3-氨基-3-(2,5-二甲基-3-噻吩)-丙酸 | 470704-56-4

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 中文名称: 3-氨基-3-(2,5-二甲基-3-噻吩)-丙酸
• 英文名称: 3-amino-3-(2,5-dimethylthien-3-yl)propanoic acid
• 英文别名: 3-Amino-3-(2,5-dimethylthiophen-3-yl)propanoic acid
• CAS: 470704-56-4
• 化学式: C₉H₁₃NO₂S
• 分子量: 199.274
• InChiKey: CUQAJVITOFFMQS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.5
• 重原子数：
  13
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  91.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-氨基-3-(2,5-二甲基-3-噻吩)-丙酸 在 三氯化铝 、 氯化亚砜 作用下， 以 乙醚 、 二氯甲烷 为溶剂， 反应 3.0h， 生成 N-(1,3-dimethyl-6-oxo-5,6-dihydro-4H-cyclopenta[c]thien-4-yl)trifluoroacetamide
  参考文献：
  名称：

  Synthesis and biological evaluation of cyclopenta[ c ]thiophene related compounds as new antitumor agents

  摘要：

  A series of 22 cyclopenta[c]thiophene related compounds was obtained by the pharmacomodulation of 6-amino-5,6- dihydro-4H-cyclopenta[c]thiophen-4-ones 1a-g. All compounds were evaluated for potential anticancer activity in the NCI's in vitro human disease-oriented tumor cell line screening panel that consisted of 60 human tumor cell lines arranged in nine subpanels, representing diverse histologies. Among these tested compounds. seven were found to be cytotoxic, especially against leukemia cell lines, allowing us to point out some structure activity relationships. These derivatives were further evaluated for potential in vivo anticancer activity in the hollow fiber assay developed at the NCI, which selected two compounds. If and 3a for standard xenograft testing. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(02)00070-6
• 作为产物：
  描述：

  2,5-二甲基噻吩 在 sodium hydroxide 、 ammonium acetate 、 三氯氧磷 作用下， 以 乙醇 、 N,N-二甲基甲酰胺 为溶剂， 反应 27.5h， 生成 3-氨基-3-(2,5-二甲基-3-噻吩)-丙酸
  参考文献：
  名称：

  Synthesis and biological evaluation of cyclopenta[ c ]thiophene related compounds as new antitumor agents

  摘要：

  A series of 22 cyclopenta[c]thiophene related compounds was obtained by the pharmacomodulation of 6-amino-5,6- dihydro-4H-cyclopenta[c]thiophen-4-ones 1a-g. All compounds were evaluated for potential anticancer activity in the NCI's in vitro human disease-oriented tumor cell line screening panel that consisted of 60 human tumor cell lines arranged in nine subpanels, representing diverse histologies. Among these tested compounds. seven were found to be cytotoxic, especially against leukemia cell lines, allowing us to point out some structure activity relationships. These derivatives were further evaluated for potential in vivo anticancer activity in the hollow fiber assay developed at the NCI, which selected two compounds. If and 3a for standard xenograft testing. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0968-0896(02)00070-6

文献信息

• Synthesis and biological evaluation of cyclopenta[ c ]thiophene related compounds as new antitumor agents
  作者：Patrick Dallemagne、Lan Pham Khanh、Abdellah Alsaı̈di、Olivier Renault、Isabelle Varlet、Valérie Collot、Ronan Bureau、Sylvain Rault

  DOI：10.1016/s0968-0896(02)00070-6

  日期：2002.7

  A series of 22 cyclopenta[c]thiophene related compounds was obtained by the pharmacomodulation of 6-amino-5,6- dihydro-4H-cyclopenta[c]thiophen-4-ones 1a-g. All compounds were evaluated for potential anticancer activity in the NCI's in vitro human disease-oriented tumor cell line screening panel that consisted of 60 human tumor cell lines arranged in nine subpanels, representing diverse histologies. Among these tested compounds. seven were found to be cytotoxic, especially against leukemia cell lines, allowing us to point out some structure activity relationships. These derivatives were further evaluated for potential in vivo anticancer activity in the hollow fiber assay developed at the NCI, which selected two compounds. If and 3a for standard xenograft testing. (C) 2002 Elsevier Science Ltd. All rights reserved.