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4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinoline | 1187313-22-9

中文名称
——
中文别名
——
英文名称
4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinoline
英文别名
4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinolone
4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinoline化学式
CAS
1187313-22-9
化学式
C15H9BrN4
mdl
——
分子量
325.167
InChiKey
VZRGZDCXYIAXFA-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

  • 密度:
    1?+-.0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    20
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    43.1
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinoline间氯过氧苯甲酸三氯氧磷 作用下, 以 二氯甲烷甲苯 为溶剂, 反应 6.0h, 生成 4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)-2-chloroquinoline
    参考文献:
    名称:
    [EN] BMP INHIBITORS AND METHODS OF USE THEREOF
    [FR] INHIBITEURS DE BMP ET LEURS PROCÉDÉS D'UTILISATION
    摘要:
    公开号:
    WO2014160203A3
  • 作为产物:
    描述:
    2-(喹啉-4-基)乙腈氢溴酸肼溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 16.0h, 生成 4-(6-bromopyrazolo[1,5-a]pyrimidin-3-yl)quinoline
    参考文献:
    名称:
    [EN] INHIBITORS OF THE BMP SIGNALING PATHWAY
    [FR] INHIBITEURS DE LA VOIE DE SIGNALISATION BMP
    摘要:
    本发明提供了BMP信号通路的小分子抑制剂。这些化合物可用于调节细胞生长、分化、增殖和凋亡,因此可用于治疗与BMP信号通路相关的疾病或症状,包括炎症、心血管疾病、血液学疾病、癌症和骨骼疾病,以及调节细胞分化和/或增殖。
    公开号:
    WO2009114180A1
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文献信息

  • [EN] THERAPEUTIC COMPOUNDS AND METHODS<br/>[FR] COMPOSÉS ET MÉTHODES THÉRAPEUTIQUES
    申请人:UNIV RUTGERS
    公开号:WO2018165569A1
    公开(公告)日:2018-09-13
    Disclosed herein are compounds of formula II: II or a salt thereof. Also disclosed are pharmaceutical compositions and therapeutic methods for treating certain diseases including cancer such as lung cancer.
    本文披露了II式化合物及其盐。还披露了包括肺癌在内的某些疾病的药物组合物和治疗方法。
  • Novel bone morphogenetic protein receptor inhibitor JL5 suppresses tumor cell survival signaling and induces regression of human lung cancer
    作者:Jenna H. Newman、David J. Augeri、Rachel NeMoyer、Jyoti Malhotra、Elaine Langenfeld、Charles B. Chesson、Natalie S. Dobias、Michael J. Lee、Saeed Tarabichi、Sachin R. Jhawar、Praveen K. Bommareddy、Sh’Rae Marshall、Evita T. Sadimin、John E. Kerrigan、Michael Goedken、Christine Minerowicz、Salma K. Jabbour、Shengguo Li、Mary O. Carayannopolous、Andrew Zloza、John Langenfeld
    DOI:10.1038/s41388-018-0156-9
    日期:2018.7
    BMP receptor inhibitors induce death of cancer cells through the downregulation of antiapoptotic proteins XIAP, pTAK1, and Id1-Id3. However, the current most potent BMP receptor inhibitor, DMH2, does not downregulate BMP signaling in vivo because of metabolic instability and poor pharmacokinetics. Here we identified the site of metabolic instability of DMH2 and designed a novel BMP receptor inhibitor, JL5. We show that JL5 has a greater volume of distribution and suppresses the expression of Id1 and pTak1 in tumor xenografts. Moreover, we demonstrate JL5-induced tumor cell death and tumor regression in xenograft mouse models without immune cells and humanized with adoptively transferred human immune cells. In humanized mice, JL5 additionally induces the infiltration of immune cells within the tumor microenvironment. Our studies show that the BMP signaling pathway is targetable in vivo and BMP receptor inhibitors can be developed as a therapeutic to treat cancer patients.
    BMP受体抑制剂通过下调抗凋亡蛋白XIAP、pTAK1和Id1-Id3来诱导癌细胞死亡。然而,目前最有效的BMP受体抑制剂DMH2由于代谢不稳定和药代动力学不佳,不能在体内下调BMP信号。在这里,我们确定了DMH2代谢不稳定的部位,并设计了一种新型的BMP受体抑制剂JL5。我们表明JL5具有更大的分布体积,并抑制肿瘤异种移植中Id1和pTak1的表达。此外,我们证明了JL5诱导的肿瘤细胞死亡和肿瘤消退在异种移植小鼠模型中,没有免疫细胞,并用人源化移植的人免疫细胞。在人源化小鼠中,JL5还诱导免疫细胞在肿瘤微环境中的浸润。我们的研究表明,BMP信号通路在体内是可靶向的,BMP受体抑制剂可以开发为治疗癌症患者的治疗方法。
  • INHIBITORS OF THE BMP SIGNALING PATHWAY
    申请人:Yu Paul B.
    公开号:US20110053930A1
    公开(公告)日:2011-03-03
    The present invention provides small molecule inhibitors of BMP signaling. These compounds may be used to modulate cell growth, differentiation, proliferation, and apoptosis, and thus may be useful for treating diseases or conditions associated with BMP signaling, including inflammation, cardiovascular disease, hematological disease, cancer, and bone disorders, as well as for modulating cellular differentiation and/or proliferation.
    本发明提供了BMP信号通路的小分子抑制剂。这些化合物可以用于调节细胞生长、分化、增殖和凋亡,因此可能有用于治疗与BMP信号通路相关的疾病或病症,包括炎症、心血管疾病、血液疾病、癌症和骨骼疾病,以及调节细胞分化和/或增殖。
  • BMP INHIBITORS AND METHODS OF USE THEREOF
    申请人:THE BRIGHAM AND WOMEN'S HOSPITAL, INC.
    公开号:US20160046633A1
    公开(公告)日:2016-02-18
    The present invention provides small molecule inhibitors of BMP signaling. These compounds may be used to modulate cell growth, differentiation, proliferation, and apoptosis, and thus may be useful for treating diseases or conditions associated with BMP signaling, including inflammation, cardiovascular disease, hematological disease, cancer, and bone disorders, as well as for modulating cellular differentiation and/or proliferation. These compounds may also be used to reduce circulating levels of ApoB-100 or LDL and treat or prevent acquired or congenital hypercholesterolemia or hyperlipoproteinemia; diseases, disorders, or syndromes associated with defects in lipid absorption or metabolism; or diseases, disorders, or syndromes caused by hyperlipidemia.
    本发明提供了BMP信号通路的小分子抑制剂。这些化合物可用于调节细胞生长、分化、增殖和凋亡,因此可用于治疗与BMP信号通路相关的疾病或病症,包括炎症、心血管疾病、血液病、癌症和骨病,以及调节细胞分化和/或增殖。这些化合物还可用于降低ApoB-100或LDL的循环水平,治疗或预防获得性或先天性高胆固醇血症或高脂蛋白血症;与脂质吸收或代谢缺陷相关的疾病、疾病或综合症;或由高脂血症引起的疾病、疾病或综合症。
  • BMP inhibitors and methods of use thereof
    申请人:The Brigham and Women's Hospital, Inc.
    公开号:US10017516B2
    公开(公告)日:2018-07-10
    The present invention provides small molecule inhibitors of BMP signaling. These compounds may be used to modulate cell growth, differentiation, proliferation, and apoptosis, and thus may be useful for treating diseases or conditions associated with BMP signaling, including inflammation, cardiovascular disease, hematological disease, cancer, and bone disorders, as well as for modulating cellular differentiation and/or proliferation. These compounds may also be used to reduce circulating levels of ApoB-100 or LDL and treat or prevent acquired or congenital hypercholesterolemia or hyperlipoproteinemia; diseases, disorders, or syndromes associated with defects in lipid absorption or metabolism; or diseases, disorders, or syndromes caused by hyperlipidemia.
    本发明提供了 BMP 信号转导的小分子抑制剂。这些化合物可用于调节细胞生长、分化、增殖和凋亡,因此可用于治疗与 BMP 信号转导相关的疾病或病症,包括炎症、心血管疾病、血液病、癌症和骨骼疾病,以及调节细胞分化和/或增殖。这些化合物还可用于降低载脂蛋白B-100或低密度脂蛋白的循环水平,治疗或预防获得性或先天性高胆固醇血症或高脂蛋白血症;与脂质吸收或代谢缺陷相关的疾病、失调或综合症;或由高脂血症引起的疾病、失调或综合症。
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