7
Collaborate with us

26 January 2026

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.

2
Discover us

22 January 2026

Meet the opnMe team at the Life Science Switzerland (LS2) Annual Meeting 2026 in Zurich. Visit our booth to discover free high‑quality molecules and opportunities for collaboration and funding. Join our talk to explore new insights into KRAS biology, SOS1 inhibition, and how open innovation accelerates scientific discovery.

15
Collaborate with us

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.

24
Collaborate with us

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.

10
Molecules for free

25 November 2025

By regulating intracellular cGMP levels, phosphodiesterase-9 (PDE9) plays a critical role in neuronal signaling, vascular function, and cell survival. By making our potent, selective, and brain-penetrant PDE9 inhibitor, BI 409306 (osoresonontrine) available to scientists free of charge, we incentivize new research to fully understand the role of the molecule in the context of disease.

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