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.
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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
We employ our advanced, specialised process to create targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology leverages molecular simulations to examine a vast array of proteins, capturing their dynamics in both isolated forms and in complexes with other proteins. Through ensemble virtual screening, we thoroughly account for the protein's conformational mobility, identifying critical binding sites within functional regions and distant allosteric locations. This detailed exploration ensures that we comprehensively assess every possible mechanism of action, with the objective of identifying novel therapeutic targets and lead compounds that span a wide spectrum of biological functions.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q99972
UPID:
MYOC_HUMAN
Alternative names:
Myocilin 55 kDa subunit; Trabecular meshwork-induced glucocorticoid response protein
Alternative UPACC:
Q99972; B2RD84; O00620; Q7Z6Q9
Background:
Myocilin, a secreted glycoprotein, plays a pivotal role in various cellular processes including cell adhesion, migration, and cytoskeleton organization. It is involved in signaling pathways that regulate these processes, impacting cell behavior significantly. Myocilin's functions extend to bone formation, muscle hypertrophy, and neurite outgrowth, showcasing its versatility in biological systems.
Therapeutic significance:
Myocilin is directly associated with Glaucoma 1, open angle, A, and contributes to Glaucoma 3, primary congenital, A. Its involvement in these eye conditions, characterized by increased intraocular pressure and optic nerve damage, highlights its potential as a target for therapeutic intervention. Understanding the role of Myocilin could open doors to potential therapeutic strategies for glaucoma, offering hope for innovative treatments.