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Friday, 20 August 2004 12:11

DATE DUE SUBMISSION:


SEPTEMBER 26, 2017 TUESDAY 23:59



Dear Students,

Announcement for those who want to join the system...


Please send an email message below...

After that you will get an access for both registration to web site and appropriate course...

Attendence is optional...!


Dear Professor,
Relevance: PHA285
I'm interested in joining to the active learning system to be implemented in PHA2855 class, and I accept that the system involves the items based on self research and homework/project preparation as explkained in the web page related to the Organic Chemistry in English Class.
Thank you,
Student Name
Student ID




Last Updated on Thursday, 21 September 2017 11:16
 
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Erdem Buyukbingol, Ph. D.

Professor of Medicinal and Pharmaceutical Chemistry

Ankara University,
Faculty of Pharmacy (ECZACILIK)
Department of Pharmaceutical Chemistry,
Tandogan 06100, Ankara, Turkey

Office Phone: +90 312-2033-067
Fax: +90 312-213-1081
e-Mails: This e-mail address is being protected from spambots. You need JavaScript enabled to view it ; This e-mail address is being protected from spambots. You need JavaScript enabled to view it

Twitter: https://twitter.com/bykbingl

Skype: ebuyukbingol

Research Interest


We design and synthesize compounds which cannot be found elsewhere!



We discovered several compounds...

Now, it's time for you to discover us!


Our recent work has concentrated on the diverse roles of melatonin, lipoic acid, coEnzyme Q10, and retinoids in terms of their antioxidant capabilities and anticancer activities leading to prevent and/or ameliorate radiation effects. In particular, we are investigating novel derivatives of above molecules as radioprotectors and anticancer compounds.


A problem of primary importance to our group is how to handle the molecular recognition prior to free radical scavenging mechanisms. We have used careful design procedures to obtain novel antioxidant molecules based on melatonin, lipoic acid and retinoids, and computer modeling studies have been employed by constructing a family of appropriate enzyme/receptor models in which dockings have been performed on the basis of hydrogen bonding, electrostatic and hydrophobic interactions.

A general interest in problems in molecular recognition and molecular design has stimulated our more recent work towards understanding the structure and biological action of what properties are more relative to scavenge the reactive oxygen species during the extreme conditions.