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Synthesis and biological evaluation of stilbene derivatives coupled to NO donors as potential antidiabetic agents.

Journal of enzyme inhibition and medicinal chemistry2018Wang B, Liu T, Wu Z, et al.
Study designOther primary literature
SubjectAnimal

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Study design
Other primary literature
Subject
Animal
Publication year
2018
Source
doi.org
Abstract display
Shown here
Publication status
Active
Status checked
17 Aug 2026
Collected
3 Aug 2026
Freshness
Current
Review stage
Automated
Record status
Published

Abstract

The work is focused on the design of drugs that prevent and treat diabetes and its complications. A novel class of stilbene derivatives were prepared by coupling NO donors of alkyl nitrate and were fully characterised by NMR and other techniques. These compounds were tested in vitro activity, including α-glucosidase inhibitory activity, aldose reductase (AR) inhibitory activity and advanced glycation end products (AGEs) formation inhibitory activity. A class of modified compounds could play a significant effect for treatment of diabetic complications. Target compounds 3e and 7c offered a potential drug design concept for the development of therapeutic or preventive agents for diabetes and its complications.

MeSH

Aldehyde ReductaseAnimalsDiabetes ComplicationsDiabetes Mellitus, ExperimentalDose-Response Relationship, DrugDrug DesignEnzyme InhibitorsGlycation End Products, AdvancedHypoglycemic AgentsMiceMice, Inbred StrainsMolecular StructureNitratesNitric OxideStilbenesStreptozocinStructure-Activity Relationshipalpha-Glucosidases

DOI 10.1080/14756366.2018.1425686

PMID 29374975

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