pyridin-2-ylmethyl 5-(3-(4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl)pentan-3-yl)-1-ethyl-1H-pyrrole-2-carboxylate

• 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: pyridin-2-ylmethyl 5-(3-(4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl)pentan-3-yl)-1-ethyl-1H-pyrrole-2-carboxylate
• 英文别名: Pyridin-2-ylmethyl 5-[3-[4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl]pentan-3-yl]-1-ethylpyrrole-2-carboxylate；pyridin-2-ylmethyl 5-[3-[4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl]pentan-3-yl]-1-ethylpyrrole-2-carboxylate
• 化学式: C₃₁H₄₀N₂O₄
• 分子量: 504.67
• InChiKey: SYRMFJYAABGDRA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  37
• 可旋转键数：
  13
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.45
• 拓扑面积：
  70.4
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  pyridin-2-ylmethyl 5-(3-(4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl)pentan-3-yl)-1-ethyl-1H-pyrrole-2-carboxylate 在 sodium tetrahydroborate 作用下， 以 甲醇 为溶剂， 反应 2.0h， 以94%的产率得到pyridin-2-ylmethyl 1-ethyl-5-(3-(4-(2-hydroxy-3,3-dimethylbutoxy)-3-methylphenyl)pentan-3-yl)-1H-pyrrole-2-carboxylate
  参考文献：
  名称：

  Novel nonsecosteroidal VDR ligands with phenyl-pyrrolyl pentane skeleton for cancer therapy

  摘要：

  A series of nonsecosteroidal vitamin D-3 receptor (VDR) ligands with phenyl-pyrrolyl pentane skeleton were synthesized for cancer therapy. In contrast to 1 alpha,25-dihydroxyvitamin D-3 (Calcitriol), these VDR ligands exhibited anti-proliferative activity without inducing hypercalcemia. These compounds were evaluated for vitamin D-3-agonistic ability and anti-proliferative activity in vitro. Among them, compounds 5k and 5i exhibited equivalent vitamin D-3-agonistic activity compared with Calcitriol. Meanwhile, compound 5k displayed promising inhibiting profile against MCF-7, HepG-2 and Caco-2 with IC50 values of 0.00586 mu M, 0.176 mu M, and 1.01 mu M (Calcitriol: 5.58 mu M, 80.83 mu M and 4.46 mu M) respectively. Compound Si inhibited proliferation of PC-3 with IC50 value of 0.00798 mu M (Calcitriol: 17.25 mu M). Additionally, neither of these compounds significantly elevated serum calcium in rats. (C) 2015 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2015.10.042
• 作为产物：
  描述：

  2-吡啶甲醇 、 5-(3-(4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl)pentan-3-yl)-1-ethylpyrrole-2-carboxylic acid 在 1-羟基苯并三唑 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 三乙胺 作用下， 以 氯仿 为溶剂， 反应 2.0h， 以77%的产率得到pyridin-2-ylmethyl 5-(3-(4-(3,3-dimethyl-2-oxobutoxy)-3-methylphenyl)pentan-3-yl)-1-ethyl-1H-pyrrole-2-carboxylate
  参考文献：
  名称：

  Novel nonsecosteroidal VDR ligands with phenyl-pyrrolyl pentane skeleton for cancer therapy

  摘要：

  A series of nonsecosteroidal vitamin D-3 receptor (VDR) ligands with phenyl-pyrrolyl pentane skeleton were synthesized for cancer therapy. In contrast to 1 alpha,25-dihydroxyvitamin D-3 (Calcitriol), these VDR ligands exhibited anti-proliferative activity without inducing hypercalcemia. These compounds were evaluated for vitamin D-3-agonistic ability and anti-proliferative activity in vitro. Among them, compounds 5k and 5i exhibited equivalent vitamin D-3-agonistic activity compared with Calcitriol. Meanwhile, compound 5k displayed promising inhibiting profile against MCF-7, HepG-2 and Caco-2 with IC50 values of 0.00586 mu M, 0.176 mu M, and 1.01 mu M (Calcitriol: 5.58 mu M, 80.83 mu M and 4.46 mu M) respectively. Compound Si inhibited proliferation of PC-3 with IC50 value of 0.00798 mu M (Calcitriol: 17.25 mu M). Additionally, neither of these compounds significantly elevated serum calcium in rats. (C) 2015 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2015.10.042

文献信息

• Novel nonsecosteroidal VDR ligands with phenyl-pyrrolyl pentane skeleton for cancer therapy
  作者：Zhixin Ge、Meixi Hao、Meng Xu、Zhigui Su、Zisheng Kang、Lingjing Xue、Can Zhang

  DOI：10.1016/j.ejmech.2015.10.042

  日期：2016.1

  A series of nonsecosteroidal vitamin D-3 receptor (VDR) ligands with phenyl-pyrrolyl pentane skeleton were synthesized for cancer therapy. In contrast to 1 alpha,25-dihydroxyvitamin D-3 (Calcitriol), these VDR ligands exhibited anti-proliferative activity without inducing hypercalcemia. These compounds were evaluated for vitamin D-3-agonistic ability and anti-proliferative activity in vitro. Among them, compounds 5k and 5i exhibited equivalent vitamin D-3-agonistic activity compared with Calcitriol. Meanwhile, compound 5k displayed promising inhibiting profile against MCF-7, HepG-2 and Caco-2 with IC50 values of 0.00586 mu M, 0.176 mu M, and 1.01 mu M (Calcitriol: 5.58 mu M, 80.83 mu M and 4.46 mu M) respectively. Compound Si inhibited proliferation of PC-3 with IC50 value of 0.00798 mu M (Calcitriol: 17.25 mu M). Additionally, neither of these compounds significantly elevated serum calcium in rats. (C) 2015 Elsevier Masson SAS. All rights reserved.