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.
Our selection of compounds is from a large virtual library of over 60 billion molecules. The production and distribution of these compounds are managed by our partner 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
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.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
Q9Y5A9
UPID:
YTHD2_HUMAN
Alternative names:
CLL-associated antigen KW-14; High-glucose-regulated protein 8; Renal carcinoma antigen NY-REN-2
Alternative UPACC:
Q9Y5A9; A6NKG4; A8K966; B4E1G7; D3DPM8; Q5VSZ9; Q8TDH0; Q9BUJ5
Background:
YTH domain-containing family protein 2 (YTHDF2) plays a pivotal role in RNA metabolism, specifically recognizing and binding N6-methyladenosine (m6A)-containing RNAs. This modification is crucial for mRNA stability and processing. YTHDF2 regulates mRNA stability by promoting degradation of m6A-containing mRNAs, influencing cellular differentiation, oocyte maturation, spermatogenesis, hematopoietic stem cell specification, neural development, hepatic lipid metabolism, and the innate immune response.
Therapeutic significance:
Understanding the role of YTH domain-containing family protein 2 could open doors to potential therapeutic strategies.