
Prestwick Drug-Fragment Library:
1456 fragments arising from
smart fragmentation of approved drugs
Acknowledged as powerful tool for successful identification of lead series, fragment-based drug design is widely implemented in industry and academia. The fragment-based drug discovery (FBDD) has emerged as an alternative approach to traditional lead identification via high-throughput screening. Unlike other screening approaches, FBDD identifies smaller compounds, which bind to different parts of a biological target.
The primary rationale for fragment-based screening is that the identified hits give access to a broader chemical space while screening a limited number of compounds. FBDD gives a better chance for the final lead compound to have standard drug-likeness parameters. On the other hand, they are simpler molecules (fragments) with fewer unavoidable interactions and, thus, a much better possibility of orienting within the binding site favorably.
To meet researchers’ expectations in this field, an in-house team of medicinal chemists has designed a unique collection of 1456 small molecules (MW<300) arising from the smart fragmentation of approved drugs (1500 drugs, up to year 2016).

Prestwick Drug-Fragment Library: An original collection of fragments derived from approved drugs
- Balanced set of Ro3 compliant (55%) and Ro3 non-compliant (45%) fragments
 - Good coverage of lead-like diversity space
 - High-quality hits increased by using fragments derived from approved drugs
 - Rapid follow-up on primary hits possible
 - Experimental solubility in DMSO (100 mM) and PBS (1 mM) assessed
 - Purity 95%+ (H NMR spectrum and LC/MS available)
 - Mean MW: 182
- 56% of fragments are exclusive to the Prestwick Drug-Fragment Library and cannot be found in any other major supplier of fragment libraries
 - >80% of the recent approved drugs contain at least one of the Prestwick Drug-Fragments Library.
 
 
Prestwick Drug Fragment Library: Examples
Prestwick Drug-Fragment Library: Multi-format and highly customizable
| Format | Comments | |
|---|---|---|
| Core set 480 cpds  | 
  | 
Representative set of the entire library Ready for Screening Highly recommanded for rapid outcomes  | 
| Complete library | 
  | 
Available for cherry picking | 
| Customized set  | 
  | 
Selection based on your own criteria (physicochemical properties, substructure or similarity search)  | 
| In any case: Resupply guaranteed up to 100mg | 
Prestwick Drug-Fragment Library: Applications in FBBD and more classical screening
- Fragment-based screening using high-concentration bioassays, surface plasmon resonance (SPR), microscale thermophoresis (MST), differential scanning fluorimetry (DSF) (also termed fluorescent thermal shift assay; FTSA), X-Ray crystallography and nuclear magnetic resonance (NMR)
 - HTS for small molecules
 - Screening on living cells or cell lysates for target identification & validation
 
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