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 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.
The library features a range of promising modulators, each detailed with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Plus, each compound is presented with its ideal docking poses, affinity scores, and activity scores, ensuring a thorough insight.
We utilise our cutting-edge, exclusive workflow to develop focused 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
Q96A57
UPID:
TM230_HUMAN
Alternative names:
-
Alternative UPACC:
Q96A57; B2RDM8; D3DVZ9; Q0VGC8; Q5TDS5; Q96ES2; Q9P0A7
Background:
Transmembrane protein 230 (TMEM230) plays a crucial role in the trafficking and recycling of synaptic vesicles, essential for neurotransmitter release and synaptic transmission. This protein's involvement in these processes underscores its importance in maintaining normal brain function and neural communication.
Therapeutic significance:
Given its association with Parkinson disease, a neurodegenerative disorder marked by the loss of dopaminergic neurons and presence of Lewy bodies, TMEM230's study is pivotal. Understanding TMEM230's role could lead to novel therapeutic strategies for managing Parkinson's disease, focusing on its genetic variants and their contribution to disease pathogenesis.