Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher activity, selectivity, and safety.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated by our partner Reaxense.
Contained in the library are leading modulators, each labelled with 38 ADME-Tox and 32 physicochemical and drug-likeness qualities. In addition, each compound is illustrated with its optimal docking poses, affinity scores, and activity scores, giving a complete picture.
We employ our advanced, specialised process to create targeted libraries for enzymes.
Fig. 1. The sreening workflow of Receptor.AI
It includes comprehensive molecular simulations of the catalytic and allosteric binding pockets and the ensemble virtual screening accounting for their conformational mobility. In the case of designing modulators, the structural changes induced by reaction intermediates are taken into account to leverage activity and selectivity.
Our library stands out due to several important features:
partner
Reaxense
upacc
Q12866
UPID:
MERTK_HUMAN
Alternative names:
Proto-oncogene c-Mer; Receptor tyrosine kinase MerTK
Alternative UPACC:
Q12866; Q9HBB4
Background:
Tyrosine-protein kinase Mer, also known as Proto-oncogene c-Mer and Receptor tyrosine kinase MerTK, plays a pivotal role in various physiological processes. It transduces signals from the extracellular matrix to the cytoplasm, engaging in cell survival, migration, differentiation, and efferocytosis. Its activation triggers a cascade involving GRB2 or PLCG2 and phosphorylation of MAPK1, MAPK2, FAK/PTK2, or RAC1. MerTK is crucial in the retinal pigment epithelium for phagocytosis of rod outer segments and modulates the innate immune response by activating STAT1.
Therapeutic significance:
Given its involvement in Retinitis pigmentosa 38, a condition marked by retinal pigment deposits and photoreceptor cell loss, understanding the role of Tyrosine-protein kinase Mer could open doors to potential therapeutic strategies. Its regulatory functions in cell processes and immune response modulation highlight its potential as a target for therapeutic intervention.