Strategic explorations of an expansive chemical space

Comprehensive Hit Finding for Any Target Class

Hit finding is often the first step in a drug discovery program which dictates the amount and type of chemical matter that will be optimized through the early stages of a program. The emergence of new therapeutic target classes and modes of action has placed even greater emphasis on the need for orthogonal screening approaches and multiple screening library types.

TandemAI’s hit identification platform is equipped with a broad array of both biological and virtual screening techniques, utilizing an extensive range of commercial and bespoke libraries. Any hits from these approaches can then be rapidly optimized using TandemAI’s predictive tools.

TandemAI offers an array of hit identification approaches that include biological screening using fragments and DEL libraries as well as virtual screening approaches with commercial and custom small molecule libraries. Our virtual screening tools can be used for structure- and ligand-based projects and incorporate 2D and 3D ligand based descriptors as well as protein-ligand docking and physics based methods.

Capabilities

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