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Rings in Clinical Trials and Drugs: Present and Future.
Shearer, Jonathan; Castro, Jose L; Lawson, Alastair D G; MacCoss, Malcolm; Taylor, Richard D.
Afiliação
  • Shearer J; UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.
  • Castro JL; UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.
  • Lawson ADG; UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.
  • MacCoss M; Bohicket Pharma Consulting Limited Liability Company, 2556 Seabrook Island Road, Seabrook Island, South Carolina29455, United States.
  • Taylor RD; UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.
J Med Chem ; 65(13): 8699-8712, 2022 07 14.
Article em En | MEDLINE | ID: mdl-35730680
ABSTRACT
We present a comprehensive analysis of all ring systems (both heterocyclic and nonheterocyclic) in clinical trial compounds and FDA-approved drugs. We show 67% of small molecules in clinical trials comprise only ring systems found in marketed drugs, which mirrors previously published findings for newly approved drugs. We also show there are approximately 450 000 unique ring systems derived from 2.24 billion molecules currently available in synthesized chemical space, and molecules in clinical trials utilize only 0.1% of this available pool. Moreover, there are fewer ring systems in drugs compared with those in clinical trials, but this is balanced by the drug ring systems being reused more often. Furthermore, systematic changes of up to two atoms on existing drug and clinical trial ring systems give a set of 3902 future clinical trial ring systems, which are predicted to cover approximately 50% of the novel ring systems entering clinical trials.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article