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9 January 2026

We now share a well-characterized small molecule inhibitor of ALPK1, BI-4286, to dissect the molecular mechanisms underlaying ALPK1 signaling in disease pathology. The focus is on select indications outside of ROSAH syndrome and infectious diseases. Submit your research proposal for a chance to access BI-4286 and receive funding.

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1 December 2025

Nociplastic pain, a subtype of chronic pain, arises from altered nociception in the absence of clear tissue damage. Its poorly understood pathogenesis and the limited efficacy of current treatments underscore the urgent need for identifying and validating innovative pharmacological approaches that target central neurobiological pathways involved in pain processing.

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17 November 2025

A large portion of the proteome remains “undruggable” with traditional small molecules and biologics. To expand the druggable target landscape in areas of high unmet medical needs, novel innovative approaches could focus on targeting intracellular mechanisms, such as influencing nuclear translocation, organelle routing, molecular condensates, and spatial-temporal control mechanisms.

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10 November 2025

opnMe now offers a way for scientists to share their feedback directly on the platform. Whether it’s about a molecule you ordered or your overall experience, your input helps us improve and inspires others in the scientific community. Together, let’s make opnMe the best it can be for researchers worldwide.

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3 November 2025

In this interview, Jeffrey Conn highlights Boehringer Ingelheim’s contributions to the discovery and optimization of selective positive allosteric modulators of mGluR1 at Vanderbilt University. He also shares his perspective on how opnMe has changed his perception of the role of open innovation initiatives in advancing drug discovery by making these research tools widely accessible to the scientific community.

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