Hit-to-lead & lead optimisation

Turn first binders into development candidates.

We continue where discovery stops: confirming your hits, building structure–activity understanding and optimising potency, stability and developability until you have a lead worth taking forward.

Hit-to-lead

From a sequence to a series.

01

Hit confirmation

Resynthesis and full characterisation of selected sequences, so every decision rests on authentic, high-purity material.

02

SAR exploration

Alanine and truncation scans, positional scanning and focused analogue libraries to map which residues drive activity.

03

Scaffold design

Cyclisation, stapling, non-natural amino acids and N-methylation to lock in the active conformation.

Lead optimisation

Balance potency with drug-like properties.

01

Potency & selectivity

Iterative design–make–test cycles, with your assays or our partners’, to improve activity on your target and selectivity against related ones.

02

Chemical stability

Solution and degradation studies by HPLC and LC-MS, with the findings fed straight back into the next round of design.

03

Half-life extension

Lipidation, PEGylation and other conjugation strategies to tune exposure and duration of action.

04

Developability

Solubility, aggregation, impurity profiling and characterisation to flag risks before development.

Biology studies, through partners

Biology from specialist partners, chemistry from us.

We focus on peptide chemistry and analytics. When your program needs biology, we arrange it with specialist partner laboratories and coordinate the work for you.

  • 01
    Cell-based assays

    Activity and potency testing of your analogues, run by a partner laboratory.

  • 02
    ADME and in vivo studies

    Metabolic stability, pharmacokinetic and mouse studies, arranged with specialist pre-clinical partners.

  • 03
    One point of contact

    We coordinate the studies, supply the material and connect the results back to your chemistry.

What you receive

A lead ready for development.

  • 01
    An optimised lead series

    Your best candidates and back-ups, with the SAR that explains them.

  • 02
    Decision-ready data

    Chemistry, stability and characterisation data, plus any partner biology results, in clear reports for go/no-go decisions.

  • 03
    Material for the next step

    Gram-scale material for in vivo studies, and a route our development team can scale towards GMP.

Have a hit? Let’s make it a lead.

Tell us about your sequence, your target profile and the decision you need to make next.