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METRICS

8
Pubs

CONTACT

PROFILES

SKILLS

RESEARCH SKILLS Data Analysis: Microsoft Excel
Microsoft PowerPoint. Synthetic Organic Chemistry Techniques: Drug design and synthesis of small & large molecules
docking studies
Manual and automatic flash chromatography (normal-phase
reverse-phase
ion-exchange
affinity-chromatography)
HPLC
ESI mass spectrometry
PH-meter
melting point determination
recrystallization
distillation. Characterization Techniques: UV/Vis spectroscopy
IR spectroscopy
NMR spectroscopy (1H & 13C
31P)
and Mass spectroscopy. Computer skills: Chemdraw
Endnote
Microsoft Office
SciFinder
Topspin. Data Analysis: Microsoft Excel
Microsoft PowerPoint. Language: English
Arabic.

LANGUAGES

EN (C1)

علي حيدر حمزة علوش

Lecturer
Pharmacy • College of Pharmacy • AL-Turath University

ABOUT

EXPERIENCE Al Yarmouk Teaching Hospital (Ministry of Health, Baghdad, Iraq, March 2009- March 2010). Pharmacist under training. Management of medicine supply and health equipment to different hospital departments. Work in concert with physicians to administer safe drug therapy regimens. Ministry of health representative to fulfill the hospital needs of medicines from the private sector. Seminar presenting and weekly report of newly admitted cases at the hospital. The University of Baghdad, College of Pharmacy (Ministry of Higher Education and Scientific Research, Baghdad, Iraq, March 2010- August 2018). Laboratory instructor in the clinical pharmacy department (March 2010- March 2011). Teaching students in the final fifth year how to conduct the patient health information. Preparing and managing exams and quizzes in clinical pharmacy courses and ethics. Laboratory instructor in the pharmaceutical chemistry department (March 2011- July 2014). Laboratory and chemicals inventory and design for undergraduate students’ organic and inorganic chemistry experiments in safety protocol procedures. Monitoring students’ progress in performing their experiment independently with the growing ability to identify unknown chemicals by following specific guidelines. Licensed pharmacist (Iraq, 2012-present). Visiting lecturer Al Yarmouk College, Pharmacy Department (Iraq, Baghdad, 2011-2012). Al Israa College, Pharmacy Department (Iraq, Baghdad, Fall 2013). Al Rafedien College, Pharmacy Department (Iraq, Baghdad, 2017-2018). Teaching assistant, The University of Toledo, Toledo, Ohio, Aug 2015-present. MBC 3310 Medicinal Chemistry I: Drug Action and Design (Fall 2015, 2016). MBC 3880 Medicinal and the Biological Chemistry Laboratory (Fall 2019, 2020). MBC 3860 Microbiology for Pharmaceutical Professionals (Spring 2019, 2020, 2021, 2023). MBC 3552 Physiological Chemistry II Cellular Metabolism and Homeostasis (Spring 2021, 2022, 2023). Design the experiments and set up the lab for the active learning synthesis section. Grading of lecture homework. Proctoring midterms and final exams.

RESEARCH INTERESTS

PROJECTS Design, Synthesis, and biological evaluation of PF543 Analogs as Two Pore Channel Blockers. More than 100 compounds were synthesized by introducing different steric and electronic chemical groups. Extensive structural-activity relationship studies were collected from the synthesized compounds.  The purity standard of the final compound was achieved by complete NMR and mass characterization along with HPLC analysis. Sea urchin egg homogenate was used as a golden standard to evaluate the inhibitory action of PF543 analogs to block NAADP- Calcium mediated release through the two-pore channel. DO.11.10 cells were used as another biological assay to explore the most potent compounds. Off-target activity, such as Sphingosine kinase II inhibition, was also studied using a human sphingosine kinase kit. Synthesis of 2’- Hydroxymethyl Cytidine as a Potential Inhibitor for Hepatitis C Virus Polymerase Enzyme. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1470333250. (Master thesis 2016). 2’-Modified nucleoside was successfully synthesized with complete characterization to work as a chain terminator targeting NS5P HCV polymerase enzyme. Docking program was helped and guided to develop other sets of Sofosbuvir analogs as potent antiviral agents. Repeat with modified synthetic procedures, synthesis of 5’-Pseudouridine radical precursors as a research tool to study the oxidative RNA damages. Developed and design new productive procedures to synthesize the fully protected Pseudouridine on the gram scale starting from protected ribose. Synthesis of cyclic-di-GMP as an essential component in some gram-negative biofilm components.

PROFESSIONAL EXPERIENCE

LAB INSTRUCTOR
COLLEGY OF PHARMACY UNIVERCITY OF BAGHDAD
ASSISTANT LECTURER
COLLEGY OF PHARMACY-UNIVERSITY OF BAGHDAD
TEACHING ASSISTANT
-USAUNIVERSITY OF TOLEDO

PUBLICATIONS (8)

  1. Synthesis, docking study, and structure-activity relationship of novel anti-tumor 1, 2, 4 triazole derivatives incorporating 2-(2, 3- dimethyl aminobenzoic acid) moiety.
  2. Multifunctional Nanoparticle-Based Nutraceuticals in Targeted Therapeutics
  3. Understanding the involvement of sphingosine kinase-1 and two-pore channels in calcium signaling in T cells. The Journal of Immunology (2023)
  4. Synthesis, docking study, and structure activity relationship of novel anti-tumor 1, 2, 4 triazole derivatives incorporating 2-(2, 3-dimethyl aminobenzoic acid) moiety. Pharmacia (2022)
  5. Investigating the Potential of Multifunctional Nanoparticle-Based Nutraceuticals in Targeted Therapeutics. Handbook of Nanotechnology in Nutraceuticals (2022)
  6. Major Drivers for COVID-19 Vaccine Acceptance: A Scoping Review. Al-Rafidain Journal of Medical Sciences (ISSN 2789-3219) (2022)
  7. Lead optimization and biological evaluation of diazenylbenzenesulfonamides inhibitors against glyoxalase-I enzyme as potential anticancer agents. Bioorganic Chemistry (2022)
  8. Design, synthesis, and molecular docking studies of 5‐bromoindole‐2‐carboxylic acid hydrazone derivatives: in vitro anticancer and VEGFR‐2 inhibitory effects. ChemistrySelect (2022)
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