Research conducted at the Stanford lab of Deep Apple founder Georgios Skiniotis has enabled broad structural exploration of GPCR inactive states without the need for extensive engineering and crystallization – an approach that opens these drug targets to rapid structure determination.
Beyond GPCRs, Deep Apple’s discovery engine is readily adaptable to all other biological targets implicated in human disease. In particular, our discovery engine is well-suited to focus on transporter and ion channel target classes.
Deep Apple’s lead programs address a high value target in the inflammatory/immune pathway and several targets for weight loss and weight maintenance, including non-GLP1 targets. The oral therapeutics Deep Apple is developing in these areas are designed to offer significant tolerability and convenience compared to existing and emerging treatment options.