Cambridge structural database pharmaceuticals solids

A number of statistical analyses of the literature have been carried out in an attempt to estimate the extent of polymorphism. A search of the Cambridge Structural Database on the keywords polymorph , form , modification and phase indicates that about 3.5% of the -350 000 entries fall into this category. Approximately 25 % of the entries are either solvates or hydrates. At the other end of the spectrum, Byrn has reported that of the >150 compounds submitted for crystal form screening and analysis to SSCI, Inc. 85 % exhibit more than one crystal form, 37% are solvates and 31 % are hydrates [40]. Other studies based on different selection criteria reveal results falling somewhere between these two extremes [41]. For instance, Griesser and Burger have collected information on about 600 polymorphic forms and solvates (including hydrates) pharmaceutical compounds that are solid at 25 °C [41c],... 

FIGURE 1.5 Multiscale modeling in computational pharmaceutical solid-state chemistry. Here DEM and FEM are discrete and finite element methods MC, Monte Carlo simulation MD, molecular dynamics MM, molecular mechanics QM, quantum mechanics, respectively statistical approaches include knowledge-based models based on database analysis (e.g., Cambridge Structure Database [32]) and quantitative structure property relationships (e.g., group contributions models [33a]). 

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