Prof. Dr. Nadhir Najim Abdullah Jafar

@alzahraa.edu.iq

Pharmacy College/ Dept. of Pharmaceutical Chemistry
University of Al-zahraa for Women

EDUCATION

Dr. organic chemistry synthesis, study Anti-cancer and Anti-Viral activity for synthetic compounds. Aim of our research is get the advantage of the molecular modeling advanced studies to define the pharmacophore core of the anticancer active analogs that are essential for designing the new analogs based on the prediction of the ligand-receptor recognition. Synthesis, structural function analysis and QSAR studies are essential for targeting the viral, cancer, bacteria and fungus.

RESEARCH INTERESTS

Synthesis Organic Compounds, Docking study, Drug development, Synthesis Fluorsences compounds.

Scopus Publications

139

Scholar Citations

Scholar h-index

Scholar i10-index

Scopus Publications

Innovative pathways in Zn-based metal-organic frameworks: Synthesis, characterization, and photocatalytic efficiency for organic dye degradation
Nadhir N.A. Jafar, Rafid Jihad Albadr, Waam Mohammed Taher, Vicky Jain, Subhash Chandra, Rekha M M, Mayank Kundlas, Girish Chandra Sharma, Anita Devi, Mariem Alwan,et al.
Elsevier BV

Design and development of green electrode using graphene oxide modified with L-hypip coated with iron NPs for enantioselective electro-organic cyanation in the presence of NaCl electrolyte
Amer Alhaj Zen, Matheel D. Al-Sabti, Zaman Abdalhussein Ibadi Alaridhee, Mohammed B. Alqaraguly, Nadhir N.A. Jafar, Majid Jabir, Hasan Majdi, Elyor Berdimurodov, Maryam hussein abdulameer, Aiham O. Altayeh,et al.
Elsevier BV

Universal data-driven models to estimate the solubility of anti-cancer drugs in supercritical carbon dioxide: Correlation development and machine learning modeling
Farag M.A. Altalbawy, Nadhir N.A. Jafar, Dharmesh Sur, Anupam Yadav, Subbulakshmi Ganesan, Aman Shankhyan, M. Ravi Kumar, Girish Chandra Sharma, Iskandar Shernazarov, Sarah Qutayba Badraldin,et al.
Elsevier BV

Gadolinium (Gd)-based nanostructures as dual-armoured materials for microbial therapy and cancer theranostics
Nadhir N. A. Jafar, Junainah Abd Hamid, Farag M. A. Altalbawy, Pawan Sharma, Abhishek Kumar, Shirin Shomurotova, Rafid Jihad Albadr, Kamil K. Atiyah Altameemi, Hawraa Mahdi Saleh, Fakhri Alajeeli,et al.
Informa UK Limited
Gadolinium (Gd) nanoparticles hold significant promise in medical theranostics due to their unique properties. This review outlines the synthesis, characterisation, and applications of Gd nanostructures in combating microbial threats and advancing cancer theragnostic strategies. Synthesis methods such as co-precipitation, microemulsion, and laser ablation are discussed, alongside TEM, SEM, and magnetic characterisation. The antimicrobial efficacy of Gd nanostructures, their potential in combination therapy, and promising anticancer mechanisms are explored. Biocompatibility, toxicity, and regulatory considerations are also evaluated. Challenges, future perspectives, and emerging trends in Gd nanostructure research are highlighted, emphasising their transformative potential in medical applications.

Novel Eco-Friendly Electrode: Copper Nanoparticle-Doped MWCNTs for Green Electro-Organic Synthesis of 1,2,3-Triazoles With ChCl/Urea as a Solvent and Cocatalyst
Ali Basem, Shomansur Sh. Sagdullaev, Zaman Abdalhussein Ibadi Alaridhee, Aiham O. Altayeh, Nadhir N. A. Jafar, Majid S. Jabir, Hasan Majdi, Ameer H. Al‐Rubaye, Moamel Dheyaa Jumaah, Lola M. Usmonova,et al.
Wiley
ABSTRACTMeticulous electrode design is pivotal in advancing greener and more sustainable electro‐organic synthesis practices. In this research, our team designed and synthesized a copper‐doped electrode on multiwalled carbon nanotubes (MWCNTs) and characterized it using Fourier transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), energy‐dispersive X‐ray spectroscopy (EDS), thermogravimetric analysis (TGA), Brunauer–Emmett–Teller (BET) analysis, X‐ray diffraction (XRD) analysis, X‐ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV) analysis. Subsequently, this electrode was utilized as a catalyst at the electrode surface, serving as a cathode in electro‐oxidation reactions in the presence of phenylacetylene, sodium azide (NaN3), and benzyl halide for the production of 1,2,3‐triazole derivatives under ambient temperature, within a 30‐min reaction time, and at atmospheric pressure, achieving an efficiency level ranging from good to excellent, specifically between 88% and 96%. The synthesized 1,2,3‐triazole derivatives were identified using proton nuclear magnetic resonance (1H NMR) spectroscopy, CHN elemental analysis, and melting point. In this paper, choline chloride/urea deep eutectic solvents (DES) serve multiple roles in the reaction mechanism. They function as solvents and co‐catalysts, generate weak bases, and provide numerous advantages in green chemistry. These advantages include low toxicity, reduced environmental risks, improved atom economy, and non‐volatility, making them safer alternatives to traditional organic solvents.

Mathematical modeling of ions adsorption from water/wastewater sources via porous materials: A machine learning-based approach
Guang Yang, Nadhir N.A. Jafar, Rafid Jihad Albadr, Mariem Alwan, Zainab Sadeq Yousif, Suhair Mohammad Husein Kamona, Safaa Mohammed Ibrahim, Usama S. Altimari, Ashwaq Talib Kareem, Raghu Jettie,et al.
Elsevier BV

Simulation study of a practical approach to enhance cadmium removal via biological treatment by controlling the concentration of MLSS
Basim K. Nile, Ahmed M. Faris, Hasan F. Alesary, Nadhir N. A. Jafar, Hani K. Ismail, Muhammad Abdulredha, Maad F. Al Juboury, Waqed H. Hassan, Luma M. Ahmed, Hussein Rasool Abid,et al.
Springer Science and Business Media LLC
AbstractThe fate of cadmium at the Muharram Aisha wastewater treatment plant in Karbala governorate, Iraq was studied using the TOXCHEM model. Cadmium, a known carcinogen, and is considered one of the most dangerous heavy metals and high concentrations, greater than permissible limits, were found in the treated wastewater. The plant operates using an activated sludge system and this was modeled via TOXCHEM with a sensitivity analysis carried out on the extended aeration system. Prior to analysis, the model was calibrated and validated for cadmium, with the adjustments leading to a mean square error (RMSE) and correlation coefficient (R) of 0.0001 and 0.81, respectively. The mass balance of cadmium in the Muharram Aisha treatment plant was found to be 4832.44 g/day (37.1726%) in the treated wastewater and 8164.52 g/day (62.804%) in the sludge, which indicated that the mix liquor suspended solid (MLSS) was the most sensitive factor. The sensitivity to cadmium was analyzed via MLSS in the extended aeration system and the results o indicated that the higher the MLSS concentration (mg/L), the greater the removal of cadmium in the treated wastewater. It was found that increasing the MLSS through a biological treatment method reduced the concentration of cadmium without the need for additional of any (potentially harmful) chemical treatments. The plant was subsequently operated for a period of 5 months with the MLSS increased from 1500 to 4500 mg/L, and this reduced the concentration of cadmium in the wastewater from 0.36 to 0.01 mg/L as a consequence. This research demonstrates how the novel application of TOXCHEM can be a useful tool in the reduction of heavy metal contamination in the environment.

Synthesis of innovative Daphne mucronata extract/Cu-MOF/PVA-PVP nanofiber as high-performance anticancer and antimicrobial agent
Ali Altharawi, Nadhir N.A. Jafar, Taibah Aldakhil, and Tareq Jwad Kazem
Elsevier BV

Recent progress in ZnO-based heterostructured photocatalysts: A review
Irshad Ahmad, R. Bousbih, Ahmed Mahal, Waheed Qamar Khan, Mohammed Aljohani, Mohammed A. Amin, Nadhir N.A. Jafar, Majid S. Jabir, Hasan Majdi, Ali S. Alshomrany,et al.
Elsevier BV

A theoretical investigation for improving the performance of non-fullerene organic solar cells through side-chain engineering of BTR non-fused-ring electron acceptors
Sidra Moeed, R. Bousbih, Ali Raza Ayub, Nadhir N.A. Jafar, Mohammed Aljohani, Majid S. Jabir, Mohammed A. Amin, Hira Zubair, Hasan Majdi, Muhammad Waqas,et al.
Elsevier BV

Microwave-assisted synthesis, characterization, and in vitro biological evaluation of a novel nanocomposite using molybdenum and [2,2′-bipyridine]-4,4′-dicarboxylic acid
Mohamed J. Saadh, Nadhir N.A. Jafar, Farag M. A. Altalbawy, Pawan Sharma, Abhishek Kumar, Hassan Thoulfikar A. Alamir, Hameed Ghazy, Maha Noori Shakir, Saad khudhur Mohammed, Khursheed Muzammil,et al.
Royal Society of Chemistry (RSC)
Novel Mo/BPDA nanocomposite with crystalline structure, high thermal stability and specific surface area was synthesized. The Mo/BPDA nanocomposite was effective against a wide range of microbial species, bone cancer cells and breast cancer cells.

Highly efficient electrocatalytic oxidation of levodopa as a Parkinson therapeutic drug based on modified screen-printed electrode
Tan Wang, Nadhir N.A. Jafar, Afrah Majeed Ahmed Al-Rihaymee, Dheyaa Yahaia Alhameedi, Fadhil A. Rasen, Furqan S. Hashim, Talib Kh Hussein, Montather F. Ramadan, Kasim Kadhim Alasedi, Muath Suliman,et al.
Elsevier BV

Synthesis and characterization of Cu-modified ox-g-C<inf>3</inf>N<inf>4</inf> nanosheets as an electrode for green synthesis of phenyl Benzofuran derivatives via C–H functionalization to C–O and C–C bond formation with an electrochemical oxidation system
Zaman Abdalhussein Ibadi Alaridhee, Dheyaa J. Jasim, Ikromjon Mamadoliyev, Moayad Jasim Mohammed, Abdul-Jabbar A. Ali, Ayat H. Athab, Salim S. Al-Rejaie, Mohamed Mohany, Majid Jabir, Hasan Majdi,et al.
Springer Science and Business Media LLC

Utilizing a copper foam electrode as the catalyst in Sonogashira C-H activation coupling reactions for the electro-oxidation synthesis of diphenylethyne derivatives
Ameer H. Al-Rubaye, Salim S. Al-Rejaie, Zaman Abdalhussein Ibadi Alaridhee, Mohamed Mohany, Hawzhen Fateh M. Ameen, Nadhir N.A. Jafar, Dheyaa J. Jasim, Hasan Majdi, Abhinav Kumar, Mohammed A. Al-Anber,et al.
Elsevier BV

Elucidating the Mechanism of Tetrahydrofuran-Diol Formation through Os(VI)-Catalyzed Oxidative Cyclization of 5,6-Dihydroxyalkenes Ligated by Citric Acid
Aqeel A. Hussein, Nadhir N. A. Jafar, and Yumiao Ma
American Chemical Society (ACS)
A computational study is reported here on the mechanism of tetrahydrofuran (THF)-diol formation from the Os(VI)-catalyzed oxidative cyclization of 5,6-dihydroxyalkene ligated with citric acid and in the presence of Bro̷nsted acid. Initiated by Os(VI) dioxo citrate formation, coordination of co-oxidant pyridine-N-oxide (PNO) and protonation of its oxo group generate the active catalyst. The catalytic cycle commences through successive steps, including dihydroxyalkene addition to the active catalyst in a concerted mechanism to form hexacoordinated alkoxy-protonated PNO-complexed Os(VI) bisglycolate as a turnover-limiting step (TLS), cyclization to Os(IV) THF-diolate, reoxidation to Os(VI) THF-diolate, and hydrolysis via a dissociative mechanism to furnish the THF-diol and regenerate the active species, sustaining the catalytic cycle through an Os(VI)/Os(IV) cycle. Despite the overall exergonic nature of catalytic cycle (ΔGrcycle = -45.0 kcal/mol), the TLS is accelerated by the formation of an open-valence 16-electron Os(VI) intermediate but decelerated by the undesired formation of a saturated/hexacoordinate 18-electron Os(VI) intermediate. Bro̷nsted acid plays crucial roles in the formation of Os(VI) citrate and the active catalyst, impediment of the second cycle, and the cyclization step. Additionally, besides its role as a co-oxidant, and in the presence of acid, PNO is found to assist the insertion of dihydroxyalkene and, importantly, in releasing the THF-diol to regenerate the active intermediate.

Generation of Surface Plasmon Polaritons (SPPs) at Chiroplasma-Metal Interface
R. Bousbih, M. S. Soliman, N. N. A. Jafar, M. S. Jabir, H. Majdi, A. S. Alshomrany, N. M. A. Hadia, M. Shaban, Y. A. El-Badry, and M. Iftikhar
Springer Science and Business Media LLC

Suzuki reaction for the synthesis of new derivatives of 4-Chloro-3,5-dimethyl phenol and their in vitro antibacterial screening
R.H. Zaooli, F.A. Hussein, N.N.A. Jafar, and S.N.K. Al-Thamir
Asian Journal of Chemistry
Many derivatives of 4-chloro-3,5-dimethylphenol have been synthesized using Suzuki reaction and characterized by IR, 1H NMR and micro elemental analysis. These compounds also tested in terms of their antibacterial properties against Staphylococcus aureus, Escherichia coli and Proteus mirabilis.

Synthesis and spectral studies of novel Palladium (O) complex with ciprofloxacin antibiotic

The antifungal effect of some 4-chloro-6-methoxy-N, N-dimethylpyrimidin-2-amine derivatives containing a heterocyclic compound on the important types of fungi
Nadhir N.A. Jafar, Ibtihial M Abdul Mahdi, Mahmoud Hussein Hadwan, and Ameer A Alameri
EManuscript Technologies
Objective: 4-methoxy-N, N-dimethyl-6-(phenylthio) pyrimidin-2-amine, 4-(benzo[d]thiazol-2-ylthio)-6-methoxy-N,N-dimethylpyrimidin-2-amine, 4-(4-(1,2,3-selenadiazol-4-yl)phenoxy)-6-methoxy-N,N 2-amine and 4-(4-(1,2,3-thiadiazol-4-yl)phenoxy)-6-methoxy-N,N 2-amine have been synthesized. Method: The prepared compounds were synthesized by nucleophilic displacement of chloride substituted in pyrimidine heterocyclic ring. Results: The synthesized compounds were being identified by different methods included TLC technique, IR, 1H-NMR and 13C-NMR spectrophotometers. All compounds confirmed by elemental analysis. The biological activity of these new compounds investigated against some fungi like Aspergillus terreus and Aspergillus niger, the results was Aspergillus terreus more effected by antifungal compare with Aspergillus niger, the effect ration 0.98, 1.32 with 200μM respectively and the compound number (2) has more effect than other compounds. Conclusion: It is concluded that synthesized dimethylpyrimidin-derivatives are biologically active and developed into useful Antifungal agents. Key words: Pyrimidine, Dimethylpyrimidin-derivatives, Heterocyclic compound, Aspergillus terreus, Aspergillus niger.

Study the effect verifies of the number of moles of acrylic acid monomer on swelling of the new prepared modified co-polymer

Microwave assisted synthesis of amide derivatives of the drug ciprofloxacin and screening the biological properties

Synthesis of new analogues of drug 'Monastrol' via Biginelli reaction

Exploration of the in vitro antiviral activity of a series of new pyrimidine analogues on the replication of HIV and HCV
Nadhir NA Jafar, Najim A Al-Masoudi, Sadiq J Baqir, Pieter Leyssen, and Christophe Pannecouque
SAGE Publications
Background: In continuation of our search for new anti-HIV and anti-HCV agents, the suggestion, synthesis and structure elucidation of a new series of 2,6-diamino-4-alkylthio- or (2-benzylhydrazinyl)-5- p-chlorophenylazopyrimidines), 2,6-diamino-4-(2-benzylhydrazinyl)-5-(aryl-[1,1′-biphenyl]-4-yl)pyrimidines, 2,6-diamino-4-(aryl)-5-(aryl[1,1′-biphenyl]-4-yl) pyrimidines), 6-(aryl)-1,3-dimethyl-5-nitro pyrimidine-2,4-dione and 6-amino-4-methoxy- N,N-dimethyl-6-arylpyrimidines were described. Methods: The anti-HIV-1 (strain IIIB) and HIV-2 (strain ROD) activity of the newly synthesized pyrimidine analogues was evaluated in vitro in human MT-4 cells using the MT-4/MTT assay. Similarly, the same compounds were evaluated in vitro for their selective antiviral activity against HCV in the Huh 5–2 replicon system (type 1b, Con1 strain). Results: None of the tested compounds exhibited inhibition of HIV-1 and HIV-2 replication in cell culture. Even though many compounds yielded a 50% effective concentration in the HCV replicon system with selectivity indexes up to 6.9, none of the compounds matched the selection criteria of a selective inhibitor of virus replication in this assay (that is, >70% inhibition at concentrations that do not elicit an anti-metabolic effect on the host cells). Conclusions: Structural modification of these compounds might optimize their anti-HCV activity by introducing diverse and potent functional groups at the pyrimidine backbone, like nitrile residue. Because of the nature of the molecules, these new derivatives will also be evaluated for their potential anti-HIV activity.

Synthesis and biological activity of new derivatives of 6-chloro-5-((4-chlorophenyl)diazenyl)pyrimidine-2,4-diamine and 4-chloro-6-methoxy-N,N-dimethylpyrimidin-2-amine
Nadhir Najimabdullah Jafar, Hussein Oleiwi Muttaleb Al-Dahmoshi, Ayad Mohammed JeburAlmamoori, Noor Salman Kadhim Al-Khafajii, and NajimAbod Al-Masoudi
Oriental Scientific Publishing Company
6-chloro-5-((4-chlorophenyl) diazenyl) pyrimidine-2, 4-diamine and 4-chloro-6-methoxy-N,Ndimethylpyrimidin-2-amine has been used as precursors for the synthesis of new pyrimidine derivatives, employing Suzuki cross-coupling reaction. Thus, treatment of pyrimidine derivative with various arylboronic acids in the presence of palladium tetraacetate, PhP3 and Na2CO3 in refluxing n-propanol afforded the target compounds. The synthesis was supported by spectroanalytical techniques. The synthesized compounds have been screened for their inhibitory activity against some microbial, the results were showed that among gram positive isolates only (1/10) isolates of S. aureus and (3/10) isolates of S. saprophyticaus were sensitive for compound 13, while (1/10) isolates of S. aureus and (1/10) isolates of S.saprophyticaus were sensitive for compound 4. All isolates of S. pyogenes were resisting to all compounds, among gram negative bacterial isolates only (2/10) isolates of E. coli and (1/10) isolates of K. pneumoniae were sensitive to compound 4. Concerning the antifungal effects of compounds 3, 4, 5, 13, 14, 15 the results revealed that, all C. albicans and C. glabrata isolate were resist these compounds.

Synthesis and anti-HIV activity of new benzimidazole, benzothiazole and carbohyrazide derivatives of the anti-inflammatory drug indomethacin
Najim A. Al-Masoudi, Nadhir N. A. Jafar, Layla J. Abbas, Sadiq J. Baqir, and Christophe Pannecouque
Walter de Gruyter GmbH
There is an urgent need for the design and development of new and safer drugs for the treatment of HIV infection, active against the currently resistant viral strains. New derivatives of the non-steroidal anti-inflammatory drug indomethacin bearing benzimidazoles, benzothiazole, purine and pyridine residues 8 - 13 were synthesized with the aim of developing new non-nucleoside reverse transcriptase inhibitors (NNRTIs).Alternatively, new imine analogs 16 - 20 were synthesized from condensation of indomethacinyl hydrazide 15, prepared from the ester 14, with various ketone precursors. Treatment of 15 with phenyl isothiocyanate or triethyl orthoformate afforded the phenylcarbonothioyl and the oxadiazole derivatives 21 and 22, respectively. The new compounds were assayed against HIV-1 and HIV-2 in MT-4 cells. Compounds 9 and 10 were the most active in inhibiting HIV-2 and HIV-1, respectively, with EC50 ≥ 17.60 μgmL−1 and > 1.15 μgmL−1 (therapeutic indexes (SI) of ≥ 3 and < 1, respectively), and are leading candidates for further development.

RECENT SCHOLAR PUBLICATIONS

Gadolinium (Gd)-based nanostructures as dual-armoured materials for microbial therapy and cancer theranostics
NNA Jafar, J Abd Hamid, F MA Altalbawy, P Sharma, A Kumar, ...
Journal of Microencapsulation, 1-27 2025

Innovative Pathways in Zn-Based Metal-Organic Frameworks: Synthesis, Characterization, and Photocatalytic Efficiency for Organic Dye Degradation
NNA Jafar, RJ Albadr, V Jain, S Chandra, R MM, M Kundlas, GC Sharma, ...
Journal of Organometallic Chemistry, 123572 2025

Design and development of green electrode using graphene oxide modified with L-hypip coated with iron NPs for enantioselective electro-organic cyanation in the presence of NaCl
AA Zen, MD Al-Sabti, ZAI Alaridhee, MB Alqaraguly, NNA Jafar, M Jabir, ...
Journal of Molecular Structure 1322, 140537 2025

Universal data-driven models to estimate the solubility of anti-cancer drugs in supercritical carbon dioxide: Correlation development and machine learning modeling
FMA Altalbawy, NNA Jafar, D Sur, A Yadav, S Ganesan, A Shankhyan, ...
Journal of CO2 Utilization 92, 103021 2025

Novel Eco‐Friendly Electrode: Copper Nanoparticle‐Doped MWCNTs for Green Electro‐Organic Synthesis of 1, 2, 3‐Triazoles With ChCl/Urea as a Solvent and Cocatalyst
A Basem, SS Sagdullaev, ZAI Alaridhee, AO Altayeh, NNA Jafar, MS Jabir, ...
Applied Organometallic Chemistry 39 (1), e7789 2025

Mathematical modeling of ions adsorption from water/wastewater sources via porous materials: A machine learning-based approach
G Yang, NNA Jafar, RJ Albadr, M Alwan, ZS Yousif, SMH Kamona, ...
Chemometrics and Intelligent Laboratory Systems 255, 105250 2024

Synthesis of innovative Daphne mucronata extract/Cu-MOF/PVA-PVP nanofiber as high-performance anticancer and antimicrobial agent
A Altharawi, NNA Jafar, T Aldakhil, TJ Kazem
Inorganic Chemistry Communications 169, 113092 2024

Recent progress in ZnO-based heterostructured photocatalysts: A review
I Ahmad, R Bousbih, A Mahal, WQ Khan, M Aljohani, MA Amin, NNA Jafar, ...
Materials Science in Semiconductor Processing 180, 108578 2024

A theoretical investigation for improving the performance of non-fullerene organic solar cells through side-chain engineering of BTR non-fused-ring electron acceptors
S Moeed, R Bousbih, AR Ayub, NNA Jafar, M Aljohani, MS Jabir, ...
Journal of Molecular Graphics and Modelling 131, 108792 2024

Highly efficient electrocatalytic oxidation of levodopa as a Parkinson therapeutic drug based on modified screen-printed electrode
T Wang, NNA Jafar, AMA Al-Rihaymee, DY Alhameedi, FA Rasen, ...
Heliyon 10 (14) 2024

Synthesis and characterization of Cu-modified ox-g-C₃N₄ nanosheets as an electrode for green synthesis of phenyl Benzofuran derivatives via C–H
ZAI Alaridhee, DJ Jasim, I Mamadoliyev, MJ Mohammed, AJA Ali, ...
Research on Chemical Intermediates 50 (7), 3053-3077 2024

Utilizing a copper foam electrode as the catalyst in Sonogashira CH activation coupling reactions for the electro-oxidation synthesis of diphenylethyne derivatives
AH Al-Rubaye, SS Al-Rejaie, ZAI Alaridhee, M Mohany, HFM Ameen, ...
Journal of Molecular Structure 1305, 137757 2024

Elucidating the Mechanism of Tetrahydrofuran-Diol Formation through Os (VI)-Catalyzed Oxidative Cyclization of 5, 6-Dihydroxyalkenes Ligated by Citric Acid
AA Hussein, NNA Jafar, Y Ma
The Journal of Organic Chemistry 89 (10), 6892-6902 2024

Generation of surface plasmon polaritons (SPPs) at chiroplasma-metal interface
R Bousbih, MS Soliman, NNA Jafar, MS Jabir, H Majdi, AS Alshomrany, ...
Plasmonics, 1-6 2024

Simulation study of a practical approach to enhance cadmium removal via biological treatment by controlling the concentration of MLSS
BK Nile, AM Faris, HF Alesary, NNA Jafar, HK Ismail, M Abdulredha, ...
Scientific Reports 14 (1), 1714 2024

Pyrimidine Derivatives as Promising Candidates for Potent Antiangiogenic: A silico Study
NNA Jafar
J Contemp Med Sci 7 (6), 353-357 2021

Suzuki Reaction for the Synthesis of New Derivatives of 4-Chloro-3,5-Dimethyl Phenol and their in vitro Antibacterial Screening
NNA Jafar
Asian Journal of Chemistry 13 (12), 2995 2019

Synthesis and Spectral Studies of Novel Palladium ( Novel Palladium ( Novel Palladium ( 0) Complex ) Complex ) Complex with Ciprofloxacin Antib
NNAJ N.S. Majeed, I.K. Kareem
International Journal of Engineering & Technology 7 ((4,36)), 722-724 2018

The Antifungal Effect of some 4-Chloro-6-Methoxy-N, N-Dimethylpyrimidin-2-Amine Derivatives Containing a Heterocyclic Compound on the Important types of Fungi
A Nadhir N. Jafar, Ibtihial M Abdul Mahdi, Mahmoud Hussein Hadwan, Ameer A
Journal of Young Pharmacists 9 (4), 463-467 2017

MOST CITED SCHOLAR PUBLICATIONS

Synthesis and anti-HIV activity of new benzimidazole, benzothiazole and carbohyrazide derivatives of the anti-inflammatory drug indomethacin
NA Al-Masoudi, NNA Jafar, LJ Abbas, SJ Baqir, C Pannecouque
Zeitschrift fr Naturforschung B 66 (9), 953-960 2011
Citations: 21

synthesis and biological activity of new derivatives of 6-chloro-5-((4- chlorophenyl) diazenyl) pyrimidine-2,4-diamine and 4-chloro-6-methoxy- N,N-dimethylpyrimidin-2-amine
NNA Jafar
IOSR Journal of Pharmacy 4, 26-36 2014
Citations: 18

Microwave assisted synthesis of amide derivatives of the drug ciprofloxacin and screening the biological properties
NNA Jafar
International Journal of ChemTech Research 9 (7), 387-395 2016
Citations: 17

Exploration of the in vitro antiviral activity of a series of new pyrimidine analogues on the replication of HIV and HCV.
NNA jafar
Antiviral chemistry and chemotheraphy 23, 103-112 2013
Citations: 17

Microwave-assisted synthesis and biological activity of ester, carbothioate and carbohydrazide derivative compounds of the drug Ciprofloxacin
NSM Nadhir N. A. Jafar *
Journal of Chemical and Pharmaceutical Sciences 10 (1), 515-521 2017
Citations: 11

Study The Effect Verifies of the Number of Moles of Acrylic Acid Monomer On Swelling of the New Prepared Modified Co-Polymer
RHZ Mohammad N AL-Baiati , Nadhir NA Jafar
Research Journal of Pharmaceutical, Biological and Chemical Sciences 7 (5 2016
Citations: 8

Generation of surface plasmon polaritons (SPPs) at chiroplasma-metal interface
R Bousbih, MS Soliman, NNA Jafar, MS Jabir, H Majdi, AS Alshomrany, ...
Plasmonics, 1-6 2024
Citations: 3

Pyrimidine Derivatives as Promising Candidates for Potent Antiangiogenic: A silico Study
NNA Jafar
J Contemp Med Sci 7 (6), 353-357 2021
Citations: 2

Criss-cross Cycloadditions on Ketazine Derived from Polyvinyl Ketone Polymer
NNA Jafar
Research Journal of Pharmaceutical, Biological and Chemical Sciences 7 (6 2016
Citations: 1

Synthesis of New Analogues of drug 'Monastrol' via Biginelli Reaction
AKM Nadhir NA Jafar*, Abbas Noor Mohammed
Research Journal of Pharmaceutical, Biological and Chemical Sciences 6 (5), 906 2015
Citations: 1

Synthesis of N-(4-Chlorophenyl)-2-methoxy-4-methylbenzamide and Spectrofluorometric Study
ANM Al-Sharify, NNA Jafar, AK Madlool
Iraqi National Journal of Chemistry 14 (56), 11-11 2014
Citations: 1