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Synthesis of 3-4-(2-furoyl)-1-piperazinyl-N- (substituted)propanamides as promising antibacterial agents with mild cytotoxicity

机译：合成3- 4-（2-（2-呋喃基）-1-哌嗪基 -N-（取代）的丙酰胺，作为具有轻度细胞毒性的有前途的抗菌剂

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Ghulam Hussain; Muhammad A Abbasi; Aziz-ur- Rehman; Sabahat Z Siddiqui; Irshad Ahmad; Rabia Malik; Muhammad Shahid; Zahid Mushtaq; Syed AA Shah;
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1. Synthesis of 3-[4-(2-furoyl)-1-piperazinyl]-N-(substituted)propanamides as promising antibacterial agents with mild cytotoxicity [J] . Ghulam Hussain, Muhammad A Abbasi, Aziz-ur-Rehman, Tropical Journal of Pharmaceutical Research . 2018,第7期

机译：3- [4-（2-呋喃基）-1-哌嗪基] -N-（取代）丙酰胺的合成作为有希望的抗菌剂，具有轻度的细胞毒性
2. Design, synthesis, molecular docking, and spectral studies of new class of carbazolyl polyhydroquinoline derivatives as promising antibacterial agents with noncytotoxicity towards human mononuclear cells from peripheral blood [J] . Venkatapathy Karuppan, Magesh Chinnaiyan J., Lavanya Gnanamani, Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry . 2020,第4期

机译：新类猪氨基喹啉喹啉衍生物的设计，合成，分子对接和光谱研究，作为对来自外周血的人单核细胞的非胞素毒性的抗菌剂
3. Design, synthesis and QSAR studies of 2-amino benzo[d]thiazolyl substituted pyrazol-5-ones: novel class of promising antibacterial agents [J] . Palkar Mahesh B., Patil Aniket, Hampannavar Girish A., Medicinal chemistry research: an international journal for rapid communications on design and mechanisms of action of biologically active agents . 2017,第9期

机译：2-氨基苯并的设计，合成和QSAR研究[D]噻唑基取代吡唑-5-唑类 - 一种：新型前列抗菌剂
4. Understanding the properties of chitosan aryl substituted thioureas in their role and potential as antibacterial agents [C] . Wan M. Khairul, Adibah Izzati Daud, Noraznawati Ismail International Symposium of Biomedical Engineering . 2018

机译：了解壳聚糖芳基取代的硫脲的性质及其作为抗菌剂的作用和潜力
5. I. Synthesis of N,N-bis(3-butenyl)amines from (2-azaallyl)nitriles. II. Synthesis of highly substituted pyrrolizidines from cyclic carbinol amides. III. Synthesis of potential phototriggered DNA crosslinking agents. [D] . Dietz, Amber L. 2005

机译：I.由（2-氮杂烯丙基）腈合成N，N-双（3-丁烯基）胺。二。由环状甲醇酰胺合成高度取代的吡咯烷核苷。三，潜在的光触发DNA交联剂的合成。
6. Novel Bi-heterocycles as Potent Inhibitors of Urease and Less Cytotoxic Agents: 3-({5-((2-Amino-13-thiazol-4-yl)methyl)-134-oxadiazol-2-yl}sulfanyl)-N-(un/substituted-phenyl)propanamides [O] . Muhammad Athar Abbasi, Muhammad Shahid Ramzan, Aziz ur-Rehman, 2020

机译：新型双杂项作为脲酶的有效抑制剂和少细胞毒性剂：3 - （{5 - （（2-氨基-13-噻唑-4-基）甲基）-134-恶二唑-2-基}磺酰基）-N-（UN /取代 - 苯基）丙烷酰胺
7. Studies on antibacterial agents. III. Synthesis and antibacterial activities of substituted 1,4-dihydro-8-methyl-4-oxoquinoline-3-carboxylic acids. [O] . Hisashi MIYAMOTO, Hiraki UEDA, Tatsuya OTSUKA, 1990

机译：研究抗菌剂。 III。取代的1,4-二氢-8-甲基-4-氧代喹啉-3-羧酸的合成及抗菌活性。

Synthesis of 3-4-(2-furoyl)-1-piperazinyl-N- (substituted)propanamides as promising antibacterial agents with mild cytotoxicity

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