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phenyl 4-(nitrooxymethyl)benzoate | 1314877-96-7

中文名称
——
中文别名
——
英文名称
phenyl 4-(nitrooxymethyl)benzoate
英文别名
Phenyl-4-(Nitrooxymethyl)Benzoate
phenyl 4-(nitrooxymethyl)benzoate化学式
CAS
1314877-96-7
化学式
C14H11NO5
mdl
——
分子量
273.245
InChiKey
GNRDQTKRXAIZQS-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):
    3.7
  • 重原子数:
    20
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    81.4
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    phenyl 4-(chloromethyl)benzoatesilver nitrate 作用下, 以 乙腈 为溶剂, 反应 4.0h, 以70.8%的产率得到phenyl 4-(nitrooxymethyl)benzoate
    参考文献:
    名称:
    New microtubule polymerization inhibitors comprising a nitrooxymethylphenyl group
    摘要:
    We have designed cancer antiproliferative compounds, starting from aniline or phenol derivative, which comprise one or two nitrooxymethylphenyl groups as do the hybrid drugs NCX4040 and NCX530. Compound 2a with p-nitrooxymethylbenzoyl-oxy and -amino groups as well as 8a with a p-nitrooxymethylbenzoylamino group showed more promising effects than NCX4040 against human colon and breast cancer cells. Since 2a and 8a, but not NCX4040, arrested human colon carcinoma HCT116 cells in the M phase, the former two compounds may inhibit cell growth differently from NCX4040. Merged images of immunofluorescence-stained a-tubulin and Hoechst-stained nuclei in human fibrosarcoma HT1080 cells showed that 2a and 8a disrupted microtubule formation just as did vincristine, the tubulin polymerization inhibitor. In experiments in vivo, the intraperitoneal administration of 8a at 80 mg/kg/day reduced the growth of HCT116 xenografts in nude mice to T/C 55%. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2011.05.031
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文献信息

  • [EN] COMPOUNDS USEFUL IN THE TREATMENT OF NEOPLASTIC DISEASES<br/>[FR] COMPOSÉS UTILES DANS LE TRAITEMENT DE MALADIES NÉOPLASIQUES
    申请人:UNIVERSITÄT ZU KÖLN
    公开号:WO2015044177A1
    公开(公告)日:2015-04-02
    The present invention refers to compounds of formula: (formula A), wherein R1 is selected from (formula I), (formula II), (formula (III), (formula IV), (formula V), or (formula B), and wherein R2, R3, R4 and R5 are as defined in the claims and X is OTBS, hydroxy, formyloxy, acetoxy, nitrooxy, nitrooxymethyl, or a halogen; and pharmaceutically acceptable salts thereof, which are useful in the treatment of neoplastic or proliferative disorders, a pharmaceutical composition comprising such a compound and a method preparing this compound.
    本发明涉及以下式的化合物:(式A),其中R1从(式I),(式II),(式III),(式IV),(式V)或(式B)中选择,并且其中R2,R3,R4和R5如权利要求中定义的那样,X为OTBS,羟基,甲酰氧基,乙酰氧基,硝基氧基,硝基甲氧基或卤素;及其药学上可接受的盐,用于治疗肿瘤性或增生性疾病,包括这种化合物的药物组合物和制备该化合物的方法。
  • COMPOUNDS USEFUL IN THE TREATMENT OF NEOPLASTIC DISEASES
    申请人:Universität zu Köln
    公开号:EP3049386A1
    公开(公告)日:2016-08-03
  • New microtubule polymerization inhibitors comprising a nitrooxymethylphenyl group
    作者:Yasuyuki Kawaratani、Tomohiko Harada、Yoshiyuki Hirata、Yasuo Nagaoka、Susumu Tanimura、Makio Shibano、Masahiko Taniguchi、Masahide Yasuda、Kimiye Baba、Shinichi Uesato
    DOI:10.1016/j.bmc.2011.05.031
    日期:2011.7
    We have designed cancer antiproliferative compounds, starting from aniline or phenol derivative, which comprise one or two nitrooxymethylphenyl groups as do the hybrid drugs NCX4040 and NCX530. Compound 2a with p-nitrooxymethylbenzoyl-oxy and -amino groups as well as 8a with a p-nitrooxymethylbenzoylamino group showed more promising effects than NCX4040 against human colon and breast cancer cells. Since 2a and 8a, but not NCX4040, arrested human colon carcinoma HCT116 cells in the M phase, the former two compounds may inhibit cell growth differently from NCX4040. Merged images of immunofluorescence-stained a-tubulin and Hoechst-stained nuclei in human fibrosarcoma HT1080 cells showed that 2a and 8a disrupted microtubule formation just as did vincristine, the tubulin polymerization inhibitor. In experiments in vivo, the intraperitoneal administration of 8a at 80 mg/kg/day reduced the growth of HCT116 xenografts in nude mice to T/C 55%. (C) 2011 Elsevier Ltd. All rights reserved.
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