has been cited by the following article(s):
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[1]
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Application of the pyrazolone derivatives as effective modulators in the opto-electronic networks
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… of Photochemistry and …,
2023 |
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[2]
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СИНТЕЗ И НЕКОТОРЫЕ БИОЛОГИЧЕСКИЕ СВОЙСТВА ПРОИЗВОДНЫХ ХРОМОФОРА ЗЕЛЕНОГО ФЛУОРЕСЦЕНТНОГО БЕЛКА
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ՏԱՍՆՀԻՆԳԵՐՈՐԴ …,
2022 |
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[3]
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Учредители: Российская академия наук
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ЖУРНАЛ ОБЩЕЙ …,
2022 |
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[4]
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Synthesis and Anticholinesterase Activity of 4-Arylidene-1-[ω-(dialkylamino) alkyl]-2-phenyl-4, 5-dihydro-1 (H)-imidazole-5-ones
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Russian Journal of …,
2022 |
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[5]
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Recent Developments and Biological Activities of 5-Oxo-Imidazolones Derivatives: A Review
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2021 |
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[6]
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Синтез и антихолинэстеразная активность функциональнозамещенных имидазол-5-онов
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2019 |
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[7]
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Синтез и антихолинэстеразные свойства (Z)-1-замещенных-2-фенил-4-(п-толуолсульфонилоксибензилиден)-5-имидазолонов
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2019 |
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[8]
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Синтез и антихолинэстеразные свойства (Z)-1-замещенных-2-фенил-4-(п-толуолсульфонилокси-бензилиден)-5-имидазолонов
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2019 |
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[9]
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Design, Synthesis and Antiproliferative Activities of Oxidative Stress Inducers Based on 2-styryl-3, 5-dihydro-4H-imidazol-4-one Scaffold
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Chemical and Pharmaceutical Bulletin,
2018 |
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[10]
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乙烯基二肽类似物的设计与合成
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2015 |
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[11]
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Dihydrooxazolones and dihydroimidazolones derived from acylglycines: syntheses, molecular structures and supramolecular assembly
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Acta Crystallographica Section C: Structural Chemistry,
2015 |
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[12]
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Antiproliferative Properties of Vinyl Dipeptides: Synthesis and MCF-7 Cell Line Testing
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Open Journal of Medicinal Chemistry,
2012 |
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[1]
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Synthesis and Anticholinesterase Activity of 4-Arylidene-1-[ω-(dialkylamino)alkyl]-2-phenyl-4,5-dihydro-1(H)-imidazole-5-ones
Russian Journal of General Chemistry,
2022
DOI:10.1134/S1070363222090043
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[2]
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Design, Synthesis and Antiproliferative Activities of Oxidative Stress Inducers Based on 2-styryl-3,5-dihydro-4H-imidazol-4-one Scaffold
Chemical and Pharmaceutical Bulletin,
2018
DOI:10.1248/cpb.c18-00398
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[3]
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Antiproliferative Properties of Vinyl Dipeptides: Synthesis and MCF-7 Cell Line Testing
Open Journal of Medicinal Chemistry,
2012
DOI:10.4236/ojmc.2012.24013
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