Abstract
Most of the nonsteroidal #anti-inflammation drugs (NSAID) have some
demerits depending on type and nature of physical conditions and limit
of doses. Herein, we report the optimization of Naproxen and its
degradants employing density functional theory (DFT) with
B3LYP/6-31g+(d,p) level theory to elucidate their thermal and molecular
orbital properties. Molecular docking and nonbonding interactions have
been performed against #prostaglandin synthase protein (5F19) to search
binding affinity and interactions of all compounds with the respective
protein. #Pharmacokinetic properties also calculated to search their
absorption, metabolism, and carcinogenicity.#Naproxen is a naphthalene nucleus bearing nonsteroidal an- ti-pyratic
and anti-inflammatory drug, that plays key role against #cyclooxygenase
(COX) leading to suppress #prostaglandins accumulation caused by various
diseases [1,2]. It has undesirable side effects upon routine medication
due to free form of terminal acid group. A bunch of modification focused
on terminal acid group protection or prodrug derivatization in order to
minimize the secondary effect [1-3]. Several degradative studies
suggested to investigate the nature of #degradant in the different
chemical and physical environment [4,5].
For more articles on BJSTR Journal please click on https://biomedres.us/
For more Medical Casereports Articles on BJSTR
Molecular Docking, Pharmacokinetic, and DFT Calculation of Naproxen and its Degradants by Moniruzzaman in BJSTR
Follow on Twitter : https://twitter.com/Biomedres01
Follow on Tumbler: https://biomedres.tumblr.com/
Like Our Pins On : https://www.pinterest.com/biomedres/