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5-methyl-6-(3-pyridylmethyl)-7,8-dihydro-1-naphthalenol

中文名称
——
中文别名
——
英文名称
5-methyl-6-(3-pyridylmethyl)-7,8-dihydro-1-naphthalenol
英文别名
5-methyl-6-(pyridin-3-ylmethyl)-7,8-dihydro-1-naphthalenol;5-Methyl-6-(pyridin-3-ylmethyl)-7,8-dihydronaphthalen-1-ol
5-methyl-6-(3-pyridylmethyl)-7,8-dihydro-1-naphthalenol化学式
CAS
——
化学式
C17H17NO
mdl
——
分子量
251.328
InChiKey
HMOMGGOLRZJBEG-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
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    33.1
  • 氢给体数:
    1
  • 氢受体数:
    2

文献信息

  • Novel dihydronaphthalene compounds and processes of producing the same
    申请人:——
    公开号:US20020032211A1
    公开(公告)日:2002-03-14
    Dihydronaphthalene compounds have excellent 17&agr;-hydroxylase/C 17-20 -lyase inhibiting activity, thromboxan A 2 synthesis inhibiting activity, and aromatase inhibiting activity and are thereby are useful as preventive and/or therapeutic agents for various male sex hormone- and female sex hormone-dependent diseases such as prostate cancer, prostatomegaly, masculinization, breast cancer, mastopathy, uterine cancer, endometriosis, and ovarian cancer, as well as myocardial infarction, angina pectoris, and bronchial asthma.
    二氢萘化合物具有优秀的17α-羟化酶/C17-20-裂解酶抑制活性,血栓素A2合成抑制活性和芳香化酶抑制活性,因此可用作预防和/或治疗各种男性激素和女性激素依赖性疾病的药物,如前列腺癌、前列腺增生、阳痿、乳腺癌、乳腺增生、子宫癌、子宫内膜异位症和卵巢癌,以及心肌梗死、心绞痛和支气管哮喘。
  • NOVEL DIHYDRONAPHTHALENE COMPOUNDS AND PROCESS FOR PRODUCING THE SAME
    申请人:Yukijirushi Nyugyo Kabushiki Kaisha
    公开号:EP1028110A1
    公开(公告)日:2000-08-16
    Dihydronaphthalene compounds have excellent 17α-hydroxylase/C17-20-lyase inhibiting activity, thromboxan A2 synthesis inhibiting activity, and aromatase inhibiting activity and are thereby are useful as preventive and/or therapeutic agents for various male sex hormone- and female sex hormone-dependent diseases such as prostate cancer, prostatomegaly, masculinization, breast cancer, mastopathy, uterine cancer, endometriosis, and ovarian cancer, as well as myocardial infarction, angina pectoris, and bronchial asthma.
    二氢萘化合物具有优异的 17α- 羟化酶/C17-20-赖氨酸酶抑制活性、血栓素 A2 合成抑制活性和芳香化酶抑制活性,因此可用作各种男性性激素和女性性激素依赖性疾病(如前列腺癌)的预防和/或治疗药物、前列腺肥大、男性化、乳腺癌、乳腺增生症、子宫癌、子宫内膜异位症和卵巢癌,以及心肌梗塞、心绞痛和支气管哮喘。
  • US6559157B2
    申请人:——
    公开号:US6559157B2
    公开(公告)日:2003-05-06
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