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 carefully select specific compounds from a vast collection of over 60 billion molecules in virtual chemical space. Our partner Reaxense helps in synthesizing and delivering these compounds.
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
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 distinguishes itself through several key aspects:
partner
Reaxense
upacc
Q9UP52
UPID:
TFR2_HUMAN
Alternative names:
-
Alternative UPACC:
Q9UP52; A6NGM7; O75422; Q1HE13; Q9HA99; Q9NX67
Background:
Transferrin receptor protein 2 plays a crucial role in iron homeostasis, mediating the cellular uptake of transferrin-bound iron. Its involvement in iron metabolism, hepatocyte function, and erythrocyte differentiation highlights its importance in maintaining iron levels within physiological ranges.
Therapeutic significance:
Given its pivotal role in iron metabolism and association with Hemochromatosis 3, a disorder characterized by iron overload, Transferrin receptor protein 2 presents a promising target for therapeutic intervention. Understanding its function could lead to novel treatments for diseases caused by iron dysregulation.