N-(3-anilinoquinoxalin-2-yl)benzenesulfonamide

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: N-(3-anilinoquinoxalin-2-yl)benzenesulfonamide
• 化学式: C₂₀H₁₆N₄O₂S
• 分子量: 376.4
• InChiKey: PKCSGOHBWGFZJZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  27
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  92.4
• 氢给体数：
  2
• 氢受体数：
  6

文献信息

• Methods of Using PI3K and MEK Modulators
  申请人：Aftab Dana T.

  公开号：US20100075947A1

  公开（公告）日：2010-03-25

  The invention provides methods of treating cancer with a combination of compounds which inhibit kinases, more specifically MEK and PI3K.

  本发明提供了一种使用抑制激酶的化合物组合来治疗癌症的方法，更具体地说是抑制MEK和PI3K的化合物组合。
• TARGETING AN HIV-1 NEF-HOST CELL KINASE COMPLEX
  申请人：Emert-Sedlak Lori

  公开号：US20110190241A1

  公开（公告）日：2011-08-04

  Drug candidates for inhibition of HIV-I replication can target Src family kinases (SFK), such as Hck, that interact with Nef protein of the virus. Compounds characterized by such inhibitory activity were identified via an assay for kinase activity of an SFK in a Nef:SFK complex. Illustrative of inhibitors identified using the kinase assay are various 2,3-diaminoquinaxolines and furo[2,3-d]pyrimidines. The inventive inhibitors were found to arrest HIV-I viral replication in vitro.

  用于抑制HIV-I复制的药物候选物可以针对Src家族激酶（SFK），如与病毒的Nef蛋白相互作用的Hck进行靶向。通过对Nef:SFK复合物中SFK的激酶活性进行测定，鉴定了具有这种抑制活性的化合物。使用激酶测定鉴定的抑制剂的例子包括各种2,3-二氨基喹啉和呋喃[2,3-d]嘧啶。这些创新的抑制剂被发现可以在体外阻止HIV-I病毒的复制。
• Method of Using PI3K and MEK Modulators
  申请人：Aftab Dana T.

  公开号：US20120302545A1

  公开（公告）日：2012-11-29

  The invention provides methods of treating cancer with a combination of compounds which inhibit kinases, more specifically MEK and PI3K.

  该发明提供了一种使用抑制激酶的化合物组合治疗癌症的方法，更具体地说是MEK和PI3K。
• N-(3-Phenylamino-quinoxalin-2-yl)-benzenesulfonamide derivatives as phosphatidylinositol 3-kinase inhibitors
  申请人：Exelixis, Inc.

  公开号：EP2364974A1

  公开（公告）日：2011-09-14

  The present invention comprises small molecule inhibitors of phosphatidylinositol 3-kinase (PI3K), which is associated with a number of malignancies such as ovarian cancer, cervical cancer, breast cancer, colon cancer, rectal cancer, and gioblastomas, among others. Accordingly, the compounds of the present invention are useful for treating, preventing, and/or inhibiting these diseases.

  本发明包括磷脂酰肌醇 3-激酶（PI3K）的小分子抑制剂，PI3K 与卵巢癌、宫颈癌、乳腺癌、结肠癌、直肠癌和巨细胞瘤等多种恶性肿瘤有关。因此，本发明的化合物可用于治疗、预防和/或抑制这些疾病。
• DRUGS TO PREVENT HPV INFECTION
  申请人：Lambert Paul F.

  公开号：US20110165220A1

  公开（公告）日：2011-07-07

  A method of inhibiting HPV virus infection is disclosed. In one embodiment, the method involves exposing a papillomavirus to an effective amount of a compound selected from the group consisting of Compound 13, Compound 14, and analogs of Compounds 13 and 14. In another embodiment, the method involves administering an inhibitor selected from the group consisting of Compound 13, Compound 14, and analogs of Compounds 13 and 14 to a susceptible tissue or cell.