Discovery of Potent, Selective, and Brain-Penetrant Small Molecule CD38 Inhibitors

Cluster of differentiation 38 (CD38) is a nicotinamide adenine dinucleotide (NAD<sup>+</sup>)-consuming ectoenzyme abundantly expressed in brain regions involved in motor control and cognition. Given the central role of NAD<sup>+</sup> in maintaining neuronal health, inhibition of CD38, resulting in NAD<sup>+</sup> elevation, has emerged as a potential therapeutic approach for neurodegenerative diseases and age-associated cognitive decline. Herein, we report the rational, structure-guided optimization of a series of small-molecule CD38 inhibitors, culminating in the identification of <b>CVN14</b>, a potent, selective, and brain-penetrant tool molecule with favorable pharmacokinetic properties for advanced preclinical evaluation. We further disclose the first high-resolution X-ray crystal structure of the <b>CVN14-</b>ADPR<b>-</b>CD38 complex, revealing an uncompetitive binding mode. <b>CVN14</b> provides a molecular tool to investigate CD38 biology in neurodegeneration and supports the development of next-generation brain-penetrant CD38 inhibitors.

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Publication Details

Journal
ACS Medicinal Chemistry Letters
Published
2026-01-29
DOI
https://doi.org/10.1021/acsmedchemlett.5c00727
Primary Topic
Calcium signaling and nucleotide metabolism
Type
article
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article

Discovery of Potent, Selective, and Brain-Penetrant Small Molecule CD38 Inhibitors

Louise Dickson, Maxine J. Roberts, Roland W. Bürli, M. Zebisch et al.
ACS Medicinal Chemistry Letters
Calcium signaling and nucleotide metabolism
article

Discovery of Potent, Selective, and Brain-Penetrant Small Molecule CD38 Inhibitors

Louise Dickson, Maxine J. Roberts, Roland W. Bürli, M. Zebisch, Kevin Doyle, Mark Carlton, Richard C. Hewer, Matthis Geitmann, Andrew Stott, V.L. Rangel, Philip Pickford, Kim L. Matthews, Lee A. Dawson, Nicola Brice, Jenna R. M. Harvey, Rosie Waters-Hall
article en

Abstract

Cluster of differentiation 38 (CD38) is a nicotinamide adenine dinucleotide (NAD<sup>+</sup>)-consuming ectoenzyme abundantly expressed in brain regions involved in motor control and cognition. Given the central role of NAD<sup>+</sup> in maintaining neuronal health, inhibition of CD38, resulting in NAD<sup>+</sup> elevation, has emerged as a potential therapeutic approach for neurodegenerative diseases and age-associated cognitive decline. Herein, we report the rational, structure-guided optimization of a series of small-molecule CD38 inhibitors, culminating in the identification of <b>CVN14</b>, a potent, selective, and brain-penetrant tool molecule with favorable pharmacokinetic properties for advanced preclinical evaluation. We further disclose the first high-resolution X-ray crystal structure of the <b>CVN14-</b>ADPR<b>-</b>CD38 complex, revealing an uncompetitive binding mode. <b>CVN14</b> provides a molecular tool to investigate CD38 biology in neurodegeneration and supports the development of next-generation brain-penetrant CD38 inhibitors.

ACS Medicinal Chemistry LettersVol. 17(2)
University of Cambridge (GB), WuXi AppTec (China) (CN), Beactica (Sweden) (SE), Evotec (United Kingdom) (GB)
Good health and well-being
Openalex Percentile: Top 75%
Calcium signaling and nucleotide metabolism
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