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(S)-4-phenyl-2-(1-phenylpropyl)isothiazolo[5,4-c]quinolin-1(2H)-one

中文名称
——
中文别名
——
英文名称
(S)-4-phenyl-2-(1-phenylpropyl)isothiazolo[5,4-c]quinolin-1(2H)-one
英文别名
(s)-4-Phenyl-2-(1-phenylpropyl)isothiazolo[5,4-c]quinolin-1(2h)-one;4-phenyl-2-[(1S)-1-phenylpropyl]-[1,2]thiazolo[5,4-c]quinolin-1-one
(S)-4-phenyl-2-(1-phenylpropyl)isothiazolo[5,4-c]quinolin-1(2H)-one化学式
CAS
——
化学式
C25H20N2OS
mdl
——
分子量
396.513
InChiKey
ASRHFTGREBNMLA-NRFANRHFSA-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):
    5.8
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    58.5
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    (S)-(-)-1-苯丙胺茴香硫醚 、 pig serum 、 L-半胱氨酸盐酸盐无水物N,N-二异丙基乙胺三氟乙酸 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下, 以 甲醇 、 aq. phosphate buffer 、 二甲基亚砜N,N-二甲基甲酰胺乙腈 为溶剂, 反应 102.5h, 生成 (S)-4-phenyl-2-(1-phenylpropyl)isothiazolo[5,4-c]quinolin-1(2H)-one
    参考文献:
    名称:
    Development of novel NK3 receptor antagonists with reduced environmental impact
    摘要:
    The neurokinin B (NKB)-neurokinin-3 receptor (NK3R) signaling positively regulates the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus. The NK3R-selective antagonists may suppress the reproductive functions of mammals. For development of novel NK3R antagonists with reduced environmental toxicity, a structure-activity relationship study of an NK3R antagonist, talnetant, was carried out. Among several talnetant derivatives with labile functional groups in the natural environment, 3-mercaptoquinoline 2f exhibited a comparable biological activity to that of the parent talnetant. Additionally, compound 2f was converted into the disulfide 3f or isothiazolone 8 by air-oxidation, both of which showed no binding affinity to NK3R. (C) 2016 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2016.05.054
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文献信息

  • 新規な化合物、薬剤およびNK3受容体拮抗剤
    申请人:国立大学法人京都大学
    公开号:JP2017081888A
    公开(公告)日:2017-05-18
    【課題】生態系へ悪影響を及ぼさずに動物の繁殖抑制をするNK3受容体拮抗体の提供。【解決手段】式(I’)で表される化合物。(R1はH、水酸基等;R2は水酸基、メルカプト基等;R3はフェニル基又はナフチル基)【選択図】なし
    提供不影响生态系统的NK3受体拮抗体,抑制动物繁殖。化合物由式(I')表示。(R1为H、羟基等;R2为羟基、巯基等;R3为苯基或萘基)。【选择图】无
  • Development of novel NK3 receptor antagonists with reduced environmental impact
    作者:Koki Yamamoto、Shiho Okazaki、Hiroaki Ohno、Fuko Matsuda、Satoshi Ohkura、Kei-ichiro Maeda、Nobutaka Fujii、Shinya Oishi
    DOI:10.1016/j.bmc.2016.05.054
    日期:2016.8
    The neurokinin B (NKB)-neurokinin-3 receptor (NK3R) signaling positively regulates the release of gonadotropin-releasing hormone (GnRH) from the hypothalamus. The NK3R-selective antagonists may suppress the reproductive functions of mammals. For development of novel NK3R antagonists with reduced environmental toxicity, a structure-activity relationship study of an NK3R antagonist, talnetant, was carried out. Among several talnetant derivatives with labile functional groups in the natural environment, 3-mercaptoquinoline 2f exhibited a comparable biological activity to that of the parent talnetant. Additionally, compound 2f was converted into the disulfide 3f or isothiazolone 8 by air-oxidation, both of which showed no binding affinity to NK3R. (C) 2016 Elsevier Ltd. All rights reserved.
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