| Literature DB >> 30946980 |
Fredrik Bergström1, Bo Lindmark2.
Abstract
The eventual candidate drug (CD) is often already synthesized during early drug discovery but not nominated until much later. To facilitate the rapid identification of a potential CD, a thoroughly worked-out CD target profile (CDTP) with criteria acceptable for the disease target product profile (TPP) is required at the start of lead generation (LG). In addition to driving the compound property optimization, the preclinical project team has to understand the ultimate goal to be able to rapidly identify and progress a potential CD. A screening cascade with meaningful and well-balanced progression criteria based on the CDTP is required to rapidly filter out unwanted compounds and to progress a potential CD through the cascade to candidate selection.Entities:
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Year: 2019 PMID: 30946980 DOI: 10.1016/j.drudis.2019.03.026
Source DB: PubMed Journal: Drug Discov Today ISSN: 1359-6446 Impact factor: 7.851