7-fluoroquinoline-3-carbaldehyde

• 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: 7-fluoroquinoline-3-carbaldehyde
• 化学式: C₁₀H₆FNO
• mdl: MFCD18433598
• 分子量: 175.162
• InChiKey: GIHIDOQMXSCYRX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  30
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  7-fluoroquinoline-3-carbaldehyde 在 sodium tetrahydroborate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 lithium chloride 作用下， 以 甲醇 、 乙腈 为溶剂， 反应 1.5h， 生成 (E)-1-(7-fluoroquinolin-3-yl)-7-(5,6,7,8-tetrahydro-1,8-naphthyridin-2-yl)hept-1-en-3-ol
  参考文献：
  名称：

  [EN] FLUORINATED TETRAHYDRONAPHTHYRIDINYL NONANOIC ACID DERIVATIVES AND USES THEREOF
  [FR] DÉRIVÉS D'ACIDE NONANOÏQUE TÉTRAHYDRONAPHTHYRIDINYLE FLUORÉS ET LEURS UTILISATIONS

  摘要：

  公开号：

  WO2016134223A3
• 作为产物：
  描述：

  2-氯-7-氟喹啉-3-甲醛 在 四(三苯基膦)钯 甲酸 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以24%的产率得到7-fluoroquinoline-3-carbaldehyde
  参考文献：
  名称：

  取代的3-喹啉烷醇的对映选择性合成及其在不对称自催化中的应用

  摘要：

  对映体富集的 3-喹啉链烷醇在将二异丙基锌添加到相应的取代的 quinoline-3-carbaldehydes 时充当不对称自催化剂，使其自身具有高达 97% 的放大对映体过量 (ee)。

  DOI：

  10.1055/s-2004-822402

文献信息

• FLUORINATED TETRAHYDRONAPHTHYRIDINYL NONANOIC ACID DERIVATIVES AND USES THEREOF
  申请人：SciFluor Life Sciences, Inc.

  公开号：US20160244447A1

  公开（公告）日：2016-08-25

  The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating fibrosis, macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.

  本发明涉及式I的氟化合物及其合成方法。本发明还涉及包含本发明中的氟化合物的制药组合物，以及通过将这些化合物和制药组合物用于需要治疗纤维化、黄斑退化、糖尿病视网膜病变（DR）、黄斑水肿、糖尿病性黄斑水肿（DME）和视网膜静脉阻塞后的黄斑水肿（RVO）的患者来进行治疗的方法。
• FLUORINATED INTEGRIN ANTAGONISTS
  申请人：SCIFLUOR LIFE SCIENCES, INC.

  公开号：US20160075698A1

  公开（公告）日：2016-03-17

  The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.

  本发明涉及式I的氟化合物及其合成方法。本发明还涉及含有本发明的氟化合物的药物组合物，并通过将这些化合物和药物组合物给予需要治疗黄斑变性、糖尿病视网膜病变（DR）、黄斑水肿、糖尿病性黄斑水肿（DME）和视网膜静脉阻塞后的黄斑水肿（RVO）的受试者来治疗这些疾病。
• Fluorinated integrin antagonists
  申请人：SciFluor Life Sciences, Inc.

  公开号：US10106537B2

  公开（公告）日：2018-10-23

  The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.

  本发明涉及式 I 的含氟化合物以及合成这些化合物的方法。本发明还涉及含有本发明含氟化合物的药物组合物，以及通过向有需要的受试者施用这些化合物和药物组合物来治疗黄斑变性、糖尿病视网膜病变（DR）、黄斑水肿、糖尿病黄斑水肿（DME）和视网膜静脉闭塞（RVO）后黄斑水肿的方法。
• Fluorinated tetrahydronaphthyridinyl nonanoic acid derivatives and uses thereof
  申请人：SciFluor Life Sciences, Inc.

  公开号：US10301307B2

  公开（公告）日：2019-05-28

  The present invention relates to fluorinated compounds of formula I and methods of synthesizing these compounds. The present invention also relates to pharmaceutical compositions containing the fluorinated compounds of the invention, and methods of treating fibrosis, macular degeneration, diabetic retinopathy (DR), macular edema, diabetic macular edema (DME), and macular edema following retinal vein occlusion (RVO), by administering these compounds and pharmaceutical compositions to subjects in need thereof.

  本发明涉及式 I 的含氟化合物以及合成这些化合物的方法。 本发明还涉及含有本发明含氟化合物的药物组合物，以及通过向有需要的受试者施用这些化合物和药物组合物来治疗纤维化、黄斑变性、糖尿病视网膜病变（DR）、黄斑水肿、糖尿病黄斑水肿（DME）和视网膜静脉闭塞（RVO）后黄斑水肿的方法。
• SAR Studies of 5-Aminopyrazole-4-carboxamide Analogues as Potent and Selective Inhibitors of <i>Toxoplasma gondii</i> CDPK1
  作者：Wenlin Huang、Kayode K. Ojo、Zhongsheng Zhang、Kasey Rivas、Rama Subba Rao Vidadala、Suzanne Scheele、Amy E. DeRocher、Ryan Choi、Matthew A. Hulverson、Lynn K. Barrett、Igor Bruzual、Latha Kallur Siddaramaiah、Keshia M. Kerchner、Matthew D. Kurnick、Gail M. Freiberg、Dale Kempf、Wim G. J. Hol、Ethan A. Merritt、Georg Neckermann、Eugenio L. de Hostos、Nina Isoherranen、Dustin J. Maly、Marilyn Parsons、J. Stone Doggett、Wesley C. Van Voorhis、Erkang Fan

  DOI：10.1021/acsmedchemlett.5b00319

  日期：2015.12.10

  We previously discovered compounds based on a 5-aminopyrazole-4-carboxamide scaffold to be potent and selective inhibitors of CDPK1 from T. gondii. The current work, through structure-activity relationship studies, led to the discovery of compounds (34 and 35) with improved characteristics over the starting inhibitor 1 in terms of solubility, plasma exposure after oral administration in mice, or efficacy on parasite growth inhibition. Compounds 34 and 35 were further demonstrated to be more effective than 1 in a mouse infection model and markedly reduced the amount of T. gondii in the brain, spleen, and peritoneal fluid, and 35 given at 20 mg/kg eliminated T. gondii from the peritoneal fluid.