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5-(benzo[c][1,2,5]thiadiazol-5-ylmethylene)-3-benzyl-2-thioxothiazolidin-4-one | 1367578-55-9

中文名称
——
中文别名
——
英文名称
5-(benzo[c][1,2,5]thiadiazol-5-ylmethylene)-3-benzyl-2-thioxothiazolidin-4-one
英文别名
5-(2,1,3-benzothiadiazol-5-ylmethylidene)-3-benzyl-2-sulfanylidene-1,3-thiazolidin-4-one
5-(benzo[c][1,2,5]thiadiazol-5-ylmethylene)-3-benzyl-2-thioxothiazolidin-4-one化学式
CAS
1367578-55-9
化学式
C17H11N3OS3
mdl
——
分子量
369.492
InChiKey
SXUSKEFYYNNDKS-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.09
  • 重原子数:
    24.0
  • 可旋转键数:
    3.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    46.09
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

反应信息

  • 作为产物:
    描述:
    3-苄基若丹宁2,1,3-苯并噻二唑-5-甲醛乙醇 为溶剂, 反应 0.92h, 以54%的产率得到5-(benzo[c][1,2,5]thiadiazol-5-ylmethylene)-3-benzyl-2-thioxothiazolidin-4-one
    参考文献:
    名称:
    The Rhodadyns, a New Class of Small Molecule Inhibitors of Dynamin GTPase Activity
    摘要:
    Six focused rhodanine-based libraries, 60 compounds in total, were synthesized and evaluated as potential dynamin I GTPase inhibitors. Twenty-six were more potent than the lead compound with 13 returning IC50 values <10 mu M, making the Rhodadyn series among the most active dynamin inhibitors reported. Two analogues were highly effective at blocking receptor-mediated endocytosis: C10 and D10 with IC50(RmE) = 7.0 +/- 2.2 and 5.9 +/- 1.0 mu M, respectively. These compounds are equipotent with the best reported in-cell dynamin inhibitors.
    DOI:
    10.1021/ml200284s
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文献信息

  • The Rhodadyns, a New Class of Small Molecule Inhibitors of Dynamin GTPase Activity
    作者:Mark J. Robertson、Gordana Hadzic、Joseph Ambrus、D. Yuri Pomè、Emily Hyde、Ainslie Whiting、Anna Mariana、Lisa von Kleist、Ngoc Chau、Volker Haucke、Phillip J. Robinson、Adam McCluskey
    DOI:10.1021/ml200284s
    日期:2012.5.10
    Six focused rhodanine-based libraries, 60 compounds in total, were synthesized and evaluated as potential dynamin I GTPase inhibitors. Twenty-six were more potent than the lead compound with 13 returning IC50 values <10 mu M, making the Rhodadyn series among the most active dynamin inhibitors reported. Two analogues were highly effective at blocking receptor-mediated endocytosis: C10 and D10 with IC50(RmE) = 7.0 +/- 2.2 and 5.9 +/- 1.0 mu M, respectively. These compounds are equipotent with the best reported in-cell dynamin inhibitors.
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同类化合物

(5-氯-2,1,3-苯并噻二唑-4-基)-氨基甲氨基硫代甲酸甲酯一氢碘 阿拉酸式苯-S-甲基 阿拉酸式苯 试剂4,7-Bis(5-bromo-2-thienyl)-5,6-bis(dodecyloxy)-2,1,3-benzothiadiazole 苯并恶唑-6-胺 苯并[d][1,2,3]噻二唑-6-羧酸 苯并[C][1,2,5]噻二唑-5-硼酸频那醇酯 苯并[C][1,2,5]噻二唑-4-磺酸钠 苯并[C][1,2,5]噻二唑-4-基甲醇 苯并[C][1,2,5]噻二唑-4,7-二基二硼酸 苯并[1,2,5]噻二唑-4-羧酸 苯并[1,2,5]噻二唑-4-磺酰氯 苯并[1,2,3]噻二唑-7-基胺 苯并[1,2,3]噻二唑-6-羧酸甲酯 苯并[1,2,3]噻二唑-5-基胺 苯并[1,2,3]噻二唑-4-基胺 苯2,1,3-噻重氮-5-羧酸酯 碘化(2,1,3-苯并硫杂(SIV)二唑-5-基)二甲基八氧代甲基铵 硫代磷酸S-[(2,1,3-苯并噻二唑-5-基)甲基]酯O,O-二钠盐 盐酸替扎尼定-d4 盐酸替扎尼定 灭草荒 替托尼定D4 替扎尼定杂质1 替扎尼定 噻唑并[4,5-f]-2,1,3-苯并噻二唑,6-甲基-(6CI,8CI) 去氢替扎尼定 全氟苯并[c][1,2,5]噻二唑 [7-[2-[2-(8-硫杂-7,9-二氮杂双环[4.3.0]壬-3,5,9-三烯-7-基)乙基二巯基]乙基]-8-硫杂-7,9-二氮杂双环[4.3.0]壬-3,5,9-三烯-2-基]甲胺 N-甲氧基-N-甲基-2,1,3-苯并噻二唑-5-酰胺 N-(5-氯-2,1,3-苯并噻二唑-4-基)硫脲 N,N'-二硫代二(亚乙基)二(2,1,3-苯并噻二唑-5-甲胺) N'-2,1,3-苯并噻二唑-4-基-N,N-二甲基酰亚胺基甲酰胺 BTQBT(升华提纯) 7H-咪唑并[4,5-g][1,2,3]苯并噻二唑 7H-咪唑并[4,5-e][1,2,3]苯并噻二唑 7-肼基[1,3]噻唑并[4,5-e][2,1,3]苯并噻二唑 7-硝基-苯并[1,2,5]噻二唑-4-基胺 7-硝基-1,2,3-苯并噻二唑 7-甲基[1,3]噻唑并[5,4-e][2,1,3]苯并噻二唑 7-甲基[1,3]噻唑并[4,5-e][2,1,3]苯并噻二唑 7-甲基[1,3]噻唑并[4,5-e][1,2,3]苯并噻二唑 7-溴苯并[c][1,2,5]噻二唑-4-磺酸 7-溴-苯并[D][1,2,3]噻二唑 7-溴-5-甲基-4-硝基-2,1,3-苯并噻二唑 7-溴-4-醛基苯并[C][1,2,5]噻二唑 7-溴-2,1,3-苯并噻二唑-4-磺酰氯 7-溴-2,1,3-苯并噻二唑-4-甲腈 7-溴-2,1,3-苯并噻二唑-4-亚磺酸 7-氯-苯并[1,2,5]噻二唑-4-基胺