Explore the Potential with AI-Driven Innovation
The focused library is created on demand with the latest virtual screening and parameter assessment technology, supported by the Receptor.AI drug discovery platform. This method is more effective than traditional methods and results in higher-quality compounds with better 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 utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
By deploying molecular simulations, our approach comprehensively covers a broad array of proteins, tracking their flexibility and dynamics individually and within complexes. Ensemble virtual screening is utilised to take into account conformational dynamics, identifying pivotal binding sites located within functional regions and at allosteric locations. This thorough exploration ensures that every conceivable mechanism of action is considered, aiming to identify new therapeutic targets and advance lead compounds throughout a vast spectrum of biological functions.
Several key aspects differentiate our library:
partner
Reaxense
upacc
Q6DJT9
UPID:
PLAG1_HUMAN
Alternative names:
Pleiomorphic adenoma gene 1 protein
Alternative UPACC:
Q6DJT9; B4DLC2; Q59GH8; Q9Y4L2
Background:
Zinc finger protein PLAG1, also known as Pleiomorphic adenoma gene 1 protein, plays a pivotal role in cell proliferation and development. It functions as a transcription factor, activating target genes like IGFII, which leads to uncontrolled cell growth. Its overexpression is linked to various tumors, including pleomorphic adenomas of the salivary gland and hepatoblastoma, a common liver tumor in children.
Therapeutic significance:
Given its role in diseases like Silver-Russell syndrome 4 and its association with tumor development, targeting PLAG1 could offer new avenues for therapeutic interventions. Understanding the role of Zinc finger protein PLAG1 could open doors to potential therapeutic strategies.