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February 5, 2026Molecules0 citationsOpen Access

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)

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MIMalliga R. Iyer

Key Points

  • To develop a novel synthetic route for a peripherally acting dual target inhibitor of CB1R and iNOS.
  • Utilize a chiral thio-substituted leaving group from a Bunte-salt reaction approach.
  • Synthesize diastereomeric compounds that are further processed to enantiopure compounds.
  • Rapidly assemble a variety of chiral sulfonyl amino compounds.
  • Successful synthesis of a selective antagonist of CB1R and an inhibitor of iNOS.
  • Demonstrated efficiency in producing diastereomeric compounds.
  • Establishment of a method for assembling chiral sulfonyl amino compounds.

Abstract

Zevaquenabant (S-MRI-1867) is a clinical-stage agent that is a peripherally restricted, potent antagonist of CB1R 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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Cite This Study

Malliga R. Iyer (2026) studied this question.

synapsesocial.com/papers/6984345ff1d9ada3c1fb2732https://doi.org/10.3390/molecules31030515
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