Antibacterial Evaluation, In Silico Study and ADMET Properties of Local Lawsonia inermis Leaves Extract Zainab Abdulhussein, Munther Muhammad-Ali, Ekhlas Jasim Tropical Journal of Natural Product Research, 2025 Plant extracts are important in the treatment of many bacterial infections, including henna extracts. Pharmacognosy have become an alternative to traditional medications because of a synergistic effect in combating bacterial infections and no multiple side effects. This investigation examined the antibacterial efficacy of Lawsonia inermis acetone extract against bacteria isolated from urinary tract infections (UTIs) and wounds, including Pseudomonas aeruginosa, Staphylococcus aureus, Klebsiella pneumonia, and Escherichia coli. To isolate the pathogenic bacteria (P. aeruginosa, S. aureus, K. pneumonia, and E. coli), clinical pathogenic samples were obtained. Acetone extract of Lawsonia inermis leaves was produced using Soxhlet extraction and the solution of solid extract was investigated by the cork borer technique which gave an inhibitory zone of 18 to 22 mm against the four species of bacteria. 16 phytocompounds (1a–1p) were identified in the extract using gas chromatography-mass spectrophotometry (GC–MS) peak area percentage (10.66-1.72%). The analysis of phytochemicals using molecular docking simulations of their antibacterial potential revealed binding affinities of – 4.38 to – 7.83 kcal/mol, – 4.67 to – 7.47 kcal/mol, – 5.06 to – 9.07 and – 4.41 to – 7.30 kcal/mol against the dihydropteroate synthase and gyrase B 24kDa proteins of E. coli, and TyrRS and gyrase B proteins of S. aureus, respectively. The extract phytochemicals were subjected to physicochemical parameters evaluation: ADMET predictions. Pharmacokinetic prediction indicates fewer adverse effects. The extract has potential antimicrobial activity, with higher levels of clinical safety based on ADMET predictions.
Synthesis, Molecular Docking Study and Antimicrobial Evaluation of Some 1,2,4-Triazole Compounds Munther Abduljaleel Muhammad Ali, Ekhlas Qanber Jasim, Abeer Issa Mohammed Indian Journal of Pharmaceutical Education and Research, 2025 Aim: The objective of this study is synthesis of 1,2,4-triazole derivatives, evaluation there in vitro antimicrobial activity and showing the molecular docking. Materials and Methods: Two series of 5-alkylthio-3-aryl-4-phenyl-1,2,4-triazoles were successfully synthesized. The 1,2,4-triazole thiol was produced via cyclization reaction using the hydrazide compounds (2-hydroxybenzohydrazide and 5-bromofuran-2-carbohydrazide), which were then employed as nucleophilic species to attract various kinds of alkyl halides to synthesis the final compounds. All produced compounds underwent spectroscopic characterization and tested their antibacterial and antifungal activities. With synthetic ligands, molecular docking studies were conducted against the proteins 1AJ0, 1JIJ, and 4ZA5 to identify the crucial interactions underlying antimicrobial activity. Results: UV-visible, FTIR, 1H-NMR and CHNS analysis were confirmed the chemical structures and purity. Initial antibacterial screening results showed that several produced compounds 1e , 1f , 2e , and 2f have good inhibitory effects, whilst some compounds 2e demonstrated high antifungal activity when compared to the control drug fluconazole. Two active substances, 1e and 2e , showed a moderate level of toxicity, with LD 50 values of 3.5 and 2.3 g/kg, respectively. The strongest compounds, 1e , 1f , 2e , and 2f , demonstrated high binding energy antibacterial and antifungal activity, which were supported by docking analysis. Conclusion: Triazole derivatives were synthesized by multi-reaction steps with high yields. Some synthesized triazole derivatives showed promising antibacterial and antifungal activities as compared with parent compounds and standard drugs. The results of antimicrobial activities of compounds were enhanced by good affinity of molecular docking of these compounds with the active site of proteins as compared with standard drugs amoxicillin and fluconazole.
Apelin, C-reactive protein, and serum protein correlation with blood pressure – a biomarker analysis Zahraa Ahmed Mutaeb, Usama H. Ramadhan, Ekhlas Qanber Jasim European Journal of Clinical and Experimental Medicine, 2025 Introduction and aim. Hypertension is a major global health burden and a leading cause of cardiovascular disease and premature death. This study aimed to evaluate the association between serum apelin, inflammatory markers, and protein metabolism parameters in hypertensive patients compared to normotensive controls. This study uniquely explores the interplay between inflammatory and protein metabolism biomarkers using advanced multivariate models in hypertensive adults, a combination not previously examined in this populationMaterial and methods. Two hundred adults aged 35–65 years were divided into hypertensive (n=100) and normotensive (n=100) groups. Serum apelin and C-reactive protein (CRP) levels were measured using enzyme-linked immunosorbent assay, while albumin and total protein were assessed via spectrophotometry. Statistical analyses included t-tests, multiple regression, structural equation modeling (SEM), and Cox regression.Results. Hypertensive patients had significantly higher blood pressure (p<0.001), CRP (7.52±4.21 vs. 1.35±0.51 mg/L; p<0.001), globulin (3.4±1.0 vs. 1.8±0.9 g/dL; p<0.001), and total protein, but lower apelin (2386.2±401.7 vs. 2873.4±572.8 pg/mL; p<0.001) and albumin levels. SEM revealed a direct association between CRP and systolic blood pressure (β=0.45, p<0.001), and a negative association between apelin and systolic pressure (β=−0.20, p=0.03). CRP (HR=1.75, p=0.005) and systolic BP (HR=1.52, p<0.001) were independent predictors of cardiovascular events.Conclusion. The findings suggest that systemic inflammation and dysregulation of serum protein metabolism are significantly associated with hypertension and cardiovascular risk. Apelin may play a protective role by mitigating the impact of inflammation on blood pressure.
Synthesis, Corrosion Inhibition Efficiency in Acidic Media, and Quantum Chemical Studies of Some Hydrazine Derivatives Huda Saleh Abood, Ekhlas Qanber Jasim, Munther Abduljaleel Muhammad-Ali Science and Technology Indonesia, 2024 In this work, four hydrazone Schiff base derivatives N-(2,4-Dinitro-phenyl)-N’-(1H-pyrrol-2-ylmethylene)-hydrazine (1a), N-Benzo [1,3] dioxol-5-ylmethylene-N’-(2,4-dinitro-phenyl)-hydrazine (1b), (E)-5-((2-(2,4-dinitrophenyl)hydrazono)methyl)-2-hydroxybenzoic acid (1c) and (E)-1-(2,4-dinitrophenyl)-2-(2-methoxybenzylidene)hydrazine (1d) were synthesized by reaction of four aldehydes namely pyrrole-2-carboxaldehyde, piperonal, 5-formylsalicylic acid, and o-vanillin with 2,4-dinitrophenyl hydrazine to produce the final compounds 1a, 1b, 1c, and 1d, respectively. These four compounds were investigated as corrosion inhibitors in aqueous mild acidic static solution. FTIR, HNMR, and elemental analysis were used to elucidate the chemical structure of the synthesized inhibitors. Using potential dynamic polarization measurements, these inhibitors’ efficiency in preventing C-steel corrosion in 1.00 M HCl was studied. The results of the experiments revealed that 1×10−3 M is the ideal concentration for 1a, 1b, 1c, and 1d, and that the corresponding inhibition efficiencies for these subunits were 80.70%, 91.30%, 91.34, and 88.80%, respectively. The best corrosion inhibitors were compounds 1b and 1c. Furthermore, studies suggested that these substances are mixed-type inhibitors and that the efficiency of the inhibition is strongly correlated with their quantity. Quantum paraments included Dipole moment, energy band gap (ΔE), value of energy of lowermost unoccupied molecular orbital (ELUMO), and energy of high most occupied molecular orbital (EHOMO) using Molecular Operating Environment MOE, Gaussian, and HyperChem software packages were determined which demonstrated strong agreement between algorithmic and practical findings.
Synthesis, Characterization, and Antibacterial Activity of Some Mesalazine Derivatives Ekhlas Qanber Jasim Science and Technology Indonesia, 2023 Mesalazine, often referred to as mesalamine or 5-aminosalicylic acid (5-ASA), and its derivatives are some of the first medications to be approved for treating digestive tract inflammations, including ulcerative colitis and mild to moderate Crohn’s disease. Sulfasalazine, discovered in 1938 for therapeutic use, was the first mesalazine derivative. High yields of four different mesalazine derivatives were synthesized, including two Schiff bases and two azo compounds. The present study involved the synthesis of Schiff bases through the reaction of mesalazine with pyrrole-2-carbaldehyde or indole-2-carbaldehyde, resulting in the formation of 5-(((1H-pyrrol-2-yl)methylene)amino)-2-hydroxybenzoic acid (1) or 5-(((1H-indol-2-yl)methylene)amino)-2hydroxybenzoic acid (2), respectively. The synthesis of azo compounds involved the coupling of mesalazine with sulfamethoxazole or pyridoxine, resulting in the formation of 5-amino-2-hydroxy-3-((4-(N-(5-methylisoxazol-3-yl)sulfamoyl)phenyl)diazenyl)benzoic acid (3) or 2-hydroxy-5-((5-hydroxy-3,4-bis(hydroxymethyl)-6-methylpyridin-2-yl)diazenyl)benzoic acid (4), respectively. The identification of the synthesized compounds was carried out using IR and 1H-NMR spectroscopy. Antibacterial assessment of the synthetic compounds was performed in vitro against gram-negative bacteria (such as Escherichia coli and Pseudomonas aeruginosa) and gram-positive bacteria (Staphylococcus aureus). The antibacterial activity studies demonstrated that against Escherichia coli and Staphylococcus aureus, the Schiff base compounds are more active than azo compounds. Compound 1 showed the highest activity, resulting in a 23 mm inhibition zone against E. coli at 1000 ug/ml. In contrast, the antibacterial activity of compound 2 was observed to be 25 mm against S. aureus at the same highest concentration.
Antibacterial Efficacy and Molecular Docking of Leaf Extract of Laurus nobilis L Against some Isolated Pathogenic UTI Bacteria Amani Abd Al-Ridha Al-Abdullah, Ekhlas Qanber Jasim, Munther Abduljaleel Muhammad-Ali Iop Conference Series Earth and Environmental Science, 2023 The objective of the current study was to analyze the chemical compositions and antibacterial properties of Laurus nobilis. The bacterial strain was isolated from urine sample of female patients have urinary tract infection in Al-Basrah Teaching Hospital. Two solvents (hot and cold aqueous and ethanol) were used to extract the dried leaves of L. nobilis. While there were differences in the inhibition zones that solvent extracts demonstrated against bacterial pathogens, all of them significantly inhibited pathogens. The diameters of the inhibition zones on Staphylococcus aureus where the alcoholic extract was in the range of 17-29 mm, 22-28 mm for hot water and 12-14 mm for cold aqueous extract. The diameters of the inhibition zones on Klebsiella pneumoniae for alcoholic extract were 18-20 mm, 19-21.5 mm for hot aqueous extract and 12-17 mm for cold water extract. The GC-MS analysis demonstrated the presence of different phytochemical compounds in the extract of Laurus nobilis. A total of 60 compounds were identified, for ethanolic extract, tris (2-methylenecyclopropyl)methanol, (3aS,6aR,9aR,9bS)-3,6,9-trimethylenedecahydroazuleno[4,5-b]furan-2(3H)-one and (3aS,6aR,9aR,9bS)-6-methyl-3,9-dimethylene-3a,4,6a,7,8,9,9a,9b-octahydroazuleno[4,5-b]furan-2(3H)-one were the major compounds with percentage values 9.64%, 8.86% and 7.43%, respectively. For hot water extract, the major three compounds were 5-(hydroxymethyl)furan-2-carbaldehyde 11.64%, 2-methyl-5-nitro-2H-1,2,3-triazol-4-amine 8.39% and tris(2-methylenecyclopropyl)methanol 6.81%. Whereas, for cold water extract, the major compounds were n-Hexadecanoic acid 26.05%, Bis(2-ethylhexyl) phthalate 22.94% and Octadecanoic acid 8.25%. Molecular docking showed that these nine major compounds had an excellent binding affinity -4.25 to -8.56 kcal/mol against S. aureus using protein 1JIJ. The binding affinity of these compounds against K. pneumoniae (protein 6PIB) were in the range - 4.03 to -8.22 kcal/mol.
Theophylline determination in pharmaceuticals using a novel high-performance liquid chromatographic process H.N.K. AL-Salman, Ekhlas Qanber Jasim, Hussein H. Hussein Neuroquantology, 2021 Objective: The current study aims to find a suitable, accurate, and faster RP-HPLC technique for the determination of theophylline, which could then be validated in accordance with the International Conference on Harmonization (ICH) guidelines. The Aim of this Study: The aim of this study was to develop an efficient, accurate, and faster RP-HPLC method for determining theophylline, which was then validated using the International Conference on Harmonization (ICH) guidelines. Methods: In the HPLC analysis, the Waters 2695 was used. The drug was isolated better using an Ion Pac zorbax 300-SCX Agilent Column, 5 m, 4.6 250 mm, with a liquid phase of Orthophosphoric acid (0.1 percent Orthophosphoric acid in HPLC acetonitrile and Methanol in the ratio of 50:50 v/v at a flow rate of 1ml/min, with discovery at 280 nm using a PDA detector. Results: Theophylline's preservation time was discovered to be 3.747 0.127 min. In the 5-25 mg/l range, the procedure was found to be linear, with a parallel coefficient (R2) of 0.9998. The LOD and LOQ of the system were determined to be (0.99 and 3) g/ml, respectively. The technique and system precisions were predicted using, and the outcomes were determined as percent RSD principles, which were noticed to be within the strict limitations. Theophylline recovery was detected to be in the 99-100 percent range, confirming the method's precision. Conclusion: Using basic ICH guidelines, the suggested RP-HPLC process was validated. The following methodology can be used successfully and easily for routine diagnostic analysis.
Synthesis, characterization, antifungal activity and structure-activity relationships: Study of some mono- And di-schiff bases Periodico Tche Quimica, 2020
The extract of pumpkin seeds as a corrosion inhibitor of mild steel alloy in acidic solution Periodico Tche Quimica, 2020
Synthesis, characterization, antimicrobial activity and theoretical studies of new polymeric schiff-base Journal of the Chemical Society of Pakistan, 2019
Analytical methods for diagnosis a mixture of narcotic substances in seized materials International Journal of Green Pharmacy, 2018
Apelin, C-reactive protein, and serum protein correlation with blood pressure‒a biomarker analysis ZA Mutaeb, UH Ramadhan, EQ Jasim European Journal of Clinical and Experimental Medicine 23 (4), 947–954-947–954 , 2025 2025
Synthesis, In silico, and Pharmacokinetic Drug Likeness of Some Schiff Bases as Hybrid Antibacterial and Antifungal Agents MA Muhammad-Ali, EQ Jasim, AH Al-Saadoon Pharmaceutical Science: New Insights and Developments Vol. 9, 100-118 , 2025 2025
Leptin and C-Reactive Protein in Hypertension: Correlation and Risk Factor with Serum Albumin, Globulin and Total Protein ZA Mutaeb, UH Ramadhan, EQ Jasim European Journal of Medical and Health Research 3 (5), 117-125 , 2025 2025
Synthesis, Molecular Docking Study and Antimicrobial Evaluation of Some 1,2,4-Triazole Compounds AIM Munther Abduljaleel Muhammad-Ali1,*, Ekhlas Qanber Jasim2 Indian Journal of Pharmaceutical Education and Research 59 (1S) , 2025 2025 Citations: 1
Antibacterial Evaluation, In Silico Study and ADMET Properties of Local Lawsonia inermis Leaves Extract. ZR Abdulhussein, MA Muhammad-Ali, EQ Jasim Tropical Journal of Natural Product Research 9 (4) , 2025 2025
Evaluation of Serum Ferritin and Vitamin D and Their Correlation with TSH in Hypothyroid Patients in Basrah City ANA Ekhlas Qanber Jasim, Marwa Jassim Abdulqader Frontiers in Health Informatics 13 (3), 3239-3248 , 2024 2024 Citations: 1
The interplay of blood electrolytes and triglycerides in type 2 diabetes mellitus EQ Jasim, HR Alnjar, UH Ramadhan, MA Muhammad-Ali DYSONA–Life Science 5 (2), 62-67 , 2024 2024
In Vitro Studies of Biosynthesized Nanoparticles of Dysphania Aqueous Leaves Extract Against Some Isolated Bacteria from Wounds and Burns and In Silico Evaluations of … AAAA Ekhlas Q. Jasim, Munther A. Muhammad-Ali Tropical Journal of Natural Product Research 8 (11) , 2024 2024 Citations: 5
Synthesis, Corrosion Inhibition Efficiency in Acidic Media, and Quantum Chemical Studies of Some Hydrazine Derivatives HS Abood, EQ Jasim, MA Muhammad-Ali Science and Technology Indonesia 9 (1), 137-147 , 2024 2024 Citations: 3
Synthesis, characterization and antibacterial activity of some mesalazine derivatives MAMA Ekhlas Qanber Jasim Science and Technology Indonesia 8 (3), 338-343 , 2023 2023 Citations: 9
Antibacterial Efficacy and Molecular Docking of Leaf Extract of Laurus nobilis L Against some Isolated Pathogenic UTI Bacteria AAAR Al-Abdullah, EQ Jasim, MA Muhammad-Ali IOP Conference Series: Earth and Environmental Science 1215 (1), 012057 , 2023 2023 Citations: 2
Synthesis, antibacterial evaluation, and docking studies of some azo compounds and schiff bases derived from sulfonamide MA Muhammad-Ali, EQ Jasim, AH Al-Saadoon Journal of Medicinal and Chemical Sciences 6 (9), 2128-2139 , 2023 2023 Citations: 10
Synthesis, Corrosion inhibition study and DFT calculation of two New Azo Compounds HK Deaf, EQ Jasim, H Rafid, KM Mohammed Egyptian Journal of Chemistry 65 (12), 481-492 , 2022 2022 Citations: 8
SÍNTESE, ESTUDO DE DOCAGEM E AVALIAÇÃO BIOLÓGICA DE DERIVADOS DA 4-AMINOANTIPIRINA-ISONIAZIDA COMO AGENTES HÍBRIDOS ANTIBACTERIANOS E ANALGÉSICOS. AE MOHAMMAD, MA MUHAMMAD-ALI, EQ JASIM Periódico Tchê Química 19 (42) , 2022 2022
Synthesis, docking study, and biological evaluation of 4-aminoantipyrine-isoniazid derivatives as a hybrid antibacterial and analgesic agents AE Mohammad, MA Muhammad-Ali, EQ Jasim 2022 Citations: 2
Spectrophotometric Determination of Salbutamol and Meptazinol in Drug Formulations Using the Berthelot Reaction EQ Jasim, MA Muhammad-Ali, HK Dhaef, MH Al-Safee Journal of Hunan University Natural Sciences 48 (7) , 2021 2021
Theophylline determination in pharmaceuticals using a novel high-performance liquid chromatographic process HNK Al-Salman, EQ Jasim, HH Hussein, FH Shari NeuroQuantology 19 (7), 196-208 , 2021 2021 Citations: 16
Development of the stable, reliable, fast and simple RP-HPLC analytical method for quantifying Diphenhydramine-Hcl (DPH) in pharmaceuticals HNK Al-Salman, EAS Alassadi, RH Fayadh, HH Hussein, EQ Jasim International Journal of Pharmaceutical Research 12 (4), 4457-4467 , 2020 2020 Citations: 12
EXTRATO DE SEMENTES DE ABÓBORA COMO INIBIDOR DE CORROSÃO DE LIGA DE AÇO LEVE EM SOLUÇÃO ÁCIDA. EQ JASIM, EA ALASADI, MA MOHAMMAD-ALI Periódico Tchê Química 17 (35) , 2020 2020
Synthesis and Antibacterial Evaluation of Some Azo-Schiff Base Ligands and Estimation the Cadmium Metal by Complexation EQ Jasim, EA Alasadi, RH Fayadh, MA Muhamman-Ali Systematic Reviews in Pharmacy 11 (6), 677-687 , 2020 2020 Citations: 9
MOST CITED SCHOLAR PUBLICATIONS
Analytical methods for diagnosis a mixture of narcotic substances in seized materials EQJHNK Al-Salman International Journal of Green Pharmacy 12 (3), 216-226 , 2018 2018 Citations: 27
Antioxidant activity of some newly prepared symmetrically azo dyes derived from sulfa drugs MA Muhammad-Ali, HH Salman, E Jasim Asian J Pharm Clin Res 12 (2), 479-83 , 2019 2019 Citations: 22
Determination and evaluation of doses of metronidazole in different quantities and formulations with multiple spectroscopic methods KS Abd-Alrassol, HNK Al-Salman, EQ Jasim, HH Hussein Sys Rev Pharm 11 (5), 130-139 , 2020 2020 Citations: 17
Theophylline determination in pharmaceuticals using a novel high-performance liquid chromatographic process HNK Al-Salman, EQ Jasim, HH Hussein, FH Shari NeuroQuantology 19 (7), 196-208 , 2021 2021 Citations: 16
Development of the stable, reliable, fast and simple RP-HPLC analytical method for quantifying Diphenhydramine-Hcl (DPH) in pharmaceuticals HNK Al-Salman, EAS Alassadi, RH Fayadh, HH Hussein, EQ Jasim International Journal of Pharmaceutical Research 12 (4), 4457-4467 , 2020 2020 Citations: 12
Synthesis, Characterization and Study of Some Tetrazole Compounds as New Corrosion Inhibitors for C-steel in 0.5 M HCl Solution EQJ Adnan Sultan Abdul-Nabi1 International Journal of Engineering Research 3 (10), 613-617 , 2014 2014 Citations: 12
Synthesis, antibacterial evaluation, and docking studies of some azo compounds and schiff bases derived from sulfonamide MA Muhammad-Ali, EQ Jasim, AH Al-Saadoon Journal of Medicinal and Chemical Sciences 6 (9), 2128-2139 , 2023 2023 Citations: 10
A Comparative Study of an In Vitro Release Patterns of Ceftaroline Fosamil from Chemically-Prepared Coated Hydroxyapatite Nanoparticles. EAS Alassadi, EQ Jasim, HNK Al-Salman, MN Mosa Systematic Reviews in Pharmacy 11 (3) , 2020 2020 Citations: 10
Synthesis, characterization and antibacterial activity of some mesalazine derivatives MAMA Ekhlas Qanber Jasim Science and Technology Indonesia 8 (3), 338-343 , 2023 2023 Citations: 9
Synthesis and Antibacterial Evaluation of Some Azo-Schiff Base Ligands and Estimation the Cadmium Metal by Complexation EQ Jasim, EA Alasadi, RH Fayadh, MA Muhamman-Ali Systematic Reviews in Pharmacy 11 (6), 677-687 , 2020 2020 Citations: 9
Synthesis, Corrosion inhibition study and DFT calculation of two New Azo Compounds HK Deaf, EQ Jasim, H Rafid, KM Mohammed Egyptian Journal of Chemistry 65 (12), 481-492 , 2022 2022 Citations: 8
Investigation of Salvadora persica roots extract as corrosion inhibitor for mild steel in 1 M HCl and in cooling water EQ Jasim, MA Mohammed-Ali, AA Hussain Chem. Mater. Res 7 (4), 147-159 , 2015 2015 Citations: 8
Corrosion Inhibition of Mild-Steel in 0.5 M HCl using some prepared 1, 2, 3-Triazoles Derivatives HK Dhaif, EQ Jasim, ZA Muhajjar, AA Shanta Mediterranean Journal of Chemistry 9 (4), 290-304 , 2019 2019 Citations: 7
Spectrophotometric determination of some phenolic compounds by formation of copper (II) complexes KS Abd-Alrassol, EQ Jasim IOP Conference Series: Materials Science and Engineering 571 (1), 012097 , 2019 2019 Citations: 7
Quantitative analysis of two penicillins in oral dosage form using modern high-performance liquid chromatography method Erfan A. S. Alassadi1, Ekhlas Qanber Jasim1, Ahmed A. A. Alsaad2 International Journal of Green Pharmacy 13 (1), 81 , 2019 2019 Citations: 7
Synthesis, characterization of some azo dyes derived from sulfa drugs and the use of them as corrosion inhibitors in 0.5 M hydrochloric acid solution AS Abdul-Nabi, EQ Jasim Journal of Basrah Researches ((Sciences)) 39 (3) , 2013 2013 Citations: 7
In Vitro Studies of Biosynthesized Nanoparticles of Dysphania Aqueous Leaves Extract Against Some Isolated Bacteria from Wounds and Burns and In Silico Evaluations of … AAAA Ekhlas Q. Jasim, Munther A. Muhammad-Ali Tropical Journal of Natural Product Research 8 (11) , 2024 2024 Citations: 5
SYNTHESIS, CHARACTERIZATION, ANTIFUNGAL ACTIVITY AND STRUCTURE--ACTIVITY RELATIONSHIPS: STUDY OF SOME MONO-AND DI-SCHIFF BASES. EQ JASIM, HK DHAIF, MAMALI MUHAMMAD-ALI, A Munther Periódico Tchê Química 17 (34) , 2020 2020 Citations: 4
Synthesis, characterization and antibacterial evaluation of 1,3,4-oxadiazole derivatives SH Derawey, MN Mosa, EQ Jasim, RMO Hraishawi INTERNATIONAL JOURNAL OF RESEARCH IN PHARMACEUTICAL SCIENCES 10 (3), 2342-2350 , 2019 2019 Citations: 4
Analytical method for detecting and estimating of lanthanide ions paired with transitional elements RH Fayadh, HNK Al-Salman, M Al-Nuaim, EQ Jasim International Journal of Green Pharmacy• Apr-Jun 13 (2), 164 , 2019 2019 Citations: 4