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Compounds categorization

Extensive research has established the relationship between the extent of distribution of compounds and their physicochemical properties. With this information, Vdss can be quite successfully predicted using in silico models [27-30], In silico prediction of distribution is based on physicochemical properties that relates to passive transmembrane diffusion and tissue binding, and it only predicts Vdss. The other factors that contribute to distribution, such as transporter-mediated distribution, were not taken into account. These algorithms are based on the assumption that all compounds will dissolve in intra- and extracellular tissue water, and the unionized portion will partition into the neutral lipids and neutral phospholipids located within tissue cells. For compounds categorized as a strong base (at least one basic group (p/fa >7), an additional mechanism of electrostatic interaction with tissue acidic phospholipids is incorporated. Acids and weak bases are assumed... [Pg.78]

The precise mechanism and sight of action of most compounds categorized as calcium inhibitory compounds, therefore, remains obscure. Future refinements in experimental models and techniques will undoubtedly will lead to the classification of calcium inhibitory compounds based upon their primary mechanism of action and specific site(s) of action (extracellular vs. intracellar). Because of the uncertainty surrounding the precise mechanisms of action of calcium inhibitory compounds, I will describe their cardiac electrical and mechanical effects illuding when possible to those compounds that are believed to act l) competitively with Ca + for specific calcium channels (e.g., Co +, Mn +, La2+, etc.) 2) at the cardiac cell membrane and possibly by one of several intracellular mechanisms (e.g., verapamil, diltiazem, nifedipine) and 3) intracellularly (e.g., 2-n-propyl and 2-n-butyl MDI). [Pg.51]

Multiplex assays do not achieve the compound throughputs possible with single measurement assays however, they produce much richer information already in primary screening, which is invaluable for compound categorization and prioritization by the medicinal chemists. A further advantage of such assays... [Pg.964]

Figure 6.26 Principal component analysis of chemical space properties for groups of compounds categorized as drugs, bioactives, natural products, fragments, diversity oriented synthesis (DOS) and Rule-of-Five. Numbered compounds representative of the various categories are given in the reference. (Reprinted with permission from Shelat, A. A., Guy, R.K. The interdependence between screening methods and screening libraries. Curr. Opin. Chem. Biol. 2007, 11, 244-251, copyright 2007, Elsevier.)... Figure 6.26 Principal component analysis of chemical space properties for groups of compounds categorized as drugs, bioactives, natural products, fragments, diversity oriented synthesis (DOS) and Rule-of-Five. Numbered compounds representative of the various categories are given in the reference. (Reprinted with permission from Shelat, A. A., Guy, R.K. The interdependence between screening methods and screening libraries. Curr. Opin. Chem. Biol. 2007, 11, 244-251, copyright 2007, Elsevier.)...
An extensive series of studies for the prediction of aqueous solubility has been reported in the literature, as summarized by Lipinski et al. [15] and jorgensen and Duffy [16]. These methods can be categorized into three types 1 correlation of solubility with experimentally determined physicochemical properties such as melting point and molecular volume 2) estimation of solubility by group contribution methods and 3) correlation of solubility with descriptors derived from the molecular structure by computational methods. The third approach has been proven to be particularly successful for the prediction of solubility because it does not need experimental descriptors and can therefore be applied to collections of virtual compounds also. [Pg.495]

Vinpocetine (2), another dmg initially categorized as a cerebral vasodilator, is a member of the vinca alkaloid family of agents (7). However, interest in this compound as a potential dmg for learning and memory deficits comes from its abiUty to act as a neuronal protectant. This compound was evaluated in 15 patients with AD over a one-year period and was ineffective in improving cognitive deficits or slowing the rate of decline (8). However, in studies of patients with chronic vascular senile cerebral dysfunction (9) and organic psycho syndrome (10), vinpocetine showed beneficial results. [Pg.93]

Salt apphed as equal parts of unionised sodium chloride and calcium chloride at 20 g total per L for 1 h, three times a week, has also been used to control fungal infections on eggs. The salt combination is first appHed one day after fertilisation to the first pick of eggs. These compounds are categorized as generally recognized as safe (GRAS). [Pg.322]

One of the early events of the apoptotic process involves the translocation of phosphatidylserine on the surface of cell membranes annexin V binding and propidium iodide uptake reveals various cellular states. After treatment with organotin(IV) compounds the cells could be categorized into populations vital cells (annexin V /P ), early apoptotic cells (annexin V /P ), late apoptotic cells (annexin V /P ), and necrotic cells (annexin V /P" ). Cells are observed with a fluorescence microscope and it is possible to observe translocation of phosphatidylserine (PS) from the inner side of the plasma membrane to the outer one and to see a green stain for annexin V FLUOS bound to PS, and a red stain for propidium iodide. [Pg.359]

Many literature preparations of difunctional compounds are extensions of the methods applicable to monofunctional compounds. As an example, the reaction RCI — ROH might be used for the preparation of diols from an appropriate dichloro compund. Such methods are difficult to categorize and may be found in either the monofunctional or difunctional sections, depending on the focus of the original paper. [Pg.18]

At first glance it may seem that like dissolves like does not apply here. Certainly, none of these complex molecules looks like water, and the resemblance to simple hydrocarbons such as cyclohexane also is remote. Keep in mind, however, that the basis for the principle is that similar compounds dissolve in each other because they have common patterns of intermolecular interactions. Example indicates that alcohols containing large nonpolar segments do not dissolve well in water. We can categorize vitamins similarly by the amounts of their stmctures that can be stabilized by hydrogen bonding to water molecules. [Pg.840]

Amino alcohols, which have a broad spectrum of biological activities, can be categorized as adrenahne-like with one chiral center at C-1 or as ephedrine-like with two chiral centers at C-1 and C-2 (Scheme 7). Although a variety of methods have been developed for the stereoselective preparation of 1,2-amino alcohols, " in most cases it is easier and more efficient to prepare these important compounds stereoselectively starting from chiral cyanohydrins (Scheme... [Pg.147]

Energy interaction between a probe and a compound is necessary for molecular properties to be observed. As a result, properties can be categorized according to the nature of the probe used to observe them. Properties revealed by low-energy interactions are schematized in Fig. 1.2, which outlines that ... [Pg.7]

Organic compounds released from plant roots have been categorized according to (a) their chemical properties, such as stability (e.g., hydrolysis and oxidation), volatility, molecular weight, solubility in water, etc. (Chap. 2) (b) the modality of their release (exudates, secreted, or lysates) (c) the way of utilization... [Pg.4]


See other pages where Compounds categorization is mentioned: [Pg.327]    [Pg.193]    [Pg.79]    [Pg.73]    [Pg.183]    [Pg.14]    [Pg.79]    [Pg.327]    [Pg.193]    [Pg.79]    [Pg.73]    [Pg.183]    [Pg.14]    [Pg.79]    [Pg.298]    [Pg.413]    [Pg.514]    [Pg.224]    [Pg.130]    [Pg.86]    [Pg.350]    [Pg.346]    [Pg.68]    [Pg.78]    [Pg.42]    [Pg.339]    [Pg.157]    [Pg.209]    [Pg.14]    [Pg.308]    [Pg.187]    [Pg.244]    [Pg.263]    [Pg.97]    [Pg.110]    [Pg.302]    [Pg.63]    [Pg.445]    [Pg.357]    [Pg.118]    [Pg.748]    [Pg.914]    [Pg.1016]    [Pg.460]   
See also in sourсe #XX -- [ Pg.187 ]




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