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N-[2-[[(2R,3S,4R,5R,6S,7R,9R,10R,11S,12S,13R)-2-ethyl-3,4,9-trihydroxy-12-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-[(2S,3R,4S,6R)-3-hydroxy-6-methyl-4-[methyl(propan-2-yl)amino]oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-14-oxo-oxacyclotetradec-6-yl]oxy]ethyl]-3H-benzimidazole-5-carboxamide | 916242-90-5

中文名称
——
中文别名
——
英文名称
N-[2-[[(2R,3S,4R,5R,6S,7R,9R,10R,11S,12S,13R)-2-ethyl-3,4,9-trihydroxy-12-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-[(2S,3R,4S,6R)-3-hydroxy-6-methyl-4-[methyl(propan-2-yl)amino]oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-14-oxo-oxacyclotetradec-6-yl]oxy]ethyl]-3H-benzimidazole-5-carboxamide
英文别名
——
N-[2-[[(2R,3S,4R,5R,6S,7R,9R,10R,11S,12S,13R)-2-ethyl-3,4,9-trihydroxy-12-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-[(2S,3R,4S,6R)-3-hydroxy-6-methyl-4-[methyl(propan-2-yl)amino]oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-14-oxo-oxacyclotetradec-6-yl]oxy]ethyl]-3H-benzimidazole-5-carboxamide化学式
CAS
916242-90-5
化学式
C49H82N4O14
mdl
——
分子量
951.208
InChiKey
YSVSPZDEDARHAM-YPVQGADQSA-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):
    5.6
  • 重原子数:
    67
  • 可旋转键数:
    13
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    244
  • 氢给体数:
    7
  • 氢受体数:
    16

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    9-dihydro-9-O-(2-aminoethyl)-N-desmethyl-N-isopropyl-hydroerythromycin A1-羟基苯并三唑1-(3-二甲基氨基丙基)-3-乙基碳二亚胺 作用下, 以 四氢呋喃 为溶剂, 反应 2.25h, 以48%的产率得到N-[2-[[(2R,3S,4R,5R,6S,7R,9R,10R,11S,12S,13R)-2-ethyl-3,4,9-trihydroxy-12-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyloxan-2-yl]oxy-10-[(2S,3R,4S,6R)-3-hydroxy-6-methyl-4-[methyl(propan-2-yl)amino]oxan-2-yl]oxy-3,5,7,9,11,13-hexamethyl-14-oxo-oxacyclotetradec-6-yl]oxy]ethyl]-3H-benzimidazole-5-carboxamide
    参考文献:
    名称:
    Motilide compounds
    摘要:
    具有如公式(I)所示结构的化合物,其中RA、RB、RC、RD、RE和RF的定义如本文所述,可用作促动力剂。
    公开号:
    US20060270616A1
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文献信息

  • 9-Dihydroerythromycin ethers as motilin agonists—Developing structure–activity relationships for potency and safety
    作者:Yaoquan Liu、Yong Li、David C. Myles、Mark Claypool、Christopher W. Carreras、Simon J. Shaw
    DOI:10.1016/j.bmc.2010.08.035
    日期:2010.11
    A series of derivatives of the amine of 9-dihydro-9-O-ethylamino-N-desmethyl-N-isopropyl erythromycin A derivatives were synthesized as motilin agonists. The compounds were developed for potency without showing antibacterial activity and inhibition of the hERG potassium channel. The formamide of the amide series was found to show the optimal combination of properties relative to carbamates, ureas, thioureas, and amines. This prompted an investigation of heterocyclic isosteres for the amide. In this series the triazole had the optimal combination of properties. From the study, two compounds met the criteria for detailed pharmacokinetic studies. (C) 2010 Elsevier Ltd. All rights reserved.
  • Motilide compounds
    申请人:Liu Yaoquan
    公开号:US20060270616A1
    公开(公告)日:2006-11-30
    Compounds having a structure according to formula (I) where R A , R B , R C , R D , R E , and R F are as defined herein, are useful as prokinetic agents.
    具有如公式(I)所示结构的化合物,其中RA、RB、RC、RD、RE和RF的定义如本文所述,可用作促动力剂。
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