All the compounds are cleaved from the beads and tested in solution. If the resin beads were intimately mixed, it is not possible to test the products separately, but rather as a mixture. If activity in a pharmacological screen is observed it is not possible to say which compound or compounds are active. In order to identify the most active component, it is necessary to resynthesize the compounds individually and thereby find the most potent. This iterative process of resynthesis and screening is one of the most simple and successful methods for identifying active compounds from libraries... Short description of history and methods of combinatorial chemistry. Events and links related to combichem.
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