{4-[(anthracen-9-ylmethyl)amino]butyl}-(4-tert-butoxycarbonylaminobutyl)carbamic acid tert-butyl ester | 855997-25-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 蒽
• 英文名称: {4-[(anthracen-9-ylmethyl)amino]butyl}-(4-tert-butoxycarbonylaminobutyl)carbamic acid tert-butyl ester
• 英文别名: tert-butyl N-[4-(anthracen-9-ylmethylamino)butyl]-N-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butyl]carbamate
• CAS: 855997-25-0
• 化学式: C₃₃H₄₇N₃O₄
• 分子量: 549.754
• InChiKey: JUPQFIULHMUCMV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.8
• 重原子数：
  40
• 可旋转键数：
  16
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.52
• 拓扑面积：
  79.9
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  {4-[(anthracen-9-ylmethyl)amino]butyl}-(4-tert-butoxycarbonylaminobutyl)carbamic acid tert-butyl ester 在 盐酸 作用下， 生成 anthracen-9-ylmethyl-4,4-triamine trihydrochloride
  参考文献：
  名称：

  Synthesis and bioevaluation of N-(arylalkyl)-homospermidine conjugates

  摘要：

  N'-(Arylalkyl)homospermidines (Ic-1f) and terminally piperazine-substituted homospermidine conjugates (2a-2e) were synthesized and evaluated for cytotoxicity in mouse leukemia L 1210, alpha-difluorometliylornithine (DFMO)-treated L 12 10, melanoma B 16, spermidine (SPD)-treated B 16, and HeLa cell lines. Results demonstrated that homospermidine was a more effective vector than piperazine-substituted homospermidine in ferrying diverse arenes into cells via the polyamine transporter. The leading compound, 9-anthracenemethyl-homospermidine (1a), was shown to induce apoptosis in B16 cells and IL-3 dependent FL5.12A proB cells. The novel conjugate 4-biphenylmethyl-homospermidine (1e) could also induce apoptosis. However, it exhibited different effect on the cell cycle of B16 cells compared to la. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.06.009
• 作为产物：
  描述：

  tert-butyl (4-aminobutyl)(4-((tert-butoxycarbonyl)amino)butyl)carbamate 在 sodium tetrahydroborate 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 生成 {4-[(anthracen-9-ylmethyl)amino]butyl}-(4-tert-butoxycarbonylaminobutyl)carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis and bioevaluation of N-(arylalkyl)-homospermidine conjugates

  摘要：

  N'-(Arylalkyl)homospermidines (Ic-1f) and terminally piperazine-substituted homospermidine conjugates (2a-2e) were synthesized and evaluated for cytotoxicity in mouse leukemia L 1210, alpha-difluorometliylornithine (DFMO)-treated L 12 10, melanoma B 16, spermidine (SPD)-treated B 16, and HeLa cell lines. Results demonstrated that homospermidine was a more effective vector than piperazine-substituted homospermidine in ferrying diverse arenes into cells via the polyamine transporter. The leading compound, 9-anthracenemethyl-homospermidine (1a), was shown to induce apoptosis in B16 cells and IL-3 dependent FL5.12A proB cells. The novel conjugate 4-biphenylmethyl-homospermidine (1e) could also induce apoptosis. However, it exhibited different effect on the cell cycle of B16 cells compared to la. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2007.06.009

文献信息

• Synthesis and Biological Evaluation of Dihydromotuporamine Derivatives in Cells Containing Active Polyamine Transporters
  作者：Navneet Kaur、Jean-Guy Delcros、Bénédicte Martin、Phanstiel

  DOI：10.1021/jm0491288

  日期：2005.6.1

  Dihydromotuporamine C (4) and its 4,4-triamine analogue (5) were synthesized in good yield using ring-closing metathesis (RCM) methods. Comparison of their biological activities (Ki determinations in L1210 cells and IC50 determinations in L1210, CHO, and CHO-MG cells) revealed that the motuporamine derivatives do not use the polyamine transporter (PAT) for cellular entry. Bioevaluation of a N1-(an

  使用闭环复分解（RCM）方法以高收率合成了二氢motuporamine C（4）及其4,4-三胺类似物（5）。比较它们的生物学活性（L1210细胞中的Ki测定和L1210，CHO和CHO-MG细胞中的IC50测定）表明，motuporamine衍生物不使用多胺转运蛋白（PAT）进入细胞。N1-（蒽-9-基甲基）-N1-（乙基）高嘧啶对照的生物评价（7）显示，N1叔胺中心的存在显着降低了多胺缀合物的PAT亲和力，并废除了其PAT-定位选择性。