![Show Menu](styles/mobile-menu.png)
![Page Background](./../common/page-substrates/page0021.png)
Page 59
Notes:
Journal of Clinical & Experimental Pathology | ISSN: 2161-0681 | Volume 8
Breast Pathology and Cancer Diagnosis
6
th
World Congress and Expo on
July 25-26, 2018 | Vancouver, Canada
Medicinal Chemistry and Rational Drugs
20
th
International Conference on
&
Using ComputerAided Drug Design and docking softwares to determine
In-Silico
Metformin Binding
site with its receptor AMP Kinase Enzym
Farah Yousef
Damascus University, Syria
M
etformin receptor has been studied for decades as this drug is one of the most popular drugs used in the treatment of
Type II diabetes Mellitus (TIIDM) in the globe. Different studies have confirmed that its receptor is AMPKinase enzyme
in the liver cells. But, no crystal structure was found yet for its binding to the proposed enzyme. What we tried here is to use
our experiences in medicinal Chemistry and Computer Aided Drug Design in a try to study Metformin binding site with
AMPKinase in silico using two docking softwares and one internet site. AMPKinase crystal structure was downloaded from
Protein Data Bank database, while Metformin structure was got from Pubchem database. After analyzing the structures and
the docking results we had, we came to a conclusion that agrees with recent biological studies about this investigation. We
hope these results help researchers in drug design field to discover and\or developing new agents for the treatment of TIIDM
considering Metformin as a lead compound for that.
Biography
Farah Yousef is a PhD student from Damascus University. She has finished her previous studies at Faculty of Pharmacy at Tishreen University, Syria. She has
published 6 articles so far in reputed journals and many Arabic articles in Arabic websites and has been serving as an editorial board member of repute in different
journals. She has participated in different Syrian and Global conferences so far.
farahyousef90@yahoo.comFarah Yousef, J Clin Exp Pathol 2018, Volume 8
DOI: 10.4172/2161-0681-C3-051