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2-methyl-3-ethyl-1,4-dihydroxynaphthalene | 38262-45-2

中文名称
——
中文别名
——
英文名称
2-methyl-3-ethyl-1,4-dihydroxynaphthalene
英文别名
2-Ethyl-3-methylnaphthalene-1,4-diol
2-methyl-3-ethyl-1,4-dihydroxynaphthalene化学式
CAS
38262-45-2
化学式
C13H14O2
mdl
——
分子量
202.253
InChiKey
IZKJOVONCILCNY-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):
    3.6
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.23
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-methyl-3-ethyl-1,4-dihydroxynaphthalene乙酸酐 生成 1,4-diacetoxy-2-ethyl-3-methyl-naphthalene
    参考文献:
    名称:
    ALBEROLA, A.;GONZALEZ, NOGAL, A. M.;MARTINEZ, DE, ILARDUYA, J. A, AN. QUIM. PUBL. REAL SOC. ESP. FIS. Y QUIM., 1980, 76, N 2, 123-126
    摘要:
    DOI:
  • 作为产物:
    描述:
    甲萘醌三乙基铝 以17%的产率得到
    参考文献:
    名称:
    ALBEROLA, A.;GONZALEZ, NOGAL, A. M.;MARTINEZ, DE, ILARDUYA, J. A, AN. QUIM. PUBL. REAL SOC. ESP. FIS. Y QUIM., 1980, 76, N 2, 123-126
    摘要:
    DOI:
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文献信息

  • Naphtalene anti-psoriatic agents
    申请人:SYNTEX (U.S.A.) INC.
    公开号:EP0282006A1
    公开(公告)日:1988-09-14
    Psoriasis in mammals is relieved by administering naphthalenes of the formula: wherein:     R¹ is lower alkoxy or optionally substituted phenoxy;     R² is hydrogen, lower alkyl, lower alkoxy, optionally substituted phenyl, optionally substituted phenoxy or optionally substituted phenylalkyl;     R³ is hydrogen, lower alkyl, lower alkoxy, halo, optionally substituted phenyl, optionally substituted phenyl-lower-alkyl or optionally substituted phenyl-lower-­alkoxy, and m is 1 or 2;     X and Y may be different or are the same, and if different are either R⁴ or -C(O)W, and if the same are both -C(O)W, wherein     R⁴ is lower alkyl or optionally substituted phenyl-lower-alkyl;     W is -OR⁵ or -NR⁶R⁷,     wherein R⁵ is alkyl, optionally substituted phenyl or optionally substituted benzyl; and R⁶ and R⁷ are independently hydrogen, lower alkyl, cycloalkyl or optionally substituted phenyl.
    哺乳动物的牛皮癣可通过服用式中的萘来缓解: 其中 R¹ 是低级烷氧基或任选取代的苯氧基; R² 是氢、低级烷基、低级烷氧基、任选取代的苯基、任选取代的苯氧基或任选取代的苯基烷基; R³ 是氢、低级烷基、低级烷氧基、卤代、任选取代的苯基、任选取代的苯基-低级烷基或任选取代的苯基-低级烷氧基,且 m 是 1 或 2; X 和 Y 可以不同或相同,如果不同,则为 R⁴ 或 -C(O)W,如果相同,则均为 -C(O)W、 其中 R⁴ 是低级烷基或任选取代的苯基-低级烷基; W 是-OR⁵或-NR⁶R⁷、 其中 R⁵ 是烷基、任选取代的苯基或任选取代的苄基;以及 R⁶ 和 R⁷ 独立地为氢、低级烷基、环烷基或任选取代的苯基。
  • Menaquinol compositions and methods of treatment
    申请人:Epizon Pharma, Inc.
    公开号:US10822295B2
    公开(公告)日:2020-11-03
    The present application discloses methods for the efficient preparation of high purity compounds of the Formula I, and their methods of use. Also disclosed herein are pharmaceutical compositions comprising a therapeutically effective amount of a menaquinol compound as disclosed above, or a mixture thereof, and a pharmaceutically acceptable excipient, wherein the composition is effective for the treatment of a condition associated with vitamin K selected from for the treatment of osteoporosis and arteriosclerosis.
    本申请公开了高效制备高纯度式 I 化合物的方法及其使用方法。 本文还公开了药物组合物,该组合物包含治疗有效量的如上所述的孟喹醇化合物或其混合物,以及药学上可接受的赋形剂,其中该组合物对治疗与维生素 K 有关的病症有效,这些病症选自骨质疏松症和动脉硬化。
  • Methods and compositions for preventing or treating tissue calcification
    申请人:Epizon Pharma, Inc.
    公开号:US10874623B2
    公开(公告)日:2020-12-29
    The invention provides methods and compositions for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) tissue calcification in a subject in need thereof and, more particularly, the invention relates to methods of using menaquinone-7 (MK-7) and/or menaquinol-7 (MKH2-7) for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) tissue calcification in a subject with diabetes, chronic kidney disease, end stage renal failure, or a subject undergoing hemodialysis and/or receiving anticoagulant therapy. The invention further provides methods and compositions for reducing one or more symptoms of chronic obstructive pulmonary disorder (COPD), including using menaquinone-7 (MK-7) and/or menaquinol-7 (MKH2-7), for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) one or more symptoms of COPD.
    本发明提供了预防或治疗(例如,减缓进展、阻止和/或逆转)有需要的受试者的组织钙化的方法和组合物,更具体地说,本发明涉及使用脑醌-7(MK-7)和/或脑醌-7(MKH2-7)预防或治疗(例如,减缓进展、阻止和/或逆转)糖尿病、慢性肾病、终末期肾衰竭或接受血液透析和/或接受抗凝血治疗的受试者的组织钙化的方法、本发明涉及使用月桂醌-7(MK-7)和/或月桂醌醇-7(MKH2-7)预防或治疗(例如,减缓、阻止和/或逆转)糖尿病、慢性肾病、终末期肾衰竭患者或接受血液透析和/或接受抗凝治疗的患者的组织钙化的方法。本发明进一步提供了用于减轻慢性阻塞性肺病(COPD)的一种或多种症状的方法和组合物,包括使用甲萘醌-7(MK-7)和/或甲萘醌醇-7(MKH2-7),用于预防或治疗(例如,减缓慢性阻塞性肺病的进展、阻止和/或逆转)慢性阻塞性肺病的一种或多种症状。
  • Leal, J. M.; Arcos, J.; Garcia, B., Zeitschrift fur Physikalische Chemie (Leipzig), 1989, vol. 270, # 5, p. 887 - 896
    作者:Leal, J. M.、Arcos, J.、Garcia, B.
    DOI:——
    日期:——
  • METHODS AND COMPOSITIONS FOR PREVENTING OR TREATING TISSUE CALCIFICATION
    申请人:Epizon Pharma, Inc.
    公开号:US20210093584A1
    公开(公告)日:2021-04-01
    The invention provides methods and compositions for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) tissue calcification in a subject in need thereof and, more particularly, the invention relates to methods of using menaquinone-7 (MK-7) and/or menaquinol-7 (MKH2-7) for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) tissue calcification in a subject with diabetes, chronic kidney disease, end stage renal failure, or a subject undergoing hemodialysis and/or receiving anticoagulant therapy. The invention further provides methods and compositions for reducing one or more symptoms of chronic obstructive pulmonary disorder (COPD), including using menaquinone-7 (MK-7) and/or menaquinol-7 (MKH2-7), for preventing or treating (e.g., slowing the progression of, arresting, and/or reversing) one or more symptoms of COPD.
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