α-Furilmonoxime as an extracting agent. I. Dissociation constant and distribution coefficient of the reagent

1967 ◽  
Vol 32 (1) ◽  
pp. 331-343 ◽  
Author(s):  
F. Vláčil
Keyword(s):  
Distribution Coefficient ◽  
Dissociation Constant

Plasminogen-Plasmin System IX. Specific Binding of Tranexamic Acid to Plasmin

1975 ◽  
Vol 33 (03) ◽  
pp. 573-585 ◽  
Author(s):  
Masahiro Iwamoto
Keyword(s):  
Tranexamic Acid ◽  
Affinity Chromatography ◽  
Dissociation Constant ◽  
Factor Xiii ◽  
Specific Binding ◽  
The Other ◽  
Inhibitory Mechanism ◽  
Binding Studies ◽  
Similar Affinity ◽  
Fibrin Structure

SummaryInteractions between tranexamic acid and protein were studied in respect of the antifibrinolytic actions of tranexamic acid. Tranexamic acid did neither show any interaction with fibrinogen or fibrin, nor was incorporated into cross-linked fibrin structure by the action of factor XIII. On the other hand, tranexamic acid bound to human plasmin with a dissociation constant of 3.5 × 10−5 M, which was very close to the inhibition constant (3.6 × 10−5 M) for this compound in inhibiting plasmin-induced fibrinolysis. The binding site of tranexamic acid on plasmin was not the catalytic site of plasmin, because TLCK-blocked plasmin also showed a similar affinity to tranexamic acid (the dissociation constant, 2.9–4.8 × 10−5 M).In the binding studies with the highly purified plasminogen and TLCK-plasmin preparations which were obtained by affinity chromatography on lysine-substituted Sepharose, the molar binding ratio was shown to be 1.5–1.6 moles tranexamic acid per one mole protein.On the basis of these and other findings, a model for the inhibitory mechanism of tranexamic acid is presented.

The Binding of Calcium Ions to Bovine Factor X by Rate Dialysis

1978 ◽  
Vol 40 (02) ◽  
pp. 350-357
Author(s):  
Robert H Yue ◽  
Menard M Gertler
Keyword(s):  
Molecular Weight ◽  
Dissociation Constant ◽  
Calcium Ions ◽  
Activation Process ◽  
Factor X ◽  
The Real ◽  
High Affinity ◽  
Binding Data ◽  
Sequential Mechanism ◽  
Bovine Factor

SummaryThe binding of Ca+2 to bovine factor X (molecular weight of 74,000) (Yue und Gertler 1977) was studied by the technique of rate dialysis and with the use of 45Ca+2. The binding data are consistent with a model of sequential mechanism. One mole of Ca+2 binds to the glycoprotein with a dissociation constant of 5.2 × 10-5 M and an additional 39 ± 4 moles of Ca+2 bind to this zymogen with a dissociation constant of 3.7 × 10-3M. The binding of the high affinity Ca+2 causes a functionally significant change in the zymogen, and (calcium) (factor X) complex is the real substrate in the activation process by the protease in Russell’s viper venom.

Mathematical modelling of salt purification by recrystallization. Countercurrent arrangement

1986 ◽  
Vol 51 (11) ◽  
pp. 2481-2488
Author(s):  
Benitto Mayrhofer ◽  
Jana Mayrhoferová ◽  
Lubomír Neužil ◽  
Jaroslav Nývlt
Keyword(s):  
Steady State ◽  
Simple Model ◽  
Mathematical Modelling ◽  
Distribution Coefficient ◽  
Mother Liquor ◽  
Equilibrium Temperature ◽  
Operating Conditions ◽  
Limiting Case

The paper presents a simple model of recrystallization with countercurrent flows of the solution and the crystals being purified. The model assumes steady-state operating conditions, an equilibrium between the outlet streams of each stage, and the same equilibrium temperature and distribution coefficient for all stages. With these assumptions, the model provides the basis for analyzing the variation in the degree of purity as a function of the number of recrystallization stages. The analysis is facilitated by the use of a diagram constructed for the limiting case of perfect removal of the mother liquor from the crystals between the stages.

The interactions of tensides with calconalide I

1991 ◽  
Vol 56 (10) ◽  
pp. 2100-2106
Author(s):  
Irena Němcová ◽  
Oldřich Valcl ◽  
Jiří Makovička
Keyword(s):  
Dissociation Constant ◽  
Absorption Spectra ◽  
Tautomeric Forms

A study was made of the effect of cationogenic, anionogenic and nonionogenic tensides on the absorption spectra and dissociation constant of calconalide I. It was found that the changes in the absorption spectra are a result of influences on the dissociation of the dye and a shift in the equilibrium between the tautomeric forms. The mechanism of the effect of the tenside on dye dissociation was also discussed.

Computational Parameters in Correlation Analysis: Gas-Water Distribution Coefficient

1999 ◽  
Vol 64 (11) ◽  
pp. 1727-1747 ◽  
Author(s):  
George R. Famini ◽  
Dalia Benyamin ◽  
Christina Kim ◽  
Rattiporn Veerawat ◽  
Leland Y. Wilson
Keyword(s):  
Correlation Analysis ◽  
Distribution Coefficient ◽  
Water Distribution ◽  
Solvation Energy ◽  
Linear Solvation Energy Relationships ◽  
Linear Solvation Energy Relationship ◽  
Energy Relationships ◽  
Linear Solvation Energy ◽  
Water Equilibrium ◽  
Linear Solvation

Theoretical linear solvation energy relationships (TLSER) combine computational molecular parameters with the linear solvation energy relationship (LSER) of Kamlet and Taft to characterize and predict properties of compounds. This paper examines the correlation of the gas-water equilibrium constant for 423 compounds with the TLSER parameters. Also, it describes new parameters designed to improve the TLSER information content.

Total weak acid concentration and effective dissociation constant of nonvolatile buffers in human plasma

2001 ◽  
Vol 91 (3) ◽  
pp. 1364-1371 ◽  
Author(s):  
Peter D. Constable
Keyword(s):  
Dissociation Constant ◽  
Human Plasma ◽  
Total Concentration ◽  
Weak Acid ◽  
Strong Ion Difference ◽  
Acid Base ◽  
Horse Plasma ◽  
Using Data ◽  
Species Specific

The strong ion approach provides a quantitative physicochemical method for describing the mechanism for an acid-base disturbance. The approach requires species-specific values for the total concentration of plasma nonvolatile buffers (Atot) and the effective dissociation constant for plasma nonvolatile buffers ( K a), but these values have not been determined for human plasma. Accordingly, the purpose of this study was to calculate accurate Atot and K a values using data obtained from in vitro strong ion titration and CO2tonometry. The calculated values for Atot (24.1 mmol/l) and K a (1.05 × 10−7) were significantly ( P < 0.05) different from the experimentally determined values for horse plasma and differed from the empirically assumed values for human plasma (Atot = 19.0 meq/l and K a = 3.0 × 10−7). The derivatives of pH with respect to the three independent variables [strong ion difference (SID), Pco 2, and Atot] of the strong ion approach were calculated as follows: [Formula: see text] [Formula: see text], [Formula: see text]where S is solubility of CO2 in plasma. The derivatives provide a useful method for calculating the effect of independent changes in SID+, Pco 2, and Atot on plasma pH. The calculated values for Atot and K a should facilitate application of the strong ion approach to acid-base disturbances in humans.

Consideration on modeling of Nb sorption onto clay minerals

2020 ◽  
Vol 108 (11) ◽  
pp. 873-877
Author(s):  
Tetsuji Yamaguchi ◽  
Saki Ohira ◽  
Ko Hemmi ◽  
Logan Barr ◽  
Asako Shimada ◽  
...  
Keyword(s):  
Distribution Coefficient ◽  
Clay Minerals ◽  
Safety Assessment ◽  
Distribution Coefficients ◽  
Surface Species ◽  
Complex Species ◽  
Intermediate Depth ◽  
Speciation Model ◽  
Surface Phases ◽  
High Distribution Coefficient

AbstractSorption distribution coefficient (Kd) of niobium-94 on minerals are an important parameter in safety assessment of intermediate-depth disposal of waste from core internals etc. The Kd of Nb on clay minerals in Ca(ClO4)2 solutions were, however, not successfully modeled in a previous study. The high distribution coefficients of Nb on illite in Ca(ClO4)2 solutions were successfully reproduced by taking Ca–Nb–OH surface species into account. Solubility of Nb was studied in Ca(ClO4)2 solutions and the results were reproduced by taking an aqueous Ca–Nb–OH complex species, CaNb(OH)6+, into account in addition to previously reported Nb(OH)6− and Nb(OH)72−. Based on this aqueous speciation model, the Ca–Nb–OH surface species responsible for the sorption of Nb on illite in Ca(ClO4)2 solutions was presumed to be X_OCaNb(OH)6. Although uncertainties exist in the speciation of aqueous Ca–Nb–OH species, the result of this study proposed a possible mechanism for high distribution coefficient of Nb on illite in Ca(ClO4)2 solutions. The mechanism includes Ca–Nb–OH complex formation in aqueous, solid and surface phases.

Sign in / Sign up

Export Citation Format

Share Document