Nedaa Abd Al hameed Abd Al Rahim received the B.Sc. in pharmacy, from the college of pharmacy / university of Baghdad (2009), and then worked as a pharmacist at the Ministry of Health, Al Karkh General Hospital, from 2010 to 2011, then in the Abu Ghraib sector from 2011 to 2012, Subsequently appointed as a pharmacy teaching assistant at the College of Pharmacy, University of Baghdad, in 2012. I obtained the M.Sc. degree in pharmaceutical chemistry from the college of pharmacy / university of Baghdad (2018), and Currently I am Ph.D. student at college of pharmacy / university of Baghdad department of pharmaceutical chemistry, Taught for 4 years at collage of pharmacy laboratory, I have supervised numerous graduation projects from 2019 to the present, I have been published 4 research articles and 4 review articles in the field of pharmacy and pharmaceutical chemistry.
• B.Sc. in pharmacy from college of pharmacy/ University of Baghdad (2009) • M.Sc. in pharmaceutical chemistry from College of Pharmacy/ University of Baghdad 2018
Laboratory technical supervisor in Pharmaceutical Chemistry/Graduate Studies lab in 2023 to present
Member, Iraqi Pharmacist Syndicate Member of committee of graduation projects assessment for fifth stage students from 2019-till now Member of committee of examination from 2018 to 2020
My research interest concerns chemical synthesis of organic compounds and their characterization, biological study, and docking study which act mainly as anti-cancer compounds by inhibition of many receptors like EGFR,VEGFR, HDAC ……ect, This is a new field of research which is really interesting and may have some significant impacts on healthcare associated diseases
Lecturer in Pharmaceutical Chemistry laboratory / college of pharmacy /University of Baghdad
Organic Chemistry II / practical In organic pharmaceutical chemistry / practical organic pharmaceutical chemistry II / practical
Supervised graduating projects from 2019 till the
- present.
Solvents are important components in the pharmaceutical and chemical industries, and they are increasingly being used in catalytic reactions. Solvents have a significant influence on the kinetics and thermodynamics of reactions, and they can significantly change product selectivity. Solvents can influence product selectivity, conversion rates, and reaction rates. However, solvents have received a lot of attention in the field of green chemistry. This is due to the large amount of solvent that is frequently used in a process or formulation, particularly during the purification steps. However, neither the solvent nor the active ingredient in a formulation is directly responsible for the reaction product's composition. Because these ch
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A new series of schiff base and aminothiadiazole derivatives of N- substituted phthalimide (I-VI) were synthesized. In this work, the intermediate 4-(1,3-dioxoisoindolin-2-yl)benzaldehyde compound (I), was formed by reaction of 4-amino benzaldehyde with phthalic anhydride in glacial acetic acid(GAA). A series of Schiff bases (IV-VI) was prepared by the reaction of benzidine with compound (I) in ethanol and presence of GAA as a catalyst to form compound (IV) which react with compound (I) and p-nitro benzyldehyde to give compound (V) and (VI) respectively. A new phthalimide thiosemi-carbazone derivative (ll) was prepared by reaction of compound (l) with thiosemi-carbazide HCl in the presence of equimolar amount of sodium acetate. Fina
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Objective: Benzoxazole derivatives have antifungal, anticancer, antibacterial, and anticonvulsant function. Encouraged by this comment, we agreed to synthesize new Benzoxazole compounds connected to the bases of Schiff's. Methods: 2,4-diaminophenol (1) was prepared by the reaction of 2,4-dinitrophenol and sodium dithionate. Compound (1) reacted with either acetic acid to afford compound (2) or with formic acid to afford compound (3). The Schiff bases were preparation from the reaction condensing reaction of compound (2) or (3) and aromatic aldehydes or ketone; [p-nitrobenzaldehyde, p-hydroxybenzaldehyde, p-chlorobenzaldehyde, p-bromoacetophenone and terephthaldehyde]. Results: FTIR and 1H-NMR spectroscopy characterized all of the pr
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