Chirality: a key parameter in chemical probes.


Journal

RSC chemical biology
ISSN: 2633-0679
Titre abrégé: RSC Chem Biol
Pays: England
ID NLM: 101768727

Informations de publication

Date de publication:
04 Oct 2023
Historique:
received: 02 06 2023
accepted: 01 08 2023
medline: 6 10 2023
pubmed: 6 10 2023
entrez: 6 10 2023
Statut: epublish

Résumé

Many small molecule bioactive and marketed drugs are chiral. They are often synthesised from commercially available chiral building blocks. However, chirality is sometimes incorrectly assigned by manufacturers with consequences for the end user ranging from: experimental irreproducibility, wasted time on synthesising the wrong product and reanalysis, to the added cost of purchasing the precursor and resynthesis of the correct stereoisomer. Further on, this could lead to loss of reputation, loss of funding, to safety and ethical concerns due to potential

Identifiants

pubmed: 37799583
doi: 10.1039/d3cb00082f
pii: d3cb00082f
pmc: PMC10549247
doi:

Types de publication

Editorial

Langues

eng

Pagination

716-721

Informations de copyright

This journal is © The Royal Society of Chemistry.

Déclaration de conflit d'intérêts

There are no conflicts to declare.

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Auteurs

Andrew McGown (A)

Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK g.kostakis@sussex.ac.uk j.spencer@sussex.ac.uk.
Sussex Drug Discovery Centre, Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK.

Jordan Nafie (J)

Biotools, Inc., 17546 Beeline Highway Jupiter Florida 33458 USA.

Mohammed Otayfah (M)

Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK g.kostakis@sussex.ac.uk j.spencer@sussex.ac.uk.

Storm Hassell-Hart (S)

Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK g.kostakis@sussex.ac.uk j.spencer@sussex.ac.uk.

Graham J Tizzard (GJ)

National Crystallography Service, School of Chemistry, University of Southampton Southampton SO17 1BJ UK.

Simon J Coles (SJ)

National Crystallography Service, School of Chemistry, University of Southampton Southampton SO17 1BJ UK.

Rebecca Banks (R)

Bio-Techne (Tocris), The Watkins Building, Atlantic Road Avonmouth Bristol BS11 9QD UK hannah.maple@bio-techne.com.

Graham P Marsh (GP)

Bio-Techne (Tocris), The Watkins Building, Atlantic Road Avonmouth Bristol BS11 9QD UK hannah.maple@bio-techne.com.

Hannah J Maple (HJ)

Bio-Techne (Tocris), The Watkins Building, Atlantic Road Avonmouth Bristol BS11 9QD UK hannah.maple@bio-techne.com.

George E Kostakis (GE)

Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK g.kostakis@sussex.ac.uk j.spencer@sussex.ac.uk.

Ilaria Proietti Silvestri (I)

Liverpool ChiroChem Ltd, The Heath Business & Technical Park Runcorn Cheshire WA7 4QX UK.

Paul Colbon (P)

Liverpool ChiroChem Ltd, The Heath Business & Technical Park Runcorn Cheshire WA7 4QX UK.

John Spencer (J)

Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK g.kostakis@sussex.ac.uk j.spencer@sussex.ac.uk.
Sussex Drug Discovery Centre, Department of Chemistry, School of Life Sciences, University of Sussex Falmer BN1 9QJ UK.

Classifications MeSH