Standard Antioxidant Research Articles

Bioactivity of fluorophenyl thiourea derivatives: Antioxidant efficacy and inhibition of key diabetes-related enzymes.

Thiourea structures, known for their wide-ranging bioactivity, have significant potential in diabetes management. In this study, it was aimed to examine the antioxidant capacities of fluorophenyl thiourea derivative compounds and their inhibition studies on α-amylase and α-glycosidase enzyme activity. Antioxidant capacity was determined using Fe3+-Fe+2, FRAP, and Cu2+-Cu+ reducing analyses, DPPH· and ABTS·+ scavenging experiments. It was observed that fluorophenyl thiourea derivative compounds exhibited quite high antioxidant activity compared to standard antioxidants such as BHA, BHT, trolox, α-tocopherol, and ascorbic acid. Additionally, this study investigated the inhibitory effects of the analysis molecules on α-glycosidase and α-amylase, which are enzymes associated with diabetes. Among these derivative molecules, 4-fluorophenyl showed the highest inhibition on α-amylase (IC50: 53.307nM) and α-glycosidase (IC50: 24.928nM). These results highlight the potential of thiourea derivatives in enzyme inhibition and antioxidant therapy, making them promising candidates for diabetes management.

In Vitro Evaluation of Endocrine-Related Adverse Effects of 5-Fluoroindole Derived Melatonin Analogues with Antioxidant Activity.

Melatonin (MLT) is a natural indolic hormone with well documented antioxidant properties, but it can also modulate the estrogen signaling pathway by inhibiting the aromatase enzyme and estrogen receptor modulating activity. This dual activity raises concerns about potential endocrine-related adverse effects when using MLT and its analogues as therapeutic agents in the prevention and treatment of oxidative stress related diseases. In this study, 34 novel 5-fluoroindole derivatives of MLT were synthesized and evaluated for their antioxidant, estrogen receptor modulatory, and aromatase inhibitory activities.Three compounds (4c, 5c, and 6c) demonstrated significant antioxidant activity, with compound 4c showing the highest efficacy in reducing intracellular reactive oxygen species (ROS) by 65 % in CHO-K1 cells and displaying DPPH radical scavenging comparable to the standard antioxidant, BHT. However, these same compounds also exhibited antiestrogenic effects in the E-Screen assay, with IC50 values of 3.36×10-5 M, 1.31×10-7 M, and 1.9×10-7 M, respectively, and inhibited aromatase activity by up to 29 % in a direct enzymatic assay. These findings indicate that, while the compounds have potent antioxidant properties, their significant antiestrogenic and aromatase inhibitory activities may pose risks for unintended endocrine related effects. Further studies are needed to better understand the implications of these activities in vivo and to balance the benefits and risks of such compounds in therapeutic applications.

Phytochemical Profile and Antioxidant Activity of Hydro-distillated from Gynostemma pentaphyllum Makino with Hydrogen Gas

Hydrogen-rich Gynostemma pentaphyllum Makino distillate (HRGD) is made by distilling G. pentaphyllum Makino with hydrogen gas to produce the final product. The study evaluated the total phenolic and flavonoid contents of HRGD, as well as its antioxidant properties, including scavenging activities for various radicals such as 2,2-diphenyl-1-picryl-hydrazyl (DPPH), superoxide anion (O2-), hydrogen peroxide radical (H2O2), nitric oxide radical (NO•) and 2,2´-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS•+), along with a ferrous ion chelating assay. Total phenolic and flavonoid contents were 42330 mg gallic acid and 36300 mg rutin equivalents/100 g, respectively. HRGD exhibited significant antioxidant and free radical scavenging activities in vitro, which were dose-dependent and superior to those of standard antioxidants. HRGD exhibited higher scavenging activities for DPPH, O2-, H2O2, NO• and ABTS•+ radicals, as well as ferrous ion chelating activity than standard antioxidants (p < 0.05). The results showed that HRGD could be an economical and readily accessible source of natural antioxidants and a possible food and pharmaceutical supplement.

Optimizing Solvent Extraction for Potent Antioxidant and Antidiabetic Activities: A Study on Ampelocissus martini Root

The selection of extraction solvents is a critical factor influencing the composition and concentration of phytochemicals in plant extracts, thereby leading to variations in their biological activities. In this study, Ampelocissus martini Planch., an edible plant traditionally used for its medicinal properties, was investigated for its phytochemical profile and biological activities. We assessed the impact of different solvents used in fractionating the aqueous methanolic root extract of the plant on its phytochemical content, as well as its antioxidant, antidiabetic, and antibacterial properties. Among the 3 fractions—ethyl acetate, butanol, and water-soluble—the butanol fraction exhibited significantly higher levels of total phenolics and proanthocyanidins, while the ethyl acetate fraction contained the highest levels of total flavonoids and saponins. The water-soluble fraction showed lower concentrations of these compounds compared to the other 2 fractions. The butanol fraction demonstrated superior antioxidant activity, outperforming other fractions and several standard antioxidants, as evidenced by DPPH, ABTS, FRAP, and CUPRAC assays. Additionally, the butanol fraction showed greater antidiabetic activity, indicated by a lower IC50 value, although it was still less effective than acarbose, a synthetic antidiabetic drug. Correlation analysis revealed a significant association between total proanthocyanidin content and the observed levels of antioxidant and antidiabetic activities across the fractions. All fractions also exhibited antibacterial activity against Gram-positive bacteria. Based on these findings, butanol emerges as the optimal solvent for extracting specific phytochemicals with potent antioxidant, antidiabetic, and antibacterial activities from the aqueous methanolic extract of A. martini root. The butanol fraction holds promise as a natural source of antioxidants for managing diabetes and its associated complications. HIGHLIGHTS Butanol extract showed strong antioxidant and antidiabetic activities, rich in proanthocyanidins. Strong link was found between proanthocyanidins and bioactivities in A. martini. Butanol fraction showed promise as a natural antioxidant for diabetes management. GRAPHICAL ABSTRACT

Pharmacological Evaluation of Anti-Inflammatory and Antioxidant Potential of Cuscuta Reflexa Methanol Extract: Role in Inhibition of Cyclooxygenase and Lipooxygenase

In this study, the antioxidant and anti-inflammatory properties of the methanol extract of Cuscuta reflexa (CRWP-M) were evaluated. The plant material was collected from Dehradun and processed to obtain the extract, which was tested for its total phenolic content, reducing power, and scavenging activities against DPPH and superoxide radicals. The extract's inhibition of cyclooxygenase-1 (COX-1), cyclooxygenase-2 (COX-2), and 5-lipoxygenase (LOX) enzymes was also assessed. Results showed that the extract contained 0.132 mg/mL of gallic acid equivalents of phenolic compounds. In the reducing power assay, the extract demonstrated lower activity compared to Quercetin and Vitamin C across all concentrations. For DPPH radical scavenging, the extract was more effective than BHT at low concentrations but less effective at higher concentrations. The extract exhibited a dose-dependent inhibition of COX-1, COX-2, and LOX, with the most significant effect on LOX (IC50 of 106.49 μg/mL). In superoxide radical scavenging, Vitamin C consistently outperformed the extract at all tested concentrations. These findings suggest that while CRWP-M has notable antioxidant and anti-inflammatory properties, its efficacy varies across different assays and is generally lower than that of standard antioxidants like Quercetin and Vitamin C.

Antioxidant and antidiabetic potential of Cystoseira myrica-mediated green metallic zinc nanoparticles using the algal extract: synthesis and characterization

Abstract Cystoseira myrica marine macroalgae (CSR) were used to produce metallic zinc nanoparticle composites by utilizing the phytochemicals naturally found in the algae. This involves homogenizing the residuals of CSR (10 g), zinc nitrate solution (5 M; 100 ml), and methanol liquid extract (100 ml) at 30 °C for 24 h of sonication and stirring, followed by filtration and drying. This resulted in a hybrid bio-composite (Zn/CSR), which demonstrated strong antioxidant and antidiabetic properties when compared to zinc oxide (ZnO) and CSR used separately. The Zn/CSR hybrid showed excellent antioxidant activity against common radicals such as DPPH (91.5 ± 1.66%), nitric oxide (90.4 ± 1.2%), ABTS (92.2 ± 1.9%), and O2 ·− (27.8 ± 1.12%) (p < 0.05), performing better than the standard antioxidant, ascorbic acid. Regarding its antidiabetic properties, the Zn/CSR composite significantly inhibited key enzymes involved in diabetes, including both commercial enzyme forms (α-amylase (80.3 ± 1.65%), α-glucosidase (96.6 ± 1.11%), amyloglucosidase (95.8 ± 1.3%)) and their crude intestinal forms (α-amylase (72.3 ± 1.5%), α-glucosidase (94.2 ± 1.7%)) (p < 0.05). This improvement increases the impact of the green CSR extract in reducing the agglomeration behaviors of the loaded metal and the formation of a capping layer from the phytochemicals on its surface, in addition to the beneficial effects of the CSR as substrate, which enhances the biological functions of the loaded metal and its interaction interfaces. The Zn/CSR composite also outperformed commercial miglitol drugs and slightly surpassed acarbose in effectiveness. Given the high cost and potential side effects of current medications, the Zn/CSR composite could be a cost-effective alternative for antioxidant and antidiabetic treatments. These findings also emphasize the role of CSR-derived phytochemicals and algae residues in enhancing the biological activity of the metal nanoparticles.

Development of Luminescent and Photosensitive Cellulose Microfibers From Palm Sprout Fibers: Antibacterial Efficacy and Dye Adsorption Potential.

A key contemporary challenge is enhancing the value of agro-industrial byproducts. Cellulose, the most abundant renewable resource, offers significant industrial potential due to its versatile properties. Produced in its pure form by various bacteria, cellulose is increasingly utilized in microscale and nanoscale fibers for composite reinforcement. In this study, cellulose microfibers were derived from palm sprout fibers through a series of treatments like pretreatment, high-pressure hydrolysis in an autoclave, and bleaching. These fibers were then characterized using techniques such as UV spectroscopy, FTIR, SEM, and XRD. The study evaluated the antibacterial properties of the treated cellulose microfibers against both gram-positive Staphylococcus aureus (07%) and gram-negative Escherichia coli (10%), finding higher effectiveness against E.coli. Additionally, the microfibers exhibited a lower EC50 value of 0.101 mg/mL, suggesting that although the microfiber extract is effective, the standard antioxidant is somewhat more potent. Adsorption studies revealed that the cellulose microfibers followed the Langmuir isotherm model, with a high determination coefficient of 0.998, and reached maximum dye adsorption for RB 160 within 120 min. In this adsorption study, 50 mg of dye was removed. These results indicate that the treated cellulose microfibers are a promising biosorbent for improving dye removal processes.

UJI AKTIVITAS ANTIOKSIDAN TEH HERBAL BUNGA TELANG DENGAN PERBEDAAN PEMANIS SEBAGAI ALTERNATIF PENGOBATAN HIPERTENSI

Hypertension can be caused by an imbalance between free radicals and antioxidants in the body. Consumption of sweetened herbal tea can affect antioxidant levels. This study aims to test the antioxidant activity of telang flower herbal tea as an alternative treatment for hypertension and hedonic testing of the formulated herbal tea. Telang flower herbal tea was formulated without sweetener, sugar sweetener, stevia leaf sweetener, sorbitol and cyclamate sweetener. Telang flower herbal tea was brewed with 70℃ water then phytochemical screening of flavonoids, saponins and tannins using standard methods and antioxidant activity using DPPH method. Hedonic test was conducted by assessing the liking of 20 panellists for herbal tea on a scale of 1-5. Unsweetened telang flower herbal tea, sugar sweetener, stevia leaf sweetener, sorbitol and cyclamate sweetener had values of 247.97 ppm; 178.38 ppm; 497.765 ppm; 164.87ppm; 224.96 ppm with hedonic test values of 3.25; 4.05; 3.55; 3.55; 3.35 respectively. The antioxidant activity of telang flower herbal tea with different sweeteners is in the weak to moderate category and panellists like herbal tea with sugar sweetener the most.

Phenolic Compound Analysis and Antioxidant Properties of O. Alborosea

The Onosma genus has been used as a treatment among the public for a long time. In this study, the content analysis and some biological activities of the plant O. Alborosea Fisch. & C.A.Mey. ssp. (O. alborosea) used in traditional medicine in our country were investigated. For this purpose, methanol and water extracts of the plant were taken and the total phenolic substance amount of each extract was determined by HPLC device. FRAP, CUPRAC reduction methods and DPPH, ABTS radical scavenging methods were used to determine antioxidant activities. According to the results of our study, it was determined that water and methanol extracts showed lower activity compared to standard antioxidants. It can be said that the reason for this is related to the ratio of the phenolic amount they contain. Since no antioxidant studies were found when the literature search related to the current plant species was conducted, it is thought that our study will guide other studies to be carried out with this plant species and is important in terms of protecting our plants, which are our genetic treasure, and transferring them to future generations.

FTIR, 1H-/13C-NMR spectral characterization, antimicrobial, anticancer, antioxidant, anti-inflammatory, PASS, SAR, and in silico properties of methyl α-D-glucopyranoside derivatives

A novel series of biologically active derivatives based on methyl α-D-glucopyranoside (MGP) has been developed, comprising 6-O-monosubstituted MGP derivatives obtained from methyl α-D-glucopyranoside. These derivatives were transformed into 2,3,4-tri-O-acyl MGP derivatives, incorporating diverse functionalities within a single molecular framework, aimed at producing new products for antimicrobial studies. All synthesized compounds were identified through spectral analyses (FTIR, 1H-NMR, and 13C-NMR) and elemental analysis. Antimicrobial in vitro testing revealed that these MGP derivatives have notable efficacy against various pathogenic microorganisms, along with the prediction of activity spectra for substances (PASS). Compounds 2 and 7 exhibited the highest inhibitory activity against Bacillus subtilis and Escherichia coli, with minimum inhibitory concentration (MIC) values ranging from 0.25 to 64.0 µg/mL and minimum bactericidal concentration (MBC) values ranging from 8.0 to 128.0 µg/mL. Moreover, these compounds demonstrated significant antioxidant properties compared with those of standard antioxidants according to the results of the DPPH free radical scavenging assay. An evaluation of the growth and proliferation of Ehrlich ascites carcinoma (EAC) cells revealed moderate cell growth inhibition by compounds 5 and 6, with IC50 values of 5958.54 and 5437.17 µg/mL, respectively, as determined via an MTT colorimetric assay. An analysis of the structure-activity relationship (SAR) revealed that the combination of the (p-CH3.C6H4CO-) and halo-aromatic [3-Cl.C6H4CO-] chains with sugar had the highest efficiency in pathogens. Molecular docking studies using AutoDock Vina highlighted compound 7 as a promising inhibitor of the carbapenemase, OmpF, and HmoB proteins, with binding energies of -11.53 kcal/mol, -2.26 kcal/mol, and -30.75 kcal/mol, respectively. A 100-ns molecular dynamics simulation study demonstrated the validity of stable conformation and binding patterns in a stimulating environment. Pharmacokinetic characterization and ADMET predictions indicated favorable drug-like properties. These substantial in vitro and in silico studies demonstrate the importance of additional investigations to confirm the efficacy of MGP derivatives as antimicrobial agents.

Phytochemistry, and Antioxidant Potential of Aqueous Extract of Terminalia chebula Fruit from the Coal-Affected Forests of Bokaro District, Jharkhand

This study investigates the ethnobotanical significance, phytochemical composition, and antioxidant potential of the aqueous extract of Terminalia chebula fruit, collected from the coal-affected forests of Bokaro District, Jharkhand. Using DPPH and NBT assays, the antioxidant activity of the extract was evaluated at various concentrations (50, 100, 250, and 500 µg/mL). The DPPH assay revealed a dose-dependent increase in radical scavenging activity, with Terminalia chebula achieving 82.3% inhibition at 500 µg/mL. In comparison, ascorbic acid, a standard antioxidant, exhibited higher inhibition rates, reaching 95.0% at the same concentration. Similarly, the NBT assay demonstrated that the extract inhibited superoxide radicals, with 78.9% inhibition at 500 µg/mL, while ascorbic acid achieved 94.4% inhibition. The phytochemical analysis indicates a rich composition of phenolic compounds, flavonoids, and tannins in the extract, which are likely responsible for its antioxidant properties. These findings support the traditional medicinal uses of Terminalia chebula, particularly in managing oxidative stress-related conditions. Overall, the study highlights the significant antioxidant potential of Terminalia chebula fruit extract, suggesting its possible applications in functional foods and natural health products. Future research should focus on isolating specific bioactive compounds and exploring their synergistic effects to fully understand the therapeutic potential of this valuable ethnobotanical resource.

New Organoruthenium(II) Complexes Containing Andrographolide‐Appended Hydrazide Derivatives: Synthesis, Spectral Characterization, Anticancer Evaluation

ABSTRACTA new set of andrographolide‐appended hydrazide derivatives (AFC, AGC, and ATC) were prepared from the reaction of andrographolide with furan‐2‐carboxylic acid hydrazide (AFC), pyridine‐3‐carboxylic acid hydrazide (AGC), and thiophene 2‐carboxylic acid hydrazide (ATC), and their corresponding ruthenium(II) complexes (Ru‐AFC, Ru‐AGC, and Ru‐ATC) were synthesized by the direct reaction of [RuCl2(η6‐p‐cymene)]2 with ligands in dichloromethane under stirring condition. The compounds were analyzed by elemental analysis, IR, UV‐Vis, 1H NMR, and ESI‐MS spectrometric techniques, and the obtained spectral data revealed that the ligands coordinated to Ru(II) ion through their enone oxygen and amine nitrogen. Antioxidant activities of the ligands and complexes were calculated against DPPH•, ABTS•+, O2−, and NO• free radicals and their results were compared with standard antioxidants. The cytotoxic activity of the synthesized ligands and complexes toward A549 and HeLa cell lines was evaluated using MTT method (MTT = 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide). Among the compounds, the complex Ru‐AGC showed better cytotoxic effect against A549 and HeLa cancer cells with IC50 values of 4.75 ± 0.17 and 6.32 ± 0.26 μM, respectively. Further, the nontoxic nature of the compounds was confirmed by using human umbilical vein endothelial (HUVEC) cells. The apoptosis was inspected with AO/EB and DAPI staining methods; further, the percentages of the apoptotic and necrotic cells were determined by flow cytometry. Overall, the biological activities of our ruthenium(II)‐arene complexes were found to be more potent than their parent ligands due to chelation, and among the complexes, Ru‐AGC showed better activity due to the presence of pyridine ring in the N‐terminal position of the ligand. The obtained results highlighted the strong possibility to develop highly active ruthenium complexes as anticancer agents.

Chemical composition and potential pharmacological applications of Centaurea acaulis L.

Our study aimed to characterize the composition of the ethyl acetate extract obtained from Centaurea acaulis L. and assess its dermatoprotective and antioxidant properties. The secondary metabolite composition was established by high-performance liquid chromatography combined with mass spectrometry. The antioxidant activity was assessed using four different assays, including DPPH, β-carotene, CUPRAC, and reducing power assays. Furthermore, the in vitro photoprotective effect was evaluated by measuring sun protection. The HPLC-TOF/MS analysis identified the presence of 19 bioactive compounds in the ethyl acetate extract. Major components such as rosmarinic acid and 4-hydroxy benzoic acid were detected, along with other compounds including caffeic acid, cichoric acid, gentisic acid, p-coumaric acid, protocatechuic acid, ferulic acid, vanilic acid, gallic acid, apigenin-7-glucoside, catechin, kaempferol, and quercetin. The ethyl acetate extract of Centaurea acaulis L. exhibited strong antioxidant activity in DPPH, β-carotene, CUPRAC, and reducing power assays, outperforming standard antioxidants such as butylated hydroxytoluene (BHT) and butylated hydroxyanisole (BHA), tannic acid, and ascorbic acid. Additionally, the extract demonstrated a high ability to absorb UV radiation, with an average sun protection factor of 40.20 ± 0.11. These findings highlight the significant antioxidant and dermatoprotective potential of the ethyl acetate extract from Centaurea acaulis L., suggesting its potential use in cosmetic and dietary additive formulations.

Integrating the in vitro antioxidant activity of Polyacrylonitrile/Polyindole composites

AbstractIn this study, five compounds belonging to the Polymer composites (PCs) family, have been prepared with different amounts of polyacrylonitrile and polyindole in the composite. The PCs have inherently bactericidal activity, owing to the nitrile and indole groups. Antioxidant activity was assessed by using reducing power activity, superoxide radical scavenging activity and hydroxyl radical scavenging activity. In our study, butylated hydroxy toluene (BHT), ascorbic acid and α‐tocopherol, which are considered synthetic standard antioxidants, were used to compare antioxidant activity. In addition, since it is known that the MDA levels resulting from the oxidation of fats in Saccharomyces cerevisiae yeast cells are inversely proportional to the antioxidant properties, it gave an idea about the in vitro antioxidant properties of the new synthesized PCs. Reducing force capacity, superoxide radical scavenging activity and hydroxyl radical scavenging activity were found to be higher at 100 μg mL−1 concentration compared to 50 μg mL−1 concentration.

3,4-Dihydropyrimidine-2(1H)-one/thione Derivatives as Anti-inflammatory and Antioxidant Agents: Synthesis, Biological Activity, and Docking Studies

aims: A series of sixteen new 4-(substituted phenyl) - 6-(substituted phenylamino)-3, 4-dihydropyrimidine-2(1H)-ones/thiones derivatives have been synthesized in two step reaction. background: Free radicals are widely known to play a significant part in the inflammatory process. Many non-steroidal anti-inflammatory medicines have been shown to work as radical scavengers or as inhibitors of free radical generation. Inflammation is a part of the vascular tissues' complicated biological reaction to adverse stimuli like bacteria, damaged cells, or irritants. The organism's protective response to damaging stimuli is inflammation, which aims to get rid of them and start the healing process. The inflammatory response has several advantageous effects, such as stopping the spread of dangerous substances to nearby tissues, getting rid of cell waste and infections, and getting the body ready for repair objective: To synthesize new derivatives as anti-inflammatory and antioxidant agents. method: In first step chalcones (I1-I6) was obtained and in the second step, these chalcones were reacted with urea and thiourea in the presence of potassium hydroxide to obtain the corresponding pyrimidinones and thiopyrimidinones. The structures of the synthesized compounds 4-(substituted phenyl)-6-(substituted phenylamino)-3,4-dihydropyrimidine-2(1H)-ones/thione derivatives are investigated by means of TLC (visualized it in Iodine chamber), IR, mass, 1H-NMR spectral and elemental analysis. The title compounds evaluated for anti-inflammatory as well as antioxidant activity. Anti-inflammatory activity in vivo was carried out by carrageenan induced rat-paw edema method and compared with standard drug diclofenac sodium and antioxidant activity was measured by DPPH, FRAP and Hydrogen peroxide (H2O2) method and compared with standard ascorbic acid. result: Electron donating groups showed better antioxidant activity as compared to electron withdrawing ones in both activities. All the compounds exhibited good to moderate activity. Compound DHPM8 shows better antioxidant activity and compound DHPM6 shows better anti-inflammatory activity while compound DHPM11 shows minimum antioxidant as well as anti-inflammatory activity than other compounds. conclusion: To better understanding, we have performed molecular docking simulation. The molecular docking studies revealed that all synthesized compound were showed good receptor binding interaction in which compound 9 had highest docking score of 9.8 due to interaction with CYS36, PRO153, TYR130, GLY45, LEU152, ARG469, LYS468 and GLU465. other: NA

EVALUATION OF TURMERIC (CURCUMA LONGA) AS A POTENT NATURAL ANTIOXIDANT FOR POULTRY

Turmeric (Curcuma longa) has attracted attention due to its potent antioxidant activities standing out among other spices. Turmeric powder is bright yellow and aromatic derived from the rhizome of the plant. It is widely used due to their positive effects on the growth and health of poultry, probably as a result of their immune-stimulatory properties. In this study the DPPH (2, 2-diphenyl-1-picrylhydrazyl) assay was used to determine the antioxidant activity of turmeric using ascorbic acid as a standard antioxidant and 2, 2-diphenyl-1-picrylhydrazyl (DPPH) as a free radical. It was observed from the results obtained that the DPPH free radical scavenging ability of turmeric was in the range of 27.23% to 60.23%. The antioxidant activity of ascorbic acid (the standard antioxidant) used in the experiment was 98.65%. It was revealed from the results that the inhibition activity of turmeric against the free radical increased with an increase in the level of the concentration of its extract from 0.2mg/ml to 1.0mg/ml. The implication of this showed that the effect of turmeric extract was dose-dependent. The values obtained for IC50 for the turmeric and vitamin C (ascorbic acid) were 0.717 and 0.320 respectively. Turmeric has the potential to serve as a natural substitute for synthetic antioxidant additives in poultry production.

DFT and molecular docking studies of 10-hydroxylstrictosamide from methanol leaves extract of Sarcocephallus latifolius (Smith, Bruce)

This work isolated 10-hydroxylstrictosamide from methanol leaves extract of Sarcocephallus latifolius and structurally elucidated with the aid of 1 and 2D-NMR, FTIR and ESI-MS techniques. The antioxidant potential of the compound against various radicals was investigated and substantiated through molecular docking study, quantum chemical predictions and DFT optimizations. Furthermore, the antioxidant mechanism was confirmed by vibrational analysis and frontier orbital calculations. The molecular docking studies of the isolated compound was compared with the standard antioxidants (BHT and DTT ligands) against the peroxiredoxin (prxs)-5 receptor, and the result revealed the high binding mode of 10-hydroxylstrictosamide. The results of theoretical data validated the experimental results. Calculated HOMO/LUMO gaps show low excitation energy for 10-hydroxystrictosamide and justified its excellent antioxidant potential. The results of the molecular docking study provided valuable insights to rationalize the action and predict the binding modes of 10-hydroxystrictosamide.

A Review on Synthesis and Biological Activities of 2‐Aminophenol‐Based Schiff Bases and Their Transition Metal Complexes

ABSTRACT2‐Aminophenol‐based Schiff bases and their metal complexes have drawn a lot of interest because of their wide range of biological activity and their uses in several fields. These Schiff bases are synthesized through the condensation of 2‐aminophenol and various carbonyl compounds, and metal complexes formed easily by coordinating Schiff bases with transition metal ions possess a wide range of intriguing properties that have rendered them promising candidates in biomedical research. These compounds have a diverse array of captivating biological properties including antibacterial, antifungal, anticancer, and antioxidant actions. Their versatile nature and potential for tailored modifications hold the promise for innovative biomedical applications. Compared to standard antibiotics and other studied compounds, C2, C8–C11, and C116 complexes, along with L16 and L17 ligands, exhibit the highest antibacterial activity, while C3 and C115 complexes demonstrate the highest antifungal activity. The metal chelate formation of the ligands enhanced the antimicrobial activity by increasing their lipophilic nature. C66, C76, and C112 complexes and L39 ligand showed higher anticancer activity than standard anticancer drugs. The metal complexes have higher anticancer activity than the ligand due to improved permeability and cellular uptake. The anticancer activity of the complexes is related to the substituents of the Schiff base ligands. In compounds containing an electron‐withdrawing group (e.g., Cl or Br or NO2), the activity is obviously better than others. Ligands L1–L3 and L5, L6, and L32 demonstrated the most potent antioxidant activity, surpassing both metal complexes and standard conventional antioxidants. The ligands showed greater antioxidant activity than the metal complexes due to their capability of donating free protons to scavenge free radicals. More study is needed to fully explore the potential of 2‐aminophenol‐based Schiff bases and their transition metal complexes for the development of new drugs. This review summarizes different synthetic methods, biological activities, and the structure–activity relationship. This study aims to conduct further research on 2‐aminophenol‐based Schiff bases and their metal complexes.

Antioxidant and Antiplasmodial Potentials of Methanol Bark Extract of <i>Entada africana </i>Via <i>in Vitro</i> Approaches

<i>Plasmodium </i>parasites, which cause malaria, continue to pose a serious threat to global health, necessitating the continuous search for novel antimalarial agents. Oxidative stress has also been linked to the pathophysiology of malaria. <i>Entada africana</i> is a plant known for its ethnomedicinal uses in treating various ailments associated with inflammation including malaria. This study aimed at evaluating the antiplasmodial and antioxidant potentials of methanol bark extract from <i>Entada africana </i>(MBEEA). <i>In vitro </i>approaches were adopted for the study.<i> Plasmodium falciparum-</i>infected erythrocyte samples were cultured in Roswell Park Memorial Institute (RPMI) 1640 media under anaerobic conditions for 72 hours. Eighteen test tubes were labeled and grouped into three replicates per group. Group I (untreated), Group II, and III were treated with chloroquine (CQ) and artemether (AR) at a concentration of 5 mg/dL. Group IV, V, and VI were treated with the extract at respective concentrations of 5 mg/dL, 10 mg/dL, and 20 mg/dL for 72 hours. The parasitemia count and the percentage parasitemia inhibition were determined by microscopic examination of Giemsa-stained smears. The antioxidant potential of the extract was assessed using <i>in vitro</i> assays, including superoxide radical scavenging activity (SRSA), hydroxyl radical scavenging activity (HRSA), 1,1-diphenyl-2-picrylhydrazyl (DPPH), and ferric reducing antioxidant power (FRAP). Microscopic examination of the treated samples revealed varying degrees of parasitemia inhibition. Group II and III treated with CQ and AR demonstrated a considerable reduction in parasitemia count with percentage inhibition of 100% and 83% respectively. The <i>E. africana</i> extract showed a concentration-dependent effect on parasitemia count. At 5 mg/dL, the extract exhibited 50% parasitemia inhibition, which increased to 100% at 10 mg/dL, and 20 mg/dL respectively. The MBEEA demonstrated significant <i>in vitro </i>antioxidant activities by scavenging DPPH, SRSA, and hydroxyl radical compared to the standard antioxidant (ascorbic acid). MBEEA thus exhibit potent antioxidant and antiplasmodial properties. This plant is therefore offers to be a promising medicinal plant in the treatment of malaria, hence it is recommended as potent antiplasmodial plant usable for treating malaria.

Synthesis and Characterization of Copper(II) and Nickel(II) Complexes with 3-(Morpholin-4-yl)propane-2,3-dione 4-Allylthiosemicarbazone Exploring the Antibacterial, Antifungal and Antiradical Properties.

The eleven new copper(II) and nickel(II) coordination compounds [Cu(L)Br]2 (1), [Cu(L)Cl] (2), [Cu(L)NO3] (3), [Ni(L)Cl] (4), [Ni(HL)2](NO3)2 (5), and [Cu(A)(L)]NO3, where A is 1,10-phenanthroline (6), 2,2'-bipyridine (7), 3,4-dimethylpyridine (8), 3-methylpyridine (9), pyridine (10) and imidazole (11) were synthesized with 3-(morpholin-4-yl)propane-2,3-dione 4-allylthiosemicarbazone (HL). The new thiosemicarbazone was characterized by NMR and FTIR spectroscopy. All the coordination compounds were characterized by elemental analysis and FTIR spectroscopy. Also, the crystal structures of HL and complexes 1, 6, 7, and 11 were determined using single-crystal X-ray diffraction analysis. Complex 1 has a dimeric molecular structure with two bromide bridging ligands, while 6, 7, and 11 are ionic compounds and comprise monomeric complex cations. The studied complexes manifest antibacterial and antifungal activities and also have an antiradical activity that, in many cases, surpasses the activity of trolox, which is used as a standard antioxidant in medicine. Copper complexes 1-3 have very weak antiradical properties (IC50 > 100 µM), but nickel complexes 4-5 are strong antiradicals with IC50 values lower than that of trolox. The mixed ligand copper complexes with additional ligand of N-heteroaromatic base are superior to complexes without these additional ligands. They are 1.4-5 times more active than trolox.