S-methyl dithiobiuret hydroiodide salt | 21347-31-9

• 分子结构分类: 有机化合物 - 有机硫化合物 - 异硫脲类
• 英文名称: S-methyl dithiobiuret hydroiodide salt
• 英文别名: methyl N'-carbamothioylcarbamimidothioate;hydroiodide
• CAS: 21347-31-9
• 化学式: C₃H₇N₃S₂*HI
• 分子量: 277.153
• InChiKey: UZMZOHVPZPAVRI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.53
• 重原子数：
  9
• 可旋转键数：
  1
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  122
• 氢给体数：
  3
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  S-methyl dithiobiuret hydroiodide salt 以 乙醇 为溶剂， 生成 缩二脲
  参考文献：
  名称：

  Reaction of S-methiodide derivatives of activated thioureas with hydroxylic compounds. Novel synthesis of mercaptans

  摘要：

  DOI：

  10.1021/jo00975a015
• 作为产物：
  描述：

  2,4-二硫代缩二脲 、 碘甲烷 以 四氢呋喃 、 甲苯 为溶剂， 以85%的产率得到S-methyl dithiobiuret hydroiodide salt
  参考文献：
  名称：

  Protease inhibitors

  摘要：

  本文披露的是一种化合物，其化学式为##STR1##，被称为2-[N-(N-苄氧羰基-L-亮氨酰)]-2'-[N'-[4-(N,N-二甲氨基甲基)苄氧羰基-L-亮氨酰]碳酰肼；以及其药用可接受的盐、水合物和溶剂合物。

  公开号：

  US05998470A1

文献信息

• Synthesis of Mono N-Substituted Guanylthioureas
  作者：Lawrence A. Reiter、Katherine E. Brighty、Rhonda A. Bryant、Miriam E. Goldsmith

  DOI：10.1080/00397919608003504

  日期：1996.4

  A convenient method for the synthesis of mono N-substituted guanylthioureas in reasonable yields from readily available starting materials has been developed. In contrast to the previously published method, the use of highly noxious hydrogen sulfide is avoided. The method allows the rapid preparation of guanylthioureas since the synthesis of each requires only a single step from a common intermediate, the S-methylated derivative of dithiobiuret.
• Anti-<i>Helicobacter pylori</i> Agents. 3. 2-[(Arylalkyl)guanidino]-4-furylthiazoles
  作者：Yousuke Katsura、Shigetaka Nishino、Mitsuko Ohno、Kazuo Sakane、Yoshimi Matsumoto、Chizu Morinaga、Hirohumi Ishikawa、Hisashi Takasugi

  DOI：10.1021/jm9900671

  日期：1999.7.1

  A series of 2-[(arylalkyl)guanidinol-4-[(5-acetamidomethyl)furan-2-yl]thiazoles and some 4-acetamidomethyl positional isomers were synthesized and evaluated for antimicrobial activity against Helicobacter pylori. Among the compounds that had potent antimicrobial activity (MIC < 0.1 mu g/mL), compounds 31 and 36 additionally possessed H2 antagonist and gastric antisecretory activities. Though compound 51, an analogue incorporating a methyl group onto the furan nucleus of 36, and compound 54, a positional isomer of 51, also showed potent anti-H. pylori activity, the H2 antagonism profile was eliminated from these compounds. Thus, two types of potent anti-H. pylori agents could be derived from the same scaffold.
• Synthesis of selenoureas and selenothiocarbamic esters from thioureas
  作者：Daniel L. Klayman、Robert J. Shine

  DOI：10.1021/jo01263a070

  日期：1969.11
• Protease inhibitors
  申请人：SmithKline Beecham Corporation

  公开号：US05998470A1

  公开（公告）日：1999-12-07

  Disclosed herein is a compound of the formula ##STR1## known as 2-[N-(N-benzyloxycarbonyl-L-leucinyl)]-2'-[N'-[4-(N,N-dimethylaminomethyl) benzyloxy]carbonyl-L-leucinyl]carbohydrazide; and pharmaceutically acceptable salts, hydrates and solvates thereof.

  本文披露的是一种化合物，其化学式为##STR1##，被称为2-[N-(N-苄氧羰基-L-亮氨酰)]-2'-[N'-[4-(N,N-二甲氨基甲基)苄氧羰基-L-亮氨酰]碳酰肼；以及其药用可接受的盐、水合物和溶剂合物。
• Reaction of S-methiodide derivatives of activated thioureas with hydroxylic compounds. Novel synthesis of mercaptans
  作者：Daniel L. Klayman、Robert J. Shine、J. David Bower

  DOI：10.1021/jo00975a015

  日期：1972.5