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    The Cambridge Structural Database now contains over 1.1 million entries of organic and metal-organic small_molecule crystal_structures, providing an invaluable resource in crystallography, structural chemistry, and drug discovery. Bryant et_al 3 highlighted the importance of particle informatics approaches when revisiting the structure of lamotrigine through a reassessment of its solid-form within the context of the crystal_structures in the CSD. An analysis of the CSD Drug Subset, which encompasses all available crystal_structures from the CSD that contain an approved drug molecule, can provide an important resource and one that can provide a potential . . .

     

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