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methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate | 265321-22-0

中文名称
——
中文别名
——
英文名称
methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate
英文别名
methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,8-dihydro-1H-pyrano[3,4-b]pyridine-3-carboxylate
methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate化学式
CAS
265321-22-0
化学式
C17H15BrFNO4
mdl
——
分子量
396.213
InChiKey
QOVXXPQZWSMIPI-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:
    512.2±50.0 °C(predicted)
  • 密度:
    1.57±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    24
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    64.6
  • 氢给体数:
    1
  • 氢受体数:
    6

上下游信息

  • 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:
    methyl 4-(3-bromo-4-fluorophenyl)-2-methyl-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate吡啶 、 pyridinium hydrobromide perbromide 作用下, 以 氯仿 为溶剂, 反应 1.0h, 以0.68 g的产率得到methyl 4-(3-bromo-4-fluorophenyl)-2-(bromomethyl)-5-oxo-4,5,6,8-tetrahydro-1H-pyrano[3,4-b]pyridine-3-carboxylate
    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
  • 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:US06642222B2
    公开(公告)日:2003-11-04
    The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.
    本发明提供了一种公式I的新化合物,可能在超极化细胞膜、打开通道、放松平滑肌细胞和抑制膀胱收缩方面有用。
  • Pyrano piperidino and thiopyrano compounds and methods of use
    申请人:——
    公开号:US20030055035A1
    公开(公告)日:2003-03-20
    1 The present invention provides novel compounds of formula I which may be useful in hyperpolarizing cell membranes, opening potassium channels, relaxing smooth muscle cells, and inhibiting bladder contractions.
    本发明提供了一种新型的化合物I,可用于超极化细胞膜、打开通道、放松平滑肌细胞和抑制膀胱收缩。
  • PYRANO, PIPERIDINO, AND THIOPYRANO COMPOUNDS AND METHODS OF USE
    申请人:ABBOTT LABORATORIES
    公开号:EP1124828A1
    公开(公告)日:2001-08-22
  • US6191140B1
    申请人:——
    公开号:US6191140B1
    公开(公告)日:2001-02-20
  • US6642222B2
    申请人:——
    公开号:US6642222B2
    公开(公告)日:2003-11-04
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