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.
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 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.
Our top-notch dedicated system is used to design specialised 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
O43405
UPID:
COCH_HUMAN
Alternative names:
COCH-5B2
Alternative UPACC:
O43405; A8K9K9; D3DS84; Q96IU6
Background:
Cochlin, identified by the alternative name COCH-5B2, is a protein that plays a pivotal role in maintaining cell shape and motility within the trabecular meshwork. This protein's unique function is crucial for the proper functioning of inner ear structures, contributing to hearing and balance.
Therapeutic significance:
Cochlin is directly associated with two forms of hearing loss: Deafness, autosomal dominant, 9 (DFNA9) and Deafness, autosomal recessive, 110 (DFNB110). Both conditions highlight Cochlin's critical role in auditory processes. Understanding the role of Cochlin could open doors to potential therapeutic strategies for these hearing impairments.