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

1-(4-(heptyloxy)phenyl)-3-(piperidin-1-yl)propan-1-one | 95000-40-1

中文名称
——
中文别名
——
英文名称
1-(4-(heptyloxy)phenyl)-3-(piperidin-1-yl)propan-1-one
英文别名
3-Piperidino-1-(4-heptyloxyphenyl)-propan-1-on;1-(4-Heptoxyphenyl)-3-piperidin-1-ylpropan-1-one
1-(4-(heptyloxy)phenyl)-3-(piperidin-1-yl)propan-1-one化学式
CAS
95000-40-1
化学式
C21H33NO2
mdl
——
分子量
331.499
InChiKey
MGBSEAVFZLXRPF-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):
    5.3
  • 重原子数:
    24
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    3

文献信息

  • [EN] 1-PHENYLPROPANONE COMPOUNDS AND USE THEREOF<br/>[FR] COMPOSÉS DE 1-PHÉNYLPROPANONE ET LEUR UTILISATION
    申请人:UNIV DEGLI STUDI PADOVA
    公开号:WO2018060947A1
    公开(公告)日:2018-04-05
    The present invention relates to a 1-phenylpropanone compound of formula (I), wherein X is CH2 or an atom selected from the group consisting of O, S and Se, n is an integer from 4 to 6, A is a substituent selected from the group consisting of 4-morpholyl, 1-piperidinyl, 4-methyl-1-piperazinyl, A being optionally substituted with a (C1-C3)alkyl or (C1-C3)acyl substituent, with the proviso that when X is CH2, n is equal to 5, for use as an antitumoral agent in the treatment of breast cancer, chronic lymphatic leukemia or neuroblastoma. The invention also concerns new 1-phenylpropanone compounds, and compounds as antitumoral agents.
    本发明涉及一种化合物,其化学式为(I),其中X为CH2或从O、S和Se组成的原子中选择的一个,n为4到6之间的整数,A为从4-吗啡基、1-哌啶基、4-甲基-1-哌嗪基中选择的取代基,A可以选择地与(C1-C3)烷基或(C1-C3)酰基取代,但当X为 时,n等于5,用作抗肿瘤剂治疗乳腺癌、慢性淋巴细胞白血病或神经母细胞瘤。该发明还涉及新的1-苯基丙酮化合物,以及作为抗肿瘤剂的化合物。
  • Anesthetic oral compositions
    申请人:Richardson-Vicks, Inc.
    公开号:EP0383481A2
    公开(公告)日:1990-08-22
    Disclosed are oral anesthetic pharmaceutical compositions compris­ing: (a) from about 0.02% to about 25% of a pharmaceutically accept­able acid salt of a β-aminopropiophenone, such as dyclonine HCl; (b) from about 0.02% to about 20% of saccharin; and (c) from about 1% to about 99% of a pharmaceutically acceptable oral carrier. Also provided are methods for providing an anesthetic effect in humans or animals which comprises orally administering to said human or animal a safe and effective amount of these pharmaceutical compositions. Also provided is a novel process for the manufacture of anesthetic lozenges contain­ing a β-aminopropiophenone along with saccharin.
    所公开的口服麻醉药物组合物包含:(a) 约 0.02% 至约 25% 的药学上可接受的 β-苯丙酮酸盐,如盐酸诺宁;(b) 约 0.02% 至约 20% 的糖精;以及 (c) 约 1% 至约 99% 的药学上可接受的口服载体。还提供了为人类或动物提供麻醉效果的方法,其中包括向所述人类或动物口服安全有效量的这些药物组合物。还提供了一种制造含有β-苯丙酮糖精的麻醉锭剂的新工艺。
  • 1-phenylpropanone compounds and use thereof
    申请人:UNIVERSITA' DEGLI STUDI DI PADOVA
    公开号:US11345673B2
    公开(公告)日:2022-05-31
    The present invention relates to a 1-phenylpropanone compound of formula (I), wherein X is CH2 or an atom selected from the group consisting of O, S and Se, n is an integer from 4 to 6, A is a substituent selected from the group consisting of 4-morpholyl, 1-piperidinyl, 4-methyl-1-piperazinyl, A being optionally substituted with a (C1-C3)alkyl or (C1-C3)acyl substituent, with the proviso that when X is CH2, n is equal to 5, for use as an antitumoral agent in the treatment of breast cancer, chronic lymphatic leukemia or neuroblastoma. The invention also concerns new 1-phenylpropanone compounds, and compounds as antitumoral agents.
    本发明涉及式(I)的 1-苯基丙酮化合物,其中 X 是 CH2 或选自 O、S 和 Se 组成的组的原子,n 是 4 至 6 的整数,A 是选自 4-吗啉基、1-哌啶基、4-甲基-1-哌嗪基组成的组的取代基、4-甲基-1-哌嗪基,A任选被(C1-C3)烷基或(C1-C3)酰基取代,但当X为 时,n等于5,用作治疗乳腺癌、慢性淋巴性白血病或神经母细胞瘤的抗肿瘤剂。本发明还涉及新的 1-苯基丙酮化合物和作为抗肿瘤剂的化合物。
  • 1-PHENYLPROPANONE COMPOUNDS AND USE THEREOF
    申请人:Universita' Degli Studi Di Padova
    公开号:EP3518927B1
    公开(公告)日:2020-08-12
  • US4139627A
    申请人:——
    公开号:US4139627A
    公开(公告)日:1979-02-13
查看更多