(Z)-ethyl 3-allyl-2-((3-(isopropoxycarbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)imino)-4-methyl-2,3-dihydrothiazole-5-carboxylate

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: (Z)-ethyl 3-allyl-2-((3-(isopropoxycarbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)imino)-4-methyl-2,3-dihydrothiazole-5-carboxylate
• 英文别名: ethyl (2Z)-4-methyl-2-[(3-propan-2-yloxycarbonyl-4,5,6,7-tetrahydro-1-benzothiophen-2-yl)imino]-3-prop-2-enyl-1,3-thiazole-5-carboxylate
• 化学式: C₂₂H₂₈N₂O₄S₂
• 分子量: 448.607
• InChiKey: DGSKOQOETSGHKK-FCQUAONHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  30
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  122
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  isopropyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate 以 乙醇 为溶剂， 生成 (Z)-ethyl 3-allyl-2-((3-(isopropoxycarbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)imino)-4-methyl-2,3-dihydrothiazole-5-carboxylate
  参考文献：
  名称：

  Design, synthesis, molecular docking and biological evaluation of thiophen-2-iminothiazolidine derivatives for use against Trypanosoma cruzi

  摘要：

  In this study, we designed and synthesized a series of thiophen-2-iminothiazolidine derivatives from thiophen-2-thioureic with good anti-Trypanosoma cruzi activity. Several of the final compounds displayed remarkable trypanocidal activity. The ability of the new compounds to inhibit the activity of the enzyme cruzain, the major cysteine protease of T. cruzi, was also explored. The compounds 3b, 4b, 8b and 8c were the most active derivatives against amastigote form, with significant IC50 values between 9.7 and 6.03 mu M. The 8c derivative showed the highest potency against cruzain 9IC(50) = 2.4 mu M). Molecular docking study showed that this compound can interact with subsites S1 and S2 simultaneously, and the negative values for the theoretical energy binding (E-b = -7.39 kcal.mol(-1)) indicates interaction 9via dipol-dipole) between the hybridized sulfur sp(3) atom at the thiazolidine ring and Gly66. Finally, the results suggest that the thiophen-2-iminothiazolidines synthesized are important lead compounds for the continuing battle against Chagas disease. (C) 2016 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2016.07.013

文献信息

• Design, synthesis, molecular docking and biological evaluation of thiophen-2-iminothiazolidine derivatives for use against Trypanosoma cruzi
  作者：E.F. Silva-Júnior、E.P.S. Silva、P.H.B. França、J.P.N. Silva、E.O. Barreto、E.B. Silva、R.S. Ferreira、C.C. Gatto、D.R.M. Moreira、J.L. Siqueira-Neto、F.J.B. Mendonça-Júnior、M.C.A. Lima、J.H. Bortoluzzi、M.T. Scotti、L. Scotti、M.R. Meneghetti、T.M. Aquino、J.X. Araújo-Júnior

  DOI：10.1016/j.bmc.2016.07.013

  日期：2016.9

  In this study, we designed and synthesized a series of thiophen-2-iminothiazolidine derivatives from thiophen-2-thioureic with good anti-Trypanosoma cruzi activity. Several of the final compounds displayed remarkable trypanocidal activity. The ability of the new compounds to inhibit the activity of the enzyme cruzain, the major cysteine protease of T. cruzi, was also explored. The compounds 3b, 4b, 8b and 8c were the most active derivatives against amastigote form, with significant IC50 values between 9.7 and 6.03 mu M. The 8c derivative showed the highest potency against cruzain 9IC(50) = 2.4 mu M). Molecular docking study showed that this compound can interact with subsites S1 and S2 simultaneously, and the negative values for the theoretical energy binding (E-b = -7.39 kcal.mol(-1)) indicates interaction 9via dipol-dipole) between the hybridized sulfur sp(3) atom at the thiazolidine ring and Gly66. Finally, the results suggest that the thiophen-2-iminothiazolidines synthesized are important lead compounds for the continuing battle against Chagas disease. (C) 2016 Elsevier Ltd. All rights reserved.