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1-(4-bromophenyl)-4-propylpiperazine | 85469-66-5

中文名称
——
中文别名
——
英文名称
1-(4-bromophenyl)-4-propylpiperazine
英文别名
——
1-(4-bromophenyl)-4-propylpiperazine化学式
CAS
85469-66-5
化学式
C13H19BrN2
mdl
——
分子量
283.211
InChiKey
GTUTVVFSBBNVBB-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):
    3.4
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    6.5
  • 氢给体数:
    0
  • 氢受体数:
    2

文献信息

  • Spiro compounds, medicinal compositions containing the same and intermediates of the compounds
    申请人:Watanabe Nobuhide
    公开号:US20050256308A1
    公开(公告)日:2005-11-17
    A spiro compound represented by the following formula (I) wherein R 1 and R 2 are the same or different and each is a hydrogen atom, a chlorine atom and the like, n is 1, 2 or 3, a bond containing a broken line is a single bond or a double bond, A is —X—(CH 2 ) q —N(R 3 )(R 4 ); a group represented by the following formula (a) and the like, wherein X is an oxygen atom or a sulfur atom, q is 2 or 3, R 3 and R 4 are the same or different and each is a C 1-6 alkyl group and the like, or R 3 and R 4 optionally form, together with the adjacent nitrogen atom, a piperidine ring and the like optionally substituted by one or two C 1-6 alkyl and the like, R 5 is a C 1-6 alkyl group and the like, R 6 is a hydrogen atom and the like, and r and t are each independently one or two, or a pharmaceutically acceptable acid addition salt thereof. The compound is useful as a selective estrogen receptor modulator having a climacteric syndrome-ameliorating effect, and can be expected to be a drug for the prophylaxis and/or treatment of osteoporosis, climacteric syndrome and breast cancer.
    以下式子(I)所表示的螺环化合物,其中R1和R2相同或不同,分别为氢原子,原子等,n为1、2或3,含有断线的键为单键或双键,A为—X—(CH2)q—N(R3)(R4);一种由以下式子(a)表示的基团等,其中X为氧原子或原子,q为2或3,R3和R4相同或不同,分别为C1-6烷基等,或R3和R4可以与相邻的氮原子共同形成哌嗪环等,可选地被1或2个C1-6烷基等取代,R5为C1-6烷基等,R6为氢原子等,r和t各自独立地为1或2,或其药学上可接受的酸盐。该化合物可作为具有缓解更年期综合症作用的选择性雌激素受体调节剂,并可望成为预防和/或治疗骨质疏松症、更年期综合症和乳腺癌的药物。
  • 3-(Pyrazolyl)-1H-Pyrrolo[2,3-b]Pyridine Derivatives as Kinase Inhibitors
    申请人:Aurigene Discovery Technologies Limited
    公开号:US20150336949A1
    公开(公告)日:2015-11-26
    The present application relates to novel 3-(pyrazolyl)-1H-pyrrolo[2,3-b]pyridine derivatives of formula (I), as protein kinase inhibitors. The invention particularly relates to compounds of formula (I), preparation of compounds and pharmaceutical compositions thereof. The invention further relates to pharmaceutically acceptable salts and compositions comprising the said novel 3-(pyrazolyl)-1H-pyrrolo[2,3-b]pyridine derivatives and their use in the treatment of various disorders.
    本申请涉及一种新型的3-(吡唑基)-1H-吡咯[2,3-b]吡啶衍生物,其为蛋白激酶抑制剂。本发明特别涉及化合物(I)的制备、化合物的制备和制药组合物。本发明还涉及药学上可接受的盐和组成物,包括所述新型3-(吡唑基)-1H-吡咯[2,3-b]吡啶衍生物及其在治疗各种疾病中的用途。
  • SPIRO COMPOUNDS, MEDICINAL COMPOSITIONS CONTAINING THE SAME AND INTERMEDIATES OF THE COMPOUNDS
    申请人:Dainippon Pharmaceutical Co., Ltd.
    公开号:EP1559707A1
    公开(公告)日:2005-08-03
    A spiro compound represented by the following formula (I) wherein R1 and R2 are the same or different and each is a hydrogen atom, a chlorine atom and the like, n is 1, 2 or 3, a bond containing a broken line is a single bond or a double bond, A is -X-(CH2)q-N(R3)(R4); a group represented by the following formula (a) and the like, wherein X is an oxygen atom or a sulfur atom, q is 2 or 3, R3 and R4 are the same or different and each is a C1-6 alkyl group and the like, or R3 and R4 optionally form, together with the adjacent nitrogen atom, a piperidine ring and the like optionally substituted by one or two C1-6 alkyl and the like, R5 is a C1-6 alkyl group and the like, R6 is a hydrogen atom and the like, and r and t are each independently one or two, or a pharmaceutically acceptable acid addition salt thereof. The compound is useful as a selective estrogen receptor modulator having a climacteric syndrome-ameliorating effect, and can be expected to be a drug for the prophylaxis and/or treatment of osteoporosis, climacteric syndrome and breast cancer.
    下式(I)代表的螺环化合物 其中 R1 和 R2 相同或不同,各自为氢原子、原子等,n 为 1、2 或 3,含有断线的键为单键或双键,A 为 -X-(CH2)q-N(R3)(R4);下式(a)代表的基团 及类似物,其中 X 是氧原子或原子,q 是 2 或 3,R3 和 R4 相同或不同且各自是 C1-6 烷基及类似物,或 R3 和 R4 与相邻的氮原子一起可选地形成可选地被一个或两个 C1-6 烷基及类似物取代的哌啶环及类似物,R5 是 C1-6 烷基及类似物,R6 是氢原子及类似物,r 和 t 独立地各自是一个或两个,或其药学上可接受的酸加成盐。该化合物可用作选择性雌激素受体调节剂,具有改善更年期综合征的作用,可望成为预防和/或治疗骨质疏松症、更年期综合征和乳腺癌的药物。
  • High dielectric anisotropy liquid crystal compound and composition containing the same
    申请人:Cheng Kung-Lung
    公开号:US20080135803A1
    公开(公告)日:2008-06-12
    The invention relates to a high dielectric anisotropy liquid crystal compound which is a pyridyl derivative with substituents of electrons push-pull effect. Furthermore, the high dielectric anisotropy liquid crystal compounds are colorless and have high thermal and photo stability as well as high compatibility in a liquid crystal host. A liquid crystal composition containing the high dielectric anisotropy liquid crystal compound can reduce threshold voltage of cholesteric reflective displays, thus saving power and extending lifetime of driver ICs.
  • US7622056B2
    申请人:——
    公开号:US7622056B2
    公开(公告)日:2009-11-24
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