3-(2-phenylethenyl)-2H-1,2,4-benzothiadiazine 1,1-dioxide | 73676-86-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 噻二嗪
• 英文名称: 3-(2-phenylethenyl)-2H-1,2,4-benzothiadiazine 1,1-dioxide
• 英文别名: 3-[(E)-2-phenylethenyl]-4H-1lambda6,2,4-benzothiadiazine 1,1-dioxide；3-[(E)-2-phenylethenyl]-4H-1λ6,2,4-benzothiadiazine 1,1-dioxide
• CAS: 73676-86-5
• 化学式: C₁₅H₁₂N₂O₂S
• 分子量: 284.338
• InChiKey: HDEOMXJXOCDQIU-ZHACJKMWSA-N

物化性质

• 熔点：
  322-324.5 °C(Solv: ethanol (64-17-5))
• 沸点：
  490.7±38.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  20
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  66.9
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  肉桂酸 、 邻氨基苯磺酰胺 在 六甲基二硅氧烷 、 phosphorus pentoxide 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 5.0h， 以2.0 g的产率得到3-(2-phenylethenyl)-2H-1,2,4-benzothiadiazine 1,1-dioxide
  参考文献：
  名称：

  Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization

  摘要：

  A novel series of 2-styrylquinazolin-4(3H-ones which inhibited tubulin polymerization and the growth of L1210 murine leukemia cells was discovered. Extensive structure-activity relationship studies suggest that the entire quinazolinone structure was required, but activity was further enhanced by halide or small hydrophobic substituents at position 6. These analogues did not substantially interfere with the binding of radiolabeled colchicine, vinblastine, or GTP to tubulin and weakly stimulated GTP hydrolysis uncoupled from polymerization. Several analogues have shown in vivo tumor growth inhibitory activity in the L1210 leukemia model, with the lead compound 5o exhibiting good antitumor activity against murine solid tumors as well as human tumor xenografts.

  DOI：

  10.1021/jm00168a029

文献信息

• TANIMOTO S.; YOSHIDA N.; SUGIMOTO T.; OKANO M., BULL. INST. CHEM. RES. KYOTO UNIV., 1979, 57, NO 5-6, 381-384
  作者：TANIMOTO S.、 YOSHIDA N.、 SUGIMOTO T.、 OKANO M.

  DOI：——

  日期：——
• JIANG, J. B.;HESSON, D. P.;DUSAK, B. A.;DEXTER, D. L.;KANG, G. J.;HAMEL, +, J. MED. CHEM., 33,(1990) N, C. 1721-1728
  作者：JIANG, J. B.、HESSON, D. P.、DUSAK, B. A.、DEXTER, D. L.、KANG, G. J.、HAMEL, +

  DOI：——

  日期：——
• IMAI, Y.;MOCHIZUKI, A.;KAKIMOTO, M., SYNTHESIS, BRD, 1983, N 10, 851
  作者：IMAI, Y.、MOCHIZUKI, A.、KAKIMOTO, M.

  DOI：——

  日期：——
• FEDENKO, V. S.;SOLOMKO, Z. F.;AVRAMENKO, V. I., XIMIYA GETEROTSIKL. SOEDIN., 1984, N 7, 907-911
  作者：FEDENKO, V. S.、SOLOMKO, Z. F.、AVRAMENKO, V. I.

  DOI：——

  日期：——
• Synthesis and biological evaluation of 2-styrylquinazolin-4(3H)-ones, a new class of antimitotic anticancer agents which inhibit tubulin polymerization
  作者：Jack B. Jiang、D. P. Hesson、B. A. Dusak、D. L. Dexter、G. J. Kang、E. Hamel

  DOI：10.1021/jm00168a029

  日期：1990.6

  A novel series of 2-styrylquinazolin-4(3H-ones which inhibited tubulin polymerization and the growth of L1210 murine leukemia cells was discovered. Extensive structure-activity relationship studies suggest that the entire quinazolinone structure was required, but activity was further enhanced by halide or small hydrophobic substituents at position 6. These analogues did not substantially interfere with the binding of radiolabeled colchicine, vinblastine, or GTP to tubulin and weakly stimulated GTP hydrolysis uncoupled from polymerization. Several analogues have shown in vivo tumor growth inhibitory activity in the L1210 leukemia model, with the lead compound 5o exhibiting good antitumor activity against murine solid tumors as well as human tumor xenografts.