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Spiro[3,4-dihydrobenzo[h]chromene-2,1'-cyclohexane]-5,6-dione | 90149-99-8

中文名称
——
中文别名
——
英文名称
Spiro[3,4-dihydrobenzo[h]chromene-2,1'-cyclohexane]-5,6-dione
英文别名
——
Spiro[3,4-dihydrobenzo[h]chromene-2,1'-cyclohexane]-5,6-dione化学式
CAS
90149-99-8
化学式
C18H18O3
mdl
——
分子量
282.339
InChiKey
PWXKORUKODHKFT-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):
    3.2
  • 重原子数:
    21
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    (2-溴乙亚基)环己烷氢氧化钾硫酸 、 potassium iodide 作用下, 反应 16.25h, 生成 Spiro[3,4-dihydrobenzo[h]chromene-2,1'-cyclohexane]-5,6-dione
    参考文献:
    名称:
    .beta.-Lapachone: synthesis of derivatives and activities in tumor models
    摘要:
    In order to find a 3,4-dihydro-2H-naphtho[1,2-b]pyran-5,6-dione more potent than the naturally occurring 2,2-dimethyl derivative [beta-lapachone (10a)], we synthesized a series of analogous compounds with modifications at position 2 of the pyran ring or at positions 8 and 9 of the benzene ring. Of the compounds tested in vitro for inhibition of RNA-dependent DNA polymerase and in mice infected with Rauscher leukemia, all retained good enzyme activity. Inhibition of the reverse transcriptase activity of the 2,2-substituted derivatives 10b-e was as strong as 10a. However, only the 2-methyl-2-phenyl derivative 10e proved to be about as potent as the 2,2-dimethyl reference compound 10a in prolonging the mean survival time of mice with Rauscher leukemia virus induced leukemia.
    DOI:
    10.1021/jm00374a010
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文献信息

  • PHARMACEUTICAL COMPOSITION FOR THE TREATMENT AND PREVENTION OF DISEASES INVOLVING IMPOTENCE
    申请人:Kwak Taehwan
    公开号:US20100239674A1
    公开(公告)日:2010-09-23
    Disclosed is a pharmaceutical composition for the treatment and/or prevention of erectile dysfunction, comprising (a) a therapeutically effective amount of a compound represented by Formula 1 or 2, and (b) a pharmaceutically acceptable carrier, a diluent or an excipient, or any combination thereof.
    本发明公开了一种用于治疗和/或预防勃起功能障碍的药物组合物,包括(a)按照式1或式2表示的化合物的治疗有效量,以及(b)药学上可接受的载体、稀释剂或赋形剂,或其任意组合。
  • Pharmaceutical Composition for the Treatment or Prevention of Diseases Involving Obesity, Diabetes, Metabolic Syndrome, Neuro-Degenerative Diseases and Mitochondria Dyfunction Diseases
    申请人:Yoo Sang-Ku
    公开号:US20080146655A1
    公开(公告)日:2008-06-19
    Provided is a pharmaceutical composition for the treatment and prevention of obesity, diabetes, metabolic syndromes, degenerative diseases and mitochondrial dysfunction-related diseases, comprising: a therapeutically effective amount of a compound represented by Formula I below, or a pharmaceutically acceptable salt, prodrug, solvate or isomer thereof, and a pharmaceutically acceptable carrier, a diluent or an excipient, or any combination thereof.
    提供一种药物组合物,用于治疗和预防肥胖、糖尿病、代谢综合征、退行性疾病和线粒体功能障碍相关疾病,包括:以下式I所表示的化合物的治疗有效量,或其药学上可接受的盐、前药、溶剂或异构体,以及药学上可接受的载体、稀释剂或赋形剂,或其任意组合。
  • PHARMACEUTICAL COMPOSITION FOR THE TREATMENT OR PREVENTION OF DISEASES INVOLVING OBESITY, DIABETES, METABOLIC SYNDROME, NEURO-DEGENERATIVE DISEASES AND MITOCHONDRIA DYSFUNCTION DISEASES
    申请人:Yoo Sang-Ku
    公开号:US20090292011A1
    公开(公告)日:2009-11-26
    Provided is a pharmaceutical composition for the treatment and prevention of obesity, diabetes, metabolic syndromes, degenerative diseases and mitochondrial dysfunction-related diseases, comprising: a therapeutically effective amount of a compound represented by Formula I below, or a pharmaceutically acceptable salt, prodrug, solvate or isomer thereof, and a pharmaceutically acceptable carrier, a diluent or an excipient, or any combination thereof.
    提供了一种用于治疗和预防肥胖、糖尿病、代谢综合征、退行性疾病以及线粒体功能障碍相关疾病的制药组合物,包含以下公式I所表示的化合物的治疗有效量,或其药学上可接受的盐、前药、溶剂或异构体,以及药学上可接受的载体、稀释剂或赋形剂,或任何组合。
  • PHARMACEUTICAL COMPOSITION FOR TREATMENT AND PREVENTION OF RESTENOSIS
    申请人:Kwak Taehwan
    公开号:US20100255054A1
    公开(公告)日:2010-10-07
    Provided is a pharmaceutical composition for the treatment and/or prevention of restenosis including (a) a therapeutically effective amount of a particular compound represented by Formula 1 and 2, or a pharmaceutically acceptable salt, prodrug, solvate or isomer thereof, and (b) a pharmaceutically acceptable carrier, a diluent or an excipient, or any combination thereof.
    提供了一种药物组合物,用于治疗和/或预防再狭窄,包括(a) 一定量的化合物,其化学式为1和2,或其药学上可接受的盐、前药、溶剂或异构体,且具有治疗效果,以及(b) 药学上可接受的载体、稀释剂或赋形剂,或任何其组合。
  • METHOD FOR THE TREATMENT AND PREVENTION OF ERECTILE DYSFUNCTION
    申请人:KWAK Taehwan
    公开号:US20120114714A1
    公开(公告)日:2012-05-10
    Disclosed is a pharmaceutical composition for the treatment and/or prevention of erectile dysfunction, comprising (a) a therapeutically effective amount of a compound represented by Formula 1 or 2, and (b) a pharmaceutically acceptable carrier, a diluent or an excipient, or any combination thereof.
    本发明公开了一种治疗和/或预防勃起功能障碍的药物组合物,包括(a)公式1或2所代表的化合物的治疗有效量,以及(b)药学上可接受的载体、稀释剂或赋形剂或其组合。
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