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排序方式: 共有163条查询结果,搜索用时 215 毫秒
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Ellis MJ Antonyuk SV Strange RW Sawers G Eady RR Hasnain SS 《Inorganic chemistry》2004,43(24):7591-7593
Copper nitrite reductases contain both an electron-transfer type 1 Cu site and a catalytic type 2 Cu site. We have mutated one of the type 2 copper ligating histidines to observe the effect on catalytic turnover. This mutation has created a unique site where Cu is ligated by 2 His Nepsilon2 atoms alone. 相似文献
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MM. J. Duflos D. Letouz G. Queguiner P. Pastour 《Journal of heterocyclic chemistry》1973,10(6):1083-1084
This communication describes the synthesis of l-methyl-2,3-diformylpyrrole. This new compound is used to prepare a new heterocycle, l-methylcyclohepta[b]pyrrol-6-one and thus allows a new synthesis of l-methylpyrrolo[2,3-d]pyridazine. 相似文献
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The synthesis of N-(dimethoxy and 3, 5-diacetoxybenzoyl) -L- amino acid hydrazides, and their reactions with some aldehydes and ketones are described. 相似文献
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Ajaj Rahaf Shubyar Nasser Alashban Yazeed El-Sayed Samar Salah Tamar Al Yafei Mohammed A. Salem 《Journal of Radioanalytical and Nuclear Chemistry》2021,330(3):923-928
Journal of Radioanalytical and Nuclear Chemistry - Groundwater is the most valuable resource in arid regions, such as UAE. Estimations of natural radionuclide concentrations are important to... 相似文献
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Lamya H. Al-Wahaibi Ahmed A. B. Mohamed Samar S. Tawfik Hanan M. Hassan Ali A. El-Emam 《Molecules (Basel, Switzerland)》2021,26(8)
The reaction of 5-(3,4-dimethoxyphenyl)-1,3,4-oxadiazole-2(3H)-thione 3 with formaldehyde solution and primary aromatic amines or 1-substituted piperazines, in ethanol at room temperature yielded the corresponding N-Mannich bases 3-arylaminomethyl-5-(3,4-dimethoxyphenyl)-1,3,4-oxadiazole-2(3H)-thiones 4a–l or 3-[(4-substituted piperazin-1-yl)methyl]-5-(3,4-dimethoxyphenyl)-1,3,4-oxadiazole-2(3H)-thiones 5a–d, respectively. The in vitro inhibitory activity of compounds 4a–l and 5a–d was assessed against pathogenic Gram-positive, Gram-negative bacteria, and the yeast-like pathogenic fungus Candida albicans. The piperazinomethyl derivatives 5c and 5d displayed broad-spectrum antibacterial activities the minimal inhibitory concentration (MIC) 0.5–8 μg/mL) and compounds 4j, 4l, 5a, and 5b showed potent activity against the tested Gram-positive bacteria. In addition, the anti-proliferative activity of the compounds was evaluated against prostate cancer (PC3), human colorectal cancer (HCT-116), human hepatocellular carcinoma (HePG-2), human epithelioid carcinoma (HeLa), and human breast cancer (MCF7) cell lines. The optimum anti-proliferative activity was attained by compounds 4l, 5a, 5c, and 5d. 相似文献
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Fayçel Jemmezi Samar Chtiba Jameleddine Khiari 《Journal of heterocyclic chemistry》2013,50(2):206-208
The symmetrical vinamidinium salts were allowed to react with malononitrile in refluxing ethanol in the presence of ammonium acetate for 12 h to afford the 2‐amino‐5‐aryl or formylpyridine‐3‐carbonitriles. 相似文献