English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

An  in vitro  antidiabetic activity on   α  -amylase and   α  –glucosidase activity of novel 10-chloro-4-(2-chlorophenyl)-12-phenyl-5,6-dihydropyrimido[4,5- a ]acridin-2-amines ( 3a – 3f ) were evaluated. Structures of the synthesized molecules were studied by FT-IR,  1 H NMR,  13 C NMR, EI-MS, and single crystal X-ray structural analysis data. An  in silico  molecular docking was performed on synthesized molecules ( 3a – 3f ). Overall studies indicate that compound  3e  is a promising compound leading to the development of selective inhibition of   α  -amylase and   α  -glucosidase.

In SilicoMolecular Docking andIn VitroAntidiabetic Studies of Dihydropyrimido[4,5-a]acridin-2-amines