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| 1255515-97-9

中文名称
——
中文别名
——
英文名称
——
英文别名
——
化学式
CAS
1255515-97-9
化学式
C37H56N8O15P2Si2
mdl
——
分子量
971.015
InChiKey
DQLUURKKERJATR-QGQJFHJHSA-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

反应信息

  • 作为反应物:
    描述:
    作用下, 以 甲醇 为溶剂, 反应 12.0h, 生成
    参考文献:
    名称:
    Synthesis of cyclic di-nucleotidic acids as potential inhibitors targeting diguanylate cyclase
    摘要:
    Five analogs of cyclic di-nucleotidic acid including c-di-GMP were synthesized and evaluated for their biological activities on Slr1143, a diguanylate cyclase of Synechocystis sp. Slr1143 was overexpressed from the recombinant plasmid which contained the gene of interest and subsequently purified by affinity chromatography. A new HPLC method capable of separating the compound and product peaks with good resolution was optimized and applied to the analysis of the compounds. Results obtained show that cyclic di-inosinylic acid 1b demonstrates a stronger inhibition on Slr1143 than c-di-GMP and is a potential inhibitor for biofilm formation. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.07.068
  • 作为产物:
    描述:
    N-甲基咪唑2,4,6-三异丙基苯磺酰氯 作用下, 以 四氢呋喃 为溶剂, 生成
    参考文献:
    名称:
    Synthesis of cyclic di-nucleotidic acids as potential inhibitors targeting diguanylate cyclase
    摘要:
    Five analogs of cyclic di-nucleotidic acid including c-di-GMP were synthesized and evaluated for their biological activities on Slr1143, a diguanylate cyclase of Synechocystis sp. Slr1143 was overexpressed from the recombinant plasmid which contained the gene of interest and subsequently purified by affinity chromatography. A new HPLC method capable of separating the compound and product peaks with good resolution was optimized and applied to the analysis of the compounds. Results obtained show that cyclic di-inosinylic acid 1b demonstrates a stronger inhibition on Slr1143 than c-di-GMP and is a potential inhibitor for biofilm formation. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.07.068
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