3-acetamidothiopropionamide | 76275-89-3

• 分子结构分类: 有机化合物 - 有机硫化合物 - 硫代酰胺
• 英文名称: 3-acetamidothiopropionamide
• 英文别名: N-(2-carbamothioylethyl)acetamide；N-(3-amino-3-sulfanylidenepropyl)acetamide
• CAS: 76275-89-3
• 化学式: C₅H₁₀N₂OS
• mdl: MFCD16300813
• 分子量: 146.213
• InChiKey: DQSVHFVQJNFOFI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1
• 重原子数：
  9
• 可旋转键数：
  3
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.6
• 拓扑面积：
  87.2
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  3-acetamidothiopropionamide 以 N,N-二甲基甲酰胺 为溶剂， 反应 7.0h， 生成 3-<2-(2-acetamidoethyl)thiazole-4-carboxamido>propyl methyl sulfide
  参考文献：
  名称：

  博来霉素类似物。与博来霉素a 2相关的噻唑酰胺的合成和质子核磁共振谱归属

  摘要：

  描述了一系列3-氨基丙基二甲基s氯化物的2-取代的噻唑-4-羧酰胺的合成，并对这些衍生物的质子核磁共振谱进行了表征。该化合物是抗肿瘤抗生素博来霉素A 2的DNA结合部分的片段和类似物，将在该家族药物中用作构效关系的探针。

  DOI：

  10.1002/jhet.5570180629

文献信息

• New 7-substituted quinolone antibacterial agents. The synthesis of 1-ethyl-1,4-dihydro-4-oxo-7-(2-thiazolyl and 4-thiazolyl)-3-quinolinecarboxylic acids
  作者：Townley P. Culbertson、John M. Domagala、Phred Peterson、Shannon Bongers、Jeffrey B. Nichols

  DOI：10.1002/jhet.5570240604

  日期：1987.11

  4-dihydro-4-oxo-7-(4-thiazolyl)-3-quinolinecarboxylic acids and 1-ethyl-1,4-dihydro-4-oxo-7-(2-thiazolyl)-3-quinolinecarboxylic acids were prepared. Also prepared was 10-[2-(aminomethyl)-4-thiazolyl]-9-fluoro-2,3-dihydro-3-methyl-7-oxo-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid. Analogs with basic amine substituents on the thiazole moiety were found to have antibacterial activity.

  一系列1-乙基-1,4-二氢-4-氧代-7-（4-噻唑基）-3-喹啉羧酸和1-乙基-1,4-二氢-4-氧代-7-（2-噻唑基制备）-3-喹啉羧酸。还制备了10- [2-（氨基甲基）-4-噻唑基] -9-氟-2,3-二氢-3-甲基-7-氧代-7 H-吡啶基[1,2,3- de ] [1 ，4]苯并恶嗪-6-羧酸。发现在噻唑部分具有碱性胺取代基的类似物具有抗菌活性。
• Synthesis and DNA binding of [3-[2'-(2-acetamidoethyl)-2,4'-bithiazole-4-carboxamido]propyl]dimethylsulfonium chloride, a fragment of bleomycin A2
  作者：Ted T. Sakai、James M. Riordan、Thomas E. Booth、Jerry D. Glickson

  DOI：10.1021/jm00135a008

  日期：1981.3

  [3-[2'-(2-Acetamidoethyl)-2,4'-bithiazole-4-carboxamido]propyl]dimethylsulfonium chloride (1), the acetyl derivative of the cationic terminal dipeptide of bleomycin A2, has been synthesized and its binding to DNA and poly(dA-dT) has been studied by proton NMR and fluorescence spectroscopy. The spectral perturbations which occur upon binding of the compound to either nucleic acid indicate that that portion of bleomycin which binds to the nucleic acid can, for the most part, be mimicked by the fragment. The data are discussed in terms of the structure of the drug and the drug-nucleic acid complex.
• CULBERTSON, TOWNLEY P.;DOMAGALA, JOHN M.;PETERSON, PHRED;BONGERS, SHANNON+, J. HETEROCYCL. CHEM., 24,(1987) N 6, 1509-1520
  作者：CULBERTSON, TOWNLEY P.、DOMAGALA, JOHN M.、PETERSON, PHRED、BONGERS, SHANNON+

  DOI：——

  日期：——