Boyapalle S, Atadja P, Seto E, Bhalla K (2005) Inhibition of histone deacetylase 6 acetylates and disrupts the chaperone function of heat shock protein 90 a novel basis for antileukemia activity of histone deacetylase inhibitors. J Biol Chem 280(29) 26729-26734 Bannister AJ, Schneider R, Kouzarides T (2002) Histone methylation Dynamic or static Cell 109 801-806... [Pg.421]

Suppose that T is an n-dimensional representation of a group of transformation operators Om acting on the functions of an n-dimensional function space and that we have basis functions flt /s,. ., fn with the property that the first m (m < n) are transformed among themselves for all Om (e.g. in 6-3, the p-orbitals Pi and p5 were transformed among themselves by all O, and so m = 2 for this case) ... [Pg.110]

Fig. 2.20. Composition (mean%) of 16 individual polycyclic aromatic hydrocarbons (PAHs) to total PAHs detected in various environmental media in (a) air (n = 24), (b) soil (n = 226), (c) freshwater (n = 46), and (d) marine sediment (n = 159), from the South Korea. Naphthalene NAP, Acenaphthylene ACY, Acenaphthene ACE, Fluorine FLU, Phenanthrene PHE, Anthracene ANT, Fluoranthene FLT, Pyrene PYR, Benz[a]ant-hracene BaA, Chrysene CHR, Benzo[6]fluoranthene BbF, Benzo[ ]fluoranthene BkF, Benzo[a]pyrene BaP, Indeno[l,2,3,c,d]pyrene I123cdP, Dibenz[a,/z]anthracene DahA, Ben-zo[g,/y ]perylene BghiP. Fig. 2.20. Composition (mean%) of 16 individual polycyclic aromatic hydrocarbons (PAHs) to total PAHs detected in various environmental media in (a) air (n = 24), (b) soil (n = 226), (c) freshwater (n = 46), and (d) marine sediment (n = 159), from the South Korea. Naphthalene NAP, Acenaphthylene ACY, Acenaphthene ACE, Fluorine FLU, Phenanthrene PHE, Anthracene ANT, Fluoranthene FLT, Pyrene PYR, Benz[a]ant-hracene BaA, Chrysene CHR, Benzo[6]fluoranthene BbF, Benzo[ ]fluoranthene BkF, Benzo[a]pyrene BaP, Indeno[l,2,3,c,d]pyrene I123cdP, Dibenz[a,/z]anthracene DahA, Ben-zo[g,/y ]perylene BghiP.
Figure 20. Examples of the field dependence of Flts. The curves are obtained from the measured magnetization curves and Eq, 9, at 6 and 14 GHz, after subtraction of the nearly field independent non-resonant absorption background. The dots represent the fit of these curves using Eqs. 8 and 10 (Gaussian distributions) yielding Figure 20. Examples of the field dependence of Flts. The curves are obtained from the measured magnetization curves and Eq, 9, at 6 and 14 GHz, after subtraction of the nearly field independent non-resonant absorption background. The dots represent the fit of these curves using Eqs. 8 and 10 (Gaussian distributions) yielding <rL 33 - 38 mT.
Fig. 4-6. Experimental measurement of ( )//()/)t and )U/i)t)j. The slope of the tangent to the curve at temperature T = (<)f/dT)i at T. This equals (DS/HDt. which equals entropy change per unit extension when the elastomer is extended isothermally at Ti. The intercept on the force axis equals (flt//(l/)T since this corresponds to T =0 in Eq. (4-39). Tlie intercept is the internal energy change per unit extension. Fig. 4-6. Experimental measurement of ( )//()/)t and )U/i)t)j. The slope of the tangent to the curve at temperature T = (<)f/dT)i at T. This equals (DS/HDt. which equals entropy change per unit extension when the elastomer is extended isothermally at Ti. The intercept on the force axis equals (flt//(l/)T since this corresponds to T =0 in Eq. (4-39). Tlie intercept is the internal energy change per unit extension.
In a similar manner, cholest-4 e, aoetoxyeholest-4-ene. and niethoxyoholest 4>ene suffer attack from the expected less hindered whereas 3 -hydioxychoIest-4-ene undergoes -epoxidation. i IJie same phenomenon appeam to operate with 7tt- and 7 -hydroxy-.- h >t( flt-G(6)-ene derivatives, ti and aJso with 7a-hydroxycholest- (4 -ene. ... [Pg.352]


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See also in sourсe #XX -- [ Pg.2043 , Pg.2044 ]




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