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 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 high-tech, dedicated method is applied to construct targeted libraries.
Fig. 1. The sreening workflow of Receptor.AI
Utilising molecular simulations, our approach thoroughly examines a wide array of proteins, tracking their conformational changes individually and within complexes. Ensemble virtual screening enables us to address conformational flexibility, revealing essential binding sites at functional regions and allosteric locations. Our rigorous analysis guarantees that no potential mechanism of action is overlooked, aiming to uncover new therapeutic targets and lead compounds across diverse 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.