Explore the Potential with AI-Driven Innovation
The specialised, focused library is developed on demand with the most recent virtual screening and parameter assessment technology, guided by the Receptor.AI drug discovery platform. This approach exceeds the capabilities of traditional methods and offers compounds with higher 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.
The library includes a list of the most promising modulators annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Also, each compound is presented with its optimal docking poses, affinity scores, and activity scores, providing a comprehensive overview.
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
O43826
UPID:
G6PT1_HUMAN
Alternative names:
Glucose-5-phosphate transporter; Glucose-6-phosphate translocase; Solute carrier family 37 member 4; Transformation-related gene 19 protein
Alternative UPACC:
O43826; O96016; Q5J7V4; Q9UI19; Q9UNS4
Background:
The Glucose-6-phosphate exchanger SLC37A4, also known as Glucose-5-phosphate transporter and Glucose-6-phosphate translocase, plays a pivotal role in glucose homeostasis. It functions as an inorganic phosphate and glucose-6-phosphate antiporter in the endoplasmic reticulum, crucial for glycogenolysis and gluconeogenesis processes.
Therapeutic significance:
SLC37A4's dysfunction is linked to metabolic disorders such as Glycogen storage disease types 1B, 1C, and 1D, and Congenital disorder of glycosylation 2W, characterized by hypoglycemia, hepatomegaly, and growth retardation. Targeting SLC37A4 could offer novel therapeutic avenues for these conditions.