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1,4-bis(3,4-diethoxyphenyl)-2,3-dimethylbutane | 119189-25-2

中文名称
——
中文别名
——
英文名称
1,4-bis(3,4-diethoxyphenyl)-2,3-dimethylbutane
英文别名
meso-1,4-bis-(3,4-diethoxy-phenyl)-2,3-dimethyl-butane;2.3-Dimethyl-1.4-bis-(3.4-diaethoxy-phenyl)-butan;meso-1,4-Bis-(3,4-diaethoxy-phenyl)-2,3-dimethyl-butan;1,1'-(2,3-Dimethylbutane-1,4-diyl)bis(3,4-diethoxybenzene);4-[4-(3,4-diethoxyphenyl)-2,3-dimethylbutyl]-1,2-diethoxybenzene
1,4-bis(3,4-diethoxyphenyl)-2,3-dimethylbutane化学式
CAS
119189-25-2
化学式
C26H38O4
mdl
——
分子量
414.585
InChiKey
LLALADYYCUXSAH-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):
    7.1
  • 重原子数:
    30
  • 可旋转键数:
    13
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    硫酸二乙酯 、 alkaline earth salt of/the/ methylsulfuric acid 在 alkaline solution 作用下, 生成 1,4-bis(3,4-diethoxyphenyl)-2,3-dimethylbutane
    参考文献:
    名称:
    Waller; Gisvold, Journal of the American Pharmaceutical Association (1912), 1945, vol. 34, p. 78,79
    摘要:
    DOI:
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文献信息

  • Pharmaceutical compositions comprising catecholic butanes
    申请人:BLOCK DRUG COMPANY, INC.
    公开号:EP0297733A2
    公开(公告)日:1989-01-04
    The invention relates to pharmaceutical compositions useful in the treatment of benign, premalignant and malignant solid tumours, especially those of the skin, and in the treatment of other disorders of the skin e.g. psoriasis and acne. The compositions comprise at least one catecholic butane. The preferred catecholic butane is nordihydroguaiaretic acid. The compositions are preferably applied topically or by intratumor or subcutaneous injection. The invention also includes sunscreening agents comprising at least one catecholic butane.
    本发明涉及可用于治疗良性、恶性前和恶性实体瘤(尤其是皮肤肿瘤)以及其他皮肤疾病(如牛皮癣和痤疮)的药物组合物。组合物包含至少一种儿茶酚丁烷。首选的儿茶酚丁烷是去氢愈创木酚酸。组合物最好局部使用或通过瘤内注射或皮下注射。本发明还包括包含至少一种儿茶酚丁烷的防晒剂。
  • COMPOSITIONS OF CATECHOLIC BUTANES WITH ZINC
    申请人:CHEMEX PHARMACEUTICALS, INC.
    公开号:EP0288534A1
    公开(公告)日:1988-11-02
  • EP0288534A4
    申请人:——
    公开号:EP0288534A4
    公开(公告)日:1989-02-23
  • USE OF CATECHOLIC BUTANE DERIVATIVES IN CANCER THERAPY
    申请人:Triact Therapeutics, Inc.
    公开号:EP2349235A1
    公开(公告)日:2011-08-03
  • Cancer Therapy
    申请人:White Thomas F.
    公开号:US20100256232A1
    公开(公告)日:2010-10-07
    The present application relates to compositions and methods for treating a proliferative disorder by administering to a subject a pharmaceutical composition of a dual kinase inhibitor. Catecholic butanes cane serve as dual kinase inhibitors for purposes of methods described herein. Subjects can be further treated by co-administering an EGFR inhibitor. The present application also relates to analyzing a sample with respect to levels of IGF-1R and EGFR and comparing levels of IGF-1R and EGFR to a control. Patients can be selected for treatment with a catecholic butane based on the assessment; optionally, patients can be further treated with an EGFR inhibitor, an IGF-1R inhibitor, or both.
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同类化合物

苯基(2,4,5-三苯基-2-环戊烯-1-基)甲酮 肠二醇 珠子草素 开环异落叶松树脂酚 安五脂素 外消旋肠二醇-13C3 去甲二氢愈创木酸 半去甲二氢愈创木酸 二甲基2,5-二苯基-3,4-二氢-2H-吡咯-3,4-二羧酸酯 二氢荜澄茄脂素 9,9'-二-O-(E)-阿魏酰开环异落叶松脂素 4-[4-(4-羟基-3-甲氧基苯基)-2,3-二甲基丁基]-2-甲氧基苯酚 2,6-二甲氧基-4-羟基苯甲醛 2,6-二甲氧基-4-[(2R,3R)-4-甲氧基-3-[(7-甲氧基-1,3-苯并二噁唑-5-基)甲基]-2-(甲氧基甲基)丁基]苯酚 2,3-双[(4-羟基-3-甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁烷-1,4-二醇 2,3-双[(3,4-二甲氧基苯基)甲基]丁二酸 2,3-双(4-羟基-3-甲氧基苄基)琥珀酸二甲酯 2,3-双(3,4-二甲氧基苄基)-4-甲氧基-4-氧代丁酸 2,3-二苄基丁烷-1,4-二醇 2,3-二甲基-1,4-二苯基丁烷-2,3-二醇 2,3-二甲基-1,4-二苯基丁烷-1,4-二酮 2,3-二异丙基-1,2-二苯基-1,4-丁二酮 2,3-二[(3-羟基苯基)甲基]丁烷-1,4-二醇 2,2,3,3-四甲基-1,4-二苯基丁烷-1,4-二酮 1,4-丁烷二酮 1,2,3,4-四苯基环戊烷 1,2,3,4-四苯基丁烷 1,2,3,4-四苯基-1,4-丁烷二酮 1,2,3,4-四-(4-甲氧基-苯基)-丁烷-1,4-二酮 1,1'-[(2S,3S)-2,3-双(甲氧基甲基)-1,4-丁二基]双[3,4-二甲氧基苯] 1,1'-(2,3-二甲基-1,4-丁烷二基)二(3,4-二甲氧基苯) 1,1',2,2',3,3'-六苯基-1,1'-联(2-环丙烯) (3,3,4,4-四甲基-2-苯基环丁烯-1-基)苯 (2R,3S)-1,4-二(4-羟基-3-甲氧基苯基)-2,3-二甲基丁烷-1-酮 (-)-二氢愈创木脂酸 (+)-开环异落叶松树脂酚 1,4-difluoro-1,2,34,-tetrahydrophenylbutane (1R*,2R*,3R*,4S*)-2,3-bis(hydroxymethyl)-1-(3,4-dimethoxyphenyl)-4-<3,4-(methylenedioxy)phenyl>butane-1,4-diol 2,5-diphenyl-3,4-dimethylhexa-1,5-diene meso-1,4-bis-(3,4-dihydroxyphenyl)-2,3-dimethylbutane bis-cyclic carbonate (2R,3R)-2-(4'-hydroxy-3'-methoxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide (2R,3R)-2-(3',4'-dihydroxybenzyl)-3-(3'',4''-dimethoxybenzyl)-4-hydroxy-N-benzylbutyramide 2,5-di(3-nitrophenyl)-3,3,4,4-tetracyanopyrrolidine 4,5-dihydroxy-2,4,5-triphenyl-3-(2-pyridyl)-1-pyrroline (+/-)-(1R,2S,3R,4R)-2,3-bis(hydroxymethyl)-1,4-bisphenyl-2-hydroxybutane-1,4-diol α,β-dimethyl-γ-phenylbutyrophenone meso-2,3-bis(3,4-dihydroxybenzyl)succinic acid (±)-1-(4-hydroxy-3-methoxyphenyl)-(2R,3S)-dimethyl-4-[3-methoxy-4-(picolinoyloxy)phenyl]butane meso-1,4-bis[3-methoxy-4-(picolinoyloxy)phenyl]-(2R,3S)-dimethylbutane