Explore the Potential with AI-Driven Innovation
Our detailed focused library is generated on demand with advanced virtual screening and parameter assessment technology powered by the Receptor.AI drug discovery platform. This method surpasses traditional approaches, delivering compounds of better quality with enhanced activity, selectivity, and safety.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q6ZMJ4
UPID:
IL34_HUMAN
Alternative names:
-
Alternative UPACC:
Q6ZMJ4; B2RC28; B2Z4A8; B2ZC70; Q8N6L2
Background:
Interleukin-34 (IL-34) is a pivotal cytokine that orchestrates the proliferation, survival, and differentiation of monocytes and macrophages. It is instrumental in the release of pro-inflammatory chemokines, playing a crucial role in innate immunity and inflammatory processes. Furthermore, IL-34 is vital in regulating osteoclast proliferation and differentiation, as well as bone resorption, through signaling via CSF1R and subsequent phosphorylation of MAPK1/ERK2 and MAPK3/ERK1.
Therapeutic significance:
Understanding the role of Interleukin-34 could open doors to potential therapeutic strategies, especially in the context of inflammatory diseases and disorders related to bone resorption.