Synthesis and in vitro antiproliferative activities of quinoline derivatives.

Broch S; Aboab B; Anizon F; Moreau P

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Synthesis and in vitro antiproliferative activities of quinoline derivatives.

机译：喹啉衍生物的合成及其体外抗增殖活性。

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摘要

The synthesis of new di- and trimeric quinoline derivatives is described as well as their in vitro antiproliferative activities toward a human fibroblast primary culture and two human solid cancer cell lines (MCF-7 and PA 1).

机译：描述了新的二聚和三聚喹啉衍生物的合成，以及它们对人成纤维细胞原代培养物和两种人实体癌细胞系（MCF-7和PA 1）的体外抗增殖活性。

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《European Journal of Medicinal Chemistry: Chimie Therapeutique》 |2010年第4期|共6页
作者
Broch S; Aboab B; Anizon F; Moreau P;
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正文语种 eng
中图分类医药、卫生;劳动卫生;
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1. Synthesis and in vitro antiproliferative activities of quinoline derivatives. [J] . Broch S, Aboab B, Anizon F, European Journal of Medicinal Chemistry: Chimie Therapeutique . 2010,第4期

机译：喹啉衍生物的合成及其体外抗增殖活性。
2. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; Structure-activity relationships of neocryptolepines and 6-methyl congeners [J] . WangL., ?witalskaM., MeiZ.-W., Bioorganic and medicinal chemistry . 2012,第15期

机译：新的11-氨基烷基氨基取代的5H-和6H-吲哚并[2,3-b]喹啉的合成及体外抗增殖活性;新隐油松和6-甲基同类物的构效关系
3. Synthesis and in vitro antiproliferative activity of new 11-aminoalkylamino-substituted 5H- and 6H-indolo[2,3-b]quinolines; Structure-activity relationships of neocryptolepines and 6-methyl congeners [J] . WangL., ?witalskaM., MeiZ.-W., Bioorganic and medicinal chemistry . 2012,第15期

机译：新的11-氨基烷基氨基取代的5H-和6H-吲哚并[2,3-b]喹啉的合成及体外抗增殖活性;新隐油松和6-甲基同类物的构效关系
4. Synthesis of tetra-and tripeptide analogs of Substance P fragments and their peptoid-peptide hybrids.Study of their antiproliferative activity in vitro [C] . Paraskevi Ch.Vakalopoulou, Helen M.Makrodouli, George P.Stavropoulos International Peptide Symposium;European Peptide Symposium . 2005

机译：物质P片段的四氢肽和三肽类似物的合成及其拟肽杂交种。其抗增殖活性在体外
5. Part one. Synthesis of phosphorus-containing amino acid analogues derived from trans-4-hydroxyproline and the study of their bioactivity in the glutamate excitatory neurotransmitter system. Part two. Synthesis, structural modifications and in vitro pharmacology of quinoline-2,4-dicarboxylic acids as proposed inhibitors of the glutamate vesicular transporter. [D] . Carrigan, Christina Nicole. 2000

机译：第一部分。反式-4-羟基脯氨酸衍生的含磷氨基酸类似物的合成及其在谷氨酸兴奋性神经递质系统中的生物活性的研究。第二部分。喹啉-2,4-二羧酸作为谷氨酸囊泡转运蛋白的抑制剂的合成，结构修饰和体外药理作用。
6. In vitro activity of ciprofloxacin compared with those of other new fluorinated piperazinyl-substituted quinoline derivatives. [O] . D L Van Caekenberghe, S R Pattyn 1984

机译：与其他新的氟化哌嗪基取代的喹啉衍生物相比环丙沙星的体外活性更高。
7. Synthesis and Antitumor Activity of Fused Quinoline Derivatives. V. Methylindolo(3,2-b)quinolines. [O] . Yasuo TAKEUCHI, Masayuki KITAOMO, Ming-rong CHANG, 1997

机译：融合喹啉衍生物的合成与抗肿瘤活性。 V.甲基吲哚（3,2-B）喹啉。

Synthesis and in vitro antiproliferative activities of quinoline derivatives.

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