Explore the Potential with AI-Driven Innovation
This comprehensive focused library is produced on demand with state-of-the-art virtual screening and parameter assessment technology driven by Receptor.AI drug discovery platform. This approach outperforms traditional methods and provides higher-quality compounds with superior 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.
Our top-notch dedicated system is used to design specialised 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.
Our library stands out due to several important features:
partner
Reaxense
upacc
O60896
UPID:
RAMP3_HUMAN
Alternative names:
Calcitonin-receptor-like receptor activity-modifying protein 3
Alternative UPACC:
O60896; Q7Z2Y1
Background:
Receptor activity-modifying protein 3, alternatively known as Calcitonin-receptor-like receptor activity-modifying protein 3, is pivotal in cardioprotection. It mitigates cardiac hypertrophy and perivascular fibrosis through a GPER1-dependent mechanism. This protein is essential for the transportation of the calcitonin gene-related peptide type 1 receptor (CALCRL) and GPER1 to the plasma membrane and serves as a receptor for adrenomedullin (AM) in conjunction with CALCRL.
Therapeutic significance:
Understanding the role of Receptor activity-modifying protein 3 could open doors to potential therapeutic strategies.