Affinity enantioselectivity

Enantioselective differences in absorption, metaboHsm, clearance, dmg— macromolecule binding affinity, and other factors, which culminate in the observed enantioselective efficacy of chiral dmgs, are considered herein. More inclusive Hsts of optically active dmgs and theit enantioselective differences are available (93). 

The first observation of the enantioselective properties of an albumin was made in 1958 (28) when it was discovered that the affinity for L-tryptophan exceeded that of the D-enantiomer by a factor of approximately 100. This led to more studies in 1973 of the separation of DL-tryptophan [54-12-6] C22H22N2O2, on BSA immobilized to Sepharose (29). After extensive investigation of the chromatographic behavior of numerous racemic compounds under different mobile-phase conditions, a BSA-SILICA hplc column (Resolvosil-R-BSA, Macherey-Nagel GmvH, Duren, Germany) was... 

All enantioselective separation techniques are based on submitting the enantiomeric mixture to be resolved to a chiral environment. This environment is usually created by the presence of a chiral selector able to interact with both enantiomers of the mixture, albeit with different affinities. These differences in the enantiomer-selector association will finally result in the separation that is sought. 

The mechanistic basis of iridium-complex-catalyzed enantioselective hydrogenation is less secure than in the rhodium case. It is well known that square-planar iridium complexes exhibit a stronger affinity for dihydrogen than their rhodium counterparts. In earlier studies, Crabtree et al. investigated the addition of H2 to their complex and observed two stereoisomeric intermediate dihydrides in the hydrogenation of the coordinated cycloocta-1,5-diene. The observations were in contrast to the course of H2 addition to Ms-phosphine iridium complexes [69]. 

Turning to enzymatic hydration, we see from the data in Table 10.1 that phenanthrene 9,10-oxide Fig. 10.10, 10.29) is an excellent substrate for epoxide hydrolase. Comparison of enzymatic hydration of the three isomeric phenanthrene oxides shows that the Vmax with the 9,10-oxide is greater than with the 1,2- or the 3,4-oxide the affinity was higher as well, as assessed by the tenfold lower Km value [90]. Furthermore, phenanthrene 9,10-oxide has a plane of symmetry and is, thus, an achiral molecule, but hydration gives rise to a chiral metabolite with high product enantioselectivity. Indeed, nucleophilic attack by epoxide hydrolase occurs at C(9) with inversion of configuration i.e., from below the oxirane ring as shown in Fig. 10.10) to yield the C-H9.S, 10.S )-9,10-dihydro-9,10-diol (10.30) [91],... 

It becomes obvious from the clustered data points that the binding constant for the 7 -enantiomer is too small to be accurately determined by this method. Hence, indirect affinity CE (resolution method) was utilized to determine the binding constant for the 7 -enantiomer. Indirect affinity CE makes use of the knowledge of the constant for one enantiomer (here, A s) and in addition of experimental separation data as obtained with the racemate of DNB-Leu in presence of the tBuCQN selector as BGE additive. By use of Equation 1.10, an enantioselectivity factor may be defined as the ratio of the binding constants of S- and 7 -enantiomers yielding the following equation ... 

The ability of proteins to form enantioselective interactions with a large variety of drugs is used in chiral affinity chromatography. Protein CSPs that are most frequently used for the enantioseparation of pharmaceuticals include bovine serum albumin (BSA), human serum albumin... 

Enantioselectivity of affinity. If a receptor has sites for three of the substituents (symbolized in B by a cone, a sphere, and a cube) on the asymmetric carbon to attach to, only one of the enantiomers will have optimal fit. Its affinity will then be higher. Thus, dexeti-mide displays an affinity at the musca-Lullmann, Color Atlas of Pharmaoology... 

Inverse enantioselectivity at another receptor. An enantiomer may possess an unfavorable configuration at one receptor that may, however, be optimal for interaction with another receptor. In the case of dobutamine, the (+)-enantiomer has affinity at p-adreno-ceptors 10 times higher than that of the (-)-enantiomer, both having agonist activity. However, the a-adrenoceptor stimulant action is due to the (-)-form (see above). 

As described for receptor interactions, enantioselectivity may also be manifested in drug interactions with enzymes and transport proteins. Enantiomers may display different affinities and reaction velocities. 

Capillary electrophoresis offers a set of important advantages that make it a premier technique for the investigation of enantioselective effects in the affinity interactions between chiral drugs and cyclodextrins. The most important advantage of CE is the inherently high separation efficiency offered by this technique. As already known, the most important contributors to peak resolution (R) are a separation selectivity (a) and an efficiency (N). A relationship between these parameters in CE is described by the following equation (2) ... 

T Arai, N Nimura, T Kinoshita. Investigation of enantioselective ofloxacin-albumin binding and displacement interactions using capillary affinity zone electrophoresis. Biomed Chromatogr 9 68—74, 1995. 

Y Tanaka, S Terabe. Studies of enantioselectivities of avidin, avidin-biotin complex and streptavidin by affinity capillary electrophoresis. Chromatographia 49 489-495, 1999. 

The optimization of enzymes strongly depends on the field of appHcation. For industrial applications, high reaction rates, stabiHty under process conditions, and regio- and enantioselectivity are the most important properties of a catalyst, whereas affinity or substrate selectivity are of second order interest for a distinct process to be catalyzed. On the other hand, enzymes with a wide range of activity can be used for the production of several products reducing... 

An example of the above mentioned cascade complexation of carboxylates by macrocyclic receptors containing metal ionic centers is the inclusion of oxalate by the dien dicobalt complex 9 (Martell, Mitsokaitis) [12]. Similarly, the -cyclodextrin (jS-CD) 10, modified with a zinc cation bound by a triamine side chain, encapsulates anions like 1-adamantylcarboxylate in its cavity, fixing them by combined electrostatic and hydrophobic interactions [13], Zinc s group achieved the enantioselective transport of the potassium salts of N-protected amino acids and dipeptides by making use of the cation affinity of... 

This study permitted us not only to determine the optimal aw value for enanti-oselectivity, but also allowed us to perform a detailed study on the interaction between water and the active site of CALB. Measurements of enantioselectivity at different aw and temperature showed that the water molecule located in the selectivity pocket had a high affinity for this particular part of the active site, with a binding energy of 9kJ mol-1, and lost all its degrees of rotation, corresponding to an entropic energy of 37Jmol-1 K-1. 

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