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Mapping protein binding sites by photoreactive fragment pharmacophores

Mapping protein binding sites by photoreactive fragment pharmacophores

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0a79f05dcd144d4ba343eaa1f806db99

Mapping protein binding sites by photoreactive fragment pharmacophores

About this item

Full title

Mapping protein binding sites by photoreactive fragment pharmacophores

Publisher

London: Nature Publishing Group UK

Journal title

Communications chemistry, 2024-07, Vol.7 (1), p.168-13, Article 168

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Fragment screening is a popular strategy of generating viable chemical starting points especially for challenging targets. Although fragments provide a better coverage of chemical space and they have typically higher chance of binding, their weak affinity necessitates highly sensitive biophysical assays. Here, we introduce a screening concept that...

Alternative Titles

Full title

Mapping protein binding sites by photoreactive fragment pharmacophores

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_0a79f05dcd144d4ba343eaa1f806db99

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_0a79f05dcd144d4ba343eaa1f806db99

Other Identifiers

ISSN

2399-3669

E-ISSN

2399-3669

DOI

10.1038/s42004-024-01252-w

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