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9U,9U-flavolipid tert-butyl ester | 1258519-46-8

中文名称
——
中文别名
——
英文名称
9U,9U-flavolipid tert-butyl ester
英文别名
——
9U,9U-flavolipid tert-butyl ester化学式
CAS
1258519-46-8
化学式
C38H68N4O9
mdl
——
分子量
724.979
InChiKey
JCOQTXKXGXWBLX-HOFJZWJUSA-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):
    5.61
  • 重原子数:
    51.0
  • 可旋转键数:
    27.0
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.76
  • 拓扑面积:
    185.81
  • 氢给体数:
    5.0
  • 氢受体数:
    9.0

反应信息

  • 作为反应物:
    描述:
    9U,9U-flavolipid tert-butyl ester三氟乙酸 作用下, 反应 0.25h, 以65%的产率得到9U,9U-flavolipid
    参考文献:
    名称:
    Synthesis and biological activities of flavolipids
    摘要:
    Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.tet.2010.09.088
  • 作为产物:
    描述:
    (E)-N'-hydroxy-N'-(7'-methyl-2'-octenoyl)-cadaverinium trifluoroacetate1,3-bis-(N-succinimidyl) 2-tert-butyl citrate三乙胺 作用下, 以 1,4-二氧六环二氯甲烷 为溶剂, 以60%的产率得到9U,9U-flavolipid tert-butyl ester
    参考文献:
    名称:
    Synthesis and biological activities of flavolipids
    摘要:
    Syntheses of the bacterial surfactants 6S 6S- 9S 9S- and 9U 9U-flavolipids confirmed the structures proposed for them from spectroscopic analysis of a flavolipid mixture and made pure flavolipids available for the first time All three synthetic flavolipids and a straight chain analogue were found to be weakly cytotoxic and to inhibit metastatic cancer cell migration with 9U 9U-fiavolipid (the most abundant natural flavolipid) having the most activity Biosynthetic routes to the branched side-chains of the flavolipids are suggested and it is proposed that branched chains are employed to hinder biodegradation (C) 2010 Elsevier Ltd All rights reserved
    DOI:
    10.1016/j.tet.2010.09.088
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