Thermo Fisher Scientific has expanded its Maybridge Fragment Range with the addition of the Maybridge Ro3 Diversity Fragment Library, which is intended to facilitate drug delivery processes.
The new library has been computationally engineered to build on the key features of the original Maybridge Ro3 Library, such as Rule of Three (Ro3) compliance, pharmacophoric enrichment and quality assurance of at least 95 per cent.
The Maybridge Ro3 Diversity Library offers both an improved structural diversity profile and experimental solubility data for every one of the 1,500 member compounds.
Full Ro3 compliance means that all 1,500 fragments have the physicochemical properties that increase the probability of successful 'hits'.
The portfolio also provides access to analogues for fragment hopping, as well as reactive analogues for rapid hit evolution and derivatisation.
Consequently, the Maybridge fragments provide an ideal starting point for a lead-optimisation, structure-based drug discovery programme and the ultimate evolution of a new molecule in the drug discovery process.
Every fragment in the new Maybridge library has been experimentally triaged to assure solubility in both DMSO (200mM) and aqueous phosphate buffer (1mM).
Aqueous solubility is a prerequisite for successful in-vitro testing, as poor solubility can compromise the robustness of the screening data through aggregation and promiscuous inhibition.
Fragment hits with poor aqueous solubility are also more likely to produce evolved analogues with inferior ADME properties, such as plasma protein binding, poor systemic distribution and an increased likelihood of candidate attrition.
The Maybridge Ro3 Diversity Fragment Library mitigates all such issues.
When building the new Maybridge library, Maybridge scientists applied Daylight-based structural fingerprinting techniques (1,024-bit length) to an Ro3-compliant set of 8,000 fragments and the fingerprinted set then clustered using industry-standard clustering software (DBClus).
The resulting representative set of 1,500 high-quality molecules consists of 819 cluster centroids and 690 singletons at a Tanimoto level of 0.66.
