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Tetrabromo-p-benzoquinone reacted with excess aromatic amines to give 2,5-dirylamino-3,6-dibromo-p-benzoquinones. The latter molecules on heating with sodium sulfide in alcohol in the presence of air gave triphenodithiazinediones.
Heating with copper powder in nitrobenzene transformed these compounds into the respective indolocarbazolediones. Comparative
antimicrobial and antifungal activities of the studied compounds were determined and discussed. 相似文献
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《Journal of Coordination Chemistry》2012,65(10):1747-1758
AbstractEight new mixed ligand complexes of dioxomolybdenum(VI) with 2-hydroxy-3-methoxy/3,5-dibromo benzaldehyde 4-phenyl/ethyl-S-methyl/butyl thiosemicarbazones (L) were synthesized. The complexes of general formula [MoO2LD] (D: methanol, pyridine) were characterized by elemental analysis, IR, UV, and 1H-NMR spectroscopy. The structure of 3a was also determined by X-ray single-crystal diffraction. The thiosemicarbazone ligands are coordinated to dioxomolybdenum(VI) center through ONN set and the sixth coordinated site of the molybdenum is occupied by the second ligand (D). The in vitro antimicrobial activities of all thiosemicarbazones and their dioxomolybdenum(VI) complexes were tested against Candida albicans, Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. 相似文献
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A series of heterocycle containing amide derivatives (1–28) were synthesised by the combination of acyl chlorides (1a, 2a) and heterocyclic/homocyclic ring containing amines, and their in vitro antifungal activity was evaluated against five plant pathogenic fungi, namely Gibberella zeae, Helminthosporium maydis, Rhizoctonia solani, Botrytis cinerea and Sclerotinia sclerotiorum. Results of antifungal activity analysis indicated that some of the products showed good to excellent antifungal activity, as compound 2 showed excellent activity against G. zeae and R. solani and potent activity against H. maydi, B. cinerea and S. sclerotiorum, and compounds 1, 8 and 10 also displayed excellent antifungal potential against H. maydi, B. cinerea and S. sclerotiorum and good activity against R. solani when compared with the standard carbendazim. 相似文献
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4-硫醚基喹唑啉类化合物的合成及抑菌活性研究 总被引:2,自引:0,他引:2
以4-氯喹唑啉和巯基化合物为原料, 丙酮作溶剂, 碳酸钾作缚酸剂, 合成了7个新型4-硫醚基喹唑啉类化合物. 采用1H NMR, 13C NMR, IR及元素分析对目标化合物的结构进行了表征. 生物活性测试表明, 化合物1d在50 μg•mL-1 药剂浓度下对小麦赤霉病菌、辣椒枯萎病菌、苹果腐烂病菌的抑菌活性分别达到69.5%, 71.9%和70.8%, EC50分别为25.88, 17.08和28.77 μg•mL-1. 相似文献
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Fourteen new 1H‐1,2,4‐triazole alcohol derivatives containing a ferrocenyl moiety were synthesized. In addition, six unexpected compounds, the hydroxyls of the title compounds, methylated by methanol, were obtained. The structures of all these new compounds were confirmed using 1H NMR spectra, 13C NMR, MS and elemental analyses. Some compounds were also confirmed with IR spectra. The antifungal and plant growth regulatory activities of the title compounds are discussed. Copyright © 2008 John Wiley & Sons, Ltd. 相似文献
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Two naphthalene pyrazole ligands were synthesized using KOH/DMSO and Cu catalyst and characterized with FT-IR, ESI-MS, 1H, and 13C NMR spectroscopies. The crystal structures of 1-(2-methylnaphthalen-1-yl)-1H-pyrazole (MeNap-Pz) ligand have been determined with X-ray crystal structure analysis. Reaction of the ligands with Cu(NO3)2x3.5H2O gave two new complexes and characterized with magnetic susceptibility, molar conductance, FT-IR, LCMS-MS, ICP-OES, NMR, thermogravimetric analysis, and ESR spectra. The spectral data of the ligands are coordinated to the metal ion through the nitrogen atoms of the pyrazole ring. Consequently, it has been determined that [Cu(MeNap-Pz)2(NO3)]NO3.2H2O complex showed square planar geometry and [Cu(NapMe-Pz)2(NO3)2].H2O complex showed octahedral geometry. All compounds were screened for in vitro antibacterial activity and copper complexes have been shown to be effective on bacteria. 相似文献
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In this study, new benzoylthiourea derivatives, (E)-N-[(2-benzamidomethyleneamino)ethylcarbamothioyl]benzamide H3L′, N-(1-(3-benzoylthioureido)propan-2-ylcarbamothioyl)-benzamide H4L″, (E)-N-[4-(benzamidomethyleneamino)phenylcarbamothioyl]benzamide H3L‴, were synthesized. Structures of the compounds were identified by spectroscopic techniques. In addition, all synthesized
compounds were evaluated for in vitro antibacterial and antifungal activity. Compound H3L‴ exhibited antibacterial activity. 相似文献
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Gülhan Turan-Zitoun Begüm Nurpelin Sağlik Ulviye Acar Çevik Serkan Levent Sinem Ilgin Weiam Hussein 《Phosphorus, sulfur, and silicon and the related elements》2013,188(11):744-751
AbstractA new series of 2-((1-furan-2-yl)ethylidene)hydrazono)-4-substitutedphenylthiazol-3(2H)-amines (2a–2o) and their Schiff bases (3a–3o) from 4-nitrobenzaldehyde were synthesized. The chemical structures of all the synthesized compounds were confirmed by their IR, 1H-NMR, 13C-NMR spectroscopy and mass spectrometry. They were screened for their antimicrobial and antifungal activities. Additionally, in vitro cytotoxic acivity of the most active antifungal compound (3o) and ketoconazole was determined in NIH/3T3 cells by MTT assay. Compound 2i (4-{3-Amino-2-[(1-(furan-2-yl)ethylidene)hydrazono]-2,3-dihydrothiazol-4-yl}phenol) showed the greatest antifungal activity among the newly synthesized derivatives. Schiff bases (3c-3n) displayed an undeniable fungicidal action against Candida parapsilosis ATCC 22019 as intense as the reference ketoconazole. In addition, the most active Schiff base 3o (2-[(1-(Furan-2-yl)ethylidene)hydrazono]-N-(4-nitrobenzylidene)-4-(2,3,4-trichloro phenyl)thiazol-3(2H)-amine) showed the highest antifungal activity against both Candida krusei ATCC 6258 and Candida parapsilosis ATCC 22019, and was as potent as ketoconazole. Moreover, compound 3o was found to be non-cytotoxic against NIH/3T3 cells. 相似文献
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Synthesis of CuS and ZnO/Zn(OH)2 nanoparticles and their evaluation for in vitro antibacterial and antifungal activities 下载免费PDF全文
Hossein Zare Khafri Mehrorang Ghaedi Arash Asfaram Hamedreza Javadian Mohammad Safarpoor 《应用有机金属化学》2018,32(7)
In this study, the copper sulfide nanoparticles (CuS‐NPs) and the zinc oxide/zinc hydroxide nanoparticles ((ZnO/Zn(OH)2‐NPs) were synthesized by a simple and low‐cost method, and the synthesized nanoparticles were characterized and identified by UV–Vis, field emission scanning electron microscopy (FE‐SEM), transmission electron microscopy (TEM) and X‐ray diffraction (XRD). The antimicrobial activity of the CuS‐NPs and the ZnO/Zn(OH)2‐NPs were examined by broth dilution to determine the minimal inhibitory concentration (MIC) of antibacterial agent required to inhibit the growth of a pathogen and the minimum bactericidal concentration (MBC) required to kill a particular bacterium. Agar disc diffusion method was used to determine the zone of inhibition. The nanoparticles demonstrated potent antibacterial activity against Klebsiella pneumonia (ATCC 1827), Acinetobacter baumannii (ATCC 150504), Escherichia coli (ATCC 33218) and Staphylococcus aureus (ATCC 25293). Antifungal activity against Aspergillus oryzae (PTCC 5164) was also obtained. The data obtained from antimicrobial activities by broth dilution and agar disc diffusion methods exhibited the CuS‐NPs were more effective than the ZnO/Zn(OH)2‐NPs. A good correlation was observed between the data obtained by both methods. 相似文献
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Twelve angular oxazole-fused coumarin derivatives were designed, synthesised and characterised by 1H NMR, 13C NMR and HRMS. The structure of compound 4a was further confirmed by X-ray single-crystal diffraction. The bioassay experiment results indicated that compounds 4f and 4l have high antifungal activity on the mycelium growth of 4 plant disease fungi. Especially, compound 4l has a stronger antifungal activity compare to the commercial fungicide, Carbendazim. The herbicidal activity experiment showed that 4a and 4b can significantly inhibit the taproot and caulis development of Chenopodium album seedling and have better activities than the commercial herbicide, Acetochlor. 相似文献
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Basma H. Amin Mohamed I. Abou-Dobara Mostafa A. Diab Essam A. Gomaa Mohammed A. El-Mogazy Adel Z. El-Sonbati Mohamed S. EL-Ghareib Mostafa A. Hussien Hanaa M. Salama 《应用有机金属化学》2020,34(8):e5689
A novel series of mixed-ligand complexes of 5,5′-{(1E,1E′)-1,4-phenelynebis(diazene-2,1-diyl)}bis(quinolin-8-ol) (H2L1) as a primary ligand and 4-aminoantipyrine(L2) as a secondary ligand with Mn(II) ion were prepared using two general formulae: [Mn2(H2L1)2(L2)2X4].4Cl (X = OH2( 1 ), ONO2−( 2 ), Cl=nil; OAc( 3 ), Cl = nil) and [Mn2(H2L1)(L2)2(O2SO2)2]( 4 ). Free ligands and their complexes were characterized. Electronic absorption spectra of the mixed-ligand complexes indicate a distorted octahedral geometry around the central metal ion, and the anions X− are in the axial positions for all compounds. The ligands behave in a neutral bidentate manner, through nitrogen atoms and oxygen atoms of the carbonyl group (L2), whereas H2L1 coordinated through nitrogen and OH groups as a neutral bidentate ligand. All complexes do not contain coordinated water molecules, but complex ( 1 ) contains four water molecules. The water molecules are removed in a single step. The complexes exhibited magnetic susceptibility corresponding to five unpaired electrons. The antimicrobial activity of the Mn(II) mixed-ligand complexes ( 1–4 ) against two gram-positive bacteria, three local gram-negative bacteria, and three fungi species was tested. Mn(II) mixed-ligand complex ( 2 ) exhibited significant antibacterial activity against Bacillus cereus, Staphylococcus aureus, Escherichia coli, Klebsiella pneumoniae, and Pseudomonas sp. Mixed-ligand complex ( 2 ) exhibited a high potential cytotoxicity against the growth of human lung cancer cells. 相似文献
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Xu Tang Zhongbo Wang Xinmin Zhong Xiaobin Wang Lijuan Chen Ming He 《Phosphorus, sulfur, and silicon and the related elements》2019,194(3):241-248
A series of benzothiazole derivatives bearing a 1,3,4-thiadiazole moiety were designed, synthesized and evaluated for their antibacterial, antifungal and antiviral activities. The bioassay results indicated that most of target compounds showed good antiviral activities against tobacco mosaic virus (TMV) and antibacterial activities against Xanthomonas oryzae pv. oryzae (Xoo) and Ralstonia solanacearum (Rs). Especially, the anti-Xoo effect of title compounds 5k (N-(5-methoxybenzo[d]thiazol-2-yl)-2-((5-(2-tolyl)-1,3,4-thiadiazol-2-yl)thio)acetamide) and the anti-Rs effect of title compounds 5a (N-(5-nitrobenzo[d]thiazol-2-yl)-2-((5-(4-(trifluorom ethyl)phenyl)-1,3,4-thiadiazol-2-yl)thio)acetmide) respectively reached 52.4% and 71.6% at 100?µg/mL, which are superior to that of bismerthiazol (32.0% and 52.3%). In addition, the protective and inactivation activities of title compound 5i (N-(5-methoxybenzo [d]thiazol-2-yl)-2-((5-(4-nitrophenyl)-1,3,4-thiadiazol-2-yl)thio)acetamide) against TMV were 79.5% and 88.3%, respectively, which are better than that of ningnanmycin (76.4% and 86.8%). The above research showed that benzothiazole derivatives bearing a 1,3,4-thiadiazole moiety may be used as potential molecular templates in searching for highly-efficient antiviral and antibacterial agents. 相似文献
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Indazoles and pyrazoles are known to be pharmaceutically relevant molecules. In particular their application as both analgesic and antitumoral drugs has been reported. In order to investigate the properties of compounds belonging to these families, we have synthesised new cycloalkylpyrazoles bearing an arylidene group on the cycloalkyl ring, with the aim of modifying the biological profile of these molecules. 相似文献
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Heterobimetallic complexes of the type [M(C6H6N2)2(M′)2(R)4]Cl2 have been synthesized by the direct reaction of [M(C6H8N2)2]Cl2 with Group 4 or 14 organometallic dichlorides Ph2M′Cl2,Me2M′Cl2 or Cp2M″Cl2 in 1:2 molar ratio in MeOH (M = Pd or Pt, M′ = Si or Sn and M″ = Ti or Zr). The compounds were characterized by elemental analysis, molecular weight determination, electronic, 1H NMR and IR spectra, magnetic susceptibilities and conductivity measurements. These studies showed that the compounds are monomers and dimagnetic in nature, with a square‐planar geometry around palladium and platinum metals. Both the free ligands and their metal complexes were screened for antimicrobial activity on different species of pathogenic fungi and bacteria and were found active in this respect.Copyright © 2001 John Wiley & Sons, Ltd. 相似文献