Antidiabetic Activity Research Articles

Anti-diabetic Activity of Spirulina and Chlorella in In vivo Experimental Rats

The effects of supplying experimental rats with unicellular green algae Chlorella and tiny filamentous cyanobacteria Spirulina, on type 2 diabetes (T2DM) were examined in the present study. Eight sets of male Sprague-Dawley albino rats, each with six individuals, were used in the investigation. Throughout the trial, Group 1 was the negative control group and was given saline regularly. Group 2 was given alloxan to induce diabetes. Spirulina was given to groups 3, 4, and 5 at dosages of 100, 200, and 300 mg/kg body weight, respectively, after diabetes induction. Similarly, groups 6, 7, and 8 received dosages of 100, 200, and 300 mg/kg body weight of Chlorella, respectively. The findings indicated that the control group had significantly higher levels of triglycerides, low-density lipoprotein (LDL), blood sugar, and very low-density lipoprotein (VLDL) and considerably lower levels of insulin, high-density lipoprotein (HDL), and phospholipids. However, rats given Spirulina (groups 3, 4, and 5) showed notably higher insulin, HDL, and phospholipids levels and significantly lower blood glucose, cholesterol, VLDL, LDL, and triglycerides levels. Rats fed with Chlorella (groups 6, 7, and 8) also showed increased effectiveness of feed ratios, greater final weights, and body weight growth percentages compared to the control group. The present study shows that supplementing with Spirulina and Chlorella improves insulin lipid patterns, blood sugar, and type 2 diabetes in vivo laboratory rats. According to the research, Spirulina and Chlorella may be used as functional meals to help control and cure diabetes.

Tauroursodeoxycholic Acid (TUDCA) Relieves Streptozotocin (STZ)-Induced Diabetic Rat Model via Modulation of Lipotoxicity, Oxidative Stress, Inflammation, and Apoptosis.

Tauroursodeoxycholic acid (TUDCA) is approved for the treatment of liver diseases. However, the antihyperglycemic effects/mechanisms of TUDCA are still less clear. The present study aimed to evaluate the antidiabetic action of TUDCA in streptozotocin (STZ)-induced type 2 diabetes mellitus (T2DM) in rats. Fifteen adult Wistar albino male rats were randomly divided into three groups (n = five in each): control, diabetic (STZ), and STZ+TUDCA. The results showed that TUDCA treatment significantly reduced blood glucose, HbA1c%, and HOMA-IR as well as elevated the insulin levels in diabetic rats. TUDCA therapy increased the incretin GLP-1 concentrations, decreased serum ceramide synthase (CS), improved the serum lipid profile, and restored the glycogen content in the liver and skeletal muscles. Furthermore, serum inflammatory parameters (such as TNF-α, IL-6, IL-1ß, and PGE-2) were substantially reduced with TUDCA treatment. In the pancreas, STZ+TUDCA-treated rats underwent an obvious enhancement of enzymatic (CAT and SOD) and non-enzymatic (GSH) antioxidant defense systems and a marked decrease in markers of the lipid peroxidation rate (MDA) and nitrosative stress (NO) compared to STZ-alone. At the molecular level, TUDCA decreased the pancreatic mRNA levels of iNOS and apoptotic-related factors (p53 and caspase-3). In conclusion, TUDCA may be useful for diabetes management and could be able to counteract diabetic disorders via anti-hyperlipidemic, antioxidant, anti-inflammatory, and anti-apoptotic actions.

Formulation and Evaluation of Electrospun Nanofiber Mats of Curcumin and Leaf Extract of Tinospora cordifolia: Designed for Accelerating Diabetic Wound Healing

Traditional herbs like Tinospora cordifolia and curcumin have many therapeutic benefits. However, curcumin’s limited bioavailability is a problem. Electrospun nanofibers are an answer because they increase the effective surface area greatly, and make drug delivery better in almost all aspects. The combination in the form of nanofibers can be greatly useful in the treatment of diabetic wound healing, where curcumin, the known antibacterial and anti-inflammatory element, plays an important role. It is observed that when combined with extract of leaves of T. cordifolia, which has known antidiabetic and wound healing actions, blended in the chitosan polymer, which is itself a weak antibacterial compound hence can be one of the solutions to the menace of bacterial resistance which is very common in diabetic wound healing. This research aims to create and test electrospun nanofiber mats of curcumin and T. cordifolia leaves extract blended in chitosan as a base polymer in the treatment of diabetic wound healing. Leaves of the plant T. cordifolia, which were collected from the institute’s botanical garden, were subjected to drying and then prone to solvent extraction using methanol and acetone, resulting in the production of bioactive extracts. The curcumin was obtained as a gift sample from Sanjay Chemicals, Mumbai. Nanofibers were electrospun from chitosan, T. cordifolia leaf extract and curcumin. Characterization included scanning electron microscope (SEM), water contact angle measurement, TGA/DSC analysis, drug release studies, fourier-transform infrared (FTIR) analysis, swelling tests and in-vitro release profiling. The nanofiber mats of curcumin and leaves extract of T. cordifolia using chitosan as a base polymer were prepared and evaluated at various parameters. The results we found are very promising. The nanofibers formed by using electrospinning techniques show good content uniformity as well as good diameter which was checked using SEM. The study confirmed no component interactions using differential scanning calorimetry (DSC). The good hydrophilicity of mats was found to ensure good retention time. The study concluded with the formation of a novel formulation that can fight the menace of bacterial resistance, which is very common in the diabetic wound healing process. The formulation will ensure not only countering bacterial resistance but also the faster healing of diabetic wounds, as T. cordifolia leaves extract is known to improve angiogenesis and tissue remodeling.

In Silico and In Vitro Alpha-amylase Activities of Previously Synthesized Pyridazine Derivatives

Diabetes mellitus is one of the fastest-growing metabolic disorders. Worldwide, one out of 10 people suffer from diabetes mellitus. In this manuscript, we establish the antidiabetic potential of previously synthesized pyridazine derivatives using in silico and in vitro experiments. Molecular docking studies of pyridazine derivatives with pullulanase Amy12, isomaltase, and alpha-amylase receptors revealed that Molecules 45, 46, and 29 showed good docking interaction scores. ADMET analysis of the top three docked pyridazine derivatives (45, 46, and 29) showed lesser solubility and poor distribution behavior. Molecules 45, 46, and 29 maintained drug-like properties with good oral bioavailability. Molecules 45 and 29 showed reproductive toxicity without any sign of mutagenicity, tumorigenicity, or other irritancy. Molecule 46 emerged as a nontoxic molecule in all aspects. In vitro alpha-amylase inhibition data of molecules 45, 46, 29, and acarbose showed IC50 values of 8.67, 8.46, 8.83, and 66.65 μg/mL, respectively. The antidiabetic activity of pyridazine derivatives is increased with the presence of phenothiazine coupled with a biphenyl group, indole with a biphenyl group, and phenothiazine with an ethylphenyl group. Establishing these pyridazine derivatives using in vivo experiments could be beneficial in managing diabetes.

Development and Assessment of Tinospora cordifolia for Anti-diabetic Activity

Development and Assessment of Tinospora cordifolia for Anti-diabetic Activity

Examination of the chemical composition and anti-diabetic activities of the oils of Abelmoschus esculentus, Peganum harmala, and Aquilaria agallocha cultivated in Muğla

In this study, the oils of Abelmoschus esculentus, Peganum harmala, and Aquilaria agallocha grown in different regions of Muğla, Türkiye were obtained using the cold pressing and maceration techniques. The oils were analyzed using Gas Chromatography-Mass Spectrometry (GC-MS) to determine their fatty acid compositions. Thirty-seven fatty acids were detected. Palmitic acid (C16:0), linoleic acid (C18:2), and oleic acid (C18:1 cis-9) were the major components in all oils. Additionally, the anti-diabetic activity of the oils was screened against α-amylase and α-glycosidase, which are the related enzymes to diabetes mellitus. Promising results regarding anti-diabetic activity for Aquilaria agallocha oils were obtained.

Chemical Composition of Extracts and Fractions from Miconia Ibaguensis (Melastomataceae) Leaves and Evaluation of Biological Activities.

The study aimed to assess the chemical composition of Miconia ibaguensis leaves extracts and fractions obtained from the ethanolic extract (EE), along with evaluating their antifungal, antibacterial, antidiabetic, and antioxidant activities. The ethyl acetate fraction (EAF) exhibited potent antifungal activity against Candida spp (1.95-3.90 μg mL-1) and potent antioxidant activity in the DPPH (1.74±0.07 μg mL-1), FRAP (654.01±42.09 μmol ETrolox/gsample), and ORAC (3698.88±37.28 μmol ETrolox/gsample) methods. The EE displayed inhibition against the α-amylase enzyme (8.42±0.05 μg mL-1). Flavonoids, hydrolysable tannins, triterpenoids, and phenolic acids, identified in the EE and fractions via (-)-HPLC-ESI-MS/MS analysis, were found to contribute to the species' biological activity potentially. These findings suggest promising avenues for further research and potential applications in pharmacology and natural products, offering new possibilities in the fight against global health issues.

Development of Potential Therapeutic Agents from Black Elderberries (the Fruits of Sambucus nigra L.).

Elderberry (Sambucus nigra L.) is a widespread deciduous shrub, of which the fruits (elderberries) are used in the food industry to produce different types of dietary supplement products. These berries have been found to show multiple bioactivities, including antidiabetic, anti-infective, antineoplastic, anti-obesity, and antioxidant activities. An elderberry extract product, Sambucol®, has also been used clinically for the treatment of viral respiratory infections. As the major components, phenolic compounds, such as simple phenolic acids, anthocyanins and other flavonoids, and tannins, show promising pharmacological effects that could account for the bioactivities observed for elderberries. Based on these components, salicylic acid and its acetate derivative, aspirin, have long been used for the treatment of different disorders. Dapagliflozin, an FDA-approved antidiabetic drug, has been developed based on the conclusions obtained from a structure-activity relationship study for a simple hydrolyzable tannin, β-pentagalloylglucoside (β-PGG). Thus, the present review focuses on the development of therapeutic agents from elderberries and their small-molecule secondary metabolites. It is hoped that this contribution will support future investigations on elderberries.

Evaluation of Anti-Infection and Anti-Diabetic Activities in Methanolic and n-Hexane Plant Extracts of Indigenously Cultivated Chenopodium album

Evaluation of Anti-Infection and Anti-Diabetic Activities in Methanolic and n-Hexane Plant Extracts of Indigenously Cultivated Chenopodium album

ADME, Molecular Targets, Docking, and Dynamic Simulation Studies of Phytoconstituents of Cymbopogon citratus (DC.)

Cymbopogon citratus (DC) Stapf. is utilized in both culinary and medicinal contexts, wherein its extracts demonstrate a range of therapeutic properties, including antidiabetic, antioxidant, and anti-inflammatory activities. This investigation aimed to computationally analyze phytochemicals of C. citratus, evaluating their pharmacokinetics and binding dynamics. The findings revealed a combination of high and low gastrointestinal absorption (GIA) for C. citratus (DC.) phytochemicals, with some exhibiting permeability across the blood-brain barrier (BBB). Xanthine dehydrogenase/oxidase (XDH) emerged as the primary human molecular target of C. citratus phytocompounds, while XDH and matrix metalloproteinase-9 (MMP9) have central connectivity in the protein interaction network. Orientin has best binding affinity with XDH (−9.083 kcal.mol−1) and MMP9 (−9.051 kcal.mol−1). Molecular dynamic simulations indicated the favorable stability and interactions of XDH with orientin and quercetin, respectively. In summary, this investigation underscores the potential of twenty-six (26) phytochemicals in C. citratus extract to combat cancer and neurodegenerative diseases through mechanisms targeting XDH and MMP9.

Developments in Organocatalysis Transformations of Unsaturated Pyrazolones

Abstract: Unsaturated pyrazolones can participate in organocatalytic reactions with various substrates to form spiro-cyclic pyrazolones, and fuzed-pyrazolone heterocycles. The present review describes progress since 2013 in the organocatalysis transformations of unsaturated pyrazolones. Pyrazolones are prevalent structural motifs in a wide variety of natural products and drug or drug-like molecules. A series of nitrogen-containing pyrazolones exhibits anti-cancer, antimicrobial, anti-inflammatory, anticonvulsant, antidepressant, antidiabetic, and an-tipyretic activities. Especially, chiral spiro-cyclic pyrazolones are recognized as targets in nat-ural products and clinical pharmaceuticals. Organocatalytic systems are powerful and reliable approaches that allow us to build structurally complex molecules in an enantioselectively and diastereoselectively manner. Avoiding the use of transition metal catalysts, readily available bifunctional organocatalysts, and the performance of the reaction at ambient temperature are other advantages of these catalytic systems. Despite considerable progress in this field, it is still one of the challenging goals for chemists to make new biologically active heterocyclic molecules.

Phytochemical profile, antioxidant, antidiabetic, and antimicrobial activities of Parkia timoriana bark extracts

Abstract. Sariwati A, Suryanti V, Sari F, Kamei I, Trisnawati EW. 2024. Phytochemical profile, antioxidant, antidiabetic, and antimicrobial activities of Parkia timoriana bark extracts. Biodiversitas 25: 2427-2433. Plants have various bioactive compounds that have pharmacological activity. Kedawung (Parkia timoriana (DC) Merr) is an indigenous plant in Indonesia that contains bioactive compounds. The leaves, bark, seeds, and roots of P. timoriana are commonly used in traditional medicine. The purpose of this study was to determine the chemical composition of P. timoriana bark extract and to assess its antioxidant, antidiabetic, and antibacterial activity. The bark of P. timoriana was extracted with various solvents that differ in polarity, such as water, methanol, ethyl acetate, and hexane. All extracts were investigated for antioxidant activities by 2,2-diphenyl-1-picrylhydrazyl) (DPPH) free-radical and 2,2’-azinobis (3-ethylbenz-thiazoline-6-sulfonic-acid) (ABTS) scavenging ability. The in-vitro antidiabetic activity was carried out by ?-amylase and ?-glucosidase inhibition. Antibacterial and antifungal activities were determined by the agar disc diffusion method. Parkia timoriana bark extracts contained alkaloids, flavonoids, steroids, tannins, terpenoids, saponins, reducing sugars, and cardiac glycosides. The ethyl acetate extract possessed the highest total phenolics, alkaloids, flavonoids, saponins, tannic acid, and terpenoids. Secondary metabolites in all extracts contributed to free radical scavenging, antidiabetic, antibacterial, and antifungal properties. The P. timoriana bark contains natural chemical compounds that might be useful as therapeutic agents for producing bioactive products and pharmaceuticals in the future.

Exploring the Pharmacological Potential of Chlorogenic acid as an Anti-Cancer Agent and a Call for Advance Research.

Chlorogenic acid (CHA) is a phenolic substance found in various edible plants, such as tea and green coffee extracts. This chemical has demonstrated significant efficacy in reducing the probability of many diseases in preclinical and clinical environments. Chlorogenic acid (CHA) possesses several pharmacological attributes, such as anticancer, hepatoprotective, antimicrobial, immune-suppressant, antioxidant, and antidiabetic activities. Its applications extend to multiple industries, such as food, chemicals, medicine, and healthcare. Studies have shown that CHA can exert its anticancer effects through numerous mechanisms. It can hinder the process of cell division, trigger cell apoptosis, and suppress an increase in cancerous cell growth. The literature research conducted for this study revealed a variety of molecular and cellular processes influencing distinct signaling pathways. These mechanisms include angiogenesis, invasion and migration, oxidative stress, inflammation, cell cycle arrest, and proliferation.However, significant issues surround the use of CHA, primarily due to its limited bioavailability in animal models. This review focuses on the chemistry, natural sources, pharmacokinetics, and underlying mechanisms of action of CHA and its clinical utility in treating life-threatening diseases, such as cancer. The manuscript provides insight into novel formulation approaches.

Effect of Steeping Temperature and Storage Period on the Bioactive Compounds plus Antioxidant and Antidiabetic Activities of Infusion from Powdered Pluchea indica Less

This study was done to determine the effects of steeping temperature and storage period on the bioactive contents plus antioxidant and antidiabetic activities of Pluchea leaf infusion. The research used a randomized block design with two factors, i.e. steeping temperature (T) and storage period (B). The Pluchea leaf blades were exposed to four steeping temperatures of 60 (T1), 70 (T2), 80 (T3), and 95 (T4) °C with the storage period of 0 (B1) and 5 (B2) yr – resulting in eight treatment combinations (T1B1, T1B2, T2B1, T2B2, T3B1, T3B2, T4B1, T4B2). Statistical analysis using a paired t-test at α ≤ 0.05 showed that treatments significantly affected the bioactive contents [total phenol (TPC), total tannin (TTC), and total flavonoid (TFC)], antioxidant [DPPH scavenging activity (DPPH) and ferric reducing antioxidant power (FRAP)] potential and antidiabetic [α-amylase (AA) and α-glucosidase (GA) inhibition] properties of the Pluchea leaf infusion. TPC, TTC, DPPH, and FRAP significantly increased for the storage period and the steeping temperatures. Then, TFC decreased during the storage period but significantly increased at higher steeping temperatures. The AA and GA of Pluchea leaf infusion increased until 70 °C of the steeping temperature but decreased until 95 °C. The DPPH and FRAP of the Pluchea leaf infusion were strongly and positively correlated with TPC and TTC. The GA and AA of Pluchea leaf infusion were not influenced by the TPC and TTC but were weakly and positively correlated with TFC. The antioxidant activity of the Pluchea leaf infusion was inversely proportional to the antidiabetic activity. The simple phenolic compounds derived from Pluchea leaf infusion at different steeping temperatures and storage included gallic acid, kaempferol, myricetin, (+)-catechin, quercetin, 3,4-di-O-caffeoylquinic acid, 3,5- di-O-caffeoylquinic acid, and 4,5-di-O-caffeoylquinic acid.

Ameliorative Effects of Curcumin on Type 2 Diabetes Mellitus.

Type 2 diabetes mellitus (T2DM), a multifactorial and complicated metabolic disorder, is a growing public health problem. Numerous studies have indicated that bioactive compounds from herbal medicine have beneficial effects on T2DM prevention and treatment, owing to their numerous biological properties. Curcumin, the major curcuminoid of turmeric, is one of the most studied bioactive components of herbal supplements, and has a variety of biological activities. Clinical trials and preclinical research have recently produced compelling data to demonstrate the crucial functions of curcumin against T2DM via several routes. Accordingly, this review systematically summarizes the antidiabetic activity of curcumin, along with various mechanisms. Results showed that effectiveness of curcumin on T2DM is due to it being anti-inflammatory, anti-oxidant, antihyperglycemic, anti-apoptotic, and antihyperlipidemic, among other activities. In light of these results, curcumin may be a promising prevention/treatment choice for T2DM.

Comparative Antimicrobial Activity and Bioactive Constituents of Oils from Rhizomes of Zingiber Officinale Roscoe Obtained by Different Extraction Methods

Ginger, known for its rich array of bioactive compounds, holds significant therapeutic potential due to its diverse medicinal properties. This study investigated the antimicrobial activity and bioactive principles present in ginger rhizome oils obtained using three different extraction methods viz: liquid-liquid extraction, cold maceration, and soxhlet extraction. The oils’ bioactive principles were identified by Gas Chromatography Mass Spectrometry (GC-MS) while their antimicrobial activity was determined by agar well diffusion technique. The GC-MS analysis revealed the presence of thirty compounds in each of the oils from liquid-liquid extraction and cold maceration, and fifty four compounds in the soxhlet-extracted oil. The most predominant compound in both liquid-liquid (31.13%) and cold maceration (16.99%) oils was oleic acid whereas the Soxhlet-extracted oil contained predominantly linoleic acid methyl ester (9.27%). Some bioactive compounds identified in these oils include δ-elemene, isoborneol, α-Bisabolol oxide, stearic acid, undecanone, palmitic acid, α-copaene, zingiberene, aromadendrene, farnesol, 2-methylhexane and farnesene which possess antioxidant, antibacterial, antifungal, antiviral, anti-inflammatory, anti-ulcer, anti-cancer, hypolipidemic, mosquito repellant, antimicrobial, and antidiabetic activities. Additionally, the oils exhibited promising antimicrobial potential against the test organisms with Staphylococcus aureus showing the least susceptibility to all the samples. Staphylococcus aureus and Candida albicans were completely resistant to the oil obtained by Soxhlet extraction at all tested concentrations. Meanwhile, Klebsiella pneumoniae (20 mm), Proteus vulgaris (18 mm), and Pseudomonas aeruginosa (17 mm), were most susceptible to the oil obtained by liquid-liquid extraction, cold maceration and soxhlet extraction, respectively. The study highlighted the significance of extraction methods on the chemical composition and antimicrobial activity of ginger rhizome oils, underscoring the importance of choosing appropriate extraction techniques to optimize the oils' therapeutic properties for specific medicinal applications.

Microalgal Derivatives as Potential Nutraceutical and Pharmaceutical: Boon to Human Beings

Background: Marine resources have diverse biological and beneficial entities for human beings. Among them, microalgae are one of the eukaryotic photosynthetic organisms found in freshwater and marine environments with an immense source of metabolites. They consist of high nutraceutical and value-added compounds for health concerns. Objective: Most microalgal species like- chlorella, spirulina, Isochrysis, Nannochloropsis, etc. are found to synthesize biologically active secondary metabolites which are having high pharmaceutical and nutraceutical value. Some of the purely extracted compounds are Lecithin, fucoxanthin, astaxanthin, and most important Sulphur polysaccharides- fucose, galactose, xylose, rhamnose, etc. are providing anti-microbial, anti-fungal, anti-viral, anti-cancer and anti-diabetic activities. Methods: Many of the prior studies demonstrated the compilation of naturally derived secondary metabolites for their potential application in most fields. Because of their wide-ranging potential for use in biopharmaceutical and nutraceutical industries, microalgae have recently gained significant interest on a global scale. Result: Microalgae are both parts of the dietary ingredients and bioactive pharmaceuticals. A number of microalgal species have been explored for their significance towards their high-value products with their exceptional pharmacological and biological properties. Conclusion: This current review discussed the uses and benefits of microalgae for the manufacture of nutraceuticals and the medicinal use of diverse bioactive compounds.

Evaluation of antioxidant, antibacterial and antidiabetic activities of different parts of Litsea polyantha extracts

Evaluation of antioxidant, antibacterial and antidiabetic activities of different parts of Litsea polyantha extracts

Effect of Black Tea Polysaccharides on Alleviating Type 2 Diabetes Mellitus by Regulating PI3K/Akt/GLUT2 Pathway.

The bioactivity of tea polysaccharides (TPs) has been widely reported, but studies to date have focused on green tea. Some human health investigations have implied that black tea may possess potential antidiabetic effects, but less is known about their potential role and related antidiabetic mechanism. The present study was, therefore, conducted to investigate the chemical properties and antidiabetic activity of TPs from black tea. Monosaccharide composition revealed that Alduronic acid (77.8 mol%) considerably predominated in the fraction. TP conformation analysis indicated that three components in TPs were all typical of high-branching structures. Oral administration of TPs could effectively alleviate fasting blood glucose in type 2 diabetes mellitus (T2D) mice, with the values 23.6 ± 1.42, 19.6 ± 2.25, and 16.4 ± 2.07 mmol/L in the 200, 400, and 800 mg/kg·BW groups, respectively. Among these TPs groups, the 800 mg/kg·BW groups significantly decreased by 37.88% when compared with the T2D+water group (p < 0.05). Further studies demonstrated that TP treatment upregulated the expression of p-Akt/p-PI3K (p < 0.001). Additionally, TP treatment significantly promoted glucose transporter protein 2 (GLUT2) translocation in the liver (p < 0.001). These findings suggest that TPs from black tea protect against T2D by activating PI3K/Akt/GLUT2 signaling and might serve as a novel therapeutic candidate for T2D.

Synthesis, characterization, DNA interaction, molecular docking, and α‐glucosidase inhibition studies of 3‐(pyrimidin‐2‐ylthio) groups substituted water soluble zinc (II) phthalocyanine

In this work, 3‐(pyrimidin‐2‐ylthio)phthalonitrile (n‐MP1), non‐peripherally 3‐(pyrimidin‐2‐ylthio) groups substituted Zn (II) phthalocyanine (n‐MP2), and its water soluble derivative (n‐MP3) have been firstly synthesized and characterized with spectral data. The interaction of the n‐MP3 complex with DNA was examined in vitro using UV–visible titrimetric and thermal denaturation assays and in silico by performing molecular docking studies. In addition, the antidiabetic activity of n‐MP3 was revealed spectroscopically by studying α‐glucosidase inhibition activities. The spectroscopic results indicated that n‐MP3 effectively binds to CT‐DNA with a Kb value of 2.0 × 105 M−1 and interacts with CT‐DNA via noncovalent binding mode. Besides, docking studies divulged that n‐MP3 exhibits a stronger binding tendency (BE: −10.64 kcal/mol) with DNA than the control compounds, (7.78 kcal/mol for ethidium bromide and −6.21 kcal/mol for cisplatin). Consequently, due to its strong DNA binding activity, n‐MP3 may be suitable for antimicrobial and anticancer applications after further toxicological test systems. Also, n‐MP3 complex inhibited the activity of α‐glucosidase with the IC50 value of 1.44 ± 0.08 μM, whereas IC50 value of acarbose was 237.24 ± 1.80 μM. Therefore, it can be said that n‐MP3 is a very effective α‐glucosidase inhibitor.