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).
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Background: Nowadays, the environmentally friendly procedures must be developed to avoid using harmful compounds in synthesis methods. Their increase interest in creating and researching silver nanoparticles (AgNPs) because of their numerous applications in many fields especially medical fields such as burn, wound healing, dental and bone implants, antibacterial, viral, fungal, and arthropodal activities. Biosynthesis of nanoparticles mediated pigments have been widely used as antimicrobial agent against microorganisms. Silver nanoparticles had synthesized by using melanin from locally isolate Pseudomonas aeruginosa, and used as antimicrobial activity against pathogenic microorganisms. Aim of the study: Isolation of Pseudomonas aeruginosa
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To synthesize new hydrazone derivatives of naproxen with enhanced anti-inflammatory activity and devoid the ulcerogenic side effects. Hydrazones were synthesized by conjugation of naproxen hydrazide with seven natural and synthetic aldehyde and ketone by using glacial acetic acid as catalyst. The synthesis has been carried out following simple methodology in excellent isolated yields.The structure of the synthesized derivatives has been characterized by elemental microanalysis (CHN), FTIR Spectroscopy, and other physicochemical properties.The anti- inflammatory activity of the synthesized compounds was evaluated in vivo using the egg-white induced edema model in rats, and the results of the biological assay was found to be comparable to Nap
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The Disi water samples were collected from different Disi aquifer wells in Jordan using a clean polyethylene container of 10-liter size. A hyper-pure germanium (HPGe) detector with high- resolution gamma-ray spectroscopy and a low background counting system was used for the identification of unknown gamma-rays emitting from radionuclides in the environmental samples. The ranges of specific activity concentrations of 226Ra and 228Ra in the Disi aquifer water were found to be from 0.302 ± 0.085 to 0.723 ± 0.207 and from 0.047 ± 0.010 to 0.525 ± 0.138 Bq L−1, with average values of 0.516 ± 0.090 and 0.287 ± 0.091 Bq L−1, respectively. The average combined radium (226Ra + 228Ra) activity and radium activity ratio (228Ra/226Ra) in Disi
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There is a continuous and massive need for newer cephalosporins that should have resistance against β-lactamases and can be used orally. An approach of using cephalexin, as a well-studied and potent antibacterial compound is considered to prepare new designed derivatives. These derivatives include the incorporation of amino acid moiety linked through an amide bond with the α-amino group of cephalexin. Certain aliphatic amino acids were used, such as glycine, alanine, valine and proline. The chemical structures of these derivatives were confirmed by IR spectroscopy and elemental analyses. All the synthesized compounds were subjected for preliminary evaluation of antimicrobial activity using well diffusion method, against certa
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Schiff base of chitosan with Para-Dimethyl aminobenzaldehyde /PVA-Ag Nanocomposite have been prepared as antimicrobial polymer. The prepared chitosan Schiff base and chitosan Schiff base / PVA-Ag nanocomposite were characterized by FT-IR, SEM analysis and biological activity. The nanocomposite showed good activity against different types of bacteria.
The study aimed to survey mushroom species from fields among herbs, palm trunks, and trees in central Iraq and to identify them on the basis of morphological and molecular characteristics. As a molecular identification result with polymerase chain reaction six species were recorded (with eight isolates): Agaricus bitorquis (Quéllt) Saccardo. 1887 (SHA14); Candolleomyces candolleanus (Fr.) D. Wächter & Melzer, 2020 (SHA15); Cyclocybe cylindracea (D.C.) Vizzini & Angelini, 2014 (SHA13); Leucoagaricus hesperius Vellinga, 2010 (SHA16); Volvariella sp. (SHA17), and Volvopluteus gloiocephalus (D. C.) Vizzini, Contu & Justo, 2011 (SHA10, SHA101 and SHA12), belonging to four families of Basidiomycetes: Agaricaceae, Pluteaceae,
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The new bidentate Schiff base ligand namely [(E)-N1-(4-methoxy benzylidene) benzene-1, 2-diamine] was prepared from condensation of 4-Methoxy benzaldehyde with O-Phenylene diamine at 1:1 molar ratio in ethanol as a solvent in presence of drops of 48% HBr. The structure of ligand (L) was characterized by, FT-IR, U.V-Vis., 1H-, 13C- NMR spectrophotometer, melting point and elemental microanalysis C.H.N. Metal complexes of the ligand (L) in general molecular formula [M(L)3], where M= Mn(II), Co(II), Ni(II),Cu(II) and Hg(II); L=(C14H14N2O) in ratio (1:3)(Metal:Ligand) were synthesized and characterized by Atomic absorption, FT- IR, U.V-Vis. spectra, molar conductivity, chloride content, melting point and magnetic susceptibility from the above d
... Show MoreThis research includes the synthesis of some new different heterocyclic derivatives of 5-Bromoisatin. New sulfonylamide, diazine, oxazole, thiazole and 1,2,3-triazole derivatives of 5-Bromoisatin have been synthesized. The synthesis process started by the reaction of 5-Bromoisatin with different reagents to obtain schiff bases of 5-Bromoisatin intermediate compounds(1, 8, 19) by using glacial acetic acid as a catalyst in three routes. The first route, 5-Bromoisatin reacted with p-aminosulfonylchloride to product compound(1), then converted to sulfonyl amide derivatives(2-7) by the reaction of compound(1) with different substituted primary aromatic amine in absolute ethanol. The second route includes the reaction of 5-Bromoisatin rea
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