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Dr. Khalid M. Al-Anazi د. خالد بن مشاي العنزي

Professor

Professor of Genetics

كلية العلوم
College of Science – Zoology Department B.O.P.: 57788, Office n. 2B 162
المنشورات
مقال فى مجلة
2016

Binding of anticancer compound glycopentalone with cell cycle macromolecules

2016, Kim, A.B. Gurung, M.A. Ali, A. Bhattacharjee, K.M. Al-Anazi, M.A.Farah, F.M. Al-Hemaid, F.M. Abou-Tarboush, J. Lee and S.Y. . . 2016

Glycosmis pentaphylla Glycopentalone Molecular docking Reverse pharmaco

​The bioactive compound, Glycopentalone isolated from Glycosmis pentaphylla (Retz) (family Rutaceae) have recently reported to have cytotoxic and apoptosis inducing effects in various human cancer cell lines. However, their mode of action have not clearly been defined; therefore, target fishing of glycopentalone using combined inverse docking and reverse pharmacophore mapping approach was attempted to identify potential targets of glycopentalone, and gain insights of its binding modes against the selected molecular targets viz; CDK-2, CDK-6, Topoisomerase I, Bcl-2, VEGFR-2, Telomere:G-Quadruplex and Topoisomerase II. These targets were chosen based on their key role in progression of cancer via regulation of cell cycle and DNA replication. Molecular docking analysis revealed that glycopentalone displayed binding energies ranging from -6.38 kcal/mol to -8.35 kcal/mol to -6.38 kcal/mol and inhibition constants ranging from 20.90µM to 0.758µM. Further, the binding affinities of glycopentalone with the targets were in order Telomere:G-quadruplex> VEGFR-2> CDK-6> CDK-2> Topoisomerase II> Topoisomerase I> Bcl-2 and its binding mode analysis revealed critical hydrogen bonds as well as hydrophobic interactions with the targets. The targets were validated by reverse pharmacophore mapping of glycopentalone against a set of 2241 known human target proteins which revealed CDK-2 and VEGFR-2 as its most favorable targets. The glycopentalone was well mapped to CDK-2 and VEGFR-2 which involve a total of six pharmacophore features (two hydrophobic centres and four hydrogen bond acceptors) and nine pharmacophore features (five hydrophobic, two hydrogen bond acceptors and two hydrogen bond donors) respectively. The present computational approaches may aid in rational identification of targets for small molecules against a large set of candidate macromolecules before experimental validation by bioassays, which will save both time and economy.

نوع عمل المنشور
KSU Research Work
مجلة/صحيفة
Genetics and Molecular Research
الصفحات
In Press
مزيد من المنشورات
publications

Psoriatic inflammation has been shown to be associated with cardiovascular dysfunction and systemic inflammation. Recently, psoriasis has also been linked to hepatic disorders, however…

بواسطة Naif O.Al-HarbiaAhmedNadeemaMohammed M.Al-HarbiaKhairy M.A.ZoheiraMushtaq A.AnsariaAhmed M.El-SherbeenybKhalid M.AlanazicMoureq R.AlotaibiaSheikh F.Ahmada
2017
publications

Objective

This study was designed to characterize the DNA polymorphisms of the melanocortin-1 receptor (MC1R) gene in indigenous Saudi Arabian sheep breeds exhibiting different…

بواسطة hmed H. Mahmoud , Ashraf M. Mashaly , Ahmed M. Rady , Khalid M. Al-Anazi , and Amgad A. Saleh.
2017
publications

ABSTRACT. The bioactive compounds proceraside A, frugoside and calotropin, which were extracted from the root bark of Calotropis procera (Aiton) W.T. Aiton (family Asclepiadaceae), were recently…

بواسطة Gurung, A.B. Gurung , M.A. Ali , A. Bhattacharjee , M. AbulFarah , F. Al-Hemaid , F.M. Abou-Tarboush , K.M. Al-Anazi , F.S.M. Al-Anazi and J. Lee, . 2016
2016