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Molecular factors

No correction for molecular weights was necessary for derivatized HMS, because the injection standards were derivatized simultaneously with the samples. However, a correction factor was needed for calculating the recovered amount of SCA since the SCA was quantitated as DMS. The correction factor (molecular weight ratio) between SCA and DMS was 1.12 (417/373 417 = molecular weight of SCA and 373 = molecular weight of DMS). To calculate the amount of SCA, use the above equation, which will yield DMS (ng), then multiply that value by 1.12 to convert to nanograms of SCA. [Pg.575]

Sum of H-bond acceptor factors (HYBOT) [23] also SumCa Sum of H-bond acceptor factors/molecular polarizability (HYBOT) [23] also SCa A... [Pg.233]

Park, L. S., Gillis, S. and Urdal, D. L. (1990). Hematopoietic growth-factor receptors. In Colony-Stimulating Factors. Molecular and Cellular Biology, eds. Dexter, T. M., Garland, J. M. and Testa, N. G., Marcel Dekker, New York, pp. 39-75. [Pg.525]

Estimation is easier and less time-consuming because use is made of empirical relationships between the BCF and physicochemical properties of the compound, such as water solubility (S) [42-48], Km, (solid organic carbon/water partition coefficient) [48], Kmw (membrane water partition coefficient), iipw (liposome water partition coefficient) [49], critical micelle concentration (CMC) [45], steric factors, molecular weight [47,48], and others. The most common regression method is the estimation of BCF from the octanol-water partition coefficient (Kovl) [18,42,44-48,50,51],... [Pg.902]

C5a is inactivated by the myeloperoxidase-H202 system, which oxidises a methionine residue (Met 70) on the molecule group A streptococcal endo-proteinases also abolish chemotactic activity of C5a and related compounds. Neutrophil lysosomal enzymes (e.g. elastase and cathepsin G) also destroy C5a chemotactic activity, but as these proteases are inhibited by the serum antiproteinases, a -antiproteinase and a2-macroglobulin, the physiological role of neutrophilic proteases in the inactivation of C5a is questionable. Two chemotactic factor inactivators have been found in human serum an a-globulin that specifically and irreversibly inactivates C5-derived chemotactic factors, and a / -globulin that inactivates bacterial chemotactic factors. These activities are heat labile (destroyed by treatment at 56 °C for 30 min) and are distinct from those attributable to anaphylatoxin inactivator. An apparently specific inhibitor of C5-derived chemotactic activity has also been described in human synovial fluid and peritoneal fluid. This factor (molecular mass of 40 kDa) is heat stable and acts directly on C5a. [Pg.81]

Table 15.5 shows the factors that influence the prioritization of hits by medicinal chemists. Three factors (molecular weight, CLOGP, and selectivity) appear on both sides of the table, as both more important and less important factors in the prioritization. At first, this appears contradictory but in fact it reflects the different schools of thought mentioned above, where some chemists use these factors to filter the hits, while others view problems in these areas as something that can be fixed at a later time. In our experience, most chemists do filter out compounds with extreme values of molecular weight and hydrophobicity. [Pg.401]

As mentioned in Sect. 2.2.3, the biodistribution of HPMA copolymers depends on many factors. Molecular weight influences the uptake in the isolated tissue of yolk sac [266] as well as the elimination in vivo [124, 125,267,268]. Nonspecific increase in the rate of polymer uptake can be achieved by incorporation of positively charged or hydrophobic comonomers into the HPMA copolymer structure, such as methacryloyloxyethyltrimethylammonium chloride [22], N-methacryloyltyrosinamide [21], or N-[2-(4-hydroxyphenyl)ethyl]acrylamide [267]. The incorporation of hydrophobic moieties may influence the solution properties of the HPMA copolymer conjugates [132,134,269]. The interaction with the cellular surface may depend on the association number and the stability of the micelles. [Pg.104]

Fragrances must be volatile to be perceived. Therefore, in addition to the nature of the functional groups and the molecular structure of a compound, the molecular mass is also an important factor. Molecular masses of ca. 200 occur relatively frequently masses over 300 are an exception. [Pg.5]

Table II. The covolume factor-molecular weight relationship for the major detonation species. Table II. The covolume factor-molecular weight relationship for the major detonation species.
The capacity of the monitor for each individual compound is based on several factors, molecular structure, vapor pressure, environmental conditions, etc. The upper exposure limit is determined and specified in lieu of a back-up section. [Pg.200]

Metz, B.A., Welters, P., Hoffman, H.J., Jensen, E.O., Schell, J. de Bruijn, F.J. (1988). Primary structure and promoter analysis of leghemoglobin gene of the stem nodulated tropical legume Sesbania rostrata conserved coding sequences, cis elements and trans-acting factors. Molecular and General Genetics 214, 181-91. [Pg.199]

Zsebo KM, Cohen AM, Murdock DC, et al. Recombinant human granulocyte colony stimulating factor molecular and biological characterization. Immunobiology 1986 372 175-184. [Pg.391]

Each type of curative on the market has a different factor (molecular weight/functionality). This value changes according to the basic chemical composition and the fundamental activity of the curative for example ... [Pg.81]

Ferrara, N. 1999. Vascular endothelial growth factor molecular and biological aspects. Curr. Top. Microbiol. Immunol. 237 1-30. [Pg.295]

Morimoto, R.I. (1998). Regulation of the heat-shock transcriptional response Cross talk between a family of heat-shock factors, molecular chaper-... [Pg.445]

In this paper we investigate the process of alternate adsorption of cationic polyelectrolyte and anionic surfactant, structure and properties of adsorbed layers depending on different factors (molecular weight of PE, concentration of polyelectrolyte and surfactant, adsorbed layer formation time, the flow rate of the solution) by measuring potential and streaming current using the capillary electrokinetic method. [Pg.96]

Dumoutier, L., Van Roost, E., Colau, D., and Renauld, J. C. (2000c). Human interleukin-10-related T cell-derived inducible factor Molecular cloning and functional characterization as an hepatocyte-stimulating factor. Proc. Natl. Acad. Sci. USA 97, 10144-10149. [Pg.217]

Because of these factors, molecular weight calculations are used mainly for systematic modifications of formulations which have unsatisfactory property balances rather than for accurate predictions of gel points under practical operating conditions. The design of branched condensation polymers still relies heavily on Xn estimates, since these are less complicated than the theoretically more accurate Xw method described in the next section of this chapter. [Pg.175]

Evidence suggests that the regulation of metallothionein levels by metal ions results from the binding of zinc (or other metal ions) to a special transcription factor (molecular weight = 105 kDa, with the subsequent binding of the zinc/transcription factor complex to d promoter that resides near the metallothionein gene. The zinc/transcription factor complex actually binds to the metal response element that resides in the promoter The sequence of the metal response element is ... [Pg.811]

Chemical reaction depends on the presence of reactive substrates and on the probability of their encounters. Thus, the possibilities of reactions can be numerous. The literature describes reactions of OH groups on the surface of kaolin with isocyanates, vulcanization of nitrile rubber by ZnO, reactions of carboxyl groups on the filler surface with amines and epoxy groups, reactions of carboxyl groups with diols," and many others.The presence of a reactant on the surface of a material particle increases the probability of chemical reaction. Other factors include statistical probabilities, surface barriers which affect contact, dilution factors, molecular mobility, and viscosity changes in the system. These are discussed in other sections of this book. [Pg.307]

Schumacher, M.A. and Brennan, R.G. (2002) Structural mechanisms of multidrug recognition and regulation by bacterial multidrug transcription factors. Molecular Microbiology. 45 (4). 885-893. [Pg.152]

K. M. Zsebo, A. M. Cohen, D. C. Murdock, T. C. Boone, H. Inoue, V. R. Chazin, D. Hines, and L. M. Souze, Recombinant human granulocyte colony-stimulating factor molecular and biological characterization. Immunobiology 172 175-184 (1986). [Pg.1031]

The dissociation of the inactive ribosome into its subunits is dependent on the activity of two initiation factors, eIF-3 and eIF-6, which keep subunits apart by binding to the 40S and the 60S subunits, respectively (Hershey, 1991 Rhoads, 1991 Merrick, 1992). eIF-3 is the largest of the initiation factors (molecular mass 600-650 kDa) comprising 8-10 different polypeptides. In comparison, eIF-6 is a single polypeptide of about 25 kDa. [Pg.251]


See other pages where Molecular factors is mentioned: [Pg.434]    [Pg.106]    [Pg.221]    [Pg.470]    [Pg.27]    [Pg.321]    [Pg.197]    [Pg.54]    [Pg.117]    [Pg.134]    [Pg.65]    [Pg.96]    [Pg.106]    [Pg.211]    [Pg.4]    [Pg.186]    [Pg.243]    [Pg.470]    [Pg.242]    [Pg.505]    [Pg.92]    [Pg.566]    [Pg.233]    [Pg.88]   
See also in sourсe #XX -- [ Pg.330 ]




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