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

7-benzyl-1,3-dioxo-1,2,3,4,5,6,7,8-octahydro-[2,7]-naphthyridine-4-carbonitrile | 1228692-26-9

中文名称
——
中文别名
——
英文名称
7-benzyl-1,3-dioxo-1,2,3,4,5,6,7,8-octahydro-[2,7]-naphthyridine-4-carbonitrile
英文别名
7-Benzyl-1,3-dioxo-4,5,6,8-tetrahydro-2,7-naphthyridine-4-carbonitrile;7-benzyl-1,3-dioxo-4,5,6,8-tetrahydro-2,7-naphthyridine-4-carbonitrile
7-benzyl-1,3-dioxo-1,2,3,4,5,6,7,8-octahydro-[2,7]-naphthyridine-4-carbonitrile化学式
CAS
1228692-26-9
化学式
C16H15N3O2
mdl
——
分子量
281.314
InChiKey
QMWMORFWGNOTGT-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

  • 熔点:
    258-260 °C
  • 沸点:
    549.2±50.0 °C(Predicted)
  • 密度:
    1.32±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    21
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.31
  • 拓扑面积:
    73.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

点击查看最新优质反应信息

文献信息

  • METHOD OF TREATING CONDITIIONS WITH KINASE INHIBITORS
    申请人:ALLERGAN, INC.
    公开号:US20130237537A1
    公开(公告)日:2013-09-12
    The present invention relates to a method of treating ophthalmic diseases and conditions, e.g. diabetic retinopathy, age-related macular degeneration, retinopathy of prematurity, etc., in a subject comprising administering to said subject a therapeutically effective amount of at least one compound of formula I or a prodrug, pharmaceutically acceptable salt, racemic mixtures or enantiomers of said compound. The compounds of formula I are capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
    本发明涉及一种治疗眼科疾病和病况的方法,例如糖尿病视网膜病变、老年性黄斑变性、早产儿视网膜病变等,在一个受试者中,包括向该受试者施用至少一种式I的化合物的治疗有效量,或者该化合物的前药、药学上可接受的盐、拉丁混合物或对映体。式I的化合物能够调节酪氨酸激酶信号传导,以调节、调制和/或抑制异常细胞增殖。
  • Synthesis of 7-benzyl-5-(piperidin-1-yl)-6,7,8,9-tetrahydro-3H-pyrazolo[3,4-c][2,7]naphthyridin-1-ylamine and its analogs as bombesin receptor subtype-3 agonists
    作者:Cheng Guo、Peter R. Guzzo、Mark Hadden、Bruce J. Sargent、Larry Yet、Yanqing Kan、Oksana Palyha、Theresa M. Kelly、Xiaoming Guan、Kim Rosko、Karen Gagen、Joseph M. Metzger、Jasminka Dragovic、Kathryn Lyons、Linus S. Lin、Ravi P. Nargund
    DOI:10.1016/j.bmcl.2010.03.065
    日期:2010.5
    The original structure of a high-throughput screening hit obtained from an external vendor was revised based on multiple NMR studies. The active compound was re-synthesized via a novel route and its structure and biological activity as a BRS-3 agonist were unambiguously confirmed. Multi-gram quantities of the hit were prepared for pharmacokinetic and efficacy studies. The synthetic strategy allowed for the preparation of multiple analogs for SAR exploration. (C) 2010 Elsevier Ltd. All rights reserved.
  • METHOD OF TREATING OPHTHALMIC CONDITIONS WITH KINASE INHIBITORS
    申请人:ALLERGAN, INC.
    公开号:EP2825166A1
    公开(公告)日:2015-01-21
  • DIHYDROPYRIDOPYRIMIDINE AND DIHYDRONAPHTHYRIDINE DERIVATIVES AS TYROSINE KINASE INHIBITORS OF ESPECIALLY VEGF AND PDGF
    申请人:ALLERGAN, INC.
    公开号:EP2825537A1
    公开(公告)日:2015-01-21
  • METHOD OF TREATING CONDITIONS WITH KINASE INHIBITORS
    申请人:Allergan, Inc.
    公开号:US20170143728A1
    公开(公告)日:2017-05-25
    The present invention relates to a method of treating ophthalmic diseases and conditions, e.g. diabetic retinopathy, age-related macular degeneration, retinopathy of prematurity, etc., in a subject comprising administering to said subject a therapeutically effective amount of at least one compound of formula I or a prodrug, pharmaceutically acceptable salt, racemic mixtures or enantiomers of said compound. The compounds of formula I are capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
查看更多