diphenylmethyl 7β-(thiophen-2-acetamido)-3-<(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl>-ceph-3-em-4-carboxylate | 56737-24-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 内酰胺类
• 英文名称: diphenylmethyl 7β-(thiophen-2-acetamido)-3-<(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl>-ceph-3-em-4-carboxylate
• 英文别名: diphenyl methyl-7β-(2-thienyl)acetamido-3-<(5-methyl-1,3,4-thiadiazol-2-yl)thiomethyl> ceph-3-em-4-carboxylate；diphenylmethyl 7β-(thiophen-2-acetamido)-3-[(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl]-ceph-3-em-4-carboxylate；benzhydryl (6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-8-oxo-7-[(2-thiophen-2-ylacetyl)amino]-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate
• CAS: 56737-24-7
• 化学式: C₃₀H₂₆N₄O₄S₄
• 分子量: 634.825
• InChiKey: XISXJUDYRAEFHT-UFHPHHKVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  42
• 可旋转键数：
  11
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  209
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  diphenylmethyl 7β-(thiophen-2-acetamido)-3-<(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl>-ceph-3-em-4-carboxylate 在 双氧水 、 溶剂黄146 、 苯甲醚 、 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 24.33h， 生成 (6R,7R)-3-[(5-methyl-1,3,4-thiadiazol-2-yl)sulfanylmethyl]-5,8-dioxo-7-[(2-thiophen-2-ylacetyl)amino]-5λ4-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
  参考文献：
  名称：

  Singh, Rajeshwar; Singh, Maya P.; Micetich, Ronald G., Collection of Czechoslovak Chemical Communications, 1991, vol. 56, # 11.1, p. 2362 - 2372

  摘要：

  DOI：
• 作为产物：
  描述：

  头孢噻吩 在 phosphate buffer pH 6.4 、 碳酸氢钠 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 7.0h， 生成 diphenylmethyl 7β-(thiophen-2-acetamido)-3-<(2-methyl-1,3,4-thiadiazol-5-yl)thiomethyl>-ceph-3-em-4-carboxylate
  参考文献：
  名称：

  Singh, Rajeshwar; Singh, Maya P.; Micetich, Ronald G., Collection of Czechoslovak Chemical Communications, 1991, vol. 56, # 11.1, p. 2362 - 2372

  摘要：

  DOI：

文献信息

• Synthesis and in vitro antimicrobial activity of 3-heteroarylsulphonylmethyl cephems: a new class of cephalosporins
  作者：MP Singh、R Singh、SN Maiti、P Spevak、N Ishida、A Hyodo、RG Micetich

  DOI：10.1016/0223-5234(96)88221-3

  日期：1995.1

  A series of 3-heteroarylsulphonylmethyl and 3-heteroarylsulphenylmethyl cephems were prepared and tested for antimicrobial activities. In contrast to the adverse effect of oxidized ring sulphur of penams and cephems on antimicrobial activities, the oxidized side-chain sulphur of 3-mercaptoheteroaryl cephems retained Gram-negative and slightly decreased Gram-positive activity. The chemical nature of the moieties substituted at C-7 and C-3 positions also influenced the antibacterial activity and spectrum. Compounds with thienyl substitution at C-7 and sulphonylmethylthiazoles or sulphonylmethylthiadiazoles at C-3 exhibited good differentials in antibacterial activity vet-sus their unoxidized counterparts.
• Singh, Rajeshwar; Singh, Maya P.; Micetich, Ronald G., Collection of Czechoslovak Chemical Communications, 1991, vol. 56, # 11.1, p. 2362 - 2372
  作者：Singh, Rajeshwar、Singh, Maya P.、Micetich, Ronald G.

  DOI：——

  日期：——