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.
From a virtual chemical space containing more than 60 billion molecules, we precisely choose certain compounds. Our collaborator, Reaxense, aids in their synthesis and provision.
In the library, a selection of top modulators is provided, each marked with 38 ADME-Tox and 32 parameters related to physicochemical properties and drug-likeness. Also, every compound comes with its best docking poses, affinity scores, and activity scores, providing a comprehensive overview.
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
O75665
UPID:
OFD1_HUMAN
Alternative names:
Oral-facial-digital syndrome 1 protein; Protein 71-7A
Alternative UPACC:
O75665; B9ZVU5; O75666; Q4VAK4
Background:
Centriole and centriolar satellite protein OFD1, also known as Oral-facial-digital syndrome 1 protein, plays a crucial role in centriole length control and ciliogenesis. It recruits essential proteins like IFT88 and CEP164 to centrioles, facilitating cilium biogenesis, a process vital for cell signaling and tissue homeostasis. OFD1's involvement in Wnt signaling and left-right axis specification underscores its significance in development.
Therapeutic significance:
OFD1's mutation is linked to diseases such as Orofaciodigital syndrome 1, Simpson-Golabi-Behmel syndrome 2, Joubert syndrome 10, and Retinitis pigmentosa 23. Understanding OFD1's role could pave the way for innovative treatments targeting these genetic disorders, highlighting the protein's therapeutic potential.