5-[[4-[bis(2-chloroethyl)amino]benzoyl]amino]-1H-indole-2-carboxylic acid | 294174-41-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 5-[[4-[bis(2-chloroethyl)amino]benzoyl]amino]-1H-indole-2-carboxylic acid
• CAS: 294174-41-7
• 化学式: C₂₀H₁₉Cl₂N₃O₃
• 分子量: 420.295
• InChiKey: XCTDSMYEXLGAGA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  28
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  85.4
• 氢给体数：
  3
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  5-[[4-[bis(2-chloroethyl)amino]benzoyl]amino]-1H-indole-2-carboxylic acid 在 氯化亚砜 、 碳酸氢钠 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 22.0h， 生成 3-[1-methyl-4[1-methyl-4[5-[4-N,N-bis(2-chloroethyl)aminobenzene-1-carboxamido]indole-2-carboxamido]-pyrrole-2-carboxamido]pyrrole-2-carboxamido]propionamidine hydrochloride
  参考文献：
  名称：

  Benzoyl and cinnamoyl nitrogen mustard derivatives of benzoheterocyclic analogues of the tallimustine: synthesis and antitumour activity

  摘要：

  A series of benzoyl and cinnamoyl nitrogen mustards tethered to different benzoheterocycles and to oligopyrroles structurally related to netropsin consisting of two pyrrole-amide units and terminating with an amidine moiety have been synthesised and a structure-activity relationship determined. Derivatives 3-10 have been evaluated for their sequence selective alkylating properties and cytotoxicity against human K562 leukaemia cells. They are 2- to 50-fold less cytotoxic than tallimustine, with compound 8 being the most potent member of this series. Among tallimustine isosters, the compounds with an indole 3 or benzothiophene 6 are 4-fold less cytotoxic than tallimustine, while the compounds with an N-methyl indole or benzofuran showed a 7- and 14-fold reduced cytotoxic potency, respectively. Our preliminary results indicate that these derivatives preferentially bind to AT-rich sequence with a sequence selectivity similar to tallimustine. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(01)00425-4
• 作为产物：
  描述：

  5-氨基吲哚-2-甲酸乙酯 在 氢氧化钾 、 三乙胺 作用下， 以 1,4-二氧六环 、 二氯甲烷 为溶剂， 反应 21.0h， 生成 5-[[4-[bis(2-chloroethyl)amino]benzoyl]amino]-1H-indole-2-carboxylic acid
  参考文献：
  名称：

  二氢新霉素二苯并杂环衍生物的合成及抗肿瘤活性

  摘要：

  设计，合成以及一系列新颖的化合物（13-22和34）的体内和体外抗白血病活性，其中不同的苯并杂环环带有氮芥子基或苯甲酰基氮芥子基或α-溴丙烯酰基烷基化据报道，部分被束缚在双霉素框架上，并讨论了构效关系。通过将氮芥子取代的，苯甲酰基氮芥子取代的或α-溴丙烯酰基取代的苯并杂环的羧酸23-32与去甲酰基二胺（33）或在一种情况下与其二吡咯类似物35偶联，可以制备新的衍生物。例外，带有相同烷基化部分的化合物的活性受苯并杂环上杂原子的种类的影响很小。所有新化合物 除了一个例外，它显示出对L1210鼠白血病细胞系的体外活性与塔利莫司汀相当或更好。氮芥子和α-溴丙烯酰基部分直接与苯并杂环环相连的化合物显示出强的细胞毒活性（IC（50）为2至14 nM），而苯并杂环的苯甲酰氮芥子衍生物显示出降低的细胞毒活性，其中一种该簇的化合物（16）是没有明显活性的唯一衍生物。化合物18（一种双氮霉素的5-氮芥子气N-

  DOI：

  10.1021/jm9911229

文献信息

• BENZOHETEROCYCLIC DISTAMYCIN DERIVATIVES, PROCESS FOR PREPARING THEM, AND THEIR USE AS ANTITUMOR AND ANTIVIRAL AGENTS
  申请人：Pharmacia Italia S.p.A.

  公开号：EP0937070B1

  公开（公告）日：2003-12-03
• US6153642A
  申请人：——

  公开号：US6153642A

  公开（公告）日：2000-11-28
• Synthesis and Antitumor Activity of New Benzoheterocyclic Derivatives of Distamycin A
  作者：Pier Giovanni Baraldi、Romeo Romagnoli、Italo Beria、Paolo Cozzi、Cristina Geroni、Nicola Mongelli、Nicoletta Bianchi、Carlo Mischiati、Roberto Gambari

  DOI：10.1021/jm9911229

  日期：2000.7.1

  tallimustine. The compounds in which the nitrogen mustard and the alpha-bromoacryloyl moieties are directly linked to benzoheterocyclic ring showed potent cytotoxic activities (IC(50) ranging from 2 to 14 nM), while benzoyl nitrogen mustard derivatives of benzoheterocycles showed reduced cytotoxic activities, and one compound (16) of this cluster was the sole derivative devoid of significant activity. Compound

  设计，合成以及一系列新颖的化合物（13-22和34）的体内和体外抗白血病活性，其中不同的苯并杂环环带有氮芥子基或苯甲酰基氮芥子基或α-溴丙烯酰基烷基化据报道，部分被束缚在双霉素框架上，并讨论了构效关系。通过将氮芥子取代的，苯甲酰基氮芥子取代的或α-溴丙烯酰基取代的苯并杂环的羧酸23-32与去甲酰基二胺（33）或在一种情况下与其二吡咯类似物35偶联，可以制备新的衍生物。例外，带有相同烷基化部分的化合物的活性受苯并杂环上杂原子的种类的影响很小。所有新化合物 除了一个例外，它显示出对L1210鼠白血病细胞系的体外活性与塔利莫司汀相当或更好。氮芥子和α-溴丙烯酰基部分直接与苯并杂环环相连的化合物显示出强的细胞毒活性（IC（50）为2至14 nM），而苯并杂环的苯甲酰氮芥子衍生物显示出降低的细胞毒活性，其中一种该簇的化合物（16）是没有明显活性的唯一衍生物。化合物18（一种双氮霉素的5-氮芥子气N-
• Benzoyl and cinnamoyl nitrogen mustard derivatives of benzoheterocyclic analogues of the tallimustine: synthesis and antitumour activity
  作者：Pier Giovanni Baraldi、Romeo Romagnoli、Maria Giovanna Pavani、Maria del Carmen Nunez、John P. Bingham、John A. Hartley

  DOI：10.1016/s0968-0896(01)00425-4

  日期：2002.5

  A series of benzoyl and cinnamoyl nitrogen mustards tethered to different benzoheterocycles and to oligopyrroles structurally related to netropsin consisting of two pyrrole-amide units and terminating with an amidine moiety have been synthesised and a structure-activity relationship determined. Derivatives 3-10 have been evaluated for their sequence selective alkylating properties and cytotoxicity against human K562 leukaemia cells. They are 2- to 50-fold less cytotoxic than tallimustine, with compound 8 being the most potent member of this series. Among tallimustine isosters, the compounds with an indole 3 or benzothiophene 6 are 4-fold less cytotoxic than tallimustine, while the compounds with an N-methyl indole or benzofuran showed a 7- and 14-fold reduced cytotoxic potency, respectively. Our preliminary results indicate that these derivatives preferentially bind to AT-rich sequence with a sequence selectivity similar to tallimustine. (C) 2002 Elsevier Science Ltd. All rights reserved.