Rings in Clinical Trials and Drugs: Present and Future.


Journal

Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531

Informations de publication

Date de publication:
14 07 2022
Historique:
pubmed: 23 6 2022
medline: 23 6 2022
entrez: 22 6 2022
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 35730680
doi: 10.1021/acs.jmedchem.2c00473
pmc: PMC9289879
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

8699-8712

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Auteurs

Jonathan Shearer (J)

UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.

Jose L Castro (JL)

UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.

Alastair D G Lawson (ADG)

UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.

Malcolm MacCoss (M)

Bohicket Pharma Consulting Limited Liability Company, 2556 Seabrook Island Road, Seabrook Island, South Carolina29455, United States.

Richard D Taylor (RD)

UCB, 216 Bath Road, SloughSL1 3WE, United Kingdom.

Classifications MeSH