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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated 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
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of biological functions.
Our library stands out due to several important features:
partner
Reaxense
upacc
A0A0U1RRI6
UPID:
CENL3_HUMAN
Alternative names:
Centromere protein V pseudogene 3
Alternative UPACC:
A0A0U1RRI6
Background:
Centromere protein V-like protein 3, alternatively known as Centromere protein V pseudogene 3, represents a unique component within the cellular machinery. Its precise role and mechanism of action remain subjects of ongoing research, highlighting its potential significance in cellular processes.
Therapeutic significance:
Understanding the role of Centromere protein V-like protein 3 could open doors to potential therapeutic strategies. Its involvement in cellular functions suggests a promising avenue for drug discovery, aiming to target diseases at their molecular roots.