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.
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 effective modulators, each annotated with 38 ADME-Tox and 32 physicochemical and drug-likeness parameters. Furthermore, each compound is shown with its optimal docking poses, affinity scores, and activity scores, offering a detailed summary.
Our top-notch dedicated system is used to design specialised 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.
Several key aspects differentiate our library:
partner
Reaxense
upacc
O75603
UPID:
GCM2_HUMAN
Alternative names:
GCM motif protein 2; Glial cells missing homolog 2
Alternative UPACC:
O75603; D3GDV6; Q5THN5
Background:
Chorion-specific transcription factor GCMb, also known as GCM motif protein 2 or Glial cells missing homolog 2, plays a pivotal role in parathyroid gland development by binding specific sequences on gene promoters to activate their transcription. This transcription factor is crucial for maintaining calcium and phosphate homeostasis.
Therapeutic significance:
GCMb is directly implicated in Hypoparathyroidism, familial isolated, 2, characterized by hypocalcemia and hyperphosphatemia, and Hyperparathyroidism 4, associated with hypercalcemia and increased bone resorption. Targeting GCMb could lead to novel treatments for these calcium homeostasis disorders.