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.
The compounds are cherry-picked from the vast virtual chemical space of over 60B molecules. The synthesis and delivery of compounds is facilitated 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 utilise our cutting-edge, exclusive workflow to develop focused libraries.
Fig. 1. The sreening workflow of Receptor.AI
Our methodology employs molecular simulations to explore a wide array of proteins, capturing their dynamic states both individually and within complexes. Through ensemble virtual screening, we address conformational mobility, uncovering binding sites within functional regions and remote allosteric locations. This thorough exploration ensures no potential mechanism of action is overlooked, aiming to discover novel therapeutic targets and lead compounds across an extensive spectrum of 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.