N-benzyl-2-(4-phenylpiperazin-1-yl)quinazolin-4-amine | 166039-49-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: N-benzyl-2-(4-phenylpiperazin-1-yl)quinazolin-4-amine
• CAS: 166039-49-2
• 化学式: C₂₅H₂₅N₅
• 分子量: 395.5
• InChiKey: RNYAMUCWYNJGMN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.4
• 重原子数：
  30
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  44.3
• 氢给体数：
  1
• 氢受体数：
  5

文献信息

• USE OF COMPOUNDS FOR PREPARING ANTI-TUBERCULOSIS AGENTS
  申请人：Wynne Graham Michael

  公开号：US20100317607A1

  公开（公告）日：2010-12-16

  Compounds of a compound of compound of general formula (I) wherein X 1 , X 2 , A, R 1 R 2 , R 3 and R 4 are as defined herein; are useful as anti-mycobacterial agents, especially agents for the treatment of tuberculosis.

  在本文中，化合物的一般公式（I）中，X1、X2、A、R1、R2、R3和R4的定义如上所述；这些化合物可用作抗分枝杆菌剂，特别是用于治疗结核病的药剂。
• COMPOSITIONS AND METHODS FOR THE TREATMENT OF DISEASE ASSOCIATED WITH TRP-P8 EXPRESSION
  申请人：Natarajan Sateesh K.

  公开号：US20120094977A1

  公开（公告）日：2012-04-19

  Provided are small-molecule Trp-p8 modulators, including Trp-p8 agonists and Trp-p8 antagonists, and compositions comprising small-molecule Trp-p8 agonists as well as methods for identifying and characterizing novel small-molecule Trp-p8 modulators and methods for decreasing viability and/or inhibiting growth of Trp-p8 expressing cells, methods for activating Trp-p8-mediated cation influx, methods for stimulating apoptosis and/or necrosis, and related methods for the treatment of diseases, including cancers such as lung, breast, colon, and/or prostate cancers as well as other diseases, such as benign prostatic hyperplasia, that are associated with Trp-p8 expression.

  提供了小分子Trp-p8调节剂，包括Trp-p8激动剂和Trp-p8拮抗剂，以及包含小分子Trp-p8激动剂的组合物，以及用于识别和表征新型小分子Trp-p8调节剂的方法，以及用于降低Trp-p8表达细胞的存活率和/或抑制生长的方法，用于激活Trp-p8介导的阳离子流入的方法，用于刺激凋亡和/或坏死的方法，以及相关的治疗疾病的方法，包括肺癌、乳腺癌、结肠癌和/或前列腺癌等癌症，以及与Trp-p8表达相关的其他疾病，例如良性前列腺增生等。
• METHODS AND COMPOSITIONS FOR INHIBITION OF THE TRANSITIONAL ENDOPLASMIC RETICULUM ATPASE
  申请人：Deshaies Raymond J.

  公开号：US20110288082A1

  公开（公告）日：2011-11-24

  Compounds of Formulas I-XLIII are identified as direct inhibitors of p97 ATPase or of the degradation of a p97-dependent ubiquitin-proteasome system (UPS) substrate. Methods and compositions are disclosed for inhibiting p97 ATPase and the degradation of a p97-dependent UPS substrate, and for identifying inhibitors thereof
• US8389730B2
  申请人：——

  公开号：US8389730B2

  公开（公告）日：2013-03-05
• US8362264B2
  申请人：——

  公开号：US8362264B2

  公开（公告）日：2013-01-29