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肽U6 | 170804-63-4

中文名称
肽U6
中文别名
——
英文名称
3',4'-diaminoflavone
英文别名
2-(3,4-diaminophenyl)-4H-1-benzopyran-4-one;2-(3,4-Diaminophenyl)chromen-4-one
肽U6化学式
CAS
170804-63-4
化学式
C15H12N2O2
mdl
——
分子量
252.272
InChiKey
JXLWTFVAFWWENR-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

物化性质

  • 沸点:
    488.4±45.0 °C(Predicted)
  • 密度:
    1.372±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    78.3
  • 氢给体数:
    2
  • 氢受体数:
    4

SDS

SDS:5e09fd8274e753126f3b01fa2557620d
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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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    肽U6丁酸盐酸 作用下, 以27%的产率得到2-(2-propyl-3H-benzimidazol-5-yl)chromen-4-one
    参考文献:
    名称:
    Synthesis and antiaggregator activity of some new derivatives of 4H-1-benzopyran-4-one
    摘要:
    A series of 2-[2-alkyl-1H-benzimidazol-5(6)-yl]-4H-1 analogues 7a-7e was synthesized by the reaction with 3',4'-diaminoflavone and aliphatic carboxylic acids. 3',4'-Diaminoflavone 6 was prepared via the reduction of 2-(4-amino-3-nitrophenyl)-4H-1-benzopyran-4-one 5a. The compounds 7a-e and 14a-f were tested in vitro for their inhibitory activities against human platelet aggregation induced by collagen, ADP and A23187. The compound with a COOR group as a side chain, 2-(2-alkyloxycarbonyl-2,3-dihydro-1,4-benzodioxin-6-yl)-4H-1-benzopyran-4-one 14a-f, has potent activity, and so compound 13 was also prepared as an analogue of series 14 and tested for its antiaggregator activity.
    DOI:
    10.1016/0223-5234(96)88270-5
  • 作为产物:
    描述:
    4-(戊酰基氨基)苯甲酸 在 palladium on activated charcoal 吡啶氢氧化钾氯化亚砜硫酸氢气硝酸 作用下, 以 四氢呋喃甲醇N,N-二甲基甲酰胺 为溶剂, -15.0~100.0 ℃ 、101.33 kPa 条件下, 反应 8.83h, 生成 肽U6
    参考文献:
    名称:
    Synthesis and antiaggregator activity of some new derivatives of 4H-1-benzopyran-4-one
    摘要:
    A series of 2-[2-alkyl-1H-benzimidazol-5(6)-yl]-4H-1 analogues 7a-7e was synthesized by the reaction with 3',4'-diaminoflavone and aliphatic carboxylic acids. 3',4'-Diaminoflavone 6 was prepared via the reduction of 2-(4-amino-3-nitrophenyl)-4H-1-benzopyran-4-one 5a. The compounds 7a-e and 14a-f were tested in vitro for their inhibitory activities against human platelet aggregation induced by collagen, ADP and A23187. The compound with a COOR group as a side chain, 2-(2-alkyloxycarbonyl-2,3-dihydro-1,4-benzodioxin-6-yl)-4H-1-benzopyran-4-one 14a-f, has potent activity, and so compound 13 was also prepared as an analogue of series 14 and tested for its antiaggregator activity.
    DOI:
    10.1016/0223-5234(96)88270-5
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文献信息

  • Synthesis and antiaggregator activity of some new derivatives of 4H-1-benzopyran-4-one
    作者:H Göker、G Ayhan、M Tunçbilek、R Ertan、G Leoncini、R Garzoglio、M Mazzei
    DOI:10.1016/0223-5234(96)88270-5
    日期:1995.1
    A series of 2-[2-alkyl-1H-benzimidazol-5(6)-yl]-4H-1 analogues 7a-7e was synthesized by the reaction with 3',4'-diaminoflavone and aliphatic carboxylic acids. 3',4'-Diaminoflavone 6 was prepared via the reduction of 2-(4-amino-3-nitrophenyl)-4H-1-benzopyran-4-one 5a. The compounds 7a-e and 14a-f were tested in vitro for their inhibitory activities against human platelet aggregation induced by collagen, ADP and A23187. The compound with a COOR group as a side chain, 2-(2-alkyloxycarbonyl-2,3-dihydro-1,4-benzodioxin-6-yl)-4H-1-benzopyran-4-one 14a-f, has potent activity, and so compound 13 was also prepared as an analogue of series 14 and tested for its antiaggregator activity.
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