Explore the Potential with AI-Driven Innovation
This extensive focused library is tailor-made using the latest virtual screening and parameter assessment technology, operated by the Receptor.AI drug discovery platform. This technique is more effective than traditional methods, offering compounds with improved activity, selectivity, and safety.
We carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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 utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Key features that set our library apart include:
partner
Reaxense
upacc
Q8WWV3
UPID:
RT4I1_HUMAN
Alternative names:
NOGO-interacting mitochondrial protein
Alternative UPACC:
Q8WWV3; Q8N9B3; Q8WZ66; Q9BRA4
Background:
Reticulon-4-interacting protein 1, mitochondrial, also known as NOGO-interacting mitochondrial protein, is pivotal in the development of the inner retina and optic nerve. It regulates retinal ganglion cell neurite outgrowth, playing a crucial role in neural connectivity.
Therapeutic significance:
Linked to Optic atrophy 10, a disease marked by progressive visual loss and potential neurological symptoms, this protein's study offers insights into novel therapeutic avenues. Understanding its function could lead to breakthroughs in treating optic nerve degeneration.