摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

8-benzyl-5-(3-bromo-4-fluorophenyl)-5,8,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6(3H,7H)-dione | 265321-19-5

中文名称
——
中文别名
——
英文名称
8-benzyl-5-(3-bromo-4-fluorophenyl)-5,8,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6(3H,7H)-dione
英文别名
8-benzyl-5-(3-bromo-4-fluorophenyl)-5,7,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6-dione
8-benzyl-5-(3-bromo-4-fluorophenyl)-5,8,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6(3H,7H)-dione化学式
CAS
265321-19-5
化学式
C24H20BrFN2O3
mdl
——
分子量
483.337
InChiKey
BZMKCBVYTUNNAQ-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.1
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    58.6
  • 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:
    8-benzyl-5-(3-bromo-4-fluorophenyl)-5,8,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6(3H,7H)-dione盐酸 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 27.0h, 生成 5-(3-bromo-4-fluorophenyl)-5,8,9,10-tetrahydro-1H-pyrano[3,4-b][1,7]naphthyridine-4,6(3H,7H)-dione hydrochloride
    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:
    5‐Amino‐2H‐pyran‐3(6H)‐one, 1, a Convenient Intermediate in the Synthesis of Pyran Containing 1,4‐Dihydropyridines
    摘要:
    5-Amino-2H-pyran-3(6H)-one, 1, is a novel intermediate that is useful in the synthesis of pyran containing dihydropyridines. The synthesis and use of I will be discussed.
    DOI:
    10.1081/scc-120027702
点击查看最新优质反应信息

文献信息

  • Pyrano, piperidino, and thiopyrano compounds and methods of use
    申请人:Abbott Laboratories
    公开号:US06191140B1
    公开(公告)日:2001-02-20
    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,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,其化学式为I。
  • 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
查看更多