The plant Conyza canadensis, which belongs to Asteraceae (Compositae) family and known as Canadian horseweed. It was used as traditional medicine in China, Pakistan, India, and Africa for the treatment of various diseases causing by bacteria, fungi, or viruses. The plant has antimicrobial, antioxidant, anticoagulant, anti-inflammatory, and anticancer pharmacological activity. This study provides the first phytochemical investigation of the plant in Iraq and is concerned with extraction, fractionation, isolation, and purification of some of the important phytochemicals detected in the plant-like phenolic acids, flavonoids, and alkaloids. Also, the literature survey has revealed that the plant has a substantial antimicrobial activity, so it was deemed desirable to make a study for the antimicrobial activity of the plant. The whole plant was collected from Baghdad city / College of Pharmacy/ University of Baghdad farm during July (2020). The aerial parts and roots were washed thoroughly, dried in shade, chopped, pulverized into a coarse powder, and then weighed. The shade-dried crushed plant materials were first defatted by maceration in hexane for 24 h. Then extracted by two extraction methods (hot method using soxhlet apparatus and cold method by maceration in solvent), using 85% aqueous ethanol as solvent extraction, and fractionated by petroleum ether, chloroform, ethyl acetate, and n-butanol. The phytochemical screening of the ethanolic extract from both extraction methods revealed alkaloids, saponin glycosides, coumarins, flavonoids, steroids, phenolic compounds, proteins, anthraquinones, terpenoids, and cardiac glycosides. However, depending on the percentage yields, the hot method yield was better than the cold method, so the extraction method by soxhlet was preferred upon maceration as it gives a higher percentage yield. The petroleum ether, chloroform, and ethyl acetate fractions were analyzed by thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC) for their steroids, alkaloids, and polyphenolic (phenolic acids and flavonoids) contents, respectively. The different chromatographic results revealed the presence of stigmasterol and β- sitosterol in petroleum ether fraction, harmine alkaloid in chloroform fraction, quercetin, quercitrin, apigenin, p-coumaric acid, and caffeic acid in ethyl acetate fraction of the Iraqi C. canadensis plant. Three polyphenolics compounds (p-coumaric acid, caffeic acid, apigenin) were isolated from ethyl acetate fraction by preparative thin-layer chromatography plates (PLC), and Harmine alkaloid was isolated from chloroform fraction by high-performance liquid chromatography (HPLC) using a fraction collector. The isolated compounds were subjected to various chromatographic and spectral analytical techniques for their identification, such as TLC, FTIR, HPLC, and high-performance thin-layer chromatography (HPTLC). Petroleum ether fraction was analyzed for the detection of coumarins by TLC. One compound was isolated, purified by PLC, symbolized as MS compound, and identified by FTIR and 1H -NMR since there is no standard available for this compound. The isolated MS compound could be pyranocoumarin glycoside. To investigate the essential oil composition of Iraqi C. canadensis, hydrodistillation of fresh aerial part of the plant was done using Clevenger-type apparatus for 3hr. The essential oils components and the hexane fraction obtained by maceration of the plant material in hexane solvent were identified using GC/MS analysis. The results of GC/MS analysis of the essential oil were abundant by hydrocarbon compounds, particularly by sesquiterpene hydrocarbon. This study also involves a preliminary determination of the antimicrobial activity of ethyl acetate fraction of the plant against two Gram-positive bacteria (Staphylococcus aureus and Staphylococcus epidermidis), two Gram-negative bacteria (Escherichia coli and Klebsiella sp.) and one fungi species (Candida albicans) by measuring the inhibition zone diameter around the hole in mm, compared with streptomycin and fluconazole standard drugs for antibacterial and antifungal activity, respectively. The antimicrobial results showed significant antibacterial activity against S.aureus (gram-positive bacteria) and important antifungal activity against Candida albicans. In contrast, no antibacterial activity was demonstrated against the tested gram-negative bacteria. Furthermore, the antibacterial activity exerted against S. epidermidis (gram-positive bacteria) was affected by dilution dimethyl sulfoxide (DMSO).
The aim of this study is to synthesize an easy, non-toxic and eco-friendly method. Silver nanoparticles which were synthesized by leaf extract of mint were characterized by UV-Visible Spectroscopy which appears UVVisible spectrum of demonstrated a peak 448 nm corresponding to surface Plasmon resonance of silver nanoparticles, Fourier Transform Infrared Spectroscopy (FTIR); functional groups involved in the silver nanoparticles synthesis were identified, the presence of silver nanoparticles was confirmed by X-ray diffraction (XRD) and Atomic Force Microscope (AFM) analysis clearly illustrated that the shape of silver nanoparticles was spherical and the size of the silver nanoparticles has been measured as 55- 85 nm. Evaluation of its antimic
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The present study was conducted to investigate the antimicrobial activity of the hot water and the hot ethanolic extracts of Thuja orientalis against some pathogenic microorganisms (Staphylococcus aureus, Pseudomonas aeruginosa, Eschericha coli, Proteus mirrablis, Salmonilla typhi, Klebsiella pneumoniae, Bacillus cereus, Bacillus subtilus, Acinobacter, Staphylococcus epidermidis and Candida albicans). Results showed that both the water and alcoholic extracts of this plant exert marked inhibitory effect against all the bacterial isolates and yeast and at different ratio, and it was shown that ethanolic extract was more effective in microbial inhibition than the water extract. Maximum inhibition (16 mm) was recorded against Staphylococcus aur
... Show MoreIn this work, N-hydroxy phthalimide derivatives (NHPID) were synthesized from the nucleuphilic substitution reactions of (NHPI) with different halides (alkyl halides, sulfonyl halides, benzoyl halides and benzyl halides). The products were distinguished using FTIR spectrum and Nuclear magnetic resonsnce (1H-NMR and 13CNMR), in addition to other characteristic methods such as sodium fution for sulfur determination. followed by measuring antibacterial (with different types of gram positive/gram negative bacteria) and antifungal activities of these compounds.
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Convolvulus arvensis is a species of bindweed that is rhizomatous and is in the morning glory family (Convolvulaceae) native to Europe and Asia. The plant is naturally grown in Iraq. The plant was reported to be used in traditional medicine from as early as 1730s.
The Aerial parts of Convolvulus arvensis were macerated in 80% ethanol for 6 days. The concentrated extract was partitioned with n-hexane, chloroform, ethyl acetate- and n-butanol successively. The n-hexane and ethyl acetate, fractions were examined for the presence of phytochemicals by thin l
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The antimicrobial potency of the crude ethanolic extracts from different Iraqi plants were evaluated . Further more, total sesquiterpene lactones and phenolic compounds were isolated and their antimicrobial activity attempted. The results indicated that crude extracts have no activity except that of Callistemon lanceolatus. Also, the sesquiterpene lactones and phenolic compounds isolated from Callistemon lanceolatus were the most significant antimicrobial active constituents of the studied plants.
The effectiveness inhibitory to extract alcohol for the leaf and flower to plant sage Salvia pratensis each of Staphylococcus aureus, streptococcus epidermidis, Salmonella typhi, Pseudomonas aeroginosa, Escherichia coli, Aspergillus niger and Candida albicans whom had any inhibition to aqueous extracts of the parts itself species bacterial and fungal. The study also demonstrated that the extract of plant containing compounds chemical such as tannins, Alkaloids, Flavonoieds, and saponins, which owns effectiveness of medical. The MIC, MBC and inhibition zones for crud extract were determinated for microbial agents.
New 2-amino thiazole ,oxodiazole, sulphonilamide and diazin derivatives of N-(α-chloro aceto)-3-(tolyl imino)-5-bromo-2-oxo-indole(2) have been synthesized .The preparation process started by the reaction of 5-bromo isatin with P-toluidine in the presence of glacial acetic acid and dimethylformamide(DMF) as a solvent to give 3-(tolyl imino)5-bromo-1H-indole-2-one.(1), Compound (1) with sodium hydride in dimethylformamide(DMF) at 0C0 gave a suspension of the sodium salt of Schiff base derivative and subsequent reaction with monochloroacetylchloride obtained the intermediate compound(2).Compound(2) was reacted with different reagents in four routes.The first route involved direct reaction with substituted 2-aminobenzothiazole u
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New schiff bases series (VIII) a-e and 1,3-thiazolidin-4-one derivatives (IX) a-e containing the 1,2,4-triazole and 1,3,4-thiazazole rings were synthesized and screening their biological activities. These compounds were identified via Fourier transform infrared (FT-IR) spectra, some via Proton nuclear magnetic resonance (1H-NMR) and mass spectra. The biological results indicated that all of these compounds did not reveal antibacterial effectiveness against (Escherichia coli and Klebsiella species) (G-). Some of these compounds showed moderate antibacterial activity against (Staphylococcus aureus, and Staphylococcus epidermidis) (G+), and all compounds exhibited moderate activity against Candida albicans.
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Antibacterial activity of CNSs against Staphylococcus aureus and Escherichia coli was estimated. Higher inhibition zone of 18 mm and 20 mm were observed against S. aureus and E.coli, respectively, at a concentration of 2 mg/ml of carbon nanosphere after 24 hrs of incubation at 37 ºC. In vitro cytotoxicity experiment was performed on two parasite strains of Leishmania donovani and Leishmania tropica by using MTT assay. L. donovani revealed more sensitiv to the CNSs than L. tropica. An intermediate level of cytotoxicity of 51.31 % was observed when 2.4 mg/ml of CNSs was incubated with L. donovani, while weak cytotoxicity of 37.20 % was shown when the
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