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3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate

中文名称
——
中文别名
——
英文名称
3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate
英文别名
[3-(dimethylamino)phenyl] 5-(3,4-dioxonaphthalen-1-yl)oxypentanoate
3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate化学式
CAS
——
化学式
C23H23NO5
mdl
——
分子量
393.4
InChiKey
VFPXCXKCFZBAEJ-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:
    29
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    72.9
  • 氢给体数:
    0
  • 氢受体数:
    6

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:
    5-[(1,2-Dioxo-1,2-dihydronaphth-4-yl)oxy]valeric Acid3-羟基-N,N-二甲基苯胺N,N'-二环己基碳二亚胺4-二甲氨基吡啶 Sodium sulfate-III乙酸乙酯 、 1H 、 2H 、 4H 作用下, 以 四氢呋喃 为溶剂, 反应 2.0h, 以Column chromatography (10% EtOAc) in benzene gave 13 as a yellow solid (70 mg, 36%), 1H NMR (CDCl3) 8.13, (d, J=7.3 Hz, 1H), 7.90 (d, J=7.4 Hz, 1H), 7.69 (t, J=6.1 Hz, 1H), 7.58 (t, J=7.6 Hz, 1H), 7.22 (dd, J=8.1, 8.1 Hz, 1H), 6.30-6.70 (m, 2H), 5.96 (s, 1H), 4.21 (t, J=5.6 Hz, 2H), 2.69 (t, J=6.5 Hz, 2H), 1.90-2.15 (m, 4H)的产率得到3-Dimethylaminophenyl 5-[(1,2-dihydro-1,2-dioxonaphth-4-yl)oxy]valerate
    参考文献:
    名称:
    Quinones as disease therapies
    摘要:
    本发明提供了新型喹喔醌化合物,以及包含这些新型喹喔醌化合物的组合物。本发明还提供了使用这些新型喹喔醌化合物治疗各种疾病,包括癌症的方法。
    公开号:
    US07253207B2
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文献信息

  • [EN] NOVEL POLYAMINE ANALOG CONJUGATES AND QUINONE CONJUGATES AS THERAPIES FOR CANCERS AND PROSTATE DISEASES<br/>[FR] NOUVEAUX CONJUGUES D'ANALOGUE DE POLYAMINE ET CONJUGUES DE QUINONE, UTILISES POUR LE TRAITEMENT DE CANCERS ET DE MALADIES DE LA PROSTATE
    申请人:SLIL BIOMEDICAL CORP
    公开号:WO2000066175A2
    公开(公告)日:2000-11-09
    Peptide conjugates in which cytocidal and cytostatic agents, such as polyamine analogs or naphthoquinones, are conjugated to a polypeptide recognized and cleaved by enzymes such as prostate-specific antigen (PSA) and cathepsin B are provided, as well as compositions comprising these conjugates. Methods of using these conjugates in the treatment of prostate diseases are also provided.
    提供一种肽共轭物,其中将细胞毒性和细胞增殖抑制剂,如多胺类似物或萘醌类化合物,与多肽共轭,该多肽可以被酶如前列腺特异性抗原(PSA)和半胱氨酸蛋白酶B识别和剪切,以及包含这些共轭物的组合物。还提供了使用这些共轭物治疗前列腺疾病的方法。
  • Novel quinones as disease therapies
    申请人:SLIL Biomedical Corporation
    公开号:US20020183512A1
    公开(公告)日:2002-12-05
    Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided.
    提供了新型喹喔醌,以及包含这些新型喹喔醌的组合物。还提供了使用这些新型喹喔醌治疗包括癌症在内的各种适应症的方法。
  • QUINONES AS DISEASE THERAPIES
    申请人:——
    公开号:US20030013677A1
    公开(公告)日:2003-01-16
    Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided.
    本发明提供了新型的醌类化合物,以及包含这些新型醌类化合物的组合物。本发明还提供了使用这些新型醌类化合物治疗各种疾病,包括癌症的方法。
  • Novel polyamine analog conjugates and quinone conjugates as therapies for cancers and prostate diseases
    申请人:SLIL Biomedical Corporation
    公开号:US20040006049A1
    公开(公告)日:2004-01-08
    Peptide conjugates in which cytocidal and cytostatic agents, such as polyamine analogs or naphthoquinones, are conjugated to a polypeptide recognized and cleaved by enzymes such as prostate-specific antigen (PSA) and cathepsin B are provided, as well as compositions comprising these conjugates. Methods of using these conjugates in the treatment of prostate diseases are also provided.
    本发明提供了肽共轭物,其中将细胞毒性和细胞增殖抑制剂,如多胺类似物或萘醌类化合物,与被酶如前列腺特异性抗原(PSA)和半胱氨酸蛋白酶B识别和切割的多肽共轭。同时提供了包含这些共轭物的组合物。本发明还提供了使用这些共轭物治疗前列腺疾病的方法。
  • Quinones as disease therapies
    申请人:Cellgate, Inc.
    公开号:US07253207B2
    公开(公告)日:2007-08-07
    Novel quinones are provided, as well as compositions comprising these novel quinones. Methods of using the novel quinones in treatment of various indications including cancer are also provided.
    本发明提供了新型喹喔醌化合物,以及包含这些新型喹喔醌化合物的组合物。本发明还提供了使用这些新型喹喔醌化合物治疗各种疾病,包括癌症的方法。
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