![](/images/graphics-bg.png)
In Silico Molecular Docking and In Vitro Antidiabetic Studies of Dihydropyrimido[4,5-a]acridin-2-amines
Joint Authors
Bharathi, A.
Gayathri, M.
Vasavi, C. S.
Roopan, Selvaraj Mohana
Gayathri, G. A.
Munusami, Punnagai
Source
Issue
Vol. 2014, Issue 2014 (31 Dec. 2014), pp.1-10, 10 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2014-06-02
Country of Publication
Egypt
No. of Pages
10
Main Subjects
Abstract EN
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, 1H NMR, 13C 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.
American Psychological Association (APA)
Bharathi, A.& Roopan, Selvaraj Mohana& Vasavi, C. S.& Munusami, Punnagai& Gayathri, G. A.& Gayathri, M.. 2014. In Silico Molecular Docking and In Vitro Antidiabetic Studies of Dihydropyrimido[4,5-a]acridin-2-amines. BioMed Research International،Vol. 2014, no. 2014, pp.1-10.
https://search.emarefa.net/detail/BIM-512467
Modern Language Association (MLA)
Bharathi, A.…[et al.]. In Silico Molecular Docking and In Vitro Antidiabetic Studies of Dihydropyrimido[4,5-a]acridin-2-amines. BioMed Research International No. 2014 (2014), pp.1-10.
https://search.emarefa.net/detail/BIM-512467
American Medical Association (AMA)
Bharathi, A.& Roopan, Selvaraj Mohana& Vasavi, C. S.& Munusami, Punnagai& Gayathri, G. A.& Gayathri, M.. In Silico Molecular Docking and In Vitro Antidiabetic Studies of Dihydropyrimido[4,5-a]acridin-2-amines. BioMed Research International. 2014. Vol. 2014, no. 2014, pp.1-10.
https://search.emarefa.net/detail/BIM-512467
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-512467