Parallel synthesis plays a crucial role in medicinal chemistry, especially in the course of hit-to-lead optimization and lead optimization, which can support quick structure-activity relationship (SAR) study and structure-property relationship (SPR) study.

In parallel synthesis, medicinal chemists need diverse analogues with the functional group unchanged. Enabled by our in-stock > 40 K building blocks, such as amine building blocks, carboxylic acid building blocks, halo building blocks, pinacol borate building blocks, etc., we provide a differentiated parallel synthesis in a FTE model. This model can help clients by both reducing time and costs.