Novel Tacrine and Hesperetin analogues: Design, Molecular docking and in silico ADME studies to identify potential Acetyl choline esterase inhibitors for Alzheimer’s disease.
Öz
Alzheimer’s disease is
considered as most prevailing and common CNS disease found in elder population
over 60 years of age. The early diagnosis of the disease prior to the
occurrence of first behavioral symptom, dementia is difficult and hence the
management of dementia and alleviation of other symptoms is the only available
treatment for the AD. Acetyl cholinesterase inhibitors (AchE) are widely used
in the treatment. In this study two series of new Tacrine(T1-T9)
and Hesperetin derivatives(H1-H9) on the basis of the structural
characteristics of acetyl cholinesterase (AchE) inhibitors were designed and screened
to identify potential analogues as Anti-Alzheimer drug on the AchE (PDB ID:1DX4) using GLIDE employing extra-precision
docking. The docking results Glide score, XPscore, docking score and binding interactions
were compared with standard drug Tacrine. From the docking results it was found
that T9 showed highest docking score among the designed compounds. The ADME
properties also predicted using Qikprop application, from the above studies
potential analogues with highest AchE inhibition and excellent pharmacokinetic
properties were identified.
Anahtar Kelimeler
Kaynakça
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Ayrıntılar
Birincil Dil
İngilizce
Konular
Eczacılık ve İlaç Bilimleri
Bölüm
Araştırma Makalesi
Yayımlanma Tarihi
31 Ocak 2020
Gönderilme Tarihi
30 Nisan 2019
Kabul Tarihi
23 Eylül 2019
Yayımlandığı Sayı
Yıl 2020 Cilt: 44 Sayı: 1