A Novel Approach for the Synthesis of Peripherally Acting Dual Target Inhibitor of Cannabinoid-1 (CB1 Receptor) and Inducible Nitric Oxide Synthase (iNOS) (S-MRI-1867/Zevaquenabant)

Zevaquenabant (<i>S</i>-MRI-1867) is a clinical-stage agent that is a peripherally restricted, potent antagonist of CB<sub>1</sub>R and an inhibitor of inducible nitric oxide synthase. A novel synthetic route to this highly selective active pharmaceutical agent is described in this paper. This route makes use of rationally installed chiral thio-substituted leaving group derived from a Bunte-salt reaction approach to yield diastereomeric compounds which are further processed to enantiopure compounds. The method will enable a rapid assembly of a variety of chiral sulfonyl amino compounds in this series.

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Publication Details

Journal
Molecules
Published
2026-02-02
DOI
https://doi.org/10.3390/molecules31030515
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00
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article

A Novel Approach for the Synthesis of Peripherally Acting Dual Target Inhibitor of Cannabinoid-1 (CB1 Receptor) and Inducible Nitric Oxide Synthase (iNOS) (S-MRI-1867/Zevaquenabant)

Malliga R. Iyer
Molecules
Asymmetric Hydrogenation and Catalysis
article

A Novel Approach for the Synthesis of Peripherally Acting Dual Target Inhibitor of Cannabinoid-1 (CB1 Receptor) and Inducible Nitric Oxide Synthase (iNOS) (S-MRI-1867/Zevaquenabant)

Malliga R. Iyer
article en

Abstract

Zevaquenabant (<i>S</i>-MRI-1867) is a clinical-stage agent that is a peripherally restricted, potent antagonist of CB<sub>1</sub>R and an inhibitor of inducible nitric oxide synthase. A novel synthetic route to this highly selective active pharmaceutical agent is described in this paper. This route makes use of rationally installed chiral thio-substituted leaving group derived from a Bunte-salt reaction approach to yield diastereomeric compounds which are further processed to enantiopure compounds. The method will enable a rapid assembly of a variety of chiral sulfonyl amino compounds in this series.

MoleculesVol. 31(3)
National Institutes of Health (US), National Institute on Alcohol Abuse and Alcoholism (US)
Openalex Percentile: Top 71%
Asymmetric Hydrogenation and Catalysis
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