Author/Authors :
Valipour, Mehdi Department of Medicinal Chemistry - Faculty of Pharmacy - Mazandaran University of Medical Sciences, Sari, Iran , Davaji, Issa Department of Medicinal Chemistry - Faculty of Pharmacy - Mazandaran University of Medical Sciences, Sari, Iran , Abedi, Niusha Department of Pharmacology & Toxicology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Rajabi, Mahsa Department of Pharmacology & Toxicology - School of Pharmacy - Shahid Beheshti University of Medical Sciences, Tehran, Iran , Tüylü Küçükkılınç, Tuba Department of Biochemistry - Faculty of Pharmacy - Hacettepe University, Sihhiye, Ankara, Turkey , Ayazgök, Beyza Department of Biochemistry - Faculty of Pharmacy - Hacettepe University, Sihhiye, Ankara, Turkey , Irannejad, Hamid Department of Medicinal Chemistry - Faculty of Pharmacy - Mazandaran University of Medical Sciences, Sari, Iran
Abstract :
Alzheimer’s disease (AD) is a neuroinflammatory based pathologic state in which β-amyloid
aggregates are major devastating agents. In this study, a series of 2-hydroxyiminoethanones
were synthesized and evaluated as anti-inflammatory in carrageenan and formalin tests and
inhibitors of β-amyloid aggregation. Compounds 1-10b were synthesized through a twostep
reaction. Results: Compounds 1-5b showed more β-amyloid disaggregation ability
than reference drugs rifampicin and donepezil and compound 2b was the best compound
in this series and could reduce the extent of amyloid aggregation to 50.9%. Interestingly,
compounds 1b and 3b showed significant anti-inflammatory activity in carrageenan-induced
paw edema compared to control group and equivalent to the reference drug indomethacin.
2-Hydeoxyiminoethanones are privileged scaffold for further drug research and development
as anti-neuroinflammatory and neuroprotective agents.
Keywords :
β-amyloid aggregation , hydroxyiminoethanone , Alzheimer′s disease , Anti- inflammatory , Synthesis