I obtained a degree in Pharmacy from the University of Baghdad in 1997 and subsequently served as a laboratory instructor at the same institution. After completing my master’s degree in Pharmaceutical chemistry in 2005, I returned as a faculty member in the Department of Pharmaceutical chemistry at the University of Baghdad College of pharmacy. In 2010, I commenced my Ph.D. studies in Pharmaceutical chemistry, which I completed in 2013. I currently serve as a faculty member with the rank of lecturer in the Department of Pharmaceutical chemistry. I possess over 20 years of experience in Pharmaceutical chemistry research and have authored more than 20 publications.
Ph.D. in Pharmaceutical chemistry Master in Pharmaceutical chemistry
faculty member in the Department of Pharmaceutical chemistry at the University of Baghdad College of pharmacy
The Training of Trainers (ToT) – University of Baghdad Member in Iraqi Pharmacist Syndicate
Pharmaceutical chemistry, organic chemistry, inorganic Pharmaceutical chemistry, medicinal chemistry
Pharmacy
inorganic Pharmaceutical chemistry, heterocyclic chemistry, organic chemistry, Pharmaceutical chemistry
2 Master students
(1)
3-coumarin/chalcone B1/B2/B3 hybrids served as malleable antecedents for the development of novel bioactive pharmacophores. In this study, the matching coumarin-chalcones hybrid was obtained from 3-acetylcoumarin (comp A) via condensation with several aromatic aldehydes in ethanolic piperidine solution. To further modify these hybrids, we reacted them with thiourea in the presence of base in ethanol, yielding pyrimidine derivatives C1, C2, and C3. Their chemical characteristics and spectroscopic data were used to characterize the newly synthesized heterocyles. The antibacterial efficacy of all freshly produced compounds was tested. Compound (C3) was shown to have the highest antibacterial activity against both gram positive and gram nega
... Show MoreMefenamic acid (MA) is one of the non-steroidal anti-inflammatory drugs, it is widely used probably due to having both anti-inflammatory and analgesic activity, the main side effects of mefenamic acid include gastrointestinal tract (GIT) disturbance mainly diarrhea, peptic ulceration, and gastric bleeding. The analgesic effects of NSAIDs are probably linked to COX-2 inhibition, while COX-1 inhibition is the major cause of this classic adverse effects. Introduction of thiazolidinone may lead to the increase in the bulkiness leads to the preferential inhibition of COX-2 rather than COX-1 enzyme. The study aimed to synthesize derivatives of mefenamic acid with more potency and to decrease the drug's potential side effects, new series of 4-t
... Show More
(1)
(1)
New hydrazone derivatives of Fenoprofen were synthesized and evaluated for their anti-inflammatory activity by means of egg white induced paw edema method. All the synthesized target compounds were characterized by FT-IR spectroscopy, 1HNMR analysis and by measure of their physical properties. The synthesis of the target compounds(H1-H4) was accomplished by multistep reaction procedures. The synthesized target compounds were show activity in reducing paw edema thickness and their anti-inflammatory effect was comparable to that of the standard (Fenoprofen) except for compound H3 which show anti-inflammatory activity higher than Fenoprofen.
(3)
(1)