spiro[perhydropyrimidine-5,5'-1',3',4',9',10',10a'-hexahydro-2'-oxa-4a'-azaphenanthrene]-2,4,6-trione

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: spiro[perhydropyrimidine-5,5'-1',3',4',9',10',10a'-hexahydro-2'-oxa-4a'-azaphenanthrene]-2,4,6-trione
• 英文别名: 1,2,4,4a-tetrahydro-spiro[[1,4]oxazino[4,3-a]quinoline-5(6H),5'(2'H)-pyrimidine]-2',4',6'(1'H,3'H)-trione；2',6'-dioxo-1,1',2,4,4a,6'-hexahydro-2'H,6H-spiro[1,4-oxazino[4,3-a]quinolin-11-ium-5,5'-pyrimidin]-4'-olate；2',6'-dioxospiro[1,2,4,4a,6,11-hexahydro-[1,4]oxazino[4,3-a]quinolin-11-ium-5,5'-pyrimidine]-4'-olate
• 化学式: C₁₅H₁₅N₃O₄
• 分子量: 301.302
• InChiKey: XJWUVBRHULWDRE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.2
• 重原子数：
  22
• 可旋转键数：
  0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  87.7
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  2-氟苯甲醛 在 N,N-二异丙基乙胺 作用下， 以 异丙醇 、 乙腈 为溶剂， 反应 12.0h， 生成 spiro[perhydropyrimidine-5,5'-1',3',4',9',10',10a'-hexahydro-2'-oxa-4a'-azaphenanthrene]-2,4,6-trione
  参考文献：
  名称：

  Design, synthesis and anticancer activity of functionalized spiro-quinolines with barbituric and thiobarbituric acids

  摘要：

  A new series of spiro-quinoline compounds have been accomplished by the reaction of barbituric acid or thiobarbituric acid with derivatives of benzisoxazole-5-carbaldehyde or 2-substituted benzaldehyde. These compounds were evaluated for their in vitro cytotoxicity on two mammalian cancer cell lines MCF-7 and KB. The compounds exhibit cytotoxicity against these cell lines in micromolar range. Among the series of compounds, 11(a-j) particularly 11b and 11e showed relatively good activity against both the tested cell lines. Compound 11b was found to exhibit the highest cytotoxic activity with IC50 value 90.2 mu M for MCF-7 and 49.8 mu M for KB cell line. Flow cytometric analysis study confirmed that these molecules induced cytotoxicity via apoptosis.

  DOI：

  10.1007/s00044-015-1408-7

文献信息

• Synthesis of Spiroheterocyclic Systems from Barbituric Acids and N,N-Disubstituted o-Aminobenzaldehydes
  作者：K. A. Krasnov、V. G. Kartsev

  DOI：10.1007/s11178-005-0263-2

  日期：2005.6

  Reactions of barbituric, 1,3-dimethylbarbituric, and 2-thiobarbituric acids with 2-(1-pyrrolidinyl)benzaldehyde, its 6- and 7-membered homologs, and 4-phenylpiperazine and morpholine analogs lead to formation of fused systems with a spirocyclic 2,4,6-trioxopyrimidine fragment. The process involves intermediate formation of labile 5-arylmethylidenebarbituric acids which exhibit t-amino effect and undergo spontaneous isomerization to give the final products. The observed spirocyclizations are characterized by an anomalously high rate.

  巴比妥酸、1,3-二甲基巴比妥酸和2-硫巴比妥酸与2-(1-吡咯烷基)苯甲醛及其6-和7-成员同系物，以及4-苯基哌嗪和吗啉类似物的反应，形成了具有螺环结构的2,4,6-三氧嘧啶片段的融合体系。该过程涉及不稳定的5-芳基甲烯基巴比妥酸的中间体形成，这些中间体表现出t-氨基效应，并自发异构化，生成最终产物。观察到的螺环化反应特征是反应速率异常高。
• TRICYCLIC TETRAHYDROQUINOLINE ANTIBACTERIAL AGENTS
  申请人：Barbachyn Michael Robert

  公开号：US20100022524A1

  公开（公告）日：2010-01-28

  The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.

  该发明涉及公式I的四氢喹啉及相关化合物，以及其制备的药物组合物，对于广泛的人类和兽医病原体具有有用的抗菌活性。
• Tricyclic tetrahydroquinoline antibacterial agents
  申请人：Barbachyn Robert Michael

  公开号：US20070161630A1

  公开（公告）日：2007-07-12

  The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.

  本发明涉及公式I的四氢喹啉及其相关化合物，以及具有对广泛的人类和兽医病原体有用的抗菌活性的制药组合物。
• Tricyclic Tetrahydroquinoline Antibacterial Agents
  申请人：Barbachyn Michael Robert

  公开号：US20110092494A1

  公开（公告）日：2011-04-21

  The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.

  该发明涉及公式I的四氢喹啉及相关化合物，以及其制备的药物组合物，对人类和兽医病原体具有有用的抗菌活性。
• US7208490B2
  申请人：——

  公开号：US7208490B2

  公开（公告）日：2007-04-24