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.
We pick out particular compounds from an extensive virtual database of more than 60 billion molecules. The preparation and shipment of these compounds are facilitated by our associate 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.
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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
P24821
UPID:
TENA_HUMAN
Alternative names:
Cytotactin; GMEM; GP 150-225; Glioma-associated-extracellular matrix antigen; Hexabrachion; JI; Myotendinous antigen; Neuronectin; Tenascin-C
Alternative UPACC:
P24821; C9IYT7; C9J575; C9J6D9; C9J848; Q14583; Q15567; Q5T7S3
Background:
Tenascin-C, also known as Cytotactin or Neuronectin, is a pivotal extracellular matrix protein that plays a crucial role in the development of the nervous system. It is involved in guiding neuron migration, axon development, synaptic plasticity, and neuronal regeneration. Tenascin-C acts as a ligand for several integrins, facilitating cell adhesion processes critical for tissue development and repair.
Therapeutic significance:
The protein's association with autosomal dominant deafness, DFNA56, highlights its clinical relevance. This condition, characterized by progressive sensorineural hearing loss, underscores the importance of Tenascin-C in auditory system function. Understanding the role of Tenascin-C could open doors to potential therapeutic strategies for hearing impairment and other neurodevelopmental disorders.