Fragment-Based Drug Discovery: Difference between revisions
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==== Ligand Linking ==== | ==== Ligand Linking ==== | ||
The final step in FBDD is to link all of the individual, optimized fragments together to form one compound with very high affinity for the target. The goal is for all of the high-binding affinity characteristics of the fragments to be represented in one final compound. | The final step in FBDD is to link all of the individual, optimized fragments together to form one compound with very high affinity for the target. The goal is for all of the high-binding affinity characteristics of the fragments to be represented in one final, high-affinity compound. | ||
</StructureSection> | </StructureSection> | ||
= References = | = References = | ||
<references/> | <references/> | ||
