| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10591160 | Bioorganic & Medicinal Chemistry Letters | 2014 | 4 Pages |
Abstract
Thirteen 2-oxazine-substituted heterocyclic derivatives were synthesized targeting 5-LOX and AChE. The test revealed that the newly synthesized compounds had potent inhibition towards both 5-LOX and AChE in lower micro molar concentration (Scheme 1, FGÂ =Â functional groups).
Related Topics
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Chemistry
Organic Chemistry
Authors
Alexey Yu. Sukhorukov, Anilkumar C. Nirvanappa, Jagadish Swamy, Sema L. Ioffe, Shivananju Nanjunda Swamy, Basappa Basappa, Kanchugarakoppal S. Rangappa,