Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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 use our state-of-the-art dedicated workflow for designing 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.
Our library is unique due to several crucial aspects:
partner
Reaxense
upacc
P02768
UPID:
ALBU_HUMAN
Alternative names:
-
Alternative UPACC:
P02768; E7ESS9; O95574; P04277; Q13140; Q645G4; Q68DN5; Q6UXK4; Q86YG0; Q8IUK7; Q9P157; Q9P1I7; Q9UHS3; Q9UJZ0
Background:
Albumin, a pivotal protein in the human body, binds various substances including water, ions, fatty acids, and hormones. Its primary role is to regulate blood's colloidal osmotic pressure, crucial for maintaining fluid balance. Albumin also plays a significant role in transporting zinc, calcium, and magnesium in the plasma, showcasing a high affinity for these ions. Additionally, it interacts with bacterial siderophores like enterobactin, influencing iron uptake and bacterial growth.
Therapeutic significance:
Albumin's involvement in diseases such as Hyperthyroxinemia, familial dysalbuminemic, and Analbuminemia, underscores its clinical importance. These conditions, resulting from genetic variants affecting albumin, highlight the protein's role in maintaining normal serum thyroxine levels and circulating serum albumin. Understanding Albumin's functions and its genetic variants opens avenues for targeted therapeutic strategies, offering hope for managing these disorders.