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vinyl 9-(3-bromo-4-fluorophenyl)-8-oxo-2,3,5,7,8,9-hexahydrothieno[3,2-b][1,7]naphthyridine-6(4H)-carboxylate 1,1-dioxide | 265321-04-8

中文名称
——
中文别名
——
英文名称
vinyl 9-(3-bromo-4-fluorophenyl)-8-oxo-2,3,5,7,8,9-hexahydrothieno[3,2-b][1,7]naphthyridine-6(4H)-carboxylate 1,1-dioxide
英文别名
Ethenyl 9-(3-bromo-4-fluorophenyl)-1,1,8-trioxo-2,3,4,5,7,9-hexahydrothieno[3,2-b][1,7]naphthyridine-6-carboxylate
vinyl 9-(3-bromo-4-fluorophenyl)-8-oxo-2,3,5,7,8,9-hexahydrothieno[3,2-b][1,7]naphthyridine-6(4H)-carboxylate 1,1-dioxide化学式
CAS
265321-04-8
化学式
C19H16BrFN2O5S
mdl
——
分子量
483.315
InChiKey
PERBORXSDKBGLS-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:
    690.8±55.0 °C(predicted)
  • 密度:
    1.73±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    101
  • 氢给体数:
    1
  • 氢受体数:
    7

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

  • 作为反应物:
    描述:
    vinyl 9-(3-bromo-4-fluorophenyl)-8-oxo-2,3,5,7,8,9-hexahydrothieno[3,2-b][1,7]naphthyridine-6(4H)-carboxylate 1,1-dioxide盐酸 作用下, 以 乙醇 为溶剂, 生成 9-(3-bromo-4-fluorophenyl)-2,3,5,6,7,9-hexahydrothieno[3,2-b][1,7]naphthyridin-8(4H)-one 1,1-dioxide hydrochloride
    参考文献:
    名称:
    Pyrano, piperidino, and thiopyrano compounds and methods of use
    摘要:
    本发明提供了一种新型的化合物,可能在超极化细胞膜、打开钾通道、放松平滑肌细胞和抑制膀胱收缩方面有用,其化学式为I。
    公开号:
    US06191140B1
  • 作为产物:
    参考文献:
    名称:
    Synthesis and Structure−Activity Relationships of a Novel Series of Tricyclic Dihydropyridine-Based KATP Openers That Potently Inhibit Bladder Contractions in Vitro
    摘要:
    Structure-activity relationships were investigated on a novel series of tricyclic dihydropyridine-containing K-ATP openers. This diverse group of analogues, comprising a variety of heterocyclic rings fused to the dihydropyridine nucleus, was designed to determine the influence on activity of hydrogen-bond-donating and -accepting groups and their stereochemical disposition. Compounds were evaluated for K-ATP activity in guinea pig bladder cells using a fluorescence-based membrane potential assay and in a pig bladder strip assay. The inhibition of spontaneous bladder contractions in vitro was also examined for a subset of compounds. All compounds studied showed greater potency to inhibit spontaneous bladder contractions relative to their potencies to inhibit contractions elicited by electrical stimulation.
    DOI:
    10.1021/jm030357o
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文献信息

  • PYRANO, PIPERIDINO, AND THIOPYRANO COMPOUNDS AND METHODS OF USE
    申请人:ABBOTT LABORATORIES
    公开号:EP1124828B1
    公开(公告)日:2008-01-02
  • US6191140B1
    申请人:——
    公开号:US6191140B1
    公开(公告)日:2001-02-20
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