5-benzylidene-7-(tert-butoxycarbonylamino)-5,7,8,9-tetrahydrobenzocyclohepten-6-one | 1023620-40-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 5-benzylidene-7-(tert-butoxycarbonylamino)-5,7,8,9-tetrahydrobenzocyclohepten-6-one
• 英文别名: 5-Benzylidene-7-(tert-butoxycarbonylamino)-5,7,8,9-tetrahydro-benzocyclohepten-6-one；tert-butyl N-(5-benzylidene-6-oxo-8,9-dihydro-7H-benzo[7]annulen-7-yl)carbamate
• CAS: 1023620-40-7
• 化学式: C₂₃H₂₅NO₃
• 分子量: 363.456
• InChiKey: GTHURXNAVJRPMT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.9
• 重原子数：
  27
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  55.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  5-benzylidene-7-(tert-butoxycarbonylamino)-5,7,8,9-tetrahydrobenzocyclohepten-6-one 在 盐酸 、 5%-palladium/activated carbon 、 氢气 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 24.0h， 以79%的产率得到7-amino 5-benzylidene-5,7,8,9-tetrahydrobenzocyclohepten-6-one
  参考文献：
  名称：

  Rapid and efficient synthesis of a novel series of substituted aminobenzosuberone derivatives as potent, selective, non-peptidic neutral aminopeptidase inhibitors

  摘要：

  Racemic 5-substituted 7-aminobenzocyclohepten-6-one were synthesized and evaluated for their ability to inhibit metalloaminopeptidase activities. Unexpectedly, 5-thio substituted compounds showed enhanced inhibition potency with K-i values in the nanomolar range against the 'one zinc' aminopeptidases from the M1 family, while most of them were rather poor inhibitors of the 'two zincs' enzymes from the M17 family. This interesting selectivity profile may guide the design of new, specific inhibitors of target mammalian aminopeptidases with one active site zinc. (C) 2012 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2012.06.041
• 作为产物：
  描述：

  7-(tert-butyloxycarbonylamino)-5,7,8,9-tetrahydro-benzocyclohepten-6-one 、 苯甲醛 在 六甲基磷酰三胺 、 正丁基锂 、 六甲基二硅氮烷 作用下， 以 四氢呋喃 、 正己烷 为溶剂， 反应 3.0h， 以53%的产率得到5-benzylidene-7-(tert-butoxycarbonylamino)-5,7,8,9-tetrahydrobenzocyclohepten-6-one
  参考文献：
  名称：

  AMINOBENZOCYCLOHEPTENE DERIVATIVES, METHODS FOR PREPARING THE SAME AND USES THEREOF IN THERAPY

  摘要：

  一种具有一般化学式（I）的化合物作为治疗癌症的活性成分，特别是肿瘤，特别是涉及金属蛋白酶抑制的疾病，如氨基肽酶-N。包括具有一般化学式（I）的化合物的药物组合物。使用一般化学式（I）的化合物进行治疗的方法。

  公开号：

  US20100069504A1

文献信息

• AMINOBENZOCYCLOHEPTENE DERIVATIVES, METHODS FOR PREPARING THE SAME AND USES THEREOF IN THERAPY
  申请人：Tarnus-Rondeau Céline

  公开号：US20100069504A1

  公开（公告）日：2010-03-18

  A compound of the general formula (I) as an active principle for treating cancer, specifically tumors, in particular diseases involving inhibition of metalloproteases, such as Aminopeptidase-N. Pharmaceutical compositions comprising the compound of general formula (I). Methods of treatment using the compound of general formula (I).

  一种具有一般化学式（I）的化合物作为治疗癌症的活性成分，特别是肿瘤，特别是涉及金属蛋白酶抑制的疾病，如氨基肽酶-N。包括具有一般化学式（I）的化合物的药物组合物。使用一般化学式（I）的化合物进行治疗的方法。
• Rapid and efficient synthesis of a novel series of substituted aminobenzosuberone derivatives as potent, selective, non-peptidic neutral aminopeptidase inhibitors
  作者：Sébastien Albrecht、Emmanuel Salomon、Albert Defoin、Céline Tarnus

  DOI：10.1016/j.bmc.2012.06.041

  日期：2012.8

  Racemic 5-substituted 7-aminobenzocyclohepten-6-one were synthesized and evaluated for their ability to inhibit metalloaminopeptidase activities. Unexpectedly, 5-thio substituted compounds showed enhanced inhibition potency with K-i values in the nanomolar range against the 'one zinc' aminopeptidases from the M1 family, while most of them were rather poor inhibitors of the 'two zincs' enzymes from the M17 family. This interesting selectivity profile may guide the design of new, specific inhibitors of target mammalian aminopeptidases with one active site zinc. (C) 2012 Elsevier Ltd. All rights reserved.