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.
Our high-tech, dedicated method is applied to construct targeted 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 stands out due to several important features:
partner
Reaxense
upacc
P22732
UPID:
GTR5_HUMAN
Alternative names:
Fructose transporter; Glucose transporter type 5, small intestine
Alternative UPACC:
P22732; Q14770; Q5T977; Q8IVB3
Background:
Solute carrier family 2, facilitated glucose transporter member 5, also known as the Fructose transporter, plays a pivotal role in monosaccharide transport. It primarily functions to facilitate fructose uptake, showing low activity with other sugars. This protein is crucial for fructose absorption in the small intestine and is implicated in the regulation of salt uptake and blood pressure in response to dietary fructose. Its ability to mediate the uptake of 2-deoxyglucose, albeit with low efficiency, highlights its specificity for fructose.
Therapeutic significance:
Understanding the role of Solute carrier family 2, facilitated glucose transporter member 5 could open doors to potential therapeutic strategies. Its involvement in the regulation of blood pressure and salt uptake in response to dietary fructose underscores its potential as a target for managing diet-induced hypertension.