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

N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-1H-indazol-4-ylurea

中文名称
——
中文别名
——
英文名称
N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-1H-indazol-4-ylurea
英文别名
1-(7-fluoro-2,2-dimethylchroman-4-yl)-3-(1H-indazol-4-yl)urea;1-(7-fluoro-2,2-dimethyl-3,4-dihydrochromen-4-yl)-3-(1H-indazol-4-yl)urea
N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-1H-indazol-4-ylurea化学式
CAS
——
化学式
C19H19FN4O2
mdl
——
分子量
354.384
InChiKey
AWVYCAFGYUVHBP-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):
    2.9
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    79
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-1H-indazol-4-ylurea2-溴乙基甲基醚 在 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 1.0h, 以23%的产率得到N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-[1-(2-methoxyethyl)-1H-indazol-4-yl]urea
    参考文献:
    名称:
    Prodrugs of compounds that inhibit TRPV1 receptor
    摘要:
    式(I)的化合物 其中A,R1,R2和R3在规范中定义,并且这些化合物可用作治疗化合物,特别用于治疗与炎症、疼痛、膀胱过度活动、尿失禁以及由TRPV1引起或加重的其他疾病或症状相关的紊乱。
    公开号:
    US20070099954A1
  • 作为产物:
    描述:
    methyl 4-(3-(7-fluoro-2,2-dimethylchroman-4-yl)ureido)-1H-indazole-1-carboxylate 在 甲醇sodium hydroxide 作用下, 反应 0.5h, 以34%的产率得到N-(7-fluoro-2,2-dimethyl-3,4-dihydro-2H-chromen-4-yl)-N'-1H-indazol-4-ylurea
    参考文献:
    名称:
    Prodrugs of compounds that inhibit TRPV1 receptor
    摘要:
    式(I)的化合物 其中A,R1,R2和R3在规范中定义,并且这些化合物可用作治疗化合物,特别用于治疗与炎症、疼痛、膀胱过度活动、尿失禁以及由TRPV1引起或加重的其他疾病或症状相关的紊乱。
    公开号:
    US20070099954A1
点击查看最新优质反应信息

文献信息

  • Chromanylurea compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor and uses thereof
    申请人:Gomtsyan Arthur
    公开号:US20060128689A1
    公开(公告)日:2006-06-15
    Compounds that are antagonists of the VR1 receptor, having formula (I) or a pharmaceutically acceptable salt, prodrug, or salt of a prodrug thereof, wherein A 1 , A 2 , A 3 , A 4 , R 7 , R 8 , R 9 , X, Y, Z, L, n, and m, are as defined herein, and are useful in disorders prevented or ameliorated by inhibiting the VR1 receptor.
    对VR1受体拮抗剂,其化学式为(I)或其药用可接受的盐、前药或前药的盐,其中A1、A2、A3、A4、R7、R8、R9、X、Y、Z、L、n和m的定义如本文所述,并且在通过抑制VR1受体预防或改善的疾病中具有用处。
  • [EN] TRPV1 ANTAGONISTS<br/>[FR] ANTAGONISTES DE TRPV1
    申请人:ABBOTT LAB
    公开号:WO2010045402A1
    公开(公告)日:2010-04-22
    Disclosed herein are compounds of formula (I), or pharmaceutically acceptable salts, solvates, prodrugs, salts of prodrugs, or combinations thereof, wherein R1, R2, R3, R4, and m are defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also disclosed.
    本文披露了式(I)的化合物,或其药用可接受的盐、溶剂化合物、前药、前药的盐或它们的组合,其中R1、R2、R3、R4和m在规范中有定义。还披露了包含这种化合物的组合物以及使用这种化合物和组合物治疗疾病和疾病的方法。
  • CHROMANYLUREA COMPOUNDS THAT INHIBIT VANILLOID RECEPTOR SUBTYPE 1 (VR1) RECEPTOR AND USES THEREOF
    申请人:Gomtsyan Arthur
    公开号:US20110152250A1
    公开(公告)日:2011-06-23
    Compounds that are antagonists of the VR1 receptor, having formula (I) or a pharmaceutically acceptable salt, prodrug, or salt of a prodrug thereof, wherein A 1 , A 2 , A 3 , A 4 , R 7 , R 8 , R 9 , X, Y, Z, L, n, and m, are as defined herein, and are useful in disorders prevented or ameliorated by inhibiting the VR1 receptor.
    具有以下式子(I)或其药学上可接受的盐、前药或前药的盐的拮抗VR1受体的化合物,在其中A1、A2、A3、A4、R7、R8、R9、X、Y、Z、L、n和m如本文所定义,并且在抑制VR1受体有益于预防或改善疾病。
  • TRPV1 ANTAGONISTS
    申请人:Gomtsyan Arthur R.
    公开号:US20100120846A1
    公开(公告)日:2010-05-13
    Disclosed herein are compounds of formula (I), or pharmaceutically acceptable salts, solvates, prodrugs, salts of prodrugs, or combinations thereof, wherein R 1 , R 2 , R 3 , R 4 , and m are defined in the specification. Compositions comprising such compounds and methods for treating conditions and disorders using such compounds and compositions are also disclosed.
    本文揭示了式(I)的化合物,或其药学上可接受的盐、溶剂、前药盐、前药的盐或其组合物,其中R1、R2、R3、R4和m在规范中被定义。还揭示了包含这些化合物的组合物以及使用这些化合物和组合物治疗疾病和病症的方法。
  • PRODRUGS OF COMPOUNDS THAT INHIBIT TRPV1 RECEPTOR
    申请人:Gomtsyan Arthur R.
    公开号:US20120277190A1
    公开(公告)日:2012-11-01
    Compounds of formula (I) wherein A, R 1 , R 2 , and R 3 are defined in the specification, and which are useful as therapeutic compounds particularly for treating disorders or conditions associated with inflammation, pain, bladder overactivity, urinary incontinence, and other disorders caused by or exacerbated by TRPV1.
    公式为(I)的化合物,其中A,R1,R2和R3在规范中有定义,并且它们可用作治疗化合物,特别是用于治疗与炎症,疼痛,膀胱过度活动,尿失禁和其他由TRPV1引起或加剧的疾病或症状。
查看更多