ethyl 5-amino-3-[(N-methyl-N-phenylamino)methyl]pyrido[3,4-b]pyrazine-7-carbamate | 83269-13-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶吡嗪类
• 英文名称: ethyl 5-amino-3-[(N-methyl-N-phenylamino)methyl]pyrido[3,4-b]pyrazine-7-carbamate
• 英文别名: ethyl N-[5-amino-3-[(N-methylanilino)methyl]pyrido[3,4-b]pyrazin-7-yl]carbamate
• CAS: 83269-13-0
• 化学式: C₁₈H₂₀N₆O₂
• 分子量: 352.396
• InChiKey: OBFVNBRZIVSPNH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  106
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  ethyl 5-amino-1,2-dihydro-3-<(N-methyl-N-phenylamino)methyl>pyrido<3,4-b>pyrazine-7-carbamate 以12%的产率得到
  参考文献：
  名称：

  TEMPLE, C. ,, JR;WHEELER, G. P.;ELLIOTT, R. D.;ROSE, J. D.;COMBER, R. N.;+, J. MED. CHEM., 1983, 26, N 1, 91-95

  摘要：

  DOI：

文献信息

• 1,2-Dihydropyrido[3,4-b]pyrazines: structure-activity relationships
  作者：Carroll Temple、Glynn P. Wheeler、Robert D. Elliott、Jerry D. Rose、Robert N. Comber、John A. Montgomery

  DOI：10.1021/jm00355a018

  日期：1983.1

  Certain derivatives containing the 1,2-dihydropyrido[3,4-b]pyrazine (1-deaza-7,8-dihydropteridine) ring system are active against experimental neoplasms in mice. The mechanism of action of these agents has been attributed to the accumulation of cells at mitosis. Identification of the structural features that are necessary for activity was accomplished by evaluation of modified 1-deazapteridines and

  某些含有1,2-二氢吡啶并[3,4-b]吡嗪（1-deaza-7,8-dihydropteridine）环系统的衍生物具有抗小鼠实验肿瘤的活性。这些试剂的作用机理已归因于有丝分裂时细胞的积累。活性必需的结构特征的鉴定是通过评估修饰的1-脱氮哌啶以及开环和开环的类似物来完成的。相对于4-氨基-1-脱氮基-7，8-二氢-6-[（（N-甲基苯胺基）甲基]蝶啶-2-氨基甲酸酯（11）和相应的6-苯基化合物（12），没有抗肿瘤活性用7,8-二氢蝶啶，3-deaza-7,8-二氢蝶啶和相应的杂芳族化合物观察到。而且，当1-deaza-7,8-dihydropteridines氧化为1-deazapteridines或还原为1-deaza-5时，活性会降低或破坏。6,7,8-四氢蝶啶。另外，用其他取代基取代4-氨基会破坏活性。似乎需要具有芳基的6位取代基，这对于活性是必要的，当在7位上取代甲基时，活性会增加。
• Combinations of drugs (e.g., a benzimidazole and pentamidine) for the treatment of neoplastic disorders
  申请人：——

  公开号：US20020165261A1

  公开（公告）日：2002-11-07

  The invention features a method for treating a patient having a cancer or other neoplasm, by administering to the patient (i) a benzimidazole or a metabolite or analog thereof; and (ii) pentamidine or a metabolite or analog thereof simultaneously or within 14 days of each other in amounts sufficient to inhibit the growth of the neoplasm.

  本发明的特点是一种治疗癌症或其他肿瘤患者的方法，其方法是同时或在 14 天内向患者施用(i) 苯并咪唑或其代谢物或类似物；(ii) 戊脒或其代谢物或类似物，其用量足以抑制肿瘤的生长。
• Soft tissue implants and drug combination compositions, and use thereof
  申请人：Hunter L. William

  公开号：US20070196421A1

  公开（公告）日：2007-08-23

  Soft tissue implants (e.g., breast, pectoral, chin, facial, lip, and nasal implants) are used in combination with an anti-scarring drug combination in order to inhibit scarring that may otherwise occur when the implant is placed within an animal.
• Anti-scarring drug combinations and use thereof
  申请人：Hunter L. William

  公开号：US20070208134A1

  公开（公告）日：2007-09-06

  The present invention provides devices or implants that comprise anti-scarring drug combinations, methods or making such devices or implants, and methods of inhibiting fibrosis between the devices or implants and tissue surrounding the devices or implants. The present invention also provides compositions that comprise anti-fibrotic drug combinations, and their uses in various medical applications including the prevention of surgical adhesions, treatment of inflammatory arthritis, treatment of scars and keloids, the treatment of vascular disease, and the prevention of cartilage loss.
• Electrical devices and anti-scarring drug combinations
  申请人：Hunter L. William

  公开号：US20070198063A1

  公开（公告）日：2007-08-23

  Electrical devices (e.g., cardiac rhythm management and neurostimulation devices) for contact with tissue are used in combination with an anti-scarring drug combination or a composition that comprises an anti-scarring drug combination to inhibit scarring that may otherwise occur when the devices are implanted within an animal.